Huberman Lab - Dr. Casey Means: Transform Your Health by Improving Metabolism, Hormone & Blood Sugar Regulation
Episode Date: May 6, 2024In this episode, my guest is Dr. Casey Means, M.D., a physician trained at Stanford University School of Medicine, an expert on metabolic health and the author of the book, "Good Energy." We discuss ...how to leverage nutrition, exercise and environmental factors to enhance your metabolic health by improving mitochondrial function, hormone and blood sugar regulation. We also explore how fasting, deliberate cold exposure and spending time in nature can impact metabolic health, how to control food cravings and how to assess your metabolic health using blood testing, continuous glucose monitors and other tools. Metabolic dysfunction is a leading cause of chronic disease, obesity and reduced lifespan around the world. Conversely, improving your mitochondrial and metabolic health can positively affect your health span and longevity. Listeners of this episode will learn low- and zero-cost tools to improve their metabolic health, physical and mental well-being, body composition and target the root cause of various common diseases. For show notes, including referenced articles and additional resources, please visit hubermanlab.com. Thank you to our sponsors AG1: https://drinkag1.com/huberman Maui Nui Venison: https://mauinuivenison.com/huberman Eight Sleep: https://eightsleep.com/huberman AeroPress: https://aeropress.com/huberman InsideTracker: https://insidetracker.com/huberman Momentous: https://livemomentous.com/huberman Timestamps 00:00:00 Dr. Casey Means 00:02:18 Sponsors: Maui Nui, Eight Sleep & AeroPress 00:06:32 Metabolism, Metabolic Dysfunction, Medicinal Blindspot 00:14:17 Trifecta of Bad Energy 00:24:02 Western Living, United States, Specialization & Medicine 00:27:57 Insulin Resistance, Tool: Mitochondrial Capacity & Exercise 00:33:33 Sponsor: AG1 00:35:03 Tools: Walking & Glucose; Frequent Movement 00:44:25 Tools: Exercises to Improve Mitochondrial Capacity; Desk Treadmill 00:51:18 Soleus Push-Ups & Fidgeting, Non-Exercise Activity Thermogenesis (NEAT) 00:57:14 Sponsor: InsideTracker 00:58:21 Tool: Blood Test Biomarkers, Vital Signs & Mitochondrial Function 01:11:16 Navigate Medical System & Blood Tests, Consumer Lab Testing 01:16:46 Tool: Environmental Factors; Food, Life as a Process 01:21:58 Tool: Ultra-Processed vs. Real Food, Obesity, Soil & Micronutrients 01:32:03 Ultra-Processed Foods: Brain & Cellular Confusion 01:39:10 Tools: Control Cravings, GLP-1 Production, Microbiome Support 01:51:42 Ozempic, GLP-1 Analogs; Root Cause & Medicine 02:00:54 Tool: Deliberate Cold & Heat Exposure, Brown Fat 02:07:27 Tool: Intermittent Fasting & Metabolic Flexibility; Insulin Sensitivity 02:17:03 Tool: Continuous Glucose Monitors (CGMs) & Awareness, Glucose Spikes 02:24:34 Tool: CGMs, Glycemic Variability, Dawn Effect, Individuality 02:33:10 Sleep; Continuous Monitoring & Biomarkers 02:37:39 Mindset & Safety, Stress & Cell Danger Response 02:44:04 Tool: Being in Nature, Sunlight, Fear 02:54:44 Zero-Cost Support, Spotify & Apple Reviews, Sponsors, YouTube Feedback, Social Media, Neural Network Newsletter Disclaimer
Transcript
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Welcome to the Huberman Lab Podcast,
where we discuss science
and science-based tools for everyday life.
I'm Andrew Huberman,
and I'm a professor of neurobiology and ophthalmology
at Stanford School of Medicine.
My guest today is Dr. Casey Means.
Dr. Casey Means did her undergraduate degree
at Stanford University and her medical degree
at Stanford University School of Medicine.
She is one of the world's foremost experts
in metabolic health.
Today we discuss how metabolic function
and dysfunction impacts our health.
In particular, we discuss mitochondria,
which are involved in energy production within our cells
and the various things that we can each and all do
to ensure proper mitochondrial function,
which is essential, not just for things
like body composition and physical and mental energy,
but also our ability to regulate hormones,
blood sugar, and much more.
We discuss how exercise, even simple exercise,
like walking, as well as sleep,
as well as more vigorous exercise,
and in particular nutrition,
including the types of foods we eat,
the timing of food intake,
and the sources and quality of those foods impact our mitochondria
and other aspects of metabolic function.
We also discuss how particular micronutrients
within specific foods can directly impact mitochondrial
and metabolic health.
Dr. Means explains how mitochondria, inflammation
and reactive oxygen species,
which are the byproducts of metabolism in our cells,
can combine to create conditions of obesity,
as well as ways that we can manage those things are the byproducts of metabolism in our cells can combine to create conditions of obesity
as well as ways that we can manage those things
or even reverse mitochondrial inflammation
and reactive oxygen species dysfunction
in order to reverse obesity, reverse diabetes,
and enhance our health in myriad ways.
By the end of today's discussion,
you'll have a clear picture of the cellular processes
that occur in the brain and body
that underlie metabolic disease and metabolic health. And most importantly, you'll have a clear picture of the cellular processes that occur in the brain and body that underlie metabolic disease and metabolic health.
And most importantly, you'll have a very clear picture
of the actionable items that we can each and all carry out
every day and every week in order to ensure metabolic health,
proper mitochondrial function,
and indeed that can also impact body composition
and overall feelings of wellbeing.
I would also like to share that Dr. Casey Means
has a terrific new book coming out.
I know it's terrific because I've read it.
It is entitled, Good Energy,
the Surprising Connection Between
Metabolism and Limitless Health.
If you're interested in the book,
we provided a link to the book in the show note captions.
Before we begin, I'd like to emphasize that this podcast
is separate from my teaching and research roles at Stanford.
It is however, part of my desire and effort to bring zero cost to consumer information about
science and science related tools to the general public. In keeping with that theme, I'd like to
thank the sponsors of today's podcast. Our first sponsor is Maui Nui Venison.
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And now for my discussion with Dr. Casey Means.
Dr. Casey Means, welcome.
Dr. Andrew Huberman, thank you so much for having me.
Really excited to talk to you today about all things health.
One of the things I love so much about your work
is that you really give people a sense of agency
through knowledge and actionable tools,
which is very near and dear to my mission and my heart.
But to kick things off,
let's talk about metabolic function and dysfunction.
I think most people hear the word metabolism
and they think, okay, the burning of energy,
maybe they think about ATP,
maybe they think about calories in, calories out,
that sort of thing.
But what are we talking about when we're talking
about metabolic function and dysfunction?
Because these are really important concepts
for everyone to understand.
Yeah, I think you're exactly right.
I think that when we hear the word metabolism,
the first thing that comes to most people's minds
is my weight, do I have a fast metabolism?
Or do I have a slow metabolism or something like basal metabolic
rate?
And I think what's really important for people to realize is that metabolism is actually
the foundation of all health.
It is the core foundational pathway that drives all other aspects of health. And it's also the core foundational pathway
that's truly getting crushed in the modern American world
and underlying nine of the 10 leading causes of death
in the United States today.
It's really quite relevant to everyone.
And the spectrum of metabolic rooted disease is vast
and actually really relevant to most Americans.
The latest research from American College of Cardiology suggests that 93% of American
adults have suboptimal metabolism, and we can go into what that means.
But fundamentally, when we're talking about metabolism, we're talking about how we convert
food energy to human energy.
So we take in a astonishing 70 metric tons or so of food in our lifetime, and that is
potential energy.
It's energy from the environment that's outside of us that through our metabolic pathways
gets converted to a currency of energy that can then be used to pay for
essentially every chemical reaction inside our body.
And the bubbling up of all of those chemical reactions is our lives.
And so when metabolism is not working properly, It's essentially creating underpowered cells. And like any city or factory or machine, not having adequate power will lead to dysfunction.
And the reason that the metabolic spectrum of disease is so vast is because we have over
200 cell types in the body. And underpowering in different cell types
is going to look like different symptoms.
Because underpowering in an astrocyte
is going to look different than underpowering
an ovarian thiccacell or an endothelial cell.
It's going to look different, but the core foundational
process that is dysfunctional can actually be the same. And I think the biggest blind spot in Western health care,
and actually the reason that health outcomes are actually
getting worse every year in the United States,
is because fundamentally we are ignoring metabolic health
and metabolic dysfunction.
We are laser focused on the downstream symptoms that result from metabolic dysfunction in
different cell types.
And we spend all of our energy focusing on those symptoms, playing whack-a-mole with
them, and really ignoring that underlying foundational root
cause of metabolic function.
And what's so fascinating to me and what
I saw in the health care system as a super subspecialist,
as an ENT surgeon, is that the more we specialize
in health care, we have over 100 specialties now
that we've just invented invented in the healthcare system. The more we specialize in healthcare, the
sicker we're actually getting. So the more we do technological innovation in
all these different specialties, the sicker we're getting, and I think what
what the real nugget there that that everyone really needs to understand is
we've bought into a system where we value specialization, and this is the game in Western medicine. But
while we've done that, what has happened is we have the worst chronic disease epidemic and the
lowest life expectancy of any high-income country in the world. And the reason is because in that
specialization, we're focused on the
downstream manifestation of underpowering of cells, the cell-specific symptoms and not
the metabolic function itself. So really our chronic disease epidemic in this country is
a metabolic dysfunction epidemic and underpowering epidemic. And that is the biggest blind spot in healthcare.
And I think a focus on metabolic function as the center of our healthcare system, it's
a completely new paradigm for health that is urgently, and I cannot overstate enough,
it's urgently needed.
We know we're not in the right paradigm right now when we have 100 isolated specialties
and yet 85 to 90% of the conditions in those specialties, if you go to the science and
look at the real physiology, is metabolic dysfunction.
So that's kind of the landscape of what metabolic dysfunction is and how it's kind of creating a
big blind spot in the healthcare system that really represents an outdated way of categorizing disease
that unfortunately is killing us, I would say. Yeah, thank you for that. I have several reflections and a question. First off, the analogy that
comes to mind is an assembly line that's constructing, let's say an automobile, and it sounds like
80 to 90% of the automobiles that are coming off that assembly line are not working well.
Tires are underlined, engines isn't working well, transmission isn't working, has a bunch of issues. And no factory, no car manufacturer would tolerate that
nor would the customers, but we're tolerating that
in ourselves, it sounds like, many people are.
And then accepting the fact that then a bunch
of other businesses are going to crop up,
like the business that aligns the tires,
the business that goes and repairs the pistons.
And essentially, when you talk about these multi-specialties
that have evolved in the medical care system,
they provide an opportunity to go and fix the problems
or try and ameliorate the problems.
But really what we need to do to make this analogy
much briefer than it otherwise would be
is just to go further up the assembly line,
figure out whether or not the hardware
is correct, the software is correct, and where the hardware and software are becoming deficient
in this analogy where we are the automobile that's essentially coming off the conveyor
broken.
And the good news is, and I know this because I've read your book and because I follow your
work very closely, the good news is that we each and all can take matters
to some extent into our own hands,
collaborate with healthcare providers
and repair metabolic dysfunction,
essentially make us metabolically functional.
So the question therefore is,
I think most people when they hear metabolism,
they think energy.
And when we hear energy, we think ATP sometimes,
but typically people think about mitochondria,
the powerhouse of the cell, so to speak.
So you've talked about the trifecta or the big three,
mitochondria, inflammation, and oxidative stress
as three critical factors underlying metabolic dysfunction.
And I'm presuming those are also the avenues to address
in order to create metabolic function.
Because ultimately what we want, of course,
is an optimistic picture that we can actually
take some control, that we have some agency in all of this,
which I believe we do.
So if you would, could you get us all on the same page
about what are mitochondria and what do they do?
Why are they so important?
Then we can turn to inflammation and oxidative stress.
Yes, absolutely.
So the mitochondria are the structure within the cells.
We have 40 trillion cells and each cell might have a handful
or many thousand mitochondria.
And they are the magical part of the cell
that does that conversion process of food breaking down
and then converting to energy, translating it
to a currency of energy our body can recognize.
And so currently, what's happening
is that our environment, the environment that our cells exist in across every single facet
of our life over the past 50 to 75 years has changed rapidly.
You look at how our food system has changed from whole real food and good soil to industrial
food.
Our sleep habits have changed.
We're sleeping less.
It's very fragmented.
Our movement patterns have changed. We're sitting 80% of the waking
day. Our time in nature has changed. We actually are indoors as Americans. 93% of
a 24-hour period. So that totally changes our relationship with light. We have 80,000
synthetic toxins in our food, water, air, personal care products, home care
products. We live a thermo-neutral existence now with our thermostats.
There's no real swings in temperature unless you're intentionally trying to.
And then our emotional health is very different.
We are very much exposed to low-grade chronic stress triggers.
So across food, sleep, movement, emotional health, toxins, light, and temperature, things
are not what they once were.
And it's changed in the blink of an eye.
I mean, the light bulb was created in 1806.
This is like 0.04% of human history
that we've even had artificial light.
So things have changed.
And the unique thing about all of these changes
in our environment is that each one of those pillars,
each of those changes in our environment synergistically directly
hurts the mitochondria through different mechanisms.
The chronic low-grade stress, the sitting,
the ultra-processed nutrient-devoid food,
even the blue light at nighttime, all of it
through different core biologic mechanisms synergistically
hits this part of the cell, the mitochondria.
So we have the food coming in, but we're not doing a good job of converting it to an energy
form we can use.
So we have these underpowered dysfunctional cells because of mitochondrial dysfunction
caused by our environment.
And of course, what happens if you've got energy substrate that you can't process, it's
going to be stored.
And that's, of course, why we have an obesity and overweight
epidemic that's affecting close to 80% of Americans.
So wild.
It's just we talk about obesity like it's the problem.
Obesity is one branch of a tree that's
rooted in this mitochondrial dysfunction that's
caused by our environment.
And just to back up a little bit,
to just sort of share kind of maybe
how I sort of started thinking about that,
I had trained as an ENT surgeon.
And I was at Stanford Medical School.
And I was so fascinated by this idea of the way
that we're defining the diseases we're treating
in a specialty like ENT is like, I saw sinusitis day in and day out, and we'd have these patients
on the table that we'd be literally drilling into their skulls to suck out sinus pus. And
that's the treatment for sinusitis. And the way we diagnose the patients is we say,
pus and that's like the treatment for sinusitis. And the way we diagnose the patients is we say like, okay, this patient has sinusitis
if they have facial pressure, puerulent pus, you know, nasal discharge, nasal obstruction,
and low sense of smell.
So if they have these symptoms, then they have this disease.
But when you actually go to the science and you actually go to the studies of like what
is actually happening to create this, what you find is a lot of papers about mitochondrial
dysfunction because sinusitis is a chronic inflammatory condition where the cells are
essentially sensing some threat and then they mount this immune response that creates swelling
and then you get pus buildup.
But we confuse the pus buildup with the disease, which is actually happening inside the cells.
And so you start looking at PubMed as a clinician through a slightly different lens of like
what's actually happening in the cells.
And what you find for almost every chronic disease we're seeing in the US is that you
will find a lot of papers on how the mitochondria are dysfunctional, lower ATP generation in
a lot of these cell types.
And then what does that do?
And this gets to your question about chronic inflammation and oxidative stress.
Well, when you've got that dysfunctional mitochondria, let's say in a nasal mucosal tissue,
that is a cell that can't do its job.
That is a cell that's underpowered.
And what could be more threatening to the body
than a cell that can't do its job?
So interestingly, those cells will
initiate a whole process, which is called the cell danger
response.
It's work that's been done by Robert Navio at UCSD,
where basically they understand the mitochondria is not
working properly.
This is, of course, caused by the environment.
And they will actually release extracellular ATP,
which is not really supposed to go outside of the cell.
And that creates a massive, innate immune response,
saying, I'm underpowered. I need help, my mitochondria
is broken, this is the cell, releases ATP outside of the cell.
Usually the concentration of ATP is a million times higher inside the cell.
So releases it almost as a neurotransmitter, a purigenic neurotransmitter that massively
activates the immune system to come and help.
But the immune system comes and is like, not much we can do for you here because the problem
is not something that the immune system can help with, like grabbing a bacteria and lysing
it or taking care of some cells infected with the virus.
The problem is outside the body.
It's the environment.
So you end up getting this tornado of dysfunction, of
mitochondrial dysfunction caused by the environment leading to the cell danger
response which leads to innate immunity. And then on top of this you get the
oxy of stress which is the third piece of the trifecta which is essentially
these mitochondria trying so hard to do their work but they're not working
properly so they create damaging metabolic byproducts called oxidative stress, free radicals,
that cause more damage.
So this is happening in the nose.
It's happening all over the American body
because of our environment.
So you've got these tornadoes of interrelated physiology
of mitochondrial dysfunction, chronic inflammation,
oxidative stress, which if you start going to the research as a clinician
who's focused on symptoms and confusing those for the disease and look at what's the pathophysiology
of arthritis, what's the pathophysiology of Alzheimer's dementia, what's the pathophysiology
of type 2 diabetes, obesity, fatty liver disease, polycystic
ovarian syndrome, erectile dysfunction?
It all traces back to this trifecta that no medication or surgery, you obviously can't
operate on oxidative stress.
You can operate on the downstream symptoms.
So that's the real secret that I really feel like we need to reorient the healthcare surround since 90% of healthcare costs go towards treating
the downstream symptoms of these.
And for every marginal dollar we're spending
on treating symptoms, we're getting,
the rates are going up because they're doing nothing
to actually affect that trifecta.
But to really make it simple,
I like to think of this trifecta of what I call trifecta of
bad energy, trifecta underlying metabolic dysfunction of chronic inflammation, mitochondrial
dysfunction, oxidative stress as chronic inflammation is biochemical fear.
It's response to a threat.
Mitochondrial dysfunction is kind of like rolling blackouts.
It's not enough power.
And the oxidative stress is like wildfires. So
it's kind of what's funny to me a little bit is like what's happening inside the cell is
almost like what's happening like in our society. It's like this is like living in California.
It's like blackouts, fire, fear, and that's literally what's happening inside our cell
because of the environment. And again, the optimistic news that you alluded to is that we actually have tons of tools and tests
that can actually help us understand
our level of metabolic health
and even give us hints about inflammation,
oxidative stress and mitochondrial dysfunction.
And it's very easy to improve
if we know what we're actually focused on.
Well, that's reassuring.
And we're definitely gonna go there.
I appreciate the analogy to living in California.
I've lived here my entire life.
I have been outside of California,
but perhaps the only thing you left out
besides rolling blackouts, fires,
and what was the other one?
Fear. And fear is high taxes.
The taxes is the health debt on the body.
So in any case, not to be too dark and pessimistic.
Well, that's the healthcare cost.
I maintain great hope
and still a lot of love for California.
It's pretty great.
It's got, it's great aspects and it's not so great aspects.
And I can say that as a lifelong California resident,
there are other wonderful places to live.
A couple of questions, first of all, about places to live.
You've been talking a lot about in the United States.
Are some of these same issues with metabolic dysfunction occurring outside of the United
States?
I would imagine so.
Yep.
Any country where we've exported the standard American diet and some of the other norms
of Western living are starting to see the same rates of chronic disease.
But it is worth not mincing words here.
Of all high income countries in the world, the United States has the worst chronic disease
rates and the lowest life expectancy, and our life expectancy is going down.
And we spend about twice as much on healthcare than the second highest spending country in
the world. So we are abjectly failing and that failure is predicated
in our cult of siloing conditions into different specialties and not focusing on this root cause.
And I want to just be super clear, there's a war being fought right now to get us to believe that siloing is the way.
Because as you alluded to, siloing is profitable.
If you can convince doctors and people
that there are 10 different symptoms or separate things,
then they're going to 10 different specialists' office.
Meanwhile, 75% of American adults
are overweight and obese, some of the highest in the world.
A full 50% of American adults now have pre-diabetes and type 2 diabetes.
50%, 30% of teens have pre-diabetes, 40% of Americans have a mental health diagnosis.
Cancer is set to reach 2 million cases this year in 2024, highest ever in recorded history.
Alzheimer's is going up.
Fatty liver disease is affecting 40% of adults, 18% of teens.
Autoimmune disease is skyrocketing.
Infertility is going up at huge rates.
All these things are going up all at once in the US,
and yes, in many of the other countries
that are eating our diet.
And there's no sign of it slowing down. And
so that's really, if you look at, if you look at the research through this, this different
lens, you'll find that all of those diseases trace back to metabolic dysfunction caused
by our environment that no, that no shot pill or surgery can really address unless we unpack
the environmental piece.
Scary picture.
I'm glad that you're-
But hopeful, because we can fix it.
Exactly, I'm glad that you are creating solutions.
And I should say, and just remind people,
I said this in my introduction,
but you're talking about siloed medical care,
you're talking about the kind of standard medical system,
but let's not forget, right?
I happen to be a faculty at Stanford, you did your medical training at Stanford, you are's not forget, right? I happen to be a faculty at Stanford,
you did your medical training at Stanford,
you are a medical doctor, right?
I mean, you have an MD and are highly trained,
you were an ENT, your nose and throat doctor.
So if anyone would be familiar with the industry
and the practice and the educational system around this,
it's you.
So you're not speaking outside your Ballywick.
So before we pivot to solutions,
I know people are eager to hear solutions,
but in order to understand how to best apply those solutions,
I do think it's worth drilling into some of the issues here,
just a little bit more.
You talked about underpowered cells.
You've also alluded to the fact that
most people are consuming enough
and probably excess amounts of caloric energy.
Yes.
So is it the lack of mitochondria
or mitochondrial dysfunction
that's at the root of the problem?
The analogy I come up with is you've got a power plant
that can convert incoming power line
to power that can be distributed to a community.
The community in this analogy being the organs
and cells of the body.
There's plenty of potential energy,
but there's something about the power plant
that is inefficient or dysfunctional.
Their shorts, their circuitry that's just not working
such that the energy that the community can benefit from the cells
and organs of the body is just not there.
So it's not a lack of input, it's a lack of conversion and output.
And the consequence of this we see in the form of excess adipose tissue and all the
downstream effects.
It's not just aesthetic, it's really all the downstream effects of visceral fat, subcutaneous
fat, et cetera.
What is it that would improve access to energy
and energy utilization in cells? Is it simply a matter of getting the mitochondria
to function better, or is it that one can actually
create more mitochondria?
This is the key question for how we can get healthy.
And it's really about creating capacity in the body
to turn more potential energy to usable energy,
as opposed to taking that potential energy
and shunting it to a storage form.
It's all just like I think about everything visually.
And I'm like, you've got the circular cell
from high school biology textbook inside,
or all the little mitochondria
with the squiggly lines inside.
And it's just like there's Xs through those mitochondria.
So instead of after glycolysis and you've got the pyruvate,
instead of going through the mitochondria,
it's being shuttled into something else.
And I mean, this is fundamentally
the cause of insulin resistance,
because when the body senses that the mitochondria
can't do that conversion process,
the cell basically says, because I can't convert this,
I don't have the capacity to convert it to usable energy.
I'm going to take the substrates and I need to block them.
I mean, you've got to turn them to basically a storage form,
which inside the cell could be toxic fats like ceramides
and diacylglycerol.
And I'm also going to block the cell from taking any more
substrates because I can't do anything with them.
That is fundamentally a route of insulin resistance.
So the body says, OK, we're going
to block the ability of the insulin receptor
to transduce its intracellular signaling pathway.
We're going to block it.
And when that insulin binds, we're not actually
going to allow for glucose to come in.
So essentially essentially insulin resistance is the cell compensating for the mitochondria being broken
and telling the insulin receptor that it's not going to be functional.
And so you don't get the gluten for you don't get the gluten receptors on the cell membrane
to allow the glucose to come in. So that's insulin resistance.
Again, we talk about that as the problem, but the problem is actually inside the cell leading
to that.
So that's why just giving someone insulin
isn't necessarily the answer.
We have to increase mitochondrial capacity
to let the flow happen through it to energy, which then
trickles up into relieving a lot of these problems.
So to answer your question, what we really
want to do to increase our metabolic capacity
from a first principles perspective, it's we need to make more mitochondria.
We need to get each mitochondria to be more functional.
And we need to have each more functional mitochondria processing more energy substrates.
It's really that simple.
And the beauty is we can do all of those things.
If you actually break down what those three things mean,
it means promoting mitophagy, the recycling of old mitochondria
to new mitochondria.
It means promoting mitochondrial biogenesis.
It means increasing the oxidative capacity
of our individual mitochondria.
It means improving mitochondrial fusion, which
is actually when mitochondria come together
to form long chains of mitochondria
that are more efficient.
So there's a lot of technicalities
like what it means to print more mitochondria,
have them each be more efficient,
and have each one do more work.
But that's really what we want to do.
And that's when it just kind of gets into the simple habits.
Like there's simple things we can do for each of those things, from mitophagy.
You know, we can focus on various types of, like, endurance exercise and high intensity
interval exercise.
There's compounds like urolithin A that promote mitophagy.
When we talk about improving our, you know, oxy of capacity, This is things like the sprint workouts.
We want to build more mitochondria.
This is resistance training, literally telling
the body to make more.
But first principles, it's how do we
get more of these working better, doing more work
every day?
And then we think about, you look at the data on walking.
And it's like people who walk more than 7,000 steps a day
have a 50% to 65% lower chance of dying in 10-year follow-ups.
And it's like, yeah, because walking is literally
a glucose disposal signal.
So you're just simply asking.
It's not a great biogenesis signal.
It's not a great mitophagy signal,
but it's a great disposal.
So if you're doing lifestyle habits that
do one of those three things, which we can of course go into more,
you're improving the cell's capacity
to do that conversion process better.
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There's a lot of great science
and a lot of great stuff related to testing
and assessment of one's metabolic health
that we should get into and will get into.
But since we touched on lifestyle
and because we've been talking about
the sort of dysfunctional dark side for a bit,
maybe we could just touch on some of the lifestyle factors
that you just mentioned because I
do think it's important that people really start to feel into their sense of agency and
here we're talking about things that are relatively low time investment.
Certainly don't have much financial cost in the sense that they could be done in gyms
and with fancy equipment but they don't require that.
Again, I want to point out that these are not
like strict prescriptives, but if you had a magic wand
and because you are interested in the health of humans,
let's talk about a few of these things
that can improve glucose disposal
and mitochondrial function, mitophagy,
the removal of dead or dysfunctional mitochondria
so they can be replaced.
Let's talk about the walking one first.
You said 7,000 steps a day.
I don't track my steps.
What are we really talking about there?
We're talking about taking the stairs
and trying to walk as much as possible.
Maybe we were gonna just give a really crude prescription.
You're a doctor, so you can prescribe things.
What would you tell people to do?
How many short walks per day?
Is it like three, is it five?
What are we talking?
I would say, I mean, at least three,
I would say aiming for more than that is good though.
There's, so to sort of just give a sense
of the picture of walking, if walking were a pill,
it would be the most impactful pill we've ever had
in all of modern medicine.
most impactful pill we've ever had in all of modern medicine. There was a paper in JAMA, 6,300 participants followed for 10 to 11 years.
And the people who simply walked 7,000 steps per day compared to less than that had an
up to 70% lower risk of all-cause mortality in the follow-up period.
So not causality, but it's pretty incredible.
They've done follow-up research with slightly different numbers
showing, again, though, like many thousands of people
in the study followed for about 10 years, 8,000 to 12,000 steps
per day was associated with 50% to 65% lower all-cause
mortality.
And this has been played out in many studies showing
about a 50% reduction in Alzheimer's dementia,
obesity, type 2 diabetes, depression, cancer,
gastric reflux, just all across the board.
And I think the key thing is that it's not about the steps.
It's about the fact that muscle contraction is medicine.
When we contract our muscles, even in a very low-grade way, like walking or doing a couple
of air squats, we're activating AMPK, and we are essentially causing that cell to have
a stimulus to push glucose channels to the cell membrane.
Most of the time the glucose channels are like in vesicles, in little bags inside the cells.
They're not on the cell membrane. So of course that's going to keep the glucose in your bloodstream
not being processed by the mitochondria. So when we think about steps, it's a proxy metric for just
moving more throughout the
day.
So, let's take two people.
You have a person who's walking for one to two minutes every 30 minutes throughout the
day.
Maybe they're exercising at the end of the day or the beginning of the day.
Maybe they're not.
That person is stimulating glucose channels to be at the membrane all day.
Now let's take another person who works out really hard for one hour in the beginning
or the end of the day.
They feel great about it.
They've checked that off their box, but they're sitting the entire rest of the day.
Yes, they have gotten the benefits from the exercise, but for a lot of that day, those
glucose channels are inside the cell, not doing the work they could be doing.
So I think about these little teeny short walking breaks
or push-up breaks or air squat breaks every 30 minutes or so
throughout the day as me essentially inside the cell
pushing the glucose channels, the cell membrane,
to make them constitutively active.
It's totally different physiology.
And it's so easy.
So it's not about the steps.
It's about muscle contraction regularly throughout
the day. And this has been shown out in actually more clinical research, which has taken, there's
been several studies, two that I think are fascinating where they basically took two groups
and they said, okay, we're going to have you walk 20 minutes before each meal, three times a day,
20 minutes after each meal. So that's also three times a day or for like two minutes every 30 minutes throughout the day.
So these are three separate groups.
Three separate groups.
So it's either 20 minutes before,
either 20 minutes after or?
Two to three minutes every 30 minutes.
Okay.
All added up to 60 minutes of walking
or light jogging a day.
I'm kind of paraphrasing two different studies
that showed the same thing.
One was jogging, one was walking,
but it was basically chunks versus short walks every
30 minutes throughout the waking day.
The groups that do the short movement regularly throughout the day, even though the total
time is the same across all the groups, have significantly lower 24-hour glucose level
averages, 24-hour insulin level averages. They are metabolically
healthier. And I believe, and the research mechanistically has shown, that it's because
we're constitutively putting these channels of the membrane to take up the substrate,
use the substrate. So this is not to replace exercise. But I think it's a reframe.
I think the concept of exercise is something we're really
very wedded to in our Western culture.
And you look at more like the Blue Zones and the centenarians.
And it's like they're kind of moving as
built into their everyday life.
So we've taken movement out of our everyday life
as these knowledge workers, as we've been industrialized.
And then we think that exercise replaces that all-day movement, but biochemically it does
not.
So I think a big part of kind of digging ourselves out of this chronic disease mess and creating
capacity for mitochondria is finding ways to take a lot of the activities we do now
seated and just find a way to do more of them moving, standing, or walking.
Or if that's tough, you really need to sit at your desk
all day, then every 30 minutes taking two minutes to do some just light movement, flex
those muscles, get the glucose channels of the membrane, get the mitochondria active.
And I think another fascinating stat is like our gym memberships in the US have doubled
since the year 2000 and obesity has gone up
in the same period.
So there's some mismatch between our obsession
with exercise and our actual outcomes that we're seeing.
And I think it's that we have not actually rebuilt
constitutive movement into our daily lives.
Very interesting.
Cause I think a lot of people are now working out
so to speak, doing resistance training
which I think is terrific.
Terrific, yeah.
Used to be such, you know,
so restricted to niche subculture stuff,
like bodybuilding, pre-season football, military, et cetera,
and now it's more ubiquitous for everybody,
men, women, young, old, that's terrific.
Same thing with things like yoga and cardiovascular training.
I mean, I like to study the history of exercise culture
and it wasn't, but in the sixties when, you know,
jogging was considered kind of like, whoa,
that's like a really esoteric niche culture thing.
So lots of change.
I love the prescriptives you gave
because it's just very straightforward.
A couple of short walks, it just makes so much sense.
And I love the visual and I hope people will really
hold it in mind.
So I'll reiterate it.
The translocation of these energy utilization stores, vesicles as you call them, these little
packets from the center of the cell out to the cell surface where then they can be involved
in metabolic processes and the utilization of energy in ways that otherwise they wouldn't end glucose disposal
being a big part of this. So I have heard that a short walk after a meal will reduce blood glucose
in a way that's really dramatic. Huge amount. 30, 35% just taking a walk around the block after meal.
That's definitely a prescription I think everyone should do because the research is so strong on it
is that building in simply a 10-minute walk around the block
or a dance party in the kitchen, moving your muscles
for 10 minutes after a meal can drastically
reduce your glucose response.
Because you're just bringing all those channels to the membrane,
you're taking up the glucose you're using.
It's a whole different physiology
than sitting on the couch after a meal.
That's very high impact.
It's high leverage if it's after a meal.
So highly recommend that.
And the levels data and clinical data has shown that out
time and time again.
Whenever I go to a city like New York,
when I am forced to walk more,
I always just feel so much better.
We also know that the optic flow that one experiences
with walking has some interesting effects
on the limbic pathways and quieting of some of the anxiety
and stress-related pathways.
This links up with things like EMDR,
although there are factors that are separate from EMDR.
Basically moving through space, not outer space,
but walking through space with optic flow
has a certain anxiety reduction function in the brain,
which there are beautiful data there in my opinion.
Okay, so that touches on walking.
You did mention higher intensity exercise.
So let's keep it within the cardiovascular realm for now.
So getting heart rate way, way up,
getting breathing hard for some minutes each week,
maybe a couple of times per week.
Seems that's a good way to increase mitochondrial function
and mitochondrial number, is that right?
Yeah, so you take sort of each type of exercise.
We've got walking, we've got resistance training,
we've got high intensity interval training,
we've got endurance training,
and then we've got sort of more like zone two.
So we've got these different flavors of how we get our heart rate up, how we get the blood
flowing, what we signal to the cells.
And each one actually has like a slightly different impact on the mitochondria.
When we think about biogenesis, we're thinking mostly like endurance exercise and really
more of that zone too.
And that is really going to be a stimulus inside the cell to print more mitochondria.
When we think about improving mitochondrial fusion, high intensity interval training is
really, really good for that.
When we think about resistance training, it's like that's like muscle hypertrophy.
We're going to be creating more muscle cells and we need more mitochondria for those.
So each one has kind of a different impact and I think this is where honestly I think the regular guidelines that we have
even by our government actually make a lot of sense. It's like work every major muscle
group three times a week in a resistance type training and then work to get 75 to 150 minutes
of moderate strenuous activity. So 75 minutes of strenuous activity
or 150 minutes per week of moderate activity.
So that actually makes a lot of sense.
80% of Americans are not meeting
those very basic guidelines
and 20% of Americans don't get
any physical activity really at all.
Activity for the average American
is 3000 to 4000 steps per day,
which is less than two miles.
So we are not even close to even meeting the basic recommendations
that are out there.
But I think those are pretty reasonable.
Resistance training, two to three times a week,
most major muscle groups, and working
to get the heart rate up moderate level for 150 minutes a week
or strenuous for 75 minutes a week.
Those are going together to be potent stimuli for biogenesis, mitophagy, mitochondrial
fusion, for increasing antioxidant enzymes that are going to protect the mitochondria
from that oxy of stress.
And the one that's just actually not in there in the sort of the basic recommendations for Americans is the walking.
And I would just absolutely add to that at least 7,000 steps per day based on what the data is showing,
which honestly would probably take less than an hour total to do.
And if you break it up throughout the day, it's just a few minutes a day. So that right there are going to be like a big
multifaceted set of signals for increasing
mitochondrial capacity in different ways.
Terrific.
What are your thoughts on under the desk treadmilling?
I don't own one of these,
but, and I try and get walks
and I definitely do my three resistance training
extra sessions per week,
different muscle groups on different days.
So it ends up being each muscle group has hit directly once
and indirectly a second time.
But I like to do a long hike once on the weekend,
run in the middle of the week, that's 30, maybe 35 minutes.
And then some VO2 max, really short workout,
12 minutes total where basically I'm just going for,
you know, the feeling that my heart is going to jump out of my chest
and I'm going to die from gasp me of air.
But luckily thus far I haven't died.
Nonetheless, the total time commitment isn't that great,
but I find that I'm at a desk a lot
and I have a standing desk.
Is it wise to get a treadmill,
to treadmill under the desk?
Seems like it would be one of the best things one could do.
I'm a massive fan of under treadmill desks
because genuinely I believe that if we move more
of our daily activities that we're doing seated indoors
to outdoors moving, it would radically change the health
of the United States with real physiology underneath it.
So there's actually been research on under desk,
standing desk that is pretty interesting.
Small studies, but they took a handful of people,
I think it was around 10, in a workplace environment.
And they had them use under desk treadmills for 2 and 1 1 at very slow speeds for two weeks. And people lost on average 2.6 pounds of fat
and put on 2.2 pounds of lean mass.
Wild.
In a very short period of time.
The study makes a somewhat wild claim
that if this were extrapolated to a year,
we anticipate that we could see a loss of 44 to 66 pounds.
Which I-
Assuming it's linear progression.
Exactly.
Which is not the case, folks.
But that's why I'm saying it was a pretty,
but that was there in the discussion.
And, but I think that short period is quite interesting.
So that's pretty significant.
And that's just for two and a half hours a day.
So I think now that they're about $150 on Amazon,
these under desk treadmills,
I think for anyone who's a knowledge worker,
it's a good thing to have at your house.
And the way I use it is like,
I basically just force myself to start my day
on the treadmill desk.
And I say to myself,
if I don't like it after five minutes,
I'll sit down if I need to sit,
but I'll start and just see how it feels.
And then an hour goes by and I've forgotten I'm even on it.
Is that right?
So you're able to work without thinking
about having to treadmill.
I am putting it at such a slow speed.
I think I'm usually walking at like one mile per hour.
I mean, it's very, very glacially slow.
I do put my aura ring on my second toe when I do this
because otherwise it doesn't count my steps because if your hands
Are at your desk they they won't count your stuff because the aura rings measuring and hand accelerometry
Yeah, but it it it's incredible how even at a 1.0 1 mile per hour speed after two to three hours
You're easily gonna get six seven eight thousand steps and then throw in a couple other
Short walks throughout the day and you're getting there easily.
So it's just a great way to build back in
what modernity took away.
And that unfortunately is unavoidable,
that regular movement for good physiology.
So I'm a big fan of them and the data suggests
that for a couple hours a day,
they can actually have an impact on body composition,
which I think is a great, easy, inexpensive thing
for people to do.
But if you don't want to buy one,
like just set those timers and build in the walks,
you know, throughout the day outside.
Terrific.
Yeah, I'm a fan of getting walks when I can.
I also, I wonder your thoughts on, there was a study,
not sure if you're familiar with it,
published out of the University of Houston,
where they looked at what they called soleus pushups,
which all the gym goers are going to roll their eyes.
Imagine sitting down and a raise,
pressing your toe against the ground and raising your heel.
So kind of like seated calf raise,
but no weight, right?
Under the desk.
And this study had some remarkable claims and conclusions,
which included, as I recall,
that the activation of this muscle, the soleus,
which makes up about 1% of the body's total musculature,
involved, caused rather a disproportionate use
of blood glucose.
So it mobilized blood glucose in a good way.
And the idea was if people would,
it's not just bouncing your knee,
but would actively push their toes against the ground
and raise their heels as they were seated and doing work,
that somehow there would be a positive effect
on metabolism and blood glucose utilization.
I talked a little bit about this on social media
and a few other podcasts.
And it was interesting to see that sort of attacks
that I got, like people really didn't like the idea
that this was any different than so-called NEAT,
non-exercise and activated thermogenesis.
So it's known that people that fidget a lot
or move around a lot, burn a lot of calories.
This actually goes back to some really beautiful work
several decades or more ago from Rothwell and Stock
who talked about like the fact that animals
and people who fidget a lot burn a lot of energy.
They tend to be thinner,
they tend to have lower adipose tissue stores
and it's because they're just burning a lot more calories.
And this is actually what people who suffer from anorexia,
which is by the way,
the most deadly of the psychiatric conditions.
So it's talking about true anorexia, which is by the way, the most deadly of the psychiatric conditions. So it's talking about true anorexia
are encouraged not to do
because they either do it spontaneously
or they learn that it's a very efficient way
to burn calories and that's not what they need.
But many people do need to burn more calories.
So, bouncing the knee,
that thing that drives everybody crazy
if you're not the one doing it,
soleus pushups.
What are your thoughts about this and that study?
We don't have to pick it apart in detail,
but I thought it was kind of interesting.
It's all coming back to just moving the body
as much as possible during the day,
contracting muscles, contracting muscles.
Contracting muscles, it's medicine.
And I find the concept of NEET just endlessly fascinating,
because we kind of come up with this term,
non-exercise activity thermogenesis.
And the data is really good about it.
It basically shows that this is a prime potential intervention
for the obesity epidemic.
And it all goes back to the cell.
It's essentially a stimulus that's
telling the body to stay metabolically active,
as opposed to keeping all those metabolic pathways dormant
during the day.
And I think that it is funny, though,
that we have these acronyms for basically,
this is just the way life was 100 years ago.
If you look at the 1800s, almost 100% of Americans
lived on a farm, basically.
Pre-industrialization,
pre-urbanization.
Most Americans, not 100% but close, lived, they grew some of their own food, they lived
either on a farm or had a large garden.
Now that number is less than 1%.
So movement was just built into everything we did.
And you think from there, what has happened?
We were outside, We were moving.
Our activities of daily living involved movement.
And if you just take the grocery example,
then it moved to maybe farmers markets and outdoor open air
markets.
Then it's supermarkets.
Then now it's literally buying food online
with the click of the button.
And now some people aren't even doing that.
They're literally on the food delivered to them
with Uber Eats.
So at every level, we've taken away movement
from everyday life.
And now we have sort of an acronym to bring it back in.
But really, it's about just giving the body stimuli
that the cells have been entrained
to expect throughout all of human history
and building the back end to our modern life.
So I think NEET, it's incredibly important.
And I think it also brings up this point that is so critical,
which is like, I really think our way out
of this chronic disease epidemic,
and even for people who are listening,
don't have a chronic disease, any real chronic symptoms
we're dealing with, and just the fact
that we're not feeling as good as we could. The way out is pretty simple. It's some of these basic things
like walking more throughout the day, moving more throughout the day, getting outside, eating clean,
unpoisoned food. A lot of these things that have the best data are so simple. And I think it's really important to just
always remember the game and the industry, it's all about how complex can we make it,
like specialization, talking about some of the minutiae. But at the end of the day, all
the simple habits that we know are healthy fundamentally improve cellular biology. And
some of these things like the neat, like the, like it's emblematic of the fact that some
of the simplest solutions are the ones that are by far the most effective.
And I think the biggest misconception in healthcare right now is that the way out and the way
to get really back to true incredible health is complicated.
Like it's really not that complicated.
We've got to move more, you know, throughout the day.
That's one of them.
And you know, on each pillar that we touched on earlier,
food, sleep, all of this, you know,
when we talk about the simple habits that we know work,
the reason they work is because they all positively impact
the mitochondria, they positively impact oxidative stress,
they positively impact inflammation.
So yeah.
I love it.
I love simple solutions that hit multiple cellular pathways
that can make everybody healthier.
I'd like to just take a quick break
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I'd like to talk about assessment, blood tests in particular.
I remember in college, I was just very curious
about blood testing and I had read a little bit about it,
but it was really hard to access.
I actually went to the student health center and said,
can I just get like my lipids measured,
some hormone stuff measured?
I was in great health, I just want to do that.
And they're like, no, like what's the issue? You know, why would you do that?
Now it's very easy to find places that will do blood tests,
but there is some cost often.
And nowadays, thanks to your efforts,
your innovative and engineering efforts
and the efforts of others,
there are ways to measure what's in your blood,
blood glucose in particular,
with continuous monitoring and with snapshot monitoring.
So let's talk about blood tests.
What do you think are the three to five things
that basically everybody, if they can,
should know about what's circulating in their blood?
I'm imagining LDL, HDL, this kind of thing.
I guess APO-B is a big favorite of our friend, Peter Attia.
Fasting blood glucose, continuous blood glucose,
post meal, et cetera, just kind of evaluating
how exercise, food, et cetera, impacts blood glucose.
And then I'll leave the other categories open
because my point here is not to answer the question.
That's what comes to mind.
You've got the big ones.
So this is key is that every single person listening,
I hope after this episode will go to their health record
or send their doctor a message
and at least get the following test.
And the first seven that I'll mention are very basic
and people might take umbrage to them,
because obviously there's a lot of debate about what's
everyone's favorite lab tests.
But I think about it as what are the basics that everyone
should know, and then what's the next tier up that
are easy to access and are cheap that will give you
a lot more richness, but which you still
might have to fight your doctor for.
So the first few that you will not
have to fight your doctor for and are often
free on an annual physical
and literally define metabolic syndrome are fasting glucose,
fasting triglycerides, HDL cholesterol, hemoglobin A1C,
total cholesterol, waist circumference and blood pressure.
Okay, sorry, I hate to interrupt
and my audience hates it even more, but I'm going to just,
could you just explain what each of those is
and what it corresponds to?
Yes. Great, thank you.
And I will say, first of all, the reason I'm choosing these,
it's not even my own choice really, it's two reasons.
One is that the two studies over the past five years
that have shown us in large populations
that the vast majority of American adults
are metabolically dysfunctional use those biomarkers.
So I think because of that, it's important to to know them and the two studies that I'm referring to are one from
UNC in 2018 which showed that based on those biomarkers 88 percent of American adults are
have suboptimal metabolism and then a follow-up study from the Journal of the American College
of Cardiology from last year showed that that number has gone to 93.2% of American adults
are suboptimal in their metabolism.
And these are the metrics that they use.
And they're very basic.
If you had to pay out of pocket, they
would be less than $100.
So let's talk through them.
Why they're great is because together, they
give you kind of like a tapestry of what's actually
happening inside the cell.
If you choose to look at them that way,
if you read the tea leaves of them, the doctors often,
if they see all these lab tests, it'll
be in an electronic health record.
We've all been through this experience.
They'll come up on the screen, and there'll either be
a green, orange, or red color next to it.
It's high, it's low, it's borderline.
And the doctor will basically, it's very algorithmic.
Oh, your LDL is high.
We need to bring it down.
Oh, your glucose is high.
We need to bring it down.
Oh, your blood pressure is high.
We need to bring it down.
But what I'm inviting people to do
is understand a little bit about each test
and then read the tea leaves of what it's telling us
about our mitochondria.
So let's start with fasting glucose.
So fasting glucose, when you look at these studies
that I'm referring to, they call optimal less than 100.
So to define whether you were in that 88% or 93%,
you had to essentially be in their optimal range
for all biomarkers not on medication.
So I'll quickly run through what their ranges were.
My ranges for optimal are tighter than these.
But fasting glucose less than 100,
triglycerides less than 150, HDL above 40 for men or 50
for women, hemoglobin 1C less than 5.7%,
total cholesterol to HDL ratio less than 3.5 to 1.
Waist circumference less than 35 inches for women or 40 inches for men.
And blood pressure less than 120 over 80.
If those things were in those ranges and you weren't on medication for blood sugar or blood
pressure or whatnot, you were considered optimally metabolically healthy.
That's now 6.8% of Americans.
All of these biomarkers are easy to change
in one to two months, I would say,
with simple lifestyle habits.
Could you remind us what hemoglobin A1C is?
I think most people are familiar with HDL cholesterol
being the quote unquote good cholesterol
and LDL being the bad cholesterol.
And as I say that, I know I'm going to get dog piled.
Yeah, oh, totally, yeah.
I'm not sure that I adhere to that. I'm not sure I don't add cholesterol. And as I say that, I know I'm going to get dog piled. Yeah, totally. I'm not sure that I adhere to that.
I'm not sure I don't adhere to that.
I'm not sure about a lot of things,
but I am sure that most people think of them that way.
So just as a, to stay functional here,
we'll frame it that way for now with the caveat
that that might not be the whole story,
isn't the whole story.
But triglycerides, fat in the blood, fatty stuff.
But so key to understand about the triglycerides.
It's not, we don't want to confuse triglycerides
with eating more fat.
Triglycerides are a storage form
of excess carbohydrates in the blood.
So this is why it can tell us something about,
and I know you and Rob Lustig talked about this at length,
but it's-
And Lane Norton. And Lane, yeah. I mean, one of the things that's really tricky, gosh, So this is why it can tell us something about, and I know you and Rob Lustig talked about this at length. But it's-
And Lane Norton.
And Lane, yeah.
I mean, one of the things that's really tricky, gosh,
is that the language around nutrition and health
is complicated because people hear the word fat,
they think body fat,
but then they also think the macronutrient fat.
We just need more words to better parse the reality.
In biology, we call the two major groups of people
lumpers and splitters.
Lumpers like to lump everything together.
It oversimplifies and complicates.
Splitters like to split everything,
give a name for everything,
individual name for everything.
It complicates.
And so there's a middle ground, right?
There's a land of reasonable people and nomenclature.
And unfortunately that does not exist on the internet
nor does it exist in any one specific subfield
of medicine or science.
I mean, so much of the confusion out in the world
is because of a lack of adequate language
in order to explain.
Okay, so the triglycerides are a reflection
of excess carbohydrate intake.
And how it's helping us with that tapestry
of understanding the trifecta of bad energy
is that if you think about it,
let's just go back to that cell and that poor mitochondria
that's being absolutely decimated by our environment.
And its capacity is low.
OK, so that mitochondria is like,
I can't process glucose or fatty acids to ATP very well.
So I'm going to block their entry into the cell.
So now you've got glucose rising in the bloodstream.
So OK, fasting glucose, that was one of our biomarkers.
If that's going up, that is a little bit
of that tapestry of maybe something's
going on inside the cell that's blocking
the entry into the cell, so it's rising the bloodstream.
OK, well where's all that?
The body does not want lots of glucose floating around
in the bloodstream because it can literally independently
cause endothelial dysfunction, which is basically
blood vessel problems.
It can cause oxidative stress in the bloodstream.
It can cause glycation, which is sugar literally just sticking to things.
The body doesn't want that glucose high in the bloodstream, so it converts it to triglycerides
to be stored in a storage form of energy.
That's a key point that I think is helpful to understand is that the body, it's always trying to like kind of keep
things in the right range so it'll convert things.
So then triglycerides, a picture in your blood
of glucose being high and triglycerides being high
is very much should signal to everyone
when they look at their labs that there's probably
something going on inside the cell that's blocking the cell from being able to use and process.
It's a sign of mitochondrial dysfunction and chronic overnutrition.
Too much substrate, not enough processing, glucose is going to go up, triglycerides are
going to go up.
And so then if you kind of squint and read the tea leaves, it's like, huh, I think metabolic
dysfunction.
And what's fascinating is that the travesty in our health care system is that a patient might go into the doctor.
And they're fasting glucose is 99,
one point under what we'd consider the normal range.
And their triglycerides are 149, one point
under what we'd consider the normal range from these things.
That doctor might say to that patient, you're totally fine.
Both glucose and triglycerides are normal.
But that's just really problematic
because they're on the upper end of normal for both of those.
And so really what that would say to me,
as someone thinking about the mitochondria,
is like this person is definitely
metabolically dysfunctional.
They're on the highest end of normal
for both triglycerides and glucose.
There's something, there's definitely insulin resistance going on here. I would much rather
see that glucose at 73 and that triglyceride at 50, which to me would say, oh, this cell's
processing through energy great and things are moving through and we're not backing
up in the bloodstream. We're not converting to triglycerides. So that's where really optimal
ranges get in. But so that's glucose and triglycerides. So that's where really optimal ranges get in.
So that's glucose and triglycerides.
Why if those are starting to creep up, it's a sign that something is happening metabolically.
And then when we look at some of the other biomarkers, so hemoglobin A1C, so that's a
marker that's looking at how many of the hemoglobin molecules that are in the red blood cells that carry oxygen, how many of those hemoglobin molecules
have sugar stuck to them?
And that's glycation.
So you're looking at glycated hemoglobin.
And you can imagine that if the concentration of glucose
is higher over time, more glucose
is going to stick to red blood cells.
And that's going to create a higher percentage of glycated hemoglobin.
So that's why that lab is represented as a percentage.
So less than 5.7 is what we want.
You want those cells nice and smooth and slippery.
No sugar stuck to them, causing dysfunction.
And because blood cells last for about 9 to 120 days, hemoglobin A1c is giving us basically
a snapshot of average blood sugar levels over 9 to 120 days.
And if that average is higher, again, probably a sign that cells are rejecting glucose from
the cell and it's causing a rise in the bloodstream.
And then just talking about one other biomarker that we talked about, which was blood pressure, people might say, well, how does blood pressure relate to what's going on inside
the cell in the mitochondria and whatnot?
And the fascinating link is that when that cell becomes insulin resistance, which again
is a compensatory mechanism for mitochondrial dysfunction, the insulin is going to rise in the blood because
the body's insulin resistant.
So the body is going to turn out more insulin to try and overcome the insulin block to drive
the sugar into the cells.
So insulin levels rise.
Well, insulin is one of the key activators of nitric oxide, which is the molecule in
the blood that dilates and relaxes blood vessels.
And so when we become insulin resistant and we're not responding to that insulin signal, we end up getting less nitric oxide activity. So this is
how kind of looking at even these very basic, very cheap biomarkers through the lens of
basic cellular physiology, we can start to see, man, my body might be like underpowered. I might
have a mitochondrial issue here. So that's a few of those tests
that we really want to shoot for.
Terrific.
And thanks for bringing up blood pressure again.
It's sort of, comes across to many people as old school,
right?
But when Atiya was here,
one of the several times he was here,
he really pushed on blood pressure
as such a key metric, right?
I mean, obviously if blood pressure is high,
you're getting less nitric oxide through
whatever means here.
Vessels and capillaries are constricted.
Cells aren't able to use the energy that's coming in.
There's excess energy, there's buildup of metabolic waste.
There's all this stuff.
And now we can start to see the picture
that's trying to emerge.
And as you mentioned briefly, these markers can be put into healthy range There's all this stuff and now we can start to see the picture that's trying to emerge.
As you mentioned briefly, these markers can be put into healthy range or maybe even fantastic
range in a very short period of time.
So we'll talk about how to go about that.
In terms of getting a basic blood test, as your physician, what's the secret code? I'll give away one that a former guest
who's also an MD shared, which is,
oftentimes if you ask your physician for a blood test,
they will say, well, unless there's a particular need
or you're struggling with something,
they won't give it to you.
But if you have a shift from baseline in a symptom
or in a number that can help,
all the physicians are going to come after me now with,
I guess with stethoscopes.
I'm willing to stand my ground.
If you want a blood test,
it's often useful to mention
that there's been some market shift.
You want to be honest, right?
But some market shift in sleep, in lifestyle,
in how you feel standing up, sitting down.
I'm not trying to lace people's minds
with ideas to create narratives here,
but oftentimes where physicians are resistant,
they'll be more amenable if they understand that,
hey, like something's changing,
and the patient's saying something's changing,
it actually would be irresponsible of them
to not give the blood test.
So there you go, bring it on, MDs.
Yeah, truly.
And I think the nice thing about these, again,
very basic tests, and there are so many other tests
that I talked about in my book
and that you've talked about on your podcast,
APO-B, uric acid, fasting insulin, HOMA-IR,
HSCRP, liver function test, GGT,
all these other tests that are great,
that can really tell us more about mitochondrial dysfunction,
oxidative stress, chronic inflammation.
But the ones I'm mentioning are the ones that you will not
have to fight with your doctor about.
Oh, good.
Everything I just mentioned, the doctor
should order on an annual physical.
And it's really about us learning to actually read
the tea leaves of what they're saying
and not look at them in this algorithmic way.
But how together, if they're creeping up
or if many of them are a little bit high,
we need to focus all of our energy
on improving mitochondrial capacity, basically,
and bring those numbers down, which
we can do very, very quickly.
Once you start getting the mitochondria
moving through more of those substrates,
a lot of them will just naturally come down.
Now, in the book, I give scripts to literally talk
to your doctor with because you are going to get pushback.
Often, if you ask for a fasting insulin,
I would say probably, I mean, even though doctors
are waking up a little bit, like maybe 85% of people
are going to have their doctor say
they won't order that for them.
So I actually think there's a huge benefit.
I hate to say it, but like going outside the system,
this is where I think innovation has been valuable.
There's a lot of amazing companies
doing direct to consumer lab testing so you can basically
avoid the hassle.
Some of them are very affordable.
Function Health is a company that's doing 110 biomarkers, including all the key metabolic
biomarkers for less than $500, and they'll do it twice a year.
You don't ever have to, and then they do interpretations.
Inside Tracker, Next Health, Levels is doing labs.
And so there's a lot of this springing up because I think people are sick of fighting
with their doctors to get a crumb of information about their health.
And it's, it's, it's, we should probably be testing these, I would say three to four
times a year.
And the beauty is that I think a lot of what keeps people down
in the health world is that they're
confused about what to do.
There's a lot of noise.
There's a lot of different strategies.
Do I do paleo, keto, carnivore, vegan, Mediterranean?
Do I do HIIT or zone two or eccentric?
It's like, there's so much noise.
And the beauty with having a plan
for understanding your biomarkers regularly
is that you can cut through all the noise.
Try a strategy, see where you stand,
retest in a few months and see if you're moving
in the right direction.
You don't have to trust your doctor, you don't in the right direction. You don't have to trust your doctor.
You don't have to trust me.
You don't have to trust anyone.
You can literally trust your own labs.
And I say to people, like, if your labs are optimal and the ranges I just mentioned are
not optimal, like, you want to actually get to better than all of those if you want to
be optimal.
If your key metabolic biomarkers are optimal,
if you feel absolutely freaking incredible
and you have no symptoms, then you're
probably doing the right strategy, whatever that is.
Vegan, keto, whatever.
And exercise in your lifestyle, because that
is showing that your cells are fundamentally working properly.
So I think that's just a really empowering message.
And now there's phenomenal companies that are cropping up
to basically help allow people to do this
on their own schedule,
which I think is really the future of health
and actually will help lessen,
I think some of the intensity of the diet wars, you know,
cause it's like people can just say like,
I trust my strategy.
I know I'm doing what's right for me.
Cause like, look at all my biomarkers and I feel great.
You know, so. doing what's right for me. Cause like, look at all my biomarkers and I feel great.
Yeah, what used to be the before and after,
pre-diet exercise, post-diet exercise, photos on social media are now starting
to also include numbers, which is kind of interesting.
I mean, obviously these aren't randomized controlled trials,
but it's cool to see people posting their numbers
of things that are not just related to aesthetics
but are, or body weight, but are related to health metrics.
It's fun.
I think it speaks to a more scientific
or at least a more quantitative approach to things.
And I think it's inspiring for people.
Thanks for putting those scripts in the book
that people can refer to.
Let's say that I go in for these blood tests,
I do the basic seven,
and I find that my fasting glucose is a little high,
my triglycerides are a little high,
my LDL is a little high,
maybe a few other things are okay.
So I'm kind of in the, you know,
not in the red zone, but I'm in the like,
should probably pay attention to these things.
What are some of the things that one can do
in order to try and move those needles
in the right direction?
I know we talked about walking and movement before.
What are a few others?
And maybe we could start to touch into nutrition
a little bit, and then we'll pivot to insulin
and blood glucose.
I think on the highest level,
it's about running through what are the science-based things
that we know in our environment can lead
to metabolic dysfunction and take
honest stock of how those factors are playing out
in your life and then choose a few
to start moving in a different direction.
So the ones that I think are ones that we can really
control and that we know based on the science
are impacting our mitochondrial metabolic health
is the food, the sleep, the movement, the emotional health,
the toxins, our relationship with light,
and our relationship with temperature.
And your journey to optimal metabolic health
might be totally different from mine,
because I might really need to focus
on the food and the sleep and the emotional health. Because I might really need to focus on the food,
and the sleep, and the emotional health.
And you might really need to focus on the toxins,
and the light, and the movement.
And so a lot of it is actually taking stock
on where the levers are in your own life.
Where are you crushing it?
And is there a lot of room for improvement?
So step one is knowing that those are the things
in our environment that we need to basically improve,
to give ourselves the best capacity.
And then, of course, checking your biomarkers
to make sure your interventions are working.
But food, I think, is one that is totally unavoidable.
Of those pillars, those seven pillars,
food is one that most of us are getting wrong
and that we really actually have to get right
to improve
our metabolic health for a lot of reasons.
I mean, our bodies are basically 100% molecularly made
from food.
That's so wild.
It's so wild.
Every time I think about that, it kind of blows my mind.
Babies are 3D printed from food basically inside a woman's body.
It's wild to me.
And then what's so cool about the body, what brings me
just immense awe every day
is that we have this conception in our Western world
that the body is like a thing
that we're with throughout our life
because we kind of look the same and we age slowly.
So it's like Casey is a thing and Andrew is a thing,
but the body is actually a process.
The body, and there's this amazing Taoist statement,
like life is a process, not an entity.
I love that.
And the way. No, I'm sorry to interrupt.
I always wish that if people could understand that with biology and health, understanding
the nouns and the names is important, but it's verbs.
It's verbs, verbs, verbs.
If you understand that things are processes or processes depending on who you are and
where you live in the world,
it all becomes so much more tractable.
Yes, and it's so much more hopeful.
Because if I'm a process, if you're a process,
then every day we're eating, we are changing the process.
Whereas if you think you're a thing, then there's no hope.
Cause I'm just, I'm Casey and that's who I am.
And I have this disease.
And I think so much in our language, actually,
of health care, both our Western sort of despeiritualized
nature, we don't really have a lot of curiosity with process.
But even the ideas, the way we talk about disease,
I have diabetes.
And we don't even talk about diabetes cures,
which now a lot of people are curing their diabetes.
We call it remission.
It's this thing that's a part of you.
And I think I just love this idea of we're evolving every day
and food is so important because, again, we
take in 70 metric tons of food in the lifetime,
2 to 3 pounds per day, 1 metric ton per year on average.
And that is like the printer ink.
That's the 3D printer ink to create tomorrow's version
of ourself, which is molecularly different than the casee
of today.
That's a hopeful message because if we can give the body food,
which I think we, again, our conception of food, I think,
is very limited.
Food is the molecular building blocks of the body.
It is the molecular building blocks of the body.
It is the cell signaling functional molecules that tell our cells what to do.
They act as transcription factors, epigenetic modifiers, cell signaling pathway intermediates,
and it's also, of course, the substrate to change what the microbiome does and the composition of the microbiome, which is basically
a pharmacy inside our bodies to create different molecules that
can affect our health.
So food is certainly a calorie is a calorie
from the concept of thermodynamics.
But from the concept of molecular information,
it has three massively important parts
that are unavoidable
for creating cellular health.
So I would just say that that is the pillar
that we can be happy to drill into of like,
what do we really do to, you know,
build as much metabolic health as possible?
Yeah, I want to focus now, if you're willing,
on food, not just macronutrients,
proteins, fats, and carbohydrates, not just calories, although that as well,
but things like timing, things like fasting,
and micronutrients, which I think is a highly
underexplored topic.
So with respect to food, gosh, I feel like we've all
been exposed to pretty much every variation of, you know,
it's all calories in calories out.
And by the way, I believe in the laws of thermodynamics.
So yes, total caloric load matters.
Total energy expenditure matters without question.
Within the framework of not consuming excess calories,
there's a lot to explore, however.
I can just say for myself, for what it's worth,
I'm not very hungry until 11 a.m., noon or one.
I'm okay not eating until then
and just water, electrolytes, and caffeine
does me just fine.
I can exercise, et cetera.
But once I start eating, I really enjoy eating
and I mostly like the proteins.
I like meat and fish and eggs
and I like cheese and vegetables and carbohydrates and fruit and all of it. I like all the proteins. I like meat and fish and eggs and I like cheese and vegetables and carbohydrates
and fruit and all of it.
I like all the stuff.
And I tend to like singular few ingredient foods.
I just naturally do.
So I've been lucky in that way,
but I know a lot of people like sandwiches, processed foods,
things that are combinations of ingredients.
What do we know about kind of,
I don't want to say optimal,
but if one, we're going to explore different ways of eating
for sake of adjusting these biomarkers
in the right direction and improving metabolic health.
Is there kind of a generic jumping off point?
Would most people, for instance,
be wise to cut back on the total number of sugars
or the total amount of sugar rather,
perhaps reduce the amount of carbohydrate
and replace it with some lean quality protein.
I mean, are there generalizations that we can make
or is it really all just about not getting excessive
calories and trying to get those calories
from the most nutrient rich sources?
Well, just drilling in on two things you just said there.
So one thing you said that was interesting was that you're lucky that you like all of
those foods.
And then the second thing was, is it just about not getting excess calories?
But I think what's interesting about both of those is that I would argue that the reason
you like those foods is because you have given your body enough whole real foods that now everything in your biology,
neurobiologically, your reward circuitry, your microbiome, your satiety hormone threshold,
all of these are now basically creating a situation in which you like those foods.
And then the caloric thing fits into that because the reason we're eating excess calories,
the reason chronic nutrition is happening, and the reason we're eating excess calories, the reason chronic nutrition is happening,
and the reason we are quite literally in the United States
eating ourselves to death for the first time in human history
is because we're not eating real food.
And we're eating 60% to 75% of our calories
of ultra-processed, nutrient depleted foods that fundamentally don't give
ourselves what they need.
And a real premise that I think is so important to realize is that our cells are brilliant.
And if the cells aren't getting what they actually need to function properly, they will
drive you to eat until they get their
needs met. Unfortunately, because the ultra processed food is designed to be
highly addictive and it's devoid of what the cells actually need for good
function, we end up eating ourselves into a grave and now almost 80% of
Americans are overweight or obese.
Close to 50% of the country is obese.
We literally gloss over this as a culture.
It has become so normal in such a short amount of time.
But I always think about the fact
that there are really no other animal species in the world
that have obesity and chronic disease epidemics.
And they don't have social media.
They don't have experts. They don't have PubMed. They don't have the FDA. They don't have social media. They don't have experts.
They don't have PubMed.
They don't have the FDA.
They don't have the USDA.
They don't have any of it.
And they have somehow figured out a way
to stay at a healthy weight and to not get heart disease.
And it's because they're eating real food that meets
the needs of their cells.
And so I think to just boil that down,
the root cause of the problem is that we have a toxic food
supply that's no longer filled with the molecular information that our body needs to know to
be satiated and to function properly.
And so through the complex biology of satiety hormones and neurobiology and microbiome function,
we are driven to eat so, so, so much more. So truly, the jumping off point for anyone on the quest to better health is to eat as
much real, unprocessed food from good soil as possible.
And really, of any dietary philosophy they want, truly, I think if someone's eating real,
unprocessed food from good soil who is plant-based or who is keto, they are going to have such a higher
chance of meeting their body's actual fundamental needs. And the good thing about biomarker
testing is they can track for themselves if they are having good cellular function with
that strategy. There's been studies that have panned this out. We know that the more
ultra-processed food you eat, the higher risk of obviously
obesity but also chronic diseases are.
But then, of course, there's an amazing study from Kevin Hall just recently where he basically
locked people up at the NIH.
For two weeks, he had them eat ultra-processed food, and for two weeks, he had them eat real
food.
And people ate 7,000 more calories in the two-week period when they were eating ultra-processed food
versus the unprocessed food.
They were locked at the NIH.
I mean, I've been to NIH quite a bit.
It's great for a day job or a day visit.
I don't know that I want to be locked there.
That sounds like the Stanford Prisoner experiment.
I say this tongue in cheek and with such admiration for what he had to do, but I think it's so
amusing that we have this totally frankenfood toxic food system that's largely ultra processed.
It took amazing Kevin Hall to basically do an NIH-funded study where people, what I say
by locked is that they were inpatients at the NIH and every had ad lib,
you know, unlimited access to food during each
of those two week interventions.
So it was two weeks of ultra processed food,
two weeks of unprocessed or mentally processed food.
And they could eat whatever they wanted,
as much as they wanted in both groups.
And then they would weigh every single bite
that was left on their trays.
They knew exactly, exactly how many calories they ate.
And literally just giving people this ultra processed food, which is devoid of what our
bodies need and therefore will drive people to eat more.
They ate 500 calories more per day for a total of 7,000 calories more in that two weeks.
And they gained about two pounds and then lost
two pounds in the unprocessed group, which makes sense, of course, because a pound is
about 3,500 calories.
And so we have to do these kind of crazy studies just to prove what we kind of know is true,
which is that this ultra-processed food environment that's cropped up over the past 50 years is
an experiment that has failed.
It has failed.
You know, close to 45% of kids are overweight or obese now.
It's not working, and that really is the root cause.
So I think a lot of food is about quality and how do we actually really meet the needs
of the cells so that our satiety hormones get secreted and we naturally stop eating.
Because just telling people eat less calories
but eat whatever you want, that just doesn't work.
We have to inspire the body to not
want to eat excess calories, which
we do by stimulating satiety hormones, helping
the microbiome, support that process,
and then change our reward circuitry, which
is done with nutrient-rich, the most nutrient-rich food we can possibly get.
And that's why I mentioned the soil because our food is drastically depleted of nutrients.
So when we look at that 70 metric tons of food we're eating in the lifetime, it's just
fascinating.
That's the information for our body, what it's going to be built from, how it's going
to function.
Well, right now, 60% to 75% is ultra-processed.
So we slash the value because the ultra-processing just like slashes the nutrients.
We slash the value of that 70 metric tons.
And then we have crappy soil because our industrial agriculture system, which means the food in
some cases has 70% less of key micronutrients in it.
So that 70 metric tons, what's actually useful for our body
becomes so much smaller.
So what we want to do is basically
expand the value of that substrate
we're putting in the body.
And that means real food unprocessed from good soil,
meet the needs of the cells, naturally don't be hungry,
maintain a healthy weight. And something I talk about is that we could, I mean, we could talk about
nutrition and the biochemistry of nutrition all day, but in my review of sort of the biology and
the biochemistry, like there's five main things I think we can strive for in our food that can
really help meet the needs of ourselves. And when it really comes,
there are obviously more things our body needs,
but if we strive for these five things,
we will ultimately, I think, eat a really healthy diet.
And that is fiber, omega-3s, adequate healthy protein,
a good amount of probiotics, and high antioxidant sources.
And if we build our diet around knowing a few things in each of those
categories that we really love and stock our kitchen with it and make our meals a mixing
and matching of each of those components, and we get a good amount of those, we will
give the body a lot of what it needs to have mitochondrial health, reduce chronic inflammation,
reduce oxy of stress.
It's interesting for me to take a step back
from nutrition as it's typically presented
and think about the brain, the hypothalamic circuitry
that drives hunger and satiety and things like that.
And to map that onto what I've heard,
and I believe to be true based on my view of the literature,
which is that we are largely,
meaning these circuits in the brain
make us largely amino acid foraging machines
because we need those amino acids
in order to carry out metabolic processes
and reconstruct any tissues that need repair and recovery,
not just from exercise, but just daily turnover,
removal of waste, et cetera.
So we're foraging for amino acids unconsciously.
We're foraging for micronutrients.
And of course we need macronutrients,
we need enough energy from proteins,
fats and carbohydrates or some either combination
of the three, I feel like I'm sort of in the dying category
of omnivores, right?
I'm neither, you know, I'm not meat-based
and I'm not plant-based, I'm omnivores.
I think most people are omnivores actually,
but omnivores aren't discussed quite as much
as the other categories, at least not on social media.
But that, we think of ourselves as getting hungry
and wanting to eat.
And I think eating the food,
some of them that I listed off before,
like meat and fish and eggs and vegetables and fruits,
and some, I do like starches, like rice, oatmeal,
some pastas, some sourdough breads and things.
I love butter.
Who doesn't love butter?
Of course, none of that stuff in excess, olive oil.
But if one looks at kind of that buffet of options,
you realize you can get some high quality amino acids, you can get some high
quality lipids, you probably want to get more of them from olive oil than from butter, but
you can get the micronutrients you need provided those food sources are healthy.
Now contrast that with a highly processed diet or even a minimally processed diet and
you can get the taste, you can get the macronutrients, you can get the calories,
but you don't, meaning the brain doesn't really have
a sense of, it can't directly map taste, calories,
micronutrients onto one another.
And so you can imagine that the neural circuits,
and here is a little bit of hypothesizing slash conjecture,
but that the neural circuits responsible
for hunger and satiety would get immensely confused
by what's in a highly processed food.
A Snickers bar, if you like sweets, tastes pretty good, but it's unclear what's in
it except sugar, except it's got a certain Snickers bar taste.
But if the circuits of the brain are really trying to drive us to get amino acids and micronutrients
for bodily health and repair,
well then highly processed
and even moderately processed food
has just got to be pure confusion.
Sorry to go long here, but it reminds me of an idea
I had once where, like, imagine if you took a pill
that greatly increased the level of dopamine
or epinephrine, acetylcholine and serotonin all at once,
that's polypharmacology.
And it might make you feel a certain way,
maybe good, maybe bad.
And then afterwards you'd probably have a bit of a crash
from as the drug wore off, no doubt you would.
But let's say you wanted more of that feeling,
you wouldn't really know what to go look for
because you don't know what was in it
because it's polypharmacology.
So I feel like highly processed food is polypharmacology.
Whereas when you are eating foods
that create a more pure experience
of micronutrients, amino acid content, calories and taste,
those four things map to one another,
that intuitively we can start to understand,
oh, I like this food and it's good for me
and this is enough of it.
I don't know anyone of reasonable size
that eats like four ribeye steaks.
They eat one.
I mean, I'm sure there's some freaks out there that do that.
But one even small piece of quality meat is very satiating.
Yeah, you will self-regulate.
Cause the body, like every other animal in the world, is exquisitely
designed to regulate hunger on a very intuitive level if we eat natural food.
I think it's almost ridiculous to talk about calories in isolation because the reason we're
eating more calories is because we're eating ultra processed food.
And so, but I love what you just said, Andrew, about the brain and the polypharmacy.
I think that literally is, I've never heard that said.
And I think it's like processed food is like polypharmacy of food.
It is the definition of processed food, which I know you talked about with Rob Lustig, the
NOVA IV criteria is literally it's breaking down foods into these constituent parts
that were never meant to be separated from each other,
like the endosperm of a wheat kernel
separate from the bran and the germ.
And then take that and like a little science experiment,
pair it up with all these other individual components
and synthetic chemicals that are made in a factory
and put them together to create this thing that the body,
I truly think our insatiable hunger, again,
we're eating ourselves to death in the United States.
That's the reality.
Our insatiable hunger and our chronic disease epidemic
fundamentally is a lot of, it's mass cellular confusion.
And when you think about what chronic inflammation is,
chronic inflammation is biochemical fear
on the cellular level.
Well, when you put this stuff into the body
that's never seen before,
obviously that's gonna generate some confusion.
And you could trace that back to what that really means
with leaky gut and all the sorts
of the real physiology of that.
But there's a wonderful book that
is called The End of Cravings by Mark Schatzer.
He also wrote The Dorito Effect.
But he talks a little bit about what
you're talking about, which is the idea that processed food is
actually the ultimate food-based variable reward.
So in the way that it in things that, I mean,
I'm speaking back expert here,
but things that the body can't predict
what the outcome is going to be are
going to kind of get you in that dopamine motivation pathway.
And that's actually what processed food is doing,
is it's every time we eat a different,
we think we're eating a tortilla,
but it's like completely different
than all the other weird tortillas,
ultra-processed tortillas on the shelf.
So every time we eat tortilla and our brain is this incredible prediction machine and
as it's coming towards our mouth, we're predicting what the load is going to be.
But we have no idea.
Is it a Coke Zero?
Is it a Diet Coke with aspartame?
Is it a regular Coke?
It all tastes the same, but the nutrients that are in our gut are totally different.
So we end up actually triggering the motivation pathways
because of processed food representing a variable reward.
Whereas every time you eat a ribeye,
your body is pretty much getting a similar thing each time.
And so the prediction matching is
going to be more conducive to getting off
the motivation treadmill for more,
which I think is so fascinating.
But I think backing up a little bit,
one concept I have for food that really helps me
is really thinking about the body's always
trying to help me be satiated and trying
to help reduce my cravings.
I literally just have to give the body what it needs. I have to stimulate the body in a way
that it will serve me in giving me satiety hormones to basically
regulate my hunger.
And again, with visuals, I think it's so helpful.
I think about these cells lining our small intestine that
literally have nutrient sensors and literal receptors
on the cell membrane in the luminal side of the gut that's facing all the food that
are just sitting there waiting to bind with these things
in our food that will stimulate the cell to make the satiety
hormone that poof, effortlessly makes us not hungry,
gets rid of that grip of attachment to cravings
that all of us are so plagued by.
And I think we have this intense conversation happening
in society right now about GLP-1 analogs and ozempic
and Menjarah and all these things, GLP-1 agonists.
But we rarely talk about the fact
that we have nutrient-sensing cells of the gut,
the L cells of the gut, that when stimulated appropriately,
will make GLP-1.
And when stimulated the way they want to be, will secrete hord will make GLP-1 and when stimulated the way they want
to be will secrete hordes of GLP-1 for us. And so how do we actually think about just literally
giving the body what it needs to stimulate the anxiety hormones and the processed foods aren't
giving us those things? You know, the things that are going to stimulate those cells, well,
the things that will, I mean, this is kind of fascinating if you don't mind going down a little road.
No, please.
Yeah.
Please.
With the GLP-1 conversation,
I feel like so missing from the conversation
is the idea that like,
from a first principles perspective,
there's three ways our body could make more GLP-1.
We make more cells that make it, L cells of the gut.
Each of those cells makes more GLP-1,
and importantly, we can also inhibit the inactivator of GLP-1, which is an enzyme called DPP-4.
So GLP-1 actually gets rapidly degraded by DPP-4 in the body.
So if we can figure out how to inhibit DPP-4, we can raise our GLP-1 levels.
What is DPP-4?
It's an enzyme that breaks down GLP-1 rapidly.
Thanks, yeah, I think you said that and I apologize.
It's so fascinating.
And so how often have you seen in the headlines,
oh, here's some strategies to inhibit your DPP4?
Never, because Ozempic is on track to be the highest grossing
med in human history.
And just like we talked about in the beginning of the episode,
the whole industry, this $4 trillion health care industry,
is desperate for us to not understand
how to do the things that drugs could do for us.
So when we look at those three first principles approaches
of how do we make more L cells, get them to produce more GLP-1
from each L cell, and then inhibit the breakdown
through the inhibition of DPP-4, for the first one,
we know that short-chain fatty acids,
which of course are the byproduct
of microbial fermentation of fiber in the diet,
stimulates the differentiation of more L cells in the gut.
So more short-chain fatty acids, more L cells.
Can we translate that into support the gut microbiome?
Eat more fiber.
Eat more fiber.
And we had Justin Sonnenberg from Stanford
on a world expert in gut microbiome
and he was a big proponent of,
based on work he's done with Chris Gardner
and others at Stanford, so happens,
of ingesting one to three servings
of low sugar fermented foods each day.
Things like sauerkraut, kimchi.
Again, low sugar variety is probably best.
Not kombucha.
Yeah, maybe not. you said not kombucha.
Yeah, because that's going to be like the highest sugar
of the fermented foods, which people often go to.
But now that becomes soda.
And pretty costly.
The sauerkraut, you can actually make your own sauerkraut.
Tim Ferriss had a great recipe for this
in the four hour chef.
You have to be careful because that, you know,
that you can create some unhealthy ferment.
You have to do it the way he describes.
So check out the recipe, it's online.
Or you can buy sauerkraut and the brines,
drinking the brine off the sauerkraut or off
seems to be good for the gut.
That's such a great point, which is that ultimately
we want the short chain fatty acids,
which is the medicine that the microbiome are making for us through the microbial fermentation process.
And we can basically do that in three ways.
One is we can eat more fiber, which is prebiotics.
We can also eat more polyphenols because we're now learning that the microbiome actually
processes the ferment polyphenols from our, which is basically you'll find those in colorful
fruits and vegetables, spices, teas, cocoa, things like that.
So fermentation of polyphenols and fiber to short chain fatty acids, which then we absorb.
And then like you just said, in a fermented food, the bacteria in that food will be making
short chain fatty acids by fermenting the food in there.
And then if we drink that, we're getting the short chain fatty acids directly. So that's the kimchi, sauerkraut, Greek yogurt, kvass, which I'm obsessed with, which is like
low sugar kombucha.
It's like made with fermenting beets basically.
That's good stuff.
It's such good stuff.
Miso, natto.
So that's one.
That has been shown to differentiate more L cells in the gut.
We also know that people with type 2 diabetes have much fewer L cells in the gut. We also know that people with type 2 diabetes have much fewer L cells in the gut.
And it's hard to know what the causality is there, but I think a safe assumption is like
if we keep our blood sugar under better control and sort of stay out of that diabetic range,
it probably lends itself.
I don't know what the chicken and the egg is there, but blood sugar stability, more
L cell differentiation.
And then actually ginseng has been shown to improve L cell differentiation. And then actually ginseng has been shown to improve L cell differentiation.
So that's just sort of one set of things.
And I don't think the dose on ginseng has been settled,
but very high antioxidant component plant.
When we look at actually stimulating more GLP-1,
you've talked about urbamate, I think,
having a mild effect on glp-1 you've talked about your Ramate. I think having like a mild effect on glp-1
But there's actually a lot of other things
in the literature protein of course
very potently stimulates these nutrient receptor cells and specifically like valine and
Glutamine seem to have a potent stimulatory effect on glp-1
So you're gonna find that in like meat and turkey and eggs and things like that.
What are your thoughts on supplementing L-glutamine? It's controversial. I know that
some people do it in an effort to relieve leaky gut, but there aren't any randomized control
trials for that. So depending on one stance on what's required for kind of a threshold for
adopting something.
You know, some people will say that's crazy.
Other people really swear by supplementing L-glutamine.
Maybe it's through this route of increasing L cells
that some of the gut relief might exist.
I guess we'd have to explore it.
So that's speculative folks.
So this is interesting.
These are ways to increase the cells that then make GLP-1.
So fiber, prebiotic, probiotic fiber and fermented foods.
Antioxidants, lowering blood sugar, ginseng.
So those are kind of the L cell ones.
The actual secretion of more GLP-1,
one of the most potent ones,
and the study that looks at this,
like the bar graphs are very clearly
statistically significant,
lots of asterisks, is actually
thylakoids.
Thylakoids.
Tell me more about thylakoids.
Thylakoids are so fascinating.
Thylakoids are actually a structure in plants that are part of the chloroplasts.
So chloroplasts, and this also is fascinating because chloroplasts are basically the plant
version of mitochondria essentially.
And thylakoids are a molecule in the chloroplast.
And there's actually been research that shows that when you eat about 100 grams of spinach,
which gives you five grams of straight thylakoid over 12 weeks daily, it led to a significant
increase in GLP-1.
And again, I don't remember the exact, it was two or threefold higher secretion. So this
is in part, so that's a direct symmetry effect of the L cells. And so this equates to 3.5 ounces
of spinach a day, which is like nothing. So just getting those-
Raw spinach or cooked spinach?
I think, I actually, I don't think it actually, it might've said in the methods, but I would
imagine raw because you want to get those undenatured th might have said in the methods, but I would imagine raw because you
want to get those undenatured thylakoids in the gut.
So just kind of another, actually,
thylakoids do a lot of other interesting stuff.
They inhibit lipase in the gut and so actually
help more fat get down to the distal small bowel
and promote satiety.
So this is one of the reasons why you talk about,
oh, the people who eat all these healthy foods and greens, they're less hungry.
It's like it's biochemistry.
Like there's stuff happening in there that is making the hunger signals go down through
things like inhibiting lipase, improving GLP-1 secretion.
So other things for GLP-1 secretion, the thylakoids, also fiber has been shown, specific amino
acids, so high protein foods,
things that involve a lot of valine and glutamine. Green tea and specifically the ECGC that is
one of the compounds in green tea, that's been shown to stimulate GLP-1. Curcumin. So
there are several things that are all in that whole food, basically things you would
associate with a healthy diet, but we actually know they stimulate GLP-1.
So those are all things I try to include in my diet.
And the last one is inhibition of DPP-4.
And that one, there's just actually, when you look at the research, there's some kind
of random foods that tend to inhibit DPP-4.
Black beans, Mexican oregano, other forms of oregano,
rosemary, guava.
And I wrote this one down because it's
a word I hadn't seen very much before I started
digging into this, but myricetin,
which is found in berries, cranberries, and peppers,
and Swiss chard.
So all that is to say, ultimately, many of us
are gripped by cravings.
And the idea of just sort of not being constantly
driven to eat more, which I would argue that about 80%
of Americans are, feels really hard to overcome.
But a lot of it is literally just communicating
to yourselves in a clear way through food to help you be satiated.
And the science can show us how to do this.
And a lot of it comes down to eating,
essentially what you were talking about, how you eat,
omnivorous protein, healthy sources with nutrient density,
and lots of colorful fruits, vegetables, spices,
herbs,
things like that. So yeah.
Yeah, it's interesting.
Again, these aren't randomized controlled trials
nor are they peer reviewed studies,
but I have a few friends who I've known for most of my life
who really struggled with their weight,
carried a lot of excess weight
and were starting to suffer health issues
in their,
even their 30s, but in their 40s.
I'm 48, so they're my peers.
And so they're about that age range.
And they've all done extremely well,
meaning they lost a tremendous amount of body fat,
are terrifically healthy now
by way of basically restricting their food intake to proteins, so fish and
meat, eggs, fruits and vegetables.
They basically just cut out starches, but I don't think it was the starches per se.
I think it was the satiety that comes from eating high-quality protein, fruits and vegetables,
and from limiting the number of highly processed foods.
And actually the toughest thing for all of them was
to stop asking me or themselves rather like,
can I include this condiment, this, this, you know?
And what's interesting is all of them now seem
to really enjoy eating foods in their more pure form.
And I'm not somebody that like pushes on this on my friends.
They just come to me and say like,
how do I lose 50 pounds without having to exercise
it all off, you know, as the only source of weight loss.
They all exercise as well,
but it's just so daunting to try and lose, you know,
20, 30, 40 pounds and to do so quickly
and then to keep it off
because they've all had the experience of going on a diet
and then you're exercising a lot.
And the point here is that I really think
there's something powerful about that relationship
between taste, macronutrient value,
micronutrient value and satiety.
I think there's really those powerful associations
because the brain is such an associative machine.
One thing that I should have said before,
and I know most people are familiar with Ozempic.
Yeah.
And its commercial names are, I forget what the-
Ozempic is the commercial name and Mungaro and Wagovi.
Yeah. Got it.
Is that GLP-1 acts more or less as an appetite suppressant.
Right, yeah.
Powerful appetite suppressant.
So many millions of people are now taking GLP-1 analogs.
Is that right?
I think there were over 20 million prescripts
in the United States last year.
Is it expensive?
It's $20,000 per year.
Does insurance cover it typically?
Right now, insurance is covering it for indications,
but there is a all-out assault
from the pharmaceutical industry to essentially classify
obesity as a genetic disease and a chronic disease
in order to be able to feed this medication more
into the insurance pathway and essentially get
more taxpayer dollars to pay for this
medication. And it is extremely expensive and it's on track to be the highest grossing
medication in human history because it's now being recommended for people with obesity,
type 2 diabetes, and then the American Academy of Pediatrics recently has talked about giving this to children as young as 12 as part of the first line for overweight.
And I think really it's such a travesty based on the conversation we've had because what
Ozempic does not do in any way, shape, or form is impact the toxic environment that
we're living in that's hurting our mitochondria.
Losing weight is different than improving
mitochondrial function.
And mitochondrial dysfunction is the root cause
of basically every chronic illness and symptom
that's torturing American lives today.
And so in many ways, it represents
like the ultimate band-aid for an environment
that is not changing.
And when you think about what we could do
with $20,000 per year, and it's a weekly injection.
So people will say, well, per person,
like, oh, it's, and it's a medication
that is intended to be taken for life,
because when people come off this medication,
many people are gaining back all of the weight or even more
weight afterwards.
And then there's been conversations, Peter T has waited on this, about loss in lean mass.
Part of the weight loss is disproportionately muscle.
And so there's a lot of concerns about it above and beyond its ability to lower the
number on the scale that we should all be very alert to. Because the reality is that the 40 trillion cells in our body
are in an environment in the Western world
right now that is not conducive to core biologic functioning.
And there is obviously no shot that
can mitigate the multi-front assault on our biology that
ultimately generates a body that's
immensely profitable for those hundred specialties of healthcare.
So we're living in this matrix and this game of a devil's bargain between a $4 trillion
healthcare and pharmaceutical industry and a $6 trillion processed food industry that
all want us to think that, you know, the answer
is found in a shot and we don't need to change anything about our lifestyle.
But of course, you know, these simple habits that we're talking about, eating real food,
moving, walking, et cetera, getting out in the sunlight, rapidly can increase our mitochondrial
capacity and, you know, are just the most disruptive thing that we can do, you know,
in our culture today is learn about metabolic health and improve it and it's just interesting to see what's
happening in the media with sort of the assault against these empowering habits
and very in favor of a medication like Ozempic and then when you trace, you know,
unfortunately incentives there, a huge percentage of these outlets that cover,
you know, Ozempic is a miracle drug,
their bills are paid by pharma, 60% of mainstream media advertising budget is pharma.
And so, you know, I just say that because I think it's a scandal that we give so much
air time to these medications and not to simple metabolic habits that can make us feel, you
know, so incredible and really change our core biology.
So walking, exercise, eating,
minimally processed or non-processed foods.
You also mentioned temperature.
Yeah.
Very, very interested in that.
But before we go a little bit further down the path
of what one can do in terms of having agency
over their metabolic health,
I just feel obligated to just entertain the possibility.
Presumably somebody who's really struggled
with their weight a long time,
maybe because of excess cravings,
challenges in regulating their appetite or whatever.
We don't know what the reasons are.
Maybe they injured their knee and they can't exercise.
I mean, this happens, right?
At least not yet.
Take a GLP analog like Ozempic,
loses some weight, probably loses some muscle also.
One would hope that that would give them the sense of,
okay, now I can move my body better.
I'll start exercising, eating better as well.
I think that I have to imagine
that there's a middle case condition
where people are not just relying on pharmaceuticals
and not just relying on behaviorals and not just relying on
behavioral routes to improve metabolic health, but can do both.
Right.
I mean, and one would hope they are if they're already taking these meds, or is it the case
that when people have a pill or an injection or a potion that gives them the effect that
they want, that they just remain sedentary?
I think we have to look at history here.
I mean, first of all,
there have been other weight loss medications
throughout history that you've talked about in the podcast,
like the FenFen.
And then there was another one, I think even before that,
that made people, their temperature go up,
that you've talked about.
Okay, yeah, so the two,
these are, I used to work on thermal regulation
as an undergrad.
So FenFen was eventually banned
because it caused some cardiac issues.
I believe it was a stimulant,
from fluoramine to, sorry, it's not Fen-Fluoramine alone.
It's a combination of things.
That's why it's called Fen-Fen.
And then dinitrophenol,
which was based on the observation
that workers in the ammunition factories
were being exposed to this stuff
and losing a lot of body fat and weight.
It actually made its way into the sports community.
It's highly deadly, highly deadly.
Just don't even, don't even look it up.
It's highly deadly.
Because the moment people start looking it up,
they started thinking about dabbling
the way the internet is now.
Dinitrophenol.
And I think it has to do with sort of
processing of the mitochondria. I think it has to do with sort of processing
of the mitochondria. I think this is happening
and that the electron chains in mitochondria.
So anyway, or free electron, look it up.
Yeah.
Excuse me.
The bottom line here is that there've been plenty
of drugs, mostly stimulants used to help people lose weight
and or that have acted directly on the mitochondria.
It has not worked out well historically.
It just hasn't.
And I think that I'm not just going to lump,
it's a different mechanism.
So I don't want to lump it in with past weight loss drugs.
However, if you look at the trends throughout history,
the medicalization and pharmacology towards chronic
issues has been an abject failure.
I don't know of, and I'm sure people can correct in the comments, but of a single chronic condition
for which the explosion of the pill to treat and manage that condition has lessened the
rates of that condition. The more SSRIs has lessened the rates of that condition.
The more SSRIs you prescribe, the more depression we have.
The more metformin we prescribe, the more type 2 diabetes rates are going up.
The more ozempic is being prescribed, obesity is going up.
This is on Wall Street.
This is on track to be a blockbuster drug.
And they're not assuming the rates of obesity
are going to go down.
That wouldn't actually make sense for the business model.
I mean, these are being talked about at the JPMorgan health
care conferences.
Do you think they're thinking that this is going to plummet?
No.
I can't think of very many chronic conditions
for which the explosion of the medication has
reduced the frequency of the disease.
That's really something to think about.
And the reason is because of exactly what we started
this conversation with.
They're not actually truly impacting or healing
the root cause physiology.
In some cases, they're worsening that root cause physiology.
They are inducing oxidative stress.
They may help with the symptomatic management, but not actually reducing that trifecta that
we talked about in the beginning.
Why do we have reason to believe that medicalizing obesity and not actually getting at the root
cause, which has to be impacted by multimodal gentle nudges in our daily life habits
and environment, that that's actually gonna reduce
the rates of the condition.
No, that's very helpful.
Okay, so I'll then return to the other question
about temperature.
What are some things that can do with temperature?
And by the way, as I do this, I can't resist any longer.
Casey, Dr. Means brought me this jar of blueberries.
People that know me know that I'm a drive-by blueberry
eater, so if there's blueberries out on a table,
I'm gonna take some.
I've never eaten during a podcast, but I'm going to now.
So I'll try and chew quietly.
Do you want some?
Sure.
Okay.
I love blueberries.
And no, I don't eat them one by one.
But I'm going to try and eat them quietly.
So we'll keep them here in the middle for the time being.
And I'm going to eat them by the handful
just because I got hungry.
And you mentioned berries earlier
and it triggered a neural circuit for me.
So what about temperature?
People that know me or even that just listened
to the podcast know that I like the cold shower thing,
cold plunge thing.
I don't do it every day.
I don't do it after resistance training workouts
for at least six hours and mostly keep it on days separate
from the resistance training because there are some data
that can inhibit hypertrophy and strength adaptations.
But I like it.
I like it, it feels good.
I feel great afterwards for many hours
and I believe there are some health effects
and I'm willing to weather the storm of naysayers
because more and more data keep emerging.
That's the case.
Not all the data are spectacular.
One paper on this actually was just retracted.
We need to do an update to an episode to,
it's not work from my lab,
but I still think that there's a lot of really terrific work on deliberate cold exposure.
What's the deal with temperature and mitochondria?
So no one has basically described this better than you.
I feel like on your platform, but I think about it very, very simply.
Throughout human history, humans have really in so many different parts of the world been exposed
to hugely fluctuating temperatures.
If you look at the Sahara Desert or a regular day in Colorado, it's like you can go from
– let's talk about the Sahara Desert.
You can go from 30 degrees to 110 degrees in the span of one day.
Even the concept of indoors is a relatively new concept in human history.
Four walls,
insulation, then central heating and cooling,
that's the last 50, 75 years in most homes.
And so this idea, our cells have evolved
to respond to big swings in temperature
that very recently we have totally pulled away.
And I think that when I think about the mitochondria
increasing their capacity, I'm thinking about, well,
how do I use different energetic signals in my environment
to essentially get the mitochondria to do better work?
And we can think about all the different types of energy
that we're exposed to, solar energy, thermal energy,
acoustic energy, mechanical energy, food energy.
That's basically what our environment is, right?
And thermal energy is a big one of those.
We can speak to our mitochondria with the language of thermal energy and say, hey, it's
cold outside.
We need you to print more of yourselves or work harder such that we can create heat inside
the body to respond to this stimulus.
And so that's
kind of the framing that I use for it. And this data is hard to know if it's totally
accurate, but our population is cooling. And I think it was data from Stanford, actually,
that was showing that our temperature has gone down like 2% or something like that in
the last 100 years. And that fundamentally is mitochondria not working
as well as they should.
Research has shown we're making less ATP in a lot of our cells.
And that's a function of mitochondrial dysfunction.
One fun fact, I don't know if you knew this,
but the body makes about 88 pounds of ATP per day
for the average American.
So we're constantly making it.
We're constantly recycling it in this basically make it, use it, make it,
use it, make it, so fast that we essentially
don't change our weight.
And of course, as it's being broken down, ATP to ADP,
we release heat.
And so I just think of cold as one of the tools in our tool
belt to talk to the mitochondria to say, make more heat.
And in a world in which our mitochondria are under siege,
I think it's a valuable, often very inexpensive one
that we can use.
Of course, it does not supplement or replace
food, sleep, exercise.
But I think it can be a very valuable tool
to stimulate through that signal to basically make more heat. And we know, of course think it can be a very valuable tool to stimulate, you know, through that signal to basically make more heat.
And you know, we know, of course, it can help.
And the data, you know, is mixed, but like increase brown fat, which is like mitochondrial
dense fat and have it do more work and whatnot.
So ultimately, brown fat is mitochondrial dense fat, and we want to, you know, help
promote that.
So that's how I use cold.
And then on the heat side, you know, just fascinating how that's kind of acting to help promote that. So that's how I use cold. And then on the heat side, just fascinating
how that's kind of acting to help metabolic health
through the activation of the heat stock proteins, some of which
have the ability to upregulate antioxidant defense systems
and quell some of that wildfire that we talked about that
can hurt our mitochondria.
So I put them lesser on my list because we
can't avoid the food and you know,
the sleep and the movement,
but I think it's a great tool that we can use.
I love it.
I will just point out that the reason the brown fat
is brown at all is because of the density of mitochondria.
It's literally browned down the microscope.
This is not the kind of fat that is subcutaneous,
although it, you know, it sits around the scapula,
neck, upper back.
There's other pockets of it
on the body too, and such an interesting tissue.
Yeah, I don't know why deliberate cold exposure
is so controversial.
I think it's because people who don't like it,
and frankly, no one likes getting in it.
The best part is getting out and how you feel afterwards,
but I think it, nothing grates on people
like deliberate cold exposure
if they don't like deliberate cold exposure.
And there's no requirement for it,
but I think it's a very interesting stimulus.
And I think there's also a very interesting relationship
between light and temperature,
because in most areas of the world,
as days get longer, meaning more sunlight available,
temperatures go up.
And nowadays we can really divorce ourselves
from all this like day lengthening
and shortening temperature fluctuations,
which is not to say that we should all be running around
in a minimal amount of clothing outdoors,
but there's just such beautiful data
from Dr. Susanna Soberg's work showing, for instance,
that deliberate cold exposure then leads
to one feeling more comfortable at cold temperatures
because you become a, you know become essentially more of a furnace,
more brown fat.
Anyway, we could go on and on,
but I think it's yet another lever of autonomy
in terms of taking control of one's health.
As you said, not as critical as food intake and quality
amount and maybe timing as well.
Speaking of timing, what are your thoughts on fasting?
And then of course, movement and exercise.
The way I conceptualize the idea of fasting,
obviously this is one where we need more words, right?
Because the word fasting is so limited.
There's so many different parts of this, but.
Skipping breakfast for me would be that,
or skipping dinner.
Sometimes I'll skip dinner, sometimes I'll skip breakfast.
Right.
I think that some of the most interesting data that I've seen has been about if we reasonably
compress our eating into daytime hours during the heart of the diurnal cycle when we are
supposed to be eating.
So essentially matching our chronobiology with our behavior, which we are diurnal organisms, so we kind of need
to respect that.
When we do that and we compress it in a moderate way, our metabolic health is better.
Some of the studies that have looked at this, one that was interesting was, and I think
very hopeful for people, is that if you take all the food, all the calories that you're going to eat, and eat them in a six hour window
versus a 12 hour window, totally same amount of calories,
exact same food.
This is a controlled experiment.
People who eat the same amount of calories in a six hour
period are going to have much lower,
statistically significantly lower glucose, 24 hour glucose
and insulin levels compared to people who just space it out
over the course of a 12-hour period.
And it makes sense, because if you're spacing that food out
over the course of 12 hours, that
is a different biochemical milieu in your body
throughout the day.
It's kind of similar to the walking.
It's like you are then stimulating insulin
several more times.
You are exposing the bloodstream to insulin and glucose just
more throughout the day and giving the bloodstream less
of an opportunity to just sort of be clear from that glucose
and that insulin.
And so compressing our eating window
seems to be helpful for metabolic health.
And it's a bang for your buck, right?
Like you can eat the same amount of food.
You just have to eat in a shorter period of time.
So for people who want to eat, you know, a lot,
maybe just consider compressing it into daytime hours,
six to eight hour window.
Yeah, for me, six is tough.
Six is tough.
The one meal per day thing is tough.
I have friends like Lex Friedman
that do the one meal per day.
I end up eating so much food at that meal
that I experience a lot of mechanical distress
as typically later in the day.
I think an eight to 10 hour window has worked well for me most days.
I know as soon as we talk about intermittent fasting, which is what, or time restricted
feeding, same thing, which is what we're talking about right now.
I'm sure somebody's going to call up the, there's been a study that's been circulating
about a massive increase in cardiovascular risk
in people doing intermittent fasting,
in particular the six hour feeding window.
I just want to point out.
Worst study.
As far as I know, I could be wrong,
but as far as I know, that study is still in abstract form.
It's not yet peer reviewed.
It's like the fact that studies that haven't been peer-reviewed aren't even close to
being peer-reviewed are being like put out there as new stories is really problematic
because I can tell you as somebody who sat on the editorial boards of many journals for
many years, I still sit on a few, reviewed countless papers.
I've submitted and had to deal with reviews on countless papers.
The fact of the matter is until the reviews are done, the revisions are made, that paper
may never see the light of day and it may end up in a journal that is barely worthy
of a placemat.
It might end up in a high-tier, high-quality journal, but it might not.
Just because there was, quote unquote, a study done means very little, but it means especially little,
maybe nothing until it's peer reviewed.
Absolutely, and the methods were very poor in that study.
It was a recall-based study, I think,
for two days of recall of people's diets,
which is notoriously very bad in terms of accuracy.
So yeah, and I think I'm not in any way suggesting
that a six-hour window is the optimal window.
I'm just sharing the data that suggests that compressing the window seems to have a favorable
effect.
And I certainly don't do six hours.
But I think when you look at what the average American is doing, which is the average American
has 11 eating events per day and 50% of Americans eat over a 15-hour window per day, and 50% of Americans
eat over a 15-hour window per day.
I can recall those, because I remember when
I was writing the book, I was like, that's a long time,
15 hours and 11 events.
And every time you're doing that,
you're going to be stimulating this glucose
rise in the bloodstream, exposing the blood vessels
to that glucose.
You're going to be turning on all the pathways with insulin
to basically store it, or you know,
and so it's strain for the body.
And so I think giving the body times intentionally
to allow insulin to come down
and to allow glucose to come down,
what that does is it generates metabolic flexibility.
It gives our body an opportunity to have space to use accessible glucose and then convert
into using stored fat.
And that ultimately is metabolic flexibility, the ability for the body, giving the body
opportunities to use glucose but then have times when there's not high glucose and insulin
around to actually get
into the fat stores.
And I think one of the reasons why
we have such a massive overweight and obesity rates
in the country is because with the way the culture of eating
right now, 11 eating events per day,
eating over the course of 15 hours per day,
I would imagine the average American body is rarely,
if ever, tapping into their fat stores for energy
in a meaningful way, because we always
have glucose available to the body.
If you think about, again, the stats about ultra processed
food, about 70% of the items on the shelves in the grocery
store are ultra processed food.
And those ultra processed foods are
built on refined added sugars and refined added grains.
So we're just, we very rarely give the body the opportunity
to rest and move into fat burning.
And that's where compressing the eating window can be valuable.
Obviously, people have talked about this before.
But fasting can be a stressor for the body,
especially if your body is not used to using fat for energy.
And so it's something to ease into and go slow.
But I think if you're slowing down enough to really hear what your body's signal are
saying, you can kind of know whether I think your fasting is working for you or not.
I can tell if I've got too many other things going on, I haven't slept well, a lot of stress stress I can tell that fasting is kind of making me jittery and not feel good versus if I'm really if I have good capacity
I can feel that it's actually making me feel really incredible
And so tune in with your body obviously and you know
You can check your biomarkers if you have a CGM on you can see what's happening in your glucose if you have a ketone
Monitor, you can see what's happening your ket ketones and really actually track, which I think makes fasting actually
even more fun.
I'll mention one other piece of data that I think
is actually really kind of fun as well with timing of eating.
There was a study that looked at people
who ate the exact same meal at 9.30 AM or 8.30 PM,
so basically after dark, essentially
in the part of the diurnal phase when we probably
shouldn't be eating, versus early in the morning, 9.30.
And the glucose and insulin responses for the same meal at 8.30 p.m. were significantly
higher than when eating at 9.30 a.m.
And so again, bang for your buck, it appears that eating in that earlier part of the day when we're active
and our chronobiology is set up for metabolism and activity,
we have a lower glucose and insulin response.
There's also some evidence that melatonin, which
is secreted as we get closer to sleep,
has somewhat of an effect on impairing our insulin
sensitivity transiently.
And so we may actually just be not absorbing the glucose from those meals effectively later at night.
So I tend to kind of move a little bit more low carb, I would say, throughout the day based on that data
and what I've seen on my continuous glucose monitor, basically just higher spikes for the same meal later in the day.
So why not just kind of move it up earlier?
Very interesting.
Something I'll definitely try.
I tend to push my carbohydrates to a little bit later in the day
for sake of sleep.
Unless, of course, I've done resistance training,
which I aim to do three times a week.
And post-resistance training, I try and get some starchy
carbohydrate just to replenish glycogen.
And that then tends to reduce my carbohydrate craving
later in the day.
I love bread and butter, bread and olive oil pastas.
And the other day I found this Argentine place
and I love the steaks there, but they had gnocchi
that it took everything I had, every neural circuit
that releases GABA, inhibition of my brain
to not order three of those orders.
It was so good. But you can walk after the gnocchi. Oh yeah, sure. brain to not order three of those orders. It was so good.
But you can walk after the gnocchi.
Oh yeah, sure.
I'll allow myself to do those things.
I'm not super restrictive,
but again, I tend to eat high quality foods.
By the way, these blueberries are amazing.
Then you figure out where you got those
because they're just tangy enough.
I'm doing everything I can to just not take the jar
and funnel them into my mouth.
Yeah, I think, you know,
if we're looking at blood sugar, blood glucose and insulin,
and as long as we're talking about that,
I did use a levels tracker and yeah, full disclosure,
they're a sponsor of the podcast regularly
and I learned a ton.
I'll tell you what I learned.
I learned that, indeed my blood sugar goes up after I eat,
that certain foods,
although the foods that did this surprise me,
certain foods tend to spike my blood sugar quite a bit.
Grapes, that shouldn't be surprising.
Food order was very powerful for me.
I know that the data on food order are a little bit mixed
and it's controversial, but I like to eat like the French.
I like some soup, then I like my entree.
I like the salad at the end.
That turned out to have the steadiest and lowest rise
in blood glucose for me.
And then across time, I also found that I love hot sauna.
I go so hot with the sauna that I've been accused
by Rogan and other people.
I'm going to turn myself into a brisket.
But after the sauna, my blood sugar spikes
presumably because I'm a bit dehydrated
and it's the concentration of blood glucose.
Is that possible?
Does that make sense?
It does make sense, but also the heat can affect
the accuracy of the sensor itself.
Ah, okay.
So that could be it too.
But yeah, basically what it allowed me to do is to make a few adjustments in terms of
foods that I eliminated or eat less of, food ordering within a meal.
And I find that I'm very susceptible to, if I don't include enough fat, dietary fat in
the meal, then my blood glucose spikes, even if it's just like tuna, right?
But by including olive oil and other things,
it really blunts it.
And of course here, we're doing correlative anic data,
but for me, I felt far better
when I included a bit more fat
and when the food order was adjusted
the way I mentioned before,
always including a little bit of fiber really helped. And that makes sense, right? Slowly absorption of the food order was adjusted the way I mentioned before, always including a little bit of fiber really helped.
And that makes sense, right?
Slowly absorption of the food presumably.
So I found that it was a very valuable experiment for me.
Again, this isn't an advertisement.
It just so happens I did this and really benefit from it.
What are some other things that one can learn from continuous monitoring of blood glucose?
What are some things to watch for that might signal a problem? And what are some fun things that
one could do to explore an experiment? Because I like to explore an experiment.
Yeah. Well, I mean, a lot of the things that you just naturally learned are the things
that have been shown in data. And like you said, some of this data, it's like small studies,
small groups of people. But for instance, adding fat and fiber to meals
has a significant and repeatable impact in populations
on lowering glucose response.
Fat, probably in some part due to slowing gastric emptying
and actually slowing the digesting process,
so the rise in the bloodstream is going to slow down.
And then fiber, both for that reason,
but also because fiber can, in a sense, create a mesh blocking the absorption of some of the glucose that's in the meal.
So literally, actually preventing you from absorbing all of the carbs. And we've actually
seen that in the levels data set, that the more fiber people include with their meals,
we see essentially a direct relationship with lowering of their glucose excursions, which
is really exciting because fiber is something
that you can add to meals very easily.
I put basil seeds, chia seeds, hemp seeds,
flax seeds on a lot of my food at this point
because it's essentially a little bit of fat, a lot of fiber,
and it just helps you get more from your meal.
So what you can learn.
So I think step one, the way I think about a glucose monitor,
first of all, I'll say the purpose of the glucose monitor
is not to have to game the system and get flat glucose.
The purpose of the glucose monitor is curiosity.
It's to start to understand how it's essentially
an MRI for how all of our different dietary and lifestyle
strategies are creating this readout of glucose
in our body, which I think can be really interesting.
And in a world where so many cards are stacked against us
with diet and lifestyle and where
there's a lot of confusion about what's right for us,
that can be very helpful in actually reducing
the confusion and the cognitive load of our choices.
We know that keeping your blood sugar
through the course of a lifetime in a low and healthy range.
So I don't mean up and down spikes during the day,
but keeping your blood sugar healthy
throughout the course of your lifetime
is probably the best thing we can do for longevity,
staying insulin sensitive, staying out
of the diabetic range.
And so one thing that the glucose monitor does for us
is just give us more awareness and agency
into what the trends of our glucose are over time,
as opposed to a literally one data point snapshot once
a year in the doctor's office, which is what the majority of us are used to.
I really love the idea that people
who are able to wear glucose monitors every now and again,
maybe once a year, maybe more than once a year,
they know what their glucose is.
And so they're never going to walk into a doctor's office
and have a bomb dropped on them about pre-diabetes or
type 2 diabetes because you have the data, which is ultimately, I hope, the world that
we can move towards for a lot of biomarkers.
So you can see trends over time, which I think is very valuable.
One thing that's fascinating in terms of early prediction of metabolic disease is that you
can see how long it takes your glucose to come down after a meal.
So in a normal, healthy, insulin-sensitive body, even if the glucose goes way up, it should
come way down very quickly because the insulin is binding to insulin receptors and the glucose
is getting taken up and it'll lower.
What is quickly over the course of?
It should be down by two hours, but from what I've actually seen in our like most insulin-sensitive
people and also in research that looks at young healthy populations, you should basically be spiking
and coming down spike about 45 minutes and come down hour and a half, 90 minutes to two
hours. But if this is after sorry, after last bite,
after last bite, although it's hard to kind of exactly know. But yeah, meal is over, I
would say about 45 minutes to go up to the peak and then start coming down very quickly.
Now, if you start to see that glucose is going up
and then trailing very slowly back down to normal,
maybe taking more than two hours, three hours,
that is going to be one of those early indicators
of potential insulin resistance.
Your body's not clearing the glucose, but that's
not a metric that we use in standard practice at all. And I've actually seen myself very insulin
sensitive. My insulin is like 2.5. And if I don't sleep and I am stressed and I have been sitting,
my glucose will take way longer to come down. I have become transiently insulin resistant.
So I think that's just fascinating to see that.
What that ultimately, the metric that we call that
is area under the curve.
You want a low area under the curve, AUC,
after a glucose spike.
So you want to spike and come down quickly.
If you shade the area under the curve, it's a small amount.
If you go up and then trail off for two to three hours,
that's going to be a lot of shading under that curve.
And high AUC is associated with insulin resistance, basically.
Another thing that you can see is essentially
glycemic variability.
And glycemic variability, GV, is a metric
of how spiky your curves are.
Fasting paper out of Michael Schneider's lab
at Stanford in 2018 called,
"'Glucotypes Reveal New Patterns of Glucose Dysregulation'."
Totally landmark study, but basically they put
conclusive glucose monitors on non-diabetic individuals who by standard criteria
of diabetes do not have diabetes.
And he showed that on a CGM, a continuous glucose monitor,
you have these low variability people that are pretty much
flat throughout the day with little teeny, little teeny
rolling hills after their meals.
You have moderately spiky people,
and then you have very spiky people
who are going up down, up down, up down, up down.
When you correlate those different patterns
of glycemic variability in non-diabetic people,
you find that the spikier they are,
the worse their biomarkers are metabolically
across the board, insulin, triglycerides, et cetera.
So basically, they're showing signs
through variability of underlying dysfunction
that you would never know from
a standard test.
Those are the people who I imagine are probably going to go on to develop diseases, and yet
based on standard criteria, their doctor's telling them that they're fine, that they're
all the same.
So he also showed in that study that non-diabetic individuals, when you have a CGM on, are going
into the diabetic range and the pre-diabetic range a fairly significant amount and we would never know that if you weren't
actually tracking like a movie of the glucose. So that's so
glycemic variability, area under the curve, those are two things. Another really
interesting thing you can know from a CGM is dawn effect. So dawn effect is
basically a term in the literature for how high your glucose rises
right when you wake up in the morning.
I don't know if you noticed this when you were wearing a CGM, but some people notice
that the second they wake up, their glucose jumps up 5, 10, 20, 30 points.
What's happening here is that the cortisol awakening response to actually get you to
wake up and get out of bed, that cortisol can cause you to dump a bunch of glucose from your liver because
it's basically saying stress hormone, cortisol, we got to get up, we need glucose to fuel
the muscles, let's dump a little glucose.
So it's normal, but what the research shows is that magnitude of Dawn effect is correlated
with insulin resistance.
So the more the dawn effect you're getting,
I think it can signal maybe the more stress you're under,
the more cortisol you have floating around,
how big your cortisol awakening response is.
But also if you imagine if you're dumping all
that glucose from your liver and your cells aren't taking it up
well because you're insulin resistant, that response,
that dawn effect is going to be higher.
So I don't have the numbers right in front of me,
but typically I would want to see a dawn effect, I think,
of less than 10 points.
So you wake up and you may very well see a rise.
This is absence of any food yet.
And you do not want to see that going up 20, 30, 40 points.
Some people see a little bump again
with caffeine in the morning because it's more cortisol.
And so that's another thing that standard stuff would never tell you.
So those are kind of some of the looking at early predictors of metabolic dysfunction.
More of the fun stuff is like actually just figuring out like how is food affecting your
body and this is where people really enjoy it and like figure out like, oh my God, this food that I thought was healthy is actually not, you know, serving me. And actually,
a lot of people I think who are trying to make healthy choices, my boyfriend, like he, when we
started dating, he started using levels, his healthy snack, he worked in Venice, would be to
go to Moon Juice and get, oh gosh, I don't want to throw Moon Juice onto the bus here.
But he would get like,
They have some tasty stuff there.
They do.
But he would get this green juice
that was sweetened with dates.
And it was like $9.
And this was like the healthy choice.
And he saw the second he put on levels
that it was causing a huge spike, like 50, 60, 70 points.
And then he was crashing.
And he was actually trying to make a good decision.
So now he's swapped his snacks out
for more grass-fed cheese and some flax crackers and maybe
a venison stick or something, like grabbing ghost stuff that
isn't spiking as glucose.
But I think it can help people figure out
which foods are doing what I want them to do
and which maybe aren't.
And same thing happened for so many of our members
with oatmeal.
Unfortunately, instant oatmeal is one of the biggest
spikers in our data set for breakfast.
And a lot of people are making that choice
because they think it's heart healthy.
And in many people, it's actually
causing a big glucose excursion and crash.
And then in some other people, it's not.
And so it's really helping with what are the sneaky spikers,
and then where's the biochemical individuality?
And there was a phenomenal paper out of Israel
from SEL about seven years ago called Personalized Nutrition
by Prediction of Glycemic Responses.
It made big waves.
But it basically showed that you and I
could eat the same handful of blueberries
and have totally different glycemic responses.
So the idea of glycemic index as a certain amount of food
with a certain amount of glucose causes a certain glucose rise,
it kind of debunked that.
And that matters because repeated sustained
glycemic variability over time is not good for our health.
We want to choose the foods or balance the foods that
are going to keep us relatively more stable.
So that's very helpful, just understanding
your personal response to food.
And then what are the lifestyle strategies
that you can use sleeping better, walking after meals,
more resistance training, cold plunging, breath work that can actually serve to modulate the food
environment to actually reduce the glucose spikes? And people find that all of those things can
positively impact glucose spikes, especially the walks after the meals. But it's been fascinating
to see a lot of women,
especially menopausal women in our community,
who find that their glucose patterns are getting worse
because estrogen's dropping.
And that's going to really take a hit on insulin sensitivity.
They start resistance training.
Glucose comes kind of right back down.
So because of the monitor, they can
feel more confident in the intervention they've chose to do to help back down. So because of the monitor, they can feel more confident in the intervention
they've chose to do to help with metabolism.
And that kind of creates a virtuous cycle.
So those are some of the big things.
Those are big.
Can I mention one more?
Please.
I know I love that I just could obviously
talk about this all day.
I think it's fascinating.
But this is just one more that I think
is fascinating because this was a paper in Nature
from last year that talked about, and this may actually be one of the
most valuable things to people, which is that, again, talking about cravings, we all want
to get off the craving grip.
This paper in Nature showed that essentially when people spike their glucose with high
carb, high starchy foods, they'll often have a big crash afterwards.
And the reason for that is because a big spike leads
to a lot of insulin secretion, and then you
soak up all the glucose.
And sometimes you can actually go below your baseline.
So a small spike usually won't lead to a crash,
but a big spike often will.
That's called reactive hypoglycemia,
postprandial hypoglycemia.
A lot of people think they're dealing with hypoglycemia,
when in fact what they're really dealing with
is that they're spiking their glucose too high
and then they're crashing.
I see.
And the paper showed that the extent of post-meal dips,
the crash after the spike, was predictive of 24-hour energy
intake and cravings for carbohydrates.
And this makes sense.
If you crash low, that is a signal to your body,
we have to get our glucose back up,
and it will drive you to eat high-energy foods,
carbohydrate-rich foods and cravings.
So one of the best things we can do,
I believe from my personal experience,
from members' experience, and with some data to support this,
is that one of the adjuncts we can use
to monitor our, to manage our cravings
is actually to like lower the extent of our spikes
so that we crash less.
And so that was a fascinating study looking at CGM data.
That's interesting.
So the CGMs can reveal things,
not just in the immediate meal period,
but can relate to sort of downstream consequences.
Yeah, again, I found it to be tremendously useful.
I'm so glad you mentioned sleep, by the way.
I'm going to resist the temptation to rattle off
20 studies showing that.
Oh God.
You know, even having too much bright light in a room
while one is sleeping at night, even dim light,
which is, you know, I don't want to scare people
into thinking they have to sleep in complete darkness,
although an eye mask can be great,
can alter morning blood glucose levels in,
I believe it was adults and kids as well,
as a study in proceedings
in the National Academy of Sciences.
I have to go back and check if it included kids,
but pretty striking.
And then there's something very clear about the fact
that when people get the early night sleep
of four to five hours,
but then don't get the REM dominating,
last hour or two of sleep in the morning
that resting blood glucose is altered.
It's so interesting to think
about what's going on in sleep.
There's at least one paper that I'm aware of
where they had people breathing into a tube during sleep
to measure what sorts of metabolism they were undergoing.
And it's interesting, during a full night's sleep,
all of us seem to transition
between different forms of metabolism.
I'll send you this paper.
It's really cool.
And I'll put a link to it in the show note caption
such that at one portion of the night,
we're relying more on, let's just call it sugars
for sake of simplicity.
Other times we're more ketone dominant.
There's a market shifts in metabolism throughout the night.
It's almost like the brain and body cycle
through all the different modes of metabolism
throughout the night.
And then almost like a rehearsal of the metabolic pathways.
If we can anthropomorphize a bit here.
But then if sleep is truncated,
it clearly has an effect on daytime fuel regulation.
Just so interesting.
So getting sufficient sleep,
getting quality sleep is absolutely key.
There's a lot for people to pay attention to,
but you've given us a lot of tractable avenues
for people to do that that are mostly behavioral.
There's a few don'ts, but mostly some dos.
We haven't mentioned that, you know,
you don't need to even perhaps belong to a gym.
It's like, and with the cold exposure thing,
I always say, you know, if anything,
it'll save you money on the heating bill.
So there's a literally potential negative cost there.
I think levels in other CGMs are really interesting
and valuable to experiment with.
What sorts of other stuff is going to soon be monitored in our blood?
Because for instance, I would love to know
continuous hormone levels,
lipid levels, blood sugar levels.
I mean, are we moving past just blood glucose
and are there soon to be other things in these monitors?
So that when we, and by the way, if you haven't used these,
it's really cool.
You just take your phone, you scan it over the sensor
and then it basically gives you a chart graph
of what's going on in your bloodstream.
And now they're all, the latest gen of each of them
are all Bluetooth now.
So no more scanning, which is kind of nice.
And the answer is yes.
There are several different analytes
that we're going to be able to track.
And Abbott, which is one of the three main manufacturers of CGMs, has announced that
they have a new product called the Lingo, which is going to actually be able to measure
ketones, lactate, and alcohol continuously, which is pretty interesting from a comprehensive
metabolic standpoint.
Different sensors for each, not all in one, so I think we'll have to like polka dot ourselves if
we're tracking all those things. And then Dexcom, which is the other main company that makes CGMs,
has just announced they're coming out with an over-the-counter non-prescription version
of a CGM called the Stellow later this year. So there's exciting things happening in the industry. And I really do think continuous monitoring,
it's going to expand to a lot of these other things
that you're talking about, hormones, et cetera.
And I mean, it really needs to.
I think that snapshots of dynamic system
are just never going to really be able to give us
a full picture on what's going on.
And what we really want to be able to do
to dig our way out of this healthcare crisis, I think, is empowerment individually and understanding
how this rapidly changing environment is affecting our own biology so we can make the targeted
choices to hopefully change the environment to be more conducive to cellular health.
And continuous monitoring is a closed loop biofeedback that can help us with that decision-making
and essentially predict failure of the system
rather than wait for failure of the system
before we do something about it.
So yeah, I think a lot's coming down the pipeline.
Love it. Yeah.
Let's talk a little bit about mindset.
This is a really interesting topic
that you include in your book.
We've had guests come on and talk about growth mindset. Stress can be about mindset. This is a really interesting topic that you include in your book. We've had guests come on and talk about growth mindset,
stress can be enhancing mindset.
I'm big on mindset because I'm interested
in how our cognitive reframing or cognitive framing
can just change the way our biology works
and vice versa, of course.
But you talk about mindset in a certain context
and one of the favorite passages around that
that I really enjoyed was the relationship between
kind of like trying to control everything and nature,
you know, and how getting into nature itself
can be valuable for us.
So maybe touch a little bit on mindset, if you will,
and what are your thoughts on nature,
literally getting out of doors?
Yeah.
So I think that mindset, and more broadly than mindset,
I think psychology and our relationship specifically
with fear and control, I think they're probably
the most under-recognized thing that is impacting
the metabolic health crisis, the chronic disease epidemic.
There has been data that's looked into this.
We know that there's studies showing that loneliness
impacts mitochondrial function and that loneliness
is a risk factor and stress is a risk factor in these things.
And something really fascinating actually with the CGM data
is that many people who wear a CGM,
I don't know if you saw this, but when you feel stressed,
it actually has a diabetogenic effect. It literally causes our blood sugar Many people who wear a CGM, I don't know if you saw this, but when you feel stressed,
it actually has a diabetogenic effect.
It literally causes our blood sugar to go up when we feel stress.
And that can be a fascinating unlock for people to realize, I kind of feel like I'm okay right
now, but my body is telling me something different.
It's telling me that biochemically, I'm actually releasing energy
stores from my liver, glucose, to fight some threat that I wasn't really aware of.
We definitely understand there's this link here, but it's certainly not made its way
into clinical practice. The way I think about it is that what we know about the cells, and
especially the mitochondria, is that the mitochondria are more than the powerhouse
of the cell.
They actually are a part of the cell that
is constantly tracking resources and threats
and are basically modulating energy resources based on that.
And the threats can be anything.
They can be a virus.
They can be, and this is all coordinated
through this thing called the cell danger response.
It can be a virus.
It can be a toxin in the environment.
It can be lack of micronutrients for the electron transport chain that it needs to do its function.
It can also be psychological threats because, of course, our psychological milieu translates
through nerves and hormones and neurotransmitters and our microbiome to affect our cellular
biology throughout our whole body, our cells cells hear every single thought that we're thinking through biochemistry.
And when a cell and a mitochondria are getting the message that there is a threat or something
to be afraid of, they are going to change metabolic function towards defense alarm threat response and away from repair,
homeostasis, building, essentially thriving.
And I think what's really maybe the most unnatural thing about our modern world, you know, the
food of course is unnatural.
70% is ultra-processed. But we also have this device in our hands, literally with us
all the time, streaming fear-inducing media
into our brains and eyeballs every waking moment of the day
if we let it.
So we're glued to our screens and our devices.
And right now, essentially, the traumas and fears
of 8 billion people all over an entire globe
are now ours to process.
And our cells and our mitochondria,
there is no escaping it.
They are going to respond to that.
And so I think a big part of the metabolic health conversation
is, how do we create a sense of safety in our bodies, no
matter what is happening outside of our bodies?
And this can come down to every person's journey will be different for this because the things
that cause a sense of threat or fear for any two people are going to be different.
And I think some of the main categories is, one, unresolved childhood trauma, like something
that I think is getting a lot more talked about these days.
But like what's embedded in our nervous system, these limiting beliefs and memories that are
really wired that create a sense of hypervigilance in us sort of all the time?
What's coming in through our devices, our phones, our computers, the media that we're
exposed to that's constantly giving a fear signal.
And I think on a broader level, a big Western one
that we don't talk about is literally
like existential fear of mortality.
We have a very despiritualized, very uniquely death-fearing
culture.
Like you look at other cultures, Eastern, indigenous,
the Stoics, they all had intense curiosity about death.
We talk about the cycles of life.
There's this real engagement with it
that we are so afraid of in the Western system,
to the extent that our entire health care system actually,
I think, we've built it around like we're not going to help
you thrive. We're just going to do whatever we
can to make sure you don't die. It's built in everywhere. And so we've got the devices,
we've got the childhood trauma, we've got the fear of mortality, we have a very horror system of
mental health care in the culture. And I think that through all these things, Americans are getting
crushed mindset and psychology wise. And that is a big, big trigger of our mitochondria,
essentially diverting resources towards defense, threat, and alarm rather than homeostasis building
repair. So again, it comes back to taking really honest stock of what
are the true fear triggers in our lives
across those and others and creating
a sense of safety in our minds and bodies
no matter what the external world looks
like, which may mean putting boundaries up to the media,
doing the therapy, doing the different modalities.
What I believe, and I talk about in the book,
getting back to the question about nature,
is one of the best things that we can do
is actually literally just go outside.
And it sounds so simple, but one of the most astonishing
stats I literally found in researching this entire book
was that the average American is spending 93.7% of their time indoors.
Wild.
93.7.
That's in a car or in a building.
So we are locked in these cages staring at fear-inducing media and our mitochondria are
like, what? I don't know where to channel my energy.
It's just short-circuiting, I think.
So many things happen when we go outside, as you know.
I mean, even what the vision system is
doing to our anxiety levels.
We are getting sunlight, which of course, for complex reasons,
is very helpful for our metabolic health separately, entrains our chronobiology,
and light from the sun is an incredible regulator
of our mitochondrial function.
But it also, it's our best teacher.
When we're out in nature and we really
look at how beautiful the world is and the cycles of nature,
we see the cycles of the
seasons and we see the awe of the sun and the trees and just all this alchemy that's
happening outside of us. We see spring to summer to fall to winter. We see the tides
moving in and out. Everything's in phases. And I think when we reflect and meditate on all the cycles and the polarities in nature,
night and day, cold and hot, new moon, quarter moon, full moon, all these things, it's actually
– it entrenches on a subconscious and conscious level that there is a fundamental harmony and
pattern to the world we're living in that is bigger than us and that is
fundamentally good and beautiful and we are locked inside of the four walls of
our house I think we get very scared we get very controllable and the system
wants it that way because when we are scared and when we are existentially
afraid we will literally do anything.
We will buy anything, do anything, watch anything that will in some way ameliorate that pain
that we're feeling.
And we will take any pill, we'll get any surgery, anything that makes us feel like we're controlling
this seemingly out of control situation.
And that's what drives us into all the dopamine loops,
the social media, the processed food, the porn, the gambling,
the alcohol, all of it.
It's all to ameliorate, I think, ultimately, fear.
And I think by actually really just spending a lot more time,
try and get that 93.7% down to like 50%, spend as much time as you can
outside.
We know that people who spend more time outside are metabolically healthier.
And I think it's for pleiotropic reasons.
But I think one of it is that it is the ultimate convincing of abundance and fundamental abundance
in our world and of awe, which I think is really the antidote to fear. And
that has a profoundly soothing effect on our psychology and the sense of scarcity that
drives a lot of the decisions that actually make us unhealthy. It's fundamentally rooted
in scarcity. And I think also when we realize we are part of nature,
again, going back to that Taoist statement,
we're a process, not an entity, realizing all the trees
around us.
And we take that walk, even in a city, we see all the trees,
all those plants, all those leaves
are making the oxygen that process,
that literally let us do oxyphosforelation.
And that sun and that leaf on the tree, the sun's energy is literally being stored in
the carbon-carbon bonds that the plants are generating in photosynthesis that ultimately
all metabolism is, is unlocking the potential energy stored from the sun to create the human
energy that lets us love and move and live and think and do all the things we love to
do.
And then it just becomes so obvious, like, of course we have to eat real food.
And of course we have to not poison our soil with pesticides.
And of course we have to care about the environment and we have to get outside and move and we
have to be in the sunlight during the day because we are the environment.
We are a process that's constantly in dynamic conversation with it.
And I think a lot of people will find that their health gets a lot better if they spend
radically more time outdoors.
And I think a lot of people might say, well, I can't.
I work on a computer.
And I'm like, you know, Rome is burning.
Like we're sick as hell right now.
We need to get creative.
Like move your computer outside, take a walking meeting,
open your mail outdoors, chop your vegetables
on your balcony at your apartment.
Like we have to find a way to connect back with our source,
understand that the world is abundant and harmonious,
re-entrench the belief in our connection
with nature and then let all of our dietary
and lifestyle strategies stem from that sense
of gratitude and awe and that will lead us right
where we need to go, which is a really, I think,
joyful experience of our health journey
that's rooted fundamentally in connection
rather than us being siloed from all of this,
which going back to the beginning of the conversation,
that's fundamentally what's wrong with the healthcare system.
It silos, and we have siloed ourselves
from all of the life giving things in our environment.
And that has ultimately led us to be very, very, very sick.
And we just, I think we gotta go back outside.
So that's one of the things,
but there's many other things we can do
to change those, our relationship with fear. But we can't change the world as a whole,
but we can change what happens inside our body in terms of how we respond to it. And
for our mitochondria's sake, we have to. We have to create a sense of safety in our bodies
for our mitochondria to do the work
we need them to do for health.
I love it.
And I love it for many reasons.
I think it was my, I know it was my friend
and former guest on this podcast, Rick Rubin,
who several times early in our friendship,
he said, back to nature, the only truth.
And I asked him what he meant by that. he said, back to nature, the only truth.
And I asked him what he meant by that. And, you know, cause Rick can be a little bit
cryptic sometimes, not always, but sometimes.
And what he was saying is, you know, it's a real thing.
You know, you can immediately feel the connectedness
between the human experience and life of other types,
plants, animals, sunlight,
the circadian rhythms and the rhythms of light and dark
because they impact us so powerfully.
I mean, if there were ever a force in the world
that impacts how we feel, it's the circadian rhythm,
it's the rising and setting of the sun,
it's the impact of light and dark,
and then all the other things that you talked about today.
I can't help but reflect on kind of your take
on kind of what a lot of, not all,
but a lot of modern society attempts to do.
It attempts to do a lot of good things too, I believe.
I'm a believer in technology,
but that if I were to translate,
it sounded like what you were saying is that
it gives us a sense
of loss of control by instilling fear.
Like we don't have control.
And then there are a number of,
let's just call them programs in the world
that then sell back the illusion of some sense of agency,
little by little, right?
Temporary agency, and then puts you back into the cycle.
And there's something about going into nature,
which just removes one from all of that,
at least temporarily, gives you a more basic understanding
of the relationship to self and things around us.
Even just looking, being able to see it to a distance,
we know is powerful for the brain, reducing anxiety.
We know being outdoors for two hours or more per day
reduces myopia and nearsightedness.
This is independent of all the other effects
of circadian rhythms, et cetera.
Anyway, and on and on.
So I second and third,
and hear all the statements you made before.
I also just have to say,
I really appreciate how you are able to tackle
the cellular biology, the molecular biology, the macroscopic things
that we can all do, walking, resistance training,
cold exposure, sleep, high intensity interval training
and make a case for each and all of those
as it relates to the underlying biochemistry.
And weave all that together in a way that then
you beautifully wrapped into
this idea of connecting to nature and not divorcing ourselves from modern life, but
really looking at the ways in which certain components of modern life are really making
us sick.
Not just the behaviors, not just the do's and the don'ts that it's kind of imparting
on us, but also kind of the psychology around it.
It's that it is quietly but powerfully oppressive is the message that I'm getting.
And that we have to take a stand against it.
And the way to take a stand against it is to do
what are very basic and fairly easy to access things,
making better choices about food, timing, quality,
amount, exercise, and on and on.
So, I'm running long in my response
to your much more eloquent description of mindset.
But what I want to say is on behalf of myself
and everyone listening, I so appreciate,
we appreciate the work that you're doing
to be a medical doctor specialized in one of these silos
and then to take a step out and say, nope, not me.
I'm going to do what I see as best for the greater good
in terms of giving people tools, giving people a sense of agency and autonomy to take control of their health.
This is in some ways a heretical idea, but luckily the numbers of folks like you are
growing and you're a real leader in this field by example and by the incredible work
you're doing with technology and information sharing.
Love love love the book. I did doing with technology and information sharing. Love, love, love the book.
I did go through it front to back.
I haven't tried the recipes yet,
but thank you for bringing the blueberries.
I'll try the recipes, at least one of them.
And I just want to thank you for sharing what you do
and for continuing to do what you do.
We need it and we appreciate it.
So thank you.
Thank you.
Thank you for joining me for today's discussion
about metabolic function with Dr. Casey Means.
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