Huberman Lab - Diet & Nutrition for Mental Health | Dr. Chris Palmer
Episode Date: November 21, 2022My guest this episode is Chris Palmer, M.D., a board-certified psychiatrist and assistant professor of psychiatry at Harvard Medical School. He explains the important connection between nutrition, met...abolism and mental health and his pioneering work using the ketogenic diet to successfully treat patients with various mental illnesses, including depression and schizophrenia. Dr. Palmer explains how the ketogenic diet is an evidenced-based treatment for epilepsy, mimics the fasted state and can offset the cognitive decline in Alzheimer’s. He describes the key roles of mitochondria in mental health, how certain conditions likely arise from mitochondrial dysfunction, and how low-carbohydrate diets increase mitochondrial turnover to improve mental health. He also explains how low-carbohydrate diets positively impact the gut microbiome and weight loss, important risk factors for mitochondrial health such as marijuana and alcohol, and the best way to increase circulating ketones depending on individual needs. We also cover how a ketogenic diet impacts mood, sleep, and fertility. Dr. Palmer’s work stands as a revolutionary approach to mental health and disease that, given the prevalence of mental health challenges, should be of interest to people of all backgrounds and ages. For the full show notes, visit hubermanlab.com. Thank you to our sponsors AG1: https://athleticgreens.com/huberman LMNT: https://drinklmnt.com/hubermanlab Waking Up: https://wakingup.com/huberman Momentous: https://livemomentous.com/huberman Timestamps (00:00:00) Dr. Chris Palmer, Mental Health & Metabolic Disorders (00:03:42) Sponsor: LMNT (00:07:18) Nutrition & Mental Health (00:20:43) Low-Carb Diets & Anti-Depression, Fasting, Ketosis (00:27:52) Schizophrenia, Depression & Ketogenic Diet (00:33:58) Sponsor: AG1 (00:35:38) Psychiatric Mediations, Diet Adherence (00:42:35) Highly Processed Foods, Ketones & Mental Health Benefits (00:46:51) Ketogenic Diet & Epilepsy Treatment (00:56:10) Ketogenic Diet & Mitochondria Health (00:57:05) Nutrition & Benefits for Neurologic/Psychiatric Disorders (01:05:44) Mitochondrial Function & Mental Health (01:15:12) InsideTracker (01:16:23) Mitophagy, Mitochondrial Dysfunction, Aging & Diet (01:25:09) Neurons, Mitochondria & Blood Glucose (01:31:54) Obesity, Ketogenic Diet & Mitochondria (01:40:00) Mitochondrial Function: Inheritance, Risk Factors, Marijuana (01:46:34) Alcohol & Ketogenic Diet (01:55:21) Brain Imaging, Alzheimer’s Disease & Ketones (02:01:05) Exogenous (Liquid) Ketones vs. Ketogenic Diet (02:06:27) Neuronal Damage, Ketones & Glucose (02:10:16) Alzheimer’s Disease, Age-Related Cognitive Decline & Ketogenic Diet (02:23:45) Ketogenic Diet & Weight Loss (02:35:47) Ketogenic Diet & Fasting, Hypomania, Sleep (02:46:37) Low Carbohydrate Diets, Menstrual Cycles, Fertility (02:52:23) Obesity Epidemic, Semaglutide & GLP-1 Medications (03:01:01) Zero-Cost Support, YouTube Feedback, Spotify & Apple Reviews, Sponsors, Momentous Supplements, Neural Network Newsletter, Social Media Disclaimer Learn more about your ad choices. Visit megaphone.fm/adchoices
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.
Today my guest is Dr. Chris Palmer.
Dr. Chris Palmer is a medical doctor specializing in psychiatry at Harvard Medical School.
He is the world expert in the relationship between metabolic disorders and psychiatric disorders.
He treats a variety of different conditions, including psychosis, including psychosis, including
schizophrenia as well as attention deficit hyperactivity disorder, obsessive compulsive disorder,
anxiety disorders, and depression, among others. He is best known for understanding the relationship
between how metabolism and these various disorders of the mind interact. And indeed today, he describes
not only his own fascinating journey into the field of psychiatry, but also his clinical and
research experience using diet, that is different forms of nutrition in order to treat
various psychiatric disorders. He describes some remarkable case studies of individuals and groups
of people who have achieved tremendous relief from the types of psychiatric disorders that I just
mentioned a few moments ago, as well as new and emerging themes as to how metabolism and the
mind interact to control things like obesity. Indeed, he raises the hypothesis that perhaps obesity
in many cases is the consequence of a brain dysfunction as opposed to the consequence of a
metabolic dysfunction that then impacts the brain.
During today's episode, he shares with us
his overriding hypotheses about the critical roles
that mitochondrial function and dysfunction play
in mental health and mental illness
and how various particular types of diets,
ranging from the ketogenic diet to modified ketogenic diet
and even just slight adjustments in carbohydrate intake
can be used in order to change mitochondrial function
and bring relief for various psychiatric illnesses.
He also highlights the essential and important theme
that various diet interventions, including the ketogenic diet,
were not first developed for sake of weight loss,
but rather were developed as treatments
for neurologic conditions such as epilepsy.
Today he shares with us how the foods that we eat
a lone ending combination and how fasting,
both intermittent fasting and more lengthy fasts,
can interact with the way that our brain functions
to strongly control the way that we think, feel, and behave.
What's wonderful is that
that Dr. Palmer not only explains the science
and his clinical expertise,
but also points to various actionable measures
that people can take in order to improve their mental health.
I'd like to mention that Dr. Palmer is also the author
of a terrific new book.
The title is Brain Energy,
a revolutionary breakthrough in understanding mental health
and improving treatment for anxiety, depression, OCD, PTSD, and more.
I've read the book and it is a terrific read.
I came away from this book with a much evolved understanding
of how the various psychiatric disorders
that I just described as well as ADHD emerge in people.
And it has completely revised my understanding
about the possible origins of various psychiatric disorders
and the best ways to treat them,
including both with medications,
but also with nutritional approaches.
If you'd like to learn more about Dr. Palmer's work
and the book, please go to chrispalmermd.com.
We also provide links to the book
and to his website in our 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
for the general public.
In keeping with that theme,
I'd like to thank the sponsors of today's podcast.
And now for my discussion with Dr. Chris Palmer.
Chris, Dr. Palmer, thank you for being here.
Thank you, Andrew, for having me.
I have a lot of questions for you.
And I'm really excited about this topic
because I think most people know what mental illness is
or they have some idea what that is.
Most people have some idea what nutrition is.
Fewer people certainly know how closely those things can interact.
And I think everybody is familiar with the feeling of a food or the ingestion of a food,
making them feel good in the short term.
We eat a food that tastes delicious to us or that we associate with something nice and we feel good,
mentally and physically.
Whereas when we eat something that gives us food poisoning or maybe even something that's just
doesn't taste that great or that we associate with a bad experience, we feel less good in the
short term. But I believe that very few people understand or are familiar with the fact that
nutrition and our mental health interact in this very intimate, maybe even causal way.
And that is something that occurs over long periods of time, meaning what I ate yesterday,
the day before, maybe even 10 years ago could be impacting the way that my brain
and body are making me feel now. So if you would, I'd love for you to just tell us about a little bit of
the history, in particular your history, with exploring the relationship between nutrition
and mental health. And then we can dive into some of the more particulars of ketogenic diets
versus other diets and some of the truly miraculous findings that you and others are coming up with
based on real patients and real experiences of people who suffer and then find relief by altering their nutrition.
Sure.
You know, this story really starts with my own personal story.
And I don't need to go into great detail, but to set the stage, when I was a kid, I definitely had mental illness.
Started with OCD.
A series of events happened in my family.
my mother had a horrible kind of psychotic break and all sorts of adverse childhood events for me.
She and I were actually homeless together for a while.
I went on to have subsequent depression, suicidality, all sorts of things.
Somehow or another, I pulled myself together and got through medical school,
actually did quite well in medical school, got an award for being one of the top students.
and then was doing my internship in residency at Harvard.
And at that point in time, I was diagnosed with metabolic syndrome.
So I had high blood pressure, horrible lipids, and pre-diabetes.
And I was doing everything right, supposedly.
I was on a low-fat diet, and I was exercising regularly.
And year after year, my doctor kept telling me, diet and exercise,
I kept asking him what diet, what exercise.
I was doing everything.
He kept telling me to do.
Everything was getting worse.
My blood pressure kept going higher.
And at some point, he kind of said,
you're going to have to go on medication.
I need to put you on something for your prediabetes,
something for your cholesterol,
and something for your blood pressure.
So three pills out of the gate.
And I'm like, I'm only my 20s.
Were you overweight?
No.
Technically, no.
I had a gut, so, you know, that's a sign of insulin resistance.
I know now.
I didn't know it then.
But, and he actually kind of leaned in at one point and said, you know, do your parents have diabetes?
Yeah.
Do your parents have high blood pressure?
Yeah.
Are your parents overweight?
Yeah.
Oh, I'm really sorry.
It's genetic.
Basically, you're screwed.
It's your genes.
You're just going to have to bite the bullet and take meds.
And as a physician, I knew what that meant.
I knew that I'm in my 20s.
If I'm already on three meds for metabolic syndrome,
I'm going to be screwed by the time I'm 40 or 50,
and I'm probably going to be having heart attacks.
And I'd heard through the rumor mill that the Atkins diet
could somehow help people improve their cholesterol
all in pre-diabetes.
I actually didn't really believe it.
I was highly skeptical.
And I, you know, I believed everything I was taught in medical school.
Why would my professors lie to me?
They knew what they were talking about.
Low-fat diet was the thing to do.
And the Atkins diet was clearly dangerous and reckless.
And but I had been trying the medical dogma for years and it wasn't working for me.
And so for whatever reason, I decided this is going to be my last.
attempt at something different.
And then I'll just bite the bullet and go on meds.
So I try the Atkins diet.
I did my own special version of it.
I still avoided red meat because I was terrified of red meat.
I tried to do a healthy version,
which is probably more like the South Beach diet.
This was before the South Beach diet was invented.
But within three months, my metabolic syndrome was completely gone.
So blood pressure normalized, lipids normalized. Did your weight change? You mentioned that you were
of healthy weight, but that you had a bit of abdominal fat. So I lost the abdominal fat. I probably lost
about 10 pounds through this process. But everything got normal. And when I went back to my doctor,
he was shocked. He actually said, what the hell are you doing? During the time before you switched to
this new diet, how was your mental health, if you don't mind me asking? Because it sounds like
you're very clear that there was metabolic syndrome or you were headed towards more severe
metabolic syndrome. You mentioned OCD. I actually am familiar with this as a kid. I had a low-level
kind of Tourette's grunt and probably obsessive still to some extent, although not full-blown
clinically diagnosed OCD. So I can relate somewhat. If you're willing, what was the context of all
that before and after this nutritional switch.
So before the nutritional switch, I was still struggling with low-grade depression and OCD.
I, again, it wasn't necessarily interfering with my ability to function because I was functioning
at a high level.
I mean, anybody looking from the outside, you're a top student.
you just got into one of the most competitive,
actually at that point it was the most competitive
residency program in the country
for psychiatry.
So they would have looked at me and said,
you're fine, but I wasn't.
I was actually on medications.
I was trying different medications,
trying to figure out how to feel better,
how to stop obsessing so much,
how to not be so depressed.
And I found that those medications,
they actually came with more side effects
for me than benefits.
I was on Prozac for a long time.
It totally messed up my sleep.
And then the psychiatrist was like,
you need pills to help you sleep now.
And I'm like, that doesn't,
that's not really resonating very well with me.
And I'm now a psychiatrist.
I'm in my psychiatry residency.
And I'm thinking, you know what?
That's just not sitting well with me,
that you're going to prescribe more and more meds
for all the side effects that you're causing.
And yet at the same time,
I wanted to feel better.
And I was learning.
chemical imbalances, this is what we do to get rid of depression and OCD, you're supposed to
take your pills, and so I was taking my pills. I was in psychotherapy. I had been in psychotherapy
on and off for years. I had received much more intensive treatment when I was younger,
and that was essentially worthless for me. It actually probably just caused harm at the end of the day.
Psychoanalysis? Various psychotherapies, not psychoanalysis,
per se, but some of them were psychoanalytically oriented psychotherapies,
was actually hospitalized at one point,
had been put on lithium and amypramine,
which is a tricyclic antidepressant and other things.
And they were actually horrible.
They were horrible.
They did nothing beneficial for me.
I gave them a decent amount of time to work.
I really wanted to feel better.
So at the time that I tried this diet, I certainly wasn't impaired in the same way.
I wasn't struggling that much, but I still had these low-grade symptoms, was trying to feel better.
And the thing that was the most striking to me after doing the diet for three months was not the fact that my metabolic syndrome was gone.
That was my goal, and it was seemingly miraculous.
achievement because I got rid of everything with one dietary change. But the thing that I noticed
was dramatic improvement in my mood, energy, concentration, and sleep. I, for the first time in my life,
I started waking up before my alarm went off and feeling rested. That never happened to me before.
I was meticulous about planning when my alarm went off
and how many times I could push the snooze button
in order to be on time for wherever I needed to be,
whether it was school or the hospital or whatever.
I had this good system.
I was never late for anything,
but that was shocking to me that I felt so good.
And, you know, one of the things that I've often said to people,
prior to the diet,
I always felt like there are two types of people in the world.
There are halves and have-nots.
There are these happy, peppy people
who just are so positive and they've got energy,
and they have the saying.
They like to work hard and play hard.
And I always understood working hard.
I totally got that because I was a hard worker
and I understood the value of hard work.
and you got to do something useful with yourself.
But I never understood who the hell wants to play hard.
Like who's got energy for that?
Like, aren't you tired from working so hard?
How on earth do these people have energy to go and play hard?
And I assumed that they were just part of the halves in the world.
And they were just lucky and privileged.
They either had good genetics,
or maybe they had good childhoods or good parents or something something that I didn't have.
The kids with genuine smiles in the yearbooks.
Yes, exactly.
Whereas the rest.
And by the way, I really appreciate you sharing some of your personal story because I think it is very important for people to hear and understand that people like yourself who are extremely high functioning and accomplished that the road.
was from everything I'm hearing and understanding very choppy internally at times and that you've
overcome a lot in order to get there. And also have been going through what sounds like a very
long iterative process of trying to figure out what works and what doesn't work to finally
arrive at a solution and then make that the basis of much of the work that you're doing today
for other people. I think it's very important because I think many people share with you this
notion that there are indeed two groups, a happy group and then faded to be unhappy group.
And it speaks to the fact that your story, rather, speaks to the fact that what we see is not
always what's going on internally with people.
And that this notion of there just being two groups, the happy or the haves and the have-nots
can't be the way that it works.
And there are probably many more people suffering than we realize.
and that there is an important need for tools
to overcome that suffering.
So I really just hear even early in our discussion,
I just wanna extend a genuine thanks
because so much of what I hear from people
is questions about health and mental health
and physical health,
but that clearly point to the fact
that many people are struggling to varying degrees.
And even the people who are in this category
of great childhood and happiness
could do far better for themselves
and then also for other people.
So thank you for that.
I want to know at the point where you realized that nutrition can play a profound role in how you feel and operate in a large number of domains, you were still a student or a resident at that point?
As a resident.
At that point, did you decide that you were going to explore this in a professional context?
Not yet.
Okay.
So what was the journey forward into the work that you're doing now?
So the next step was that I just had friends and family who saw me,
saw that I had improved my health, saw that I lost some weight pretty easily.
In particular, I remember like my sister and sister-in-law,
they got really pissed at me one Thanksgiving because I could resist all the pumpkin pie
and apple pie and everything else.
They were like, how the hell are you doing that?
How are you resisting all of this food?
And I said, I don't crave it anymore.
I don't want it. I'm fine. I'm having turkey and green beans, and that's good enough for me.
So I got them to do the diet, and they too noticed dramatic improvement in their moods and energy and sleep and everything else.
So within a few years, the primary thing I noticed is this powerful antidepressant effect.
And now I'm, you know, an attending physician. I've got all.
All these patients in my clinical practice with treatment-resistant mental illness, I'm in a tertiary
care hospital, so I almost never get somebody off the street with their first episode of depression.
Out of the gate, as part of my career, I get treatment-resistant mental disorders.
So I get people who've already been to six-plus psychiatrists, therapists.
They've usually tried dozens of different medications.
They've been in decades of psychotherapy.
They've often had ECT and other things.
and nothing's working.
And I'm thinking, you know, well, we're kind of out of options for these other people
and this diet is having this really powerful antidepressant effect.
I think I'm going to try it and just see if any of my patients are game to try it
to see if it might help them.
Sure enough, it did.
Didn't help everyone and not everybody was interested and or able to do it.
But some of the ones who were able to do it ended up having a remarkable
and powerful antidepressant effect.
One woman actually became hypomanic within a month,
and she had been depressed pretty much nonstop for over five years,
chronically depressed, suicidal, in and out of hospitals.
And I saw her become hypomanic, and I'm thinking,
wow, this really is a powerful antidepressant effect.
Like, this is amazing.
This is like a medication, but better because it actually is working for her.
but I laid low at that point
because at that point
we didn't have many clinical trials
of the safety or efficacy of the Atkins diet
for even weight loss or diabetes
let alone any mental disorders
and so I really actually felt like I'm on the fringe here
and this is not going to be met with praise by anyone
so I'm just going to lay low
I'm going to offer it to patients
And I went along that way up until 2016.
I may just ask about the diet.
When you say Atkins diet, so this is low to zero starch, so low carbohydrate diet,
certainly low sugar.
Yeah.
And was it traditional Atkins?
Were you tailoring it to the individual patient,
depending on their psychiatric symptoms, whether or not they were overweight or not overweight.
I'm assuming you're not a nutritionist.
So how did you prescribe a nutrition plan for your patients?
And what was involved in making sure that they adhered to that?
Maybe even some of the things you observed in terms of who was more willing to try this or not try this.
Any observations or even data?
So early on I was winging it.
And I was, you know, the first few patients, it was try this Atkins diet.
I want to see ketosis.
So I was going for ketones.
So they were pricking their finger and they were doing a blood ketone test?
I didn't know about blood ketone monitors if they existed back then.
So I was, we were using urine strips.
Which are not quite as accurate, but still useful as a general guide from what I understand.
Is that right?
Absolutely.
And so, so I was.
strongly recommending that patients achieve urinary ketosis. And the interesting thing is I noticed a
pattern that when they were trying the diet and not getting ketones, they often did not get a
clinical benefit. It was once they got into ketosis that I began to notice the clinical benefit
and the powerful antidepressant effect. So probably any nutrition plan, aka diet, that
elevated ketones in the urine to the point where you would say this person is in ketosis,
or they would say, I'm in ketosis.
That was a step in the right direction, independent of exactly what they were eating or not eating
to get there, including fasting.
At that time, probably fasting wasn't as popular now, thanks to the incredible work,
I think it's incredible.
And he is a former colleague.
And I know there's a lot of controversy about fasting, but I think for many people,
fasting is a powerful tool for others.
less useful tool, but of Sachin Panda and others.
But fasting certainly will limit your carbohydrate intake and get you into ketosis, correct?
It will.
Did you have any patients fast or do intermittent fasting?
I did.
And I had some patients who did what Atkins had called a fat fast where they eat primarily fat.
So they either fast and or they eat primarily fats to try to get.
into a state of ketosis. So for some patients, it was actually quite easy to get into ketosis,
especially overweight and obese patients. They have a lot of fat stores on their body,
and actually limiting carbohydrates usually results in high levels of ketosis for them.
And they probably feel better, too, I imagine, because when we limit our starch intake,
we start to excrete a lot of water. People can get some pretty quick weight loss,
that even though it may not be fat loss, makes them feel literally a little lighter.
and maybe a little more energetic.
Is that right?
Absolutely.
And as the years went on,
you know, the field was advancing.
More research was coming out.
People were getting a little more sophisticated
with blood ketone monitoring,
with different versions of ketogenic diets.
And I was evolving my practice.
The thing that completely upended
everything that I knew as a psychiatrist, though,
was when I helped a patient in 2016 lose weight.
So this was a patient,
33-year-old man with schizoaffective disorder.
He had been my patient for eight years now.
Could you clarify for people what schizoaffective disorders?
I'm not a clinician, but as I recall,
it's like a low level of schizophrenia,
so there might be some auditory hallucinations.
If I met this person,
I might think they're kind of different, quote-unquote, weird,
but they would not seem necessarily at the scary to me and typically to other people.
And I mean that with respect, of course, but oftentimes people with schizophrenia can seem just like you don't even know how to interact with them because their world seems so altered.
Because they have all these so-called positive symptoms, hallucinations, and they're talking to people that no one else can see, et cetera.
Is that schizoaffective?
So no, actually.
So schizoaffective is the same as schizophrenia, essentially.
The only difference is it's schizophrenia with superimposed mood episodes.
Oh, so it's actually more severe than...
It can be.
Okay, so I have it backwards.
So schizoaffective disorder is essentially schizophrenia plus some mood episodes.
Maybe I'm thinking of schizotipel.
Schizophren is the low-grade kind of mild paranoia or kind of eccentric beliefs and other things.
Okay.
So folks out there, I have my nomenclature backward.
Schizophrenia is the quote-unquote low-level schizophrenia or schizoid-like.
Schizoaffective is as or more.
Full-blown schizophrenia plus full-blown, usually bipolar symptoms.
And now it's absolutely clear who the clinician in the room is.
Thank you for that reminder.
No worry.
So this man had schizoaffective disorder.
He had daily auditory hallucinations.
he had paranoid delusions.
He could not go out in public
without being terrified.
He was convinced
that there were these powerful families,
that they had technologies
that could control his thoughts.
They could broadcast his thoughts to other people.
They were trying to hurt him.
They had targeted him for some reason.
He wasn't quite sure why.
He had some suspicions and beliefs about
maybe when he did this bad thing
when he was 11 years old,
that's why they decided to target.
him. This man was tormented by his illness, tormented. It ruined his life. He had already tried
17 different medications and none of them stopped his symptoms. But they did cause him to gain a lot of
weight. These are the medications, as I recall, for schizophrenia, the classical ones are dopamine
receptor blockers, cause people to huge increases in prolactin. That's why sometimes men will get
breast development and they'll put on a lot of weight and they'll be catatonic or
movement disorders.
It make you feel like, I have to imagine, given how good most things that release dopamine
make us feel that blocking dopamine receptors with antipsychotics makes people feel lousy.
Horrible.
And it's a huge challenge in our field because a lot of patients don't want to take them.
And then you get these rebound effects.
If patients are on them for several months and then they stop them cold turkey, they can get wildly psychotic and ill,
end up aggressive or hospitalized or sometimes dead.
So that's him.
He weighs 340 pounds.
And for whatever reason, he gets it in his head.
I'm never going to get a girlfriend if I don't lose some weight.
He also recognizes I'm never going to get a girlfriend because I'm a loser.
I'm schizophrenic.
I live with my father.
I have nothing going for me.
But I could,
least try to address one of these awful, horrible things about myself, and maybe I could lose
some weight. So he asked for my help. For a variety of reasons, we ended up deciding to try the
ketogenic diet. Now, at this point, I have no anticipation that the ketogenic diet is going to do
anything for his psychiatric symptoms, because this man has so effective disorder. That's not
depression. Depression is very different. They're totally different disorders.
So he decides to give it a try.
Within two weeks, not only does he start losing weight,
but I begin to notice this dramatic antidepressant effect.
He's making better eye contact.
He's smiling more.
He's talking a lot more.
I'm thinking, like, what's gotten into you?
Like, you're coming to life.
Like, I've never heard you talk this much.
I've never seen you so excited or present or alive.
I haven't changed his meds at all.
The thing that upended everything that I knew as a psychiatrist was six to eight weeks in.
He spontaneously starts reporting, you know those voices that I hear all the time?
They're going away.
And he says, you know, you know how I always thought that there were all these families who were controlling my thoughts
and out to get me and they had targeted me?
And I'm thinking, oh, yeah, we've been talking about that for eight years.
We could talk about that again.
he says
you know what
now that I think about it
I don't think that's true
and now that I say it it sounds kind of crazy
it probably never was
I've probably had schizophrenia
all along like everybody's been trying to tell me
and I think it's going away
that man went on
he's now lost 160 pounds
and kept it off to this day
wow
he was able to do things he had not been able to do since the time of his diagnosis.
He was able to complete a certificate program.
He was able to go out in public and not be paranoid.
He performed improv in front of a live audience.
At one point, he was able to move out of his father's home and live independently.
And that completely blew my mind as a psychiatrist.
and I went on a scientific journey to understand what in the hell just happened.
That is indeed mind-blowing.
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I have a couple of questions.
First of all, did he stay on any kind of antipsychotic or other men?
medication. If so, were the dosages adjusted, excuse me, while undergoing this remarkable transition.
Because as we know, it's not an either-or medication or nutrition changes. It can be both.
And then the other question is one of adherence. You know, I think about someone with
schizoaffective disorder who's suffering from all the sorts of things that you described.
How does somebody like that organize themselves in order to stay on?
on a ketogenic diet.
And I say this with all the seriousness in the world,
I think there are a lot of people who do not have
schizo-type or schizoaffective disorder
who have trouble, they claim adhering to a ketogenic diet.
It's not the easiest diet, certainly in its extreme form.
At first, it's not the easiest diet to stick to.
So how did he do it?
This sounds like a remarkable individual.
And I'd also like to just,
know your general thoughts about adherence to things when people are back on their heels mentally.
You know, how do they get motivated and stick to something?
So the questions were medication, yes or no, if yes, dosage adjusted, yes or no.
And if people are suffering from depression or full-blown psychotic episodes,
how does one ensure that they continue to adhere to a diet?
So in terms of medications, he has remained on medication.
So early on, I wasn't adjusting anything.
I was just in disbelief and shocked that this was happening.
I didn't know what was going on.
Over the years, we have slowly but surely tried to taper him off his meds.
He has been on meds for decades.
He started medications when he was a young child.
his brain is developed in response to all sorts of psychiatric medications.
And it has not been easy to try to get him off.
So we continue to try to get him off medication.
And it's challenging and difficult.
And I just want to say for any listeners,
getting off your meds is very difficult and dangerous.
And you need to do it with supervision,
with a mental health professional or a prescriber
because it is dangerous.
When people reduce their meds too much,
they can get wildly symptomatic.
Is that true for depression as well?
It's true for any psychiatric medication.
The brain makes adaptations in response to psychiatric medications.
And when you stop them cold turkey,
some people are fine,
but I wouldn't recommend finding out
because I've seen patients,
when they stop antidepressants,
I've seen patients get floridly depressed and suicidal
within three months.
I had one patient almost quit her job
because she became convinced that, you know,
well, my life sucks and it's all because of my boss,
and I know that she's just, you know,
a horrible human being and she's abusing me.
And I was like, whoa, whoa, whoa,
I think this is related to your medication change.
We got her back on her meds.
Within three days, she said, oh, my God, I can't believe that happened.
Like, I almost quit my job.
And that would have been the most illogical and irrational decision I've ever made in my entire life.
But somehow it seemed so real just several days ago.
And now that I'm back on this medication.
And it doesn't mean that she needs the meds,
but it doesn't mean that he needs the meds.
It means that meds need to be adjusted very safely and cautiously and gradually.
So that's the medication piece.
The adherence piece was not easy for him and for other patients.
It is very rare that I have a patient who I can say,
do the ketogenic diet, come see me in three months and let me know how it's going.
That almost never happens.
It has happened, I think, on two occasions.
But that is, if I understand correctly, what perhaps not you, but many psychiatrists do with medication.
It's, here's your prescription.
Let's talk in a month or three months.
Yes.
So that's a variable that is probably worth us exploring a little bit here as the conversation continues.
Absolutely.
You know, that frequent contact and making micro adjustments or macro adjustments to medication or nutrition could be meaningful.
Absolutely.
So with this particular patient, you know, early on he was actually pretty adherent.
I was seeing him once a week.
And so I could do a lot of education.
I was weighing him.
I was checking his ketones.
I was checking his glucose levels.
You know, at that point, I had a blood ketone monitor in my office.
So I knew whether he was compliant or not, which is so beneficial in doing clinical work and research on this diet.
It's the only diet where within seconds I can have an objective biomarker of compliance or noncompliance.
Such a key point.
And again, it brings to mind for me the parallel with medication, I mean a patient can say they're taking their medication.
And unless they're in a hospital setting where somebody's checking under their tongue and, you know, all of this, they very well could not be taking it or taking more.
and you and I both know that blood draws for neurotransmitter levels are complicated because you want to know what's in the brain and what's functional in the brain.
And I have to imagine that most people there are prescribed drugs for any number of different psychiatric conditions are not giving blood every time they talk to their psychiatrist or psychologist.
No.
No. And when we've looked at, you know, on that front, when we've looked at studies of compliance, the majority of patients are at least,
somewhat non-compliant with prescription medications.
It's not on purpose.
They forgot.
They take it at night.
They were out late.
They were off their routine.
They forgot to brush their teeth because that's when they take their meds.
And so because they, you know, it was so late, they just crashed when they got home.
They forgot to take their meds.
Happens all the time.
If it's a medication that people take more than once a day, the noncompliant,
rates are much higher because it's just easy to forget. So it's not that people are willfully,
you know, disobeying their doctors or anything else. It's just hard to remember to take meds
consistently every day. When you say measuring ketones, I want to drill into this a little bit
because it does seem that the presence of ketones and somebody being quote unquote in ketosis
turns out to be the key variable. Certainly in your book, that's what I, one of the major
takeaways, although there were many important takeaways, that people get into ketosis.
Do they have to stay in ketosis? So, for instance, I've followed the, I don't any longer,
but I've tried in the past the so-called cyclic ketogenic diet where every third or fourth
day get some pasta, rice, et cetera. And that, it's not, that was interesting as an experiment.
But to stay in ketosis, what sort of blood levels of ketones do you like to see in your patients?
What is the range that you think most people could aspire to?
So it really depends on the patient and what I'm treating, quite honestly.
So, and I don't think every patient needs the ketogenic diet.
For some patients, simply getting rid of junk food can make a huge difference in a mood disorder, for instance.
So a junk food meaning highly processed food, food they could last on the shelf a very long time.
Highly processed foods that are usually high in both sugar, carbohydrates and carbs and fats.
Those seem to be the worst foods. That combination, high sugar, high fat, seems to be the worst combination for metabolic health.
And lo and behold, we've got emerging data that strongly suggests.
it's also bad for mental health.
Depression and anxiety are the most common mental disorders,
and so we have the best data for those disorders.
But we actually have a lot of data with even bipolar disorder and schizophrenia
that insulin resistance in particular,
and insulin signaling in the brain is impaired in people with chronic mental disorders
kind of across the board,
all the way from chronic anxiety, depression,
to bipolar to schizophrenia and even Alzheimer's disease.
We know that patients with all of those disorders
have impaired glucose metabolism
and that the insulin signaling system in the brain,
which is different than insulin signaling in the periphery,
seems to somehow possibly be playing a role.
So to step back from that.
So for some patients,
I might just want to decrease glucose and insulin levels.
and I can do that by getting rid of sweets.
For other patients, like patients with schizoaffective disorder
or schizophrenia or bipolar disorder, especially if it's chronic,
if I'm using it as a brain treatment,
then I do want a ketogenic diet,
and I usually want reasonably high levels of blood ketones.
Usually, for depression, I want to see at least greater than probably 0.8 millimole.
for psychotic disorders and bipolar disorder,
I usually want to see levels greater than 1.5.
That's what I'm shooting for, if at all possible.
And so, yeah, I think that's what I'd go for.
Yeah, so, and sorry, I didn't mean to imply that people need to be in ketosis
in order to see some mental health benefits from changing their diet.
You make very clear in your book and we'll go into this in more detail that avoiding insulin
resistance, reversing insulin resistance and essentially trying to reverse what earlier
you described as this metabolic syndrome, which is a bunch of different things, is the target.
And for some people, getting rid of highly processed foods and focusing mainly on non-processed
or minimally processed foods will really help.
for others going straight to the full-blown ketogenic diet will be of most benefit.
I'd like to back up a little bit in history and get to something which I find incredibly interesting,
which is epilepsy and the longstanding use of ketogenic diet and fasting to treat epilepsy.
And the reason I want to kind of rewind to that point in history is that I think that for a lot of listeners
and people out there who are familiar with how changing your diet or changing your exercise
can positively impact sleep and weight and all these things.
And it cascades into feeling better.
That makes perfect sense.
But for a lot of the world still, the idea that changing or using nutrition as a dissection
tool or as a treatment tool to understand and treat mental illness is still a kind of
heretical idea that to them it kind of falls in the okay well that's like a woo science or something
like that now obviously your board certified physician and psychiatrist is arguably one of the
finest medical schools in the world Harvard medical school you know even the home on the
Stanford side we acknowledge we acknowledge our east coast uh you're the Harvard of the west coast
we're not going to talk we're not going to talk we're the Stanford of the east coast that argument
could go back and forth a number of times but you know this is
You're a serious clinician and a serious scientist and you're a serious thinker.
But for a lot of people out there, the notion of using diet, they immediately think,
ah, well, that makes perfect sense.
Or I think there's a category of people who think, well, yeah, didn't Atkins die of a heart attack?
You know, I hear that a lot, you know?
So, like, that was crazy, you know, like people immediately discard the Atkins diet for that reason,
which I do think is throwing the baby out with the bathwater,
but it's an interesting thing nonetheless.
And then I think that the majority of people sit in the middle
and just want to see science and medicine come up with treatments that work.
And I have to say I'm very relieved to hear what you said earlier,
which was you never said that people should come off their medication
and just become going a ketogenic diet and everything will be cured.
You're certainly not saying that.
No.
And rather you're saying, if I understand correctly,
that nutrition needs to be considered one of the major tools in the landscape of effective
tools and that it can be very effective, evidenced by the story that you shared, and there
are many other stories in there as well, of truly miraculous transformations.
So let's talk about epilepsy and how the ketogenic diet is not just used for epilepsy, but is one
of the oldest, if not the oldest examples of the use of nutrition to treat a, you know,
condition of the nervous system that can be incredibly debilitating even deadly yeah and the reality is
that this literature and this clinical history and all of the research we have was the godsend that i
needed to do the work that i'm doing otherwise i would have been discredited on day one
chris palmer's claiming that a dietary change can influence schizophrenia or a schizoaffective disorder
that's impossible and he's a quack
But the thing that immediately got me credibility was I didn't focus on it as a diet.
I did a deep dive into the epilepsy literature.
So the ketogenic diet, unbeknownst to most people, was actually developed 100 years ago, 1921, by a physician for one and only one purpose to treat epilepsy.
It wasn't developed as a weight loss diet.
It wasn't developed as the diet that all human beings should follow.
And the reason it was developed is because of this longstanding observation
since the time of Hippocrates that fasting can stop seizures.
Now, fasting is not a healthy diet.
Fasting is the process of no diet.
So we now understand a tremendous amount of science.
Most people think going without food is bad, and they equate it with starvation.
But in fact, when we go without food, it causes tremendous shifts in metabolism, both brain and body metabolism.
And it puts the body into a mode of autophagy and conservation of resources and all sorts of things that are beneficial to human health.
And this is why fasting has been used as a therapeutic intervention in almost every culture and almost every religion for millennia.
But for the most part, that was all thought to be religious folklore.
That was just crazy talk.
And those stupid people way back then thought God cured everything.
And so they fasted and they just assumed that they were getting better.
Well, in 1921, one physician used intermittent fasting on a child with seizures and found that, oh, lo and behold, this religious folklore stuff has something to it.
It actually worked.
The problem with fasting is that you can only fast for so long before you starve to death, and that's not a very effective treatment.
And this child was ingesting water, correct?
Yes.
It was just food elimination fasting.
Food elimination.
So no special does.
diet. So it was, but the problem with fasting for epilepsy is that as soon as people start
eating a normal diet again, their seizures usually come right back, oftentimes with a vengeance.
And so it can be a good short-term intervention. You know, the fasting can take a few days,
because it can take a few days to get ketosis. And then you can get some relief from chronic seizures,
but it's not a good long-term treatment because, again, people will starve to death.
As soon as they start eating, seizures come back.
So it was actually Dr. Russell Wilder at the Mayo Clinic
who developed the ketogenic diet with one and only one purpose.
He wanted to see, can we mimic the fasting state
using this special diet to see if it might stop seizures long term?
And lo and behold, it worked.
You know, early results were extraordinarily positive.
50% of patients who used the ketogenic diet became seizure-free, and another 35% had a 50% or greater
reduction in their seizure frequency. So about 85% efficacy rate.
Sorry to interrupt. I didn't mean to do that there. Was it just for pediatric epilepsy or
for adult epilepsy as well?
So back in the 1920s, we didn't have many anti-epilepsy treatments, and a lot of adults were
struggling as well. So they were using it on anybody who would do the diet.
By the 1950s, pharmaceuticals were coming out, and we had many more anti-convulsant treatments.
And there's no question they work for a lot of people.
That's great.
And taking a pill is so much easier than doing this diet.
So the diet pretty much fell out of favor, and nobody was using it from the 1950s to about the 70s.
But lo and behold, even to this day, people with epilepsy, about 30% don't respond to
the current treatments that we have available.
30% will have treatment-resistant
epilepsy, which means they continue
to have seizures no matter how many
anti-convulsants they're taking,
even if they've had brain surgery.
It just doesn't stop their seizures.
And so in the 1970s,
the ketogenic diet was resurrected
at Johns Hopkins
for these treatment-resistant cases.
And lo and behold, it works.
Not for all of them, but it works
in about one-third
become seizure-free.
And these are people who've tried everything
and nothing's working.
So one-third becomes seizure-free.
Another third get a clinical benefit,
meaning a 50% or greater reduction
in their seizure frequency.
And the other third, it doesn't seem to work.
It's not always clear
if that's because of noncompliance
or if that's because the diet's just not working,
but about a third, a third, a third.
Seizure freedom, reduction in seizures,
or it just doesn't work.
And so the reality, the godsend for me is that we have decades of neuroscience research on the ketogenic diet and what it is doing to the brain.
We know that the ketogenic diet is influencing neurotransmitter levels, in particular glutamate, GABA, adenosine.
It changes calcium channel regulation and calcium levels, which is really important in the function of cells.
It changes gene expression.
It reduces brain inflammation.
It changes the gut microbiome.
And there are, you know, gut microbiome is a huge topic right now.
And there are some researchers who argue that is the primary benefit of the ketogenic diet.
It's changing the gut microbiome in beneficial ways.
So it's doing a lot of things.
It obviously improves insulin resistance, lowers glucose levels, lowers insulin levels,
which improves insulin signaling.
The key for my research that I've outlined, the real magic, is that this diet stimulates two processes that relate to mitochondria.
It stimulates a process called mitophagy, which is getting rid of old and defective mitochondria and replacing them with new ones.
And it also stimulates a process called mitochondrial biogenesis, which means that after people have done the ketogenic.
diet for a while, months or years, many of their cells in their bodies and brains will have
more mitochondria and those mitochondria will be healthier. And I believe that is the reason
the ketogenic diet is such a powerful treatment, not only for epilepsy, but also for people
with chronic mental disorders. Would you mind listening off a few of the mental disorders?
And I know this is not meant to be inside ball, but we should distinguish between psychiatric disorders and neurological symptoms and diseases.
You know, the fields of psychiatry and neurology, hopefully someday will just merge.
But for instance, typically if somebody is presenting with something that looks like Alzheimer's dementia, they'll talk to a neurologist, whereas if somebody is presenting with symptoms like schizophrenia and bipolar, they'll talk to a psychiatrist.
But if you wouldn't mind wearing a dual hat, could you just quickly list off some of the
neurologic and psychiatric disorders for which ketogenic, or let's just say nutrition changes,
have been shown to improve symptoms significantly?
And then maybe we can dive into a couple of these, as well as get more deeply into
these two very interesting aspects of mitochondrial function and repair and turnover.
Yeah.
So the field, you know, in terms of nutritional psychiatry, it's a broad field, and it's in its infancy, is the real answer.
If you're looking for randomized controlled trials, documenting efficacy in large numbers of patients with these disorders, we don't have them.
They're underway now, but we don't have them yet.
What we do have are case studies.
We have a lot of mechanistic science papers
by some of the leading neuroscientists and psychiatrists in the world
and neurologists in the world
kind of outlining this is everything we know that the ketogenic diet's doing.
These are the problems in the brains of people
with these chronic mental or neurological disorders,
so we know that they should work.
But the disorders range from chronic depression
to, we've got a trial underway for PTSD.
We've got one actually decent pilot trial
from the National Institutes of Health
for the ketogenic diet for alcohol use disorder, of all things,
and we can go into that a little more.
We've got a couple of pilot trials
of the ketogenic diet for Alzheimer's disease.
We've got, and those are randomized controlled trials.
We've got case studies of the ketogenic diet for chronic depression, bipolar disorder, and schizophrenia.
The largest study that we've got in that mental health sphere is a pilot study of 31 patients admitted to a French hospital.
The 28 of those patients were able to do the diet and stay on the diet.
So 10% off the bat, non-compliant, couldn't do the diet.
So we need to include that.
But of the 28 patients who were able to do,
and these are 28 patients with treatment-resistant mental disorders,
chronic depression, bipolar, and schizophrenia.
Of the patients who were able to do the ketogenic diet,
100% had at least some improvement in symptoms.
46% had remission of illness.
Remission of illness.
That does not happen with current treatment.
and 64% I think were discharged on less medicine than they went into the hospital on.
So it wasn't that the people were prescribing more medicine and that's why they were being discharged on less medication.
We've got at least, again, the hardcore scientists are going to say, show us the randomized controlled trials with hundreds of patients.
And we've got five randomized controlled trials underway now, funded primarily through philanthropy.
I can tell you that we've talked about that one index patient.
But at this point, I have now treated dozens of patients, and I've heard from hundreds of patients
who've been treated by other clinicians, researchers, or I've just heard from patients from around the world who have shared
stories of complete remission of long, chronic mental disorders, like bipolar disorder
and schizophrenia, off of psychiatric meds, some of them, not all of them, but some of them are
able to get off all psychiatric meds and remain in remission.
Again, I think I didn't say this before, but it's really important to mention for people who might
be unfamiliar with the mental health field and its connection with epilepsy. The reason that's,
it's such an important connection is that we use epilepsy treatments in psychiatric patients every
day in tens of millions of people. So a lot of people don't know this, but I'll list off some
names that a lot of your listeners may have heard of, and they probably know them as psychiatric drugs,
but in fact these are epilepsy drugs. Depakot, tegretol, lemictal, tamedal, tern.
topomax, nirontin or gabapentin, valium, clonopin, Xanax.
Those are all medications that stop seizures.
And many of them were developed initially for seizures.
But we in the mental health field quickly steal them
and start using them in tens of millions of people,
even if they're off-label.
So that means we don't have research studies
documenting that they're effective.
but we go ahead and use them anyway
because the reality is far too many patients aren't getting better
with the FDA approved treatments that we do have to offer.
So psychiatrists are just winging it in some cases
and we're just throwing whatever we can at them
and we absolutely include epilepsy treatments.
So in many ways, using the ketogenic diet
as a treatment for serious mental disorders
is nothing new at all.
It's an established evidence-based treatment for epilepsy.
We use evidence-based treatment.
for epilepsy across the board for a wide range of mental disorders. And so in many ways,
that's all I'm doing with the ketogenic diet. It just happens to be a diet. I love it. I love it.
And I should say, I love it because we had a guest on here early days of the podcast. He's a colleague
of mine at Stanford. He's a bioengineer and a psychiatrist, phenomenal scientists and psychiatrists
Carl Diceroy won the Lasker Prize and so on and so forth.
And he made a really important point, which should have been obvious to me, but wasn't until he said it,
which was, you know, the psychiatrist has tools, just like the surgeon has tools,
but the tools are language and observing behavior.
You know, those are the dissection tools for what's going on in someone's brain.
And then as a neuroscientist, you know, I'm familiar with the neurotransmitters and neuromodulators.
And you mentioned that, you know, there are these tools of, you know, altering brain chemistry,
which are of the sorts of drugs you just listed off, or antidepressants, or antipsychotics that fall
into these major bins of adjusting dopamine or adjusting serotonin or some combination of dopamine,
serotonin, epinephrine, adenosine, and on and on and on.
And it seems to me it's an incredible field, but that the field is still very much in its infancy,
that it wasn't but 100 years ago that people were measuring bumps on the head as a way to diagnose,
you know, phrenology and that there's still so much to learn.
And so when I hear you say, you know, adjusting nutrition or putting people into a ketogenic state
or even just eliminating highly processed food, sugars, et cetera,
taking care of metabolic syndrome and then observing tremendous relief in clinical syndromes
or symptoms rather of psychiatric disorders, it makes perfect sense to me.
It's yet another dissection tool and a tool for altering brain chemistry.
I think that if I think about the landscape, the sort of sociology out there of, again,
there seem to be these bins, like a third of people saying, of course, you know, diet and exercise
and social connection and limiting stress, like that's the good stuff.
That's the stuff that we know really works.
And then about a third of people are sort of unclear.
And then a third of people think, well, if it's not a prescription drug, then it just has no place in medicine.
And hopefully that's changing.
And certainly the work that you're doing is going to be important in that transition that I think we will see.
I'd like to talk about mitophagy and mitochondrial biogenesis.
I think most people learn that the mitochondria are the energy factories of cells and that indeed they are.
As a neuroscientist, what I know about them is that they are present everywhere in neurons,
not just in the so-called cell body, but you can find mitochondria in the furthest little bits of neurons.
neurons and neurons can be quite big, very large, in fact, meters long or more in some cases
and some species, including us, depending how tall somebody is. It could be many meters
or several meters, rather. And that mitochondria do a lot of stuff besides just produce energy.
Because I think people hear mitochondria energy and they think, oh, so these patients felt better,
they lost weight, they have more energy and then they're doing better. But here we're talking
about remission of auditory hallucinations, people feeling suicidal and then changing their diet
and feeling like life is something they can deal with and maybe even function extremely well and,
et cetera. So maybe we could just talk about mitochondria for a moment and then talk about these
two major effects. What are some of the other things that mitochondria are important for in neurons
and maybe other cells of the brain? Because as an access point for all this, I think it would be
great if people could learn a little mitochondrial biology.
Yeah, no.
So I guess the first thing that I'll say is that, you know, this field is one of the most
cutting edge fields in medicine right now.
20 years ago or so, I think the majority of research scientists thought of mitochondria
as nothing more than little batteries.
they take food and oxygen and turn it into ATP,
and that's really important.
Yeah, we get that, but they're just little batteries.
That's all they are.
And so one of the reasons that this work is so important
is because it combines cutting-edge research
in the metabolic field and the aging field,
and we can start to pair it with the mental health.
and neurological health field.
So
mitochondria,
one scientist
gave me this analogy,
he said,
if you think of the cell
as a computer,
a lot of people think of mitochondria
as the power cord to that computer
because they're providing the power.
And they are, in fact,
the power cord to that computer.
But actually,
their real function
is the motherboard of that computer.
So mitochondria
are directing and allocating
resources throughout a cell. That is their primary function. And then they happen to be powerhouses
as well. And so to give some clear examples, mitochondria play a direct role in the production
and release and regulation of some really key neurotransmitters, including serotonin, dopamine,
glutamate, astiolene. Those are pretty powerful neurotransmitters. I would consider those, I would consider those,
the, I know you listed more than three, but the sort of primary colors of neurotransmission.
Yes.
You know, any one of those in excess or deficiency is going to have profound negative effects
on a nervous system.
Or it's going to alter the way that people and animals feel, think, move, remember, etc.
And so as part, so mitochondria are providing both some of the building blocks, if you
will for some of those molecules.
They're part of the Krebs citric acid cycle.
Some of the intermediate products actually go into making those neurotransmitters.
Much more importantly, mitochondria provide the energy for the production of those neurotransmitters.
And fascinatingly, mitochondria are directly related to the release of neurotransmitters.
ATP alone is not enough.
There have been some research studies that have actually found that mitochondrial,
move along the membrane of the synapse to release batches of vesicles of neurotransmitters
and that if the mitochondria are removed from the synapse and researchers flood that cell with
ATP, neurotransmitters usually are not getting released.
Mitochondria are doing other things.
We don't entirely even understand what all they're doing or how they're doing it.
But they're doing other things than just providing the power.
Another really important example is that mitochondria are actually the primary regulators of epigenetics.
If you look at any one factor, so one study actually found that they're responsible for the expression of about 60% of the genes in a cell.
And so, and mitochondria do this through a lot of ways that have been known for years,
and sometimes decades.
So mitochondria are directly related to the levels of reactive oxygen species in a cell.
They are managing calcium regulation in cells.
And we know that those things play a role in epigenetic expression.
We know the levels of ATP to ADP or AMP also play a role.
And mitochondria are doing those things.
But it turns out mitochondria are actually doing much more sophisticated things than even those
in terms of gene expression, mitochondria at least play a role in all of the aspects of the human
stress response. So when humans are stressed either physically or psychologically, you know,
there are several things that happen, increased cortisol, increased adrenaline, noradrenaline,
inflammation, and gene expression, in particular in the hippocampus, occur with the stress response.
And one group of researchers actually genetically modified mitochondria in four different ways
and found that all of the stress response,
all those four buckets of stress response were impacted in one way or another,
implying that mitochondria are somehow playing a role in those.
In terms of their role in cortisol,
we know that mitochondria actually have the enzyme required for the synthesis of steroid hormones.
So that includes cortisol, estrogen, testosterone, and progesterone, some names that maybe everybody's heard of.
And so that means that if mitochondria are in short supply or dysfunctional, the production of those hormones may become dysregulated.
Mitochondria play a direct role in inflammation, and they turn the inflammatory.
system both on, or they at least play a role in turning the inflammatory system both on and off.
I think I'm not going to be able to quote the exact study and author, but one paper in cell
actually identified mitochondria as the key regulator in turning certain inflammatory cells
off and that when you inhibit mitochondrial function, those cells don't turn off.
That mitochondrial levels of reactive oxygen species are a key signaling.
process to turn the inflammatory process off.
Another study found that macrophages, so macrophages are an important immune cell that play a
role in healing.
So if you cut yourself, your body will get, you know, send inflammation that way and send immune cells
that way to try to heal your skin.
And macrophages play an important role in that healing.
One group of researchers tried to figure out, how do mass.
macrophages know to switch between the different phases of wound healing. Because the macrophages do
different things in the different phases of wound healing. And the conclusion of all of their research
was that it's mitochondria. Mitochondria are sending the essential signals that change the state
of the macrophages to induce these different phases of wound healing. So I've just talked about
neurotransmitters, hormones, epigenetic expression, inflammation.
For anybody familiar with the mental health field, they know these are like some of the key
variables that researchers have been struggling with for decades trying to figure out how do
these fit together. We know that all of those buckets can be disrupted in people with
mental disorders.
And our field has struggled to understand, but how do they fit together?
How can we make sense of this disruption?
And I believe once you understand the science of mitochondria, you can actually connect all
of the dots of the mental illness puzzle.
Super interesting little subcellar goodies these mitochondria are.
I come from a field where people are often divided into lumpers and splitters.
And I'm somewhere in between.
For those of you don't know, lumpers are people that like to make things really simple lists
of no more than three functions or dividing brain areas into no more than three
splitters of people that like to subdivide into a ton of detail.
There's a history of scientists being splitters in order to be able to name things after
themselves because there's more territory.
to go around if you're splitting than if you're lumping.
But we are doing neither here.
What I'm hearing is that mitochondria,
in addition to being important sources of energy production
and output in cells,
which of course they are,
probably have other roles
and that maybe someday,
what we call mitochondria will actually be two or three different
little subseller organelles.
Like there may be little bits in there that are controlling gene expression
and little bits in there that are controlling neurotransylase.
mensmere production. At least for now, the name is mitochondria. And thank you, by the way,
for illustrating some of the other things that they do. Because in the landscape of science
education, oftentimes people think, okay, energy production, there'll be a picture or a cartoon
of mitochondria, like flexing its muscles. People go, okay, energy, mitochondria, mighty mitochondria.
And then they'll think, oh, you know, they're just sort of like a dumb jock portion of the cell, right?
They're not doing anything sophisticated. And everything you listed off is that they are doing many
sophisticated, intricate things within cells. So I think how things are cartooned and discussed actually
has an impact and not just on the general public, but on the medical field and on the science fields.
Anyway, that's more science sociology. But now that everyone is well aware that mitochondria are doing
a large number of very important things in a very regulated way, let's talk about mitophagy.
You know, a few years ago because a Nobel Prize was given for autophagy, sometimes called autophagy,
people. You can say it either way. People know hopefully what it means is more important,
which is the gobbling up of one's own cells that are dead or injured. And this idea of
autophagy of cells being eaten up or within a system, nervous system or other system,
has come up again and again. I actually wasn't aware that mitophagy could be such an important
lever. So tell us about mitophagy, which I have to presume is the
intentional or not gobbling up of mitochondria, presumably to replace them with newer,
healthier mitochondria. Is that right? It is. So in many ways, mitophagy is a subset of autophagy,
but it's got its own name because it is specific to mitochondria. There do appear to be
some unique regulators of mitophagy compared to autophagy more broadly. Mitochondriac. Mitochondria actually
are playing a role in autophagy itself.
And this makes sense because one of the, so the global picture of autophagy is stimulated by
fasting states or fasting mimicking states.
So when your body senses that you don't have enough food, it actually hunkers down and
starts to recycle dead old parts.
in this kind of carefully orchestrated way,
and it takes them to lysosomes, they get degraded,
and then those degradation products get used
for either energy or to build new things.
Autophagy is always occurring at a low level,
but you can really hyper-stimulate the process
through fasting, calorie restriction,
fasting-mimicking diets, other things.
And this is why fasting and, you know,
calorie restriction is so kind of such hot topics in the medical field now is because we
they've been shown to induce longevity and we think it's probably through that process that you're
stimulating the body to um it kind of become lean and conservative in terms of its allocation of resources
and the body doesn't just destroy the healthiest tissue along with the old
dead stuff. It has these processes
that identify the old and defective
parts first, and they go first.
And that's what's beautiful about
the whole thing. And that's why
fasting is so important.
So mitophagy
we know
plays a really important role
because
so there's this
term called mitochondrial dysfunction
which some researchers
are actually wanting to get rid of and move away
from because as you just said,
mitochondria do so many different things and different mitochondria even within the same cell may
very well be specializing in different tasks and mitochondria from one cell to another are sometimes
doing very different things like not all mitochondria can produce cortisol that's specific to specific
cells where those genes are getting turned on so it's not like all mitochondria are producing
cortisol just the ones in your adrenal gland for instance are producing cortisol
But there is this term mitochondrial dysfunction, and it has long been known for decades
that mitochondrial dysfunction is associated with everything that ails us, essentially.
So in the 1950s, we had a theory of aging that was based on reactive oxygen species.
And that essentially, and that's where all the inflammation,
is bad for you comes from.
And where all the noise about antioxidants.
Yes.
Like in the 90s, it contains antioxidants.
Not to say antioxidants are bad, but they are certainly not the be-all end-all of health.
They are not.
But that's exactly where that research came from,
is that researchers were narrowing in on these reactive oxygen species
are highly, highly correlated with all of the diseases of aging and poor health
outcomes. Turns out they're also highly, highly correlated with all chronic mental disorders,
interestingly. And so researchers used antioxidants to see if, well, maybe if we can stop,
somehow tame these reactive oxygen species will improve health outcomes. Doesn't seem to work.
By the 1970s, our understanding of mitochondria and their role in the production of reactive oxygen
species expanded and that led to the mitochondrial theory of aging. So in the 1970s, we had this
mitochondrial theory of aging based primarily and exclusively on reactive oxygen species. Fast forward a
couple of decades, that was disproven because we now know reactive oxygen species aren't
all bad. They actually serve a signaling process. They're a normal part of human functioning and
cellular function. So they're not all bad, but we still know high levels of reactive oxygen.
species are bad for you. Fast forward to just, I think, maybe last year with this expanded
role of all of the different things mitochondria are doing, so David Sinclair published a paper
in one of the cell journals, I think, saying that, oh, mitochondria are actually the unifying
link of everything that we know about aging. Mitochondria are the cause, or defective mitochondria,
or defective mitochondrial function,
mitochondrial dysfunction,
is possibly the unifying cause
of aging and all of the aging-related disorders.
So mitophagy is trying to address all that,
is trying to say, okay, this is bad,
we don't want defective mitochondria,
and how can we get rid of old ones or defective ones
and replace them with new ones?
and I think the most powerful signal and tool that we have right now
is in fact related to diet.
It's calorie restriction.
That is the oldest, truest kind of best proven way
to prevent aging in a wide variety of animal species.
Fasting and intermittent fasting.
and again, you can only do those things for so long,
and then fasting, mimicking diets,
can also stimulate this process of mitophagy.
Before we talk about mitochondrial biogenesis,
if, and I certainly accept the idea that mitochondria
are extremely important in physical health and mental health.
That's for me is a straightforward conclusion at this point
based on what you've said, whatever, at elsewhere, et cetera.
And if various diets, including ketogenic diet, including fasting,
reducing sugar intake, et cetera, can assist in mitochondrial function and mitophagy,
and that's at least one of the levers by which diet can positively impact mental health
and physical health,
can we conclude that there's something special about low blood glucose in the brain?
right i mean that the the sort of common pathway of all of those things fasting ketogenesis for some people
maybe they for maybe some people manage have great insulin management so just removing sweets
you know refined sugars you know brings down their blood glucose level substantially they don't
need to go on a ketogenic diet in order to relieve a low level depression or something like that
it seems like the the common theme here is that glucose levels in the brain need to be reduced
which for me is surprising because neurons love glucose.
I mean, there are some really nice studies,
one that I can think of recently that was published in neurons.
If you just look at the tuning of a neuron,
how well a neuron in the brain represent some visual image in the environment.
Here we can just generalize in saying more action potentials,
more electrical signals from the neuron generally correlates
with better high fidelity representation.
It's like sort of, you know, if everyone's time someone says,
shout and then someone shouts the neuron as like the one responding to the order. And these neurons
just when there's high glucose, they are faithful representatives of what's out there in the world.
But then when you fast an animal, they become less faithful representatives of what's out there.
And yet when I've done intermittent fasting and I do a kind of modified version of it,
my mental clarity is far better than when I've had a big bowl of pasta, probably for other reasons
relate to serotonin and tryptophan. And so I think,
For the typical listener out there, I have to imagine, it's got to be a little confusing, right?
We hear neurons love glucose. They live on glucose. And here we're saying, let's deprive them of some glucose,
or let's just bring glucose levels down, or let's switch the fuel source of the brain from glucose to ketones.
And now the brain really works the way it's supposed to. So this raises a little bit of a just so story question.
Like, why would it be the case that neurons love glucose and yet if there's too much glucose,
us around, they become sick. And of course, with any, why would it be story, as I always say,
you know, I wasn't consulted at the design phase and I'm going to presume that you weren't
consulted the design phase either. And that if any of us say that we are, then we are probably
the patients that need evaluation. So I think there's a name for that, right? There's delusion, right?
Okay, I'm going to my first correct clinical assessment of myself. So how do I get my head around
this, right? You've got me sold on modicondria, not that I needed to be sold, but
that's an easy, like yes, yes, absolutely yes. The idea that diet can impact mental health and
physical health. Yes, absolutely by way of mitochondria, at least in part. Great. But then neurons
love glucose. So what's going on or what do you think is going on? I am not convinced that
glucose is the real story. Glucose may in fact
to be a symptom.
So we know that parts of the brain,
there have been a couple of studies
that just came out in the last couple of weeks, I think,
documenting that actually astrocytes
in the hypothalamus
play a key role in glucose regulation
throughout the body.
And it appears to be a metabolic
role, which in my mind,
implies that the mitochondria in those astrocytes are probably playing a key role.
Because we know mitochondria play a key role in sensing glucose levels.
They play a key role in the release of insulin from the pancreas.
But mitochondria in the brain is also playing a role in kind of balancing how much glucose is around.
And so it's a difficult question because I think in some cases, high glucose levels are actually a symptom of metabolic dysfunction somewhere in the body or brain.
And when I think about, well, what does that mean?
In my mind, most of the evidence currently is pointing to mitochondrial dysfunction somewhere in the body or brain that is the most of the evidence currently is pointing to mitochondrial dysfunction somewhere in the body or brain that is the
likely cause of that dysregulation of glucose levels.
But we know that if you consume massive amounts of junk food, sugar, and other things,
that you can get dysregulation of glucose levels.
The conundrum, though, is that that's not a universal response.
And what about the typical person?
Like, I've never really liked junk food that much.
Maybe as a kid, I can recall liking candy.
But I was a sandwich for lunch person for a long time.
And as I've changed that out for salad and maybe a small piece of meat with my salad or something like that,
I feel far better during the day, far more alert.
But I do eat carbohydrates.
I eat starches typically at night, but I tend to do some very hard training at some point during the day.
So I imagine I have some glycogen to repack.
Okay, that's me.
I only mention that because I'm not in ketosis as far as I know.
I haven't, unless you brought the strips, I haven't done the blood glucose test today.
So what about the typical person who's an omnivore eating, you know, some rice, some pasta,
pasta salads, you know, people that are that are eating not junk food, massive amounts of
sugar, but have blood glucose that's in kind of moderate range. Do you think, and here feel free
to speculate, do you think that those people might feel far better,
or even a little bit better if they were in a lower glucose state.
And I asked this because I think there are a lot of people out there who suffer from full-blown depression,
but there are also a lot of people who suffer from like moodiness and feeling not so great,
subclinical depression.
Yes. Burnout is what I would call it.
Yeah.
And just feeling like some days are great and then other days they feel lousy for reasons they don't understand.
Yeah.
And those make for less dramatic case studies.
and yet I have to assume that that description will nets a large fraction of the general public.
So the way that I kind of break this field, and I'm probably getting too nerdy right now,
but I kind of break this field into cause, what's the actual root cause,
and what are effective treatments?
And I really see them as two separate things.
just because the ketogenic diet is an effective treatment
does not imply that the cause of the problem was eating carbohydrates
and I think that's a really important distinction
there are many people who disagree with me on that there's no doubt about it
and everybody's heard people say sugar is the cause of everything that ails you
or carbs are the cause of everything that ails you if everybody does a low-carb diet
or a ketogenic diet.
And then they go to, so it must be sugar that was the cause.
I don't see it as clearly black and white as that.
The calorie restriction, ketogenic diet, carbohydrate restriction
are inducing metabolic changes in the brain and body.
And regardless of what the person was eating,
they are inducing metabolic changes that can be really beneficial to brain health.
So let me just give a clear black and white example of this,
and then I can speak to the broader topic that you brought up about just a general population.
The easy example of the ketogenic diet being an effective intervention
for somebody who was not following a bad diet is an infant with epilepsy.
There are lots of infants who have uncontrollable.
seizures. They are drinking breast milk. To the best of our knowledge, that is the primary
most beneficial food source an infant could be consuming. Now, some might say, well,
maybe the mother's, you know, whatever, I don't buy that. The mother's breast milk is, in fact,
the optimal food source for that infant. And yet that infant is still seizing. If we put that
infant on a ketogenic diet, a lot of those infants seizures will stop. It doesn't mean that the
cause of the infant seizures was a bad diet, but it means a dietary intervention can change
brain metabolism and improve symptoms in that person. So going to your broader question about
adults modern day, the real answer is, you know, there was just this conference in London, the
Royal College of Obesity Medicine or something like that.
That's not the name, but something along those lines.
The conclusion of that conference, it invited the greatest minds in obesity medicine.
The overarching conclusion of that conference was, we don't know what causes obesity.
It's really important that we sit with that.
We don't know what causes obesity.
They don't think excess caloric intake beyond one's daily metabolic needs is causing obesity.
Some will argue that.
And so some will say, yes, it's all energy balance.
But why do we have an epidemic of obesity?
Well, that's the gazillion dollar question.
And junk, some will say it's all the junk food.
But we had junk food in the 1970s.
When I was growing up, I grew up on Kool-Aid.
Twinkies and King Dongs and Ho-Hos and...
Oh, I'm re-watching the Mad Men series now.
I love that series and I'm re-watching it.
And I happen to know someone who worked on that series.
They research everything for the props and the costumes, everything, but right down to diet.
And if you look at the diet, it was terrible.
It was mostly, yes, there was a lot of excessive amounts of drinking and cigarette smoking,
but the diets were terrible.
It was prepackaged foods.
It was frozen dinners.
I mean, that really came to prominence in the 70s and 80s.
but even in the 50s, and from what I've been reading, even in the 30s and 40s,
you know, people were not eating grass-fed meat and Brazil nuts with a little bit of broccoli
rabbi on the side.
No.
No.
Not the typical intake.
So something out there, or maybe multiple things are at play to increase obesity.
And at the end of the day, I believe some will call this special.
but I actually think we've got a tremendous amount of evidence that continues to point in this direction.
I believe that mitochondria are the key to the obesity epidemic,
that there is something in our environment.
So that is either our food, environmental toxins,
stress levels, poor sleep, not getting adequate sunlight,
whatever you want to speculate on, all of the above,
All of those things are known to impair mitochondrial function.
And if parts of your brain that regulate metabolism and that regulate eating behaviors are not metabolically healthy,
it means that they will not stop you from eating, or it means that your metabolism will not rise to the challenge of 10 donuts.
because some people can eat 10 donuts and go on staying thin and healthy.
Although I totally agree, although I would just like to say that it seems to me that compared
to when I was growing up, and again, I haven't run the statistics, there are fewer and fewer
of those individuals around now.
Just as when I was growing up, it was one or two kids in class that were quite overweight,
and then there were some that were mildly overweight, but most were of healthy weight.
nowadays that's dramatically altered the landscape is dramatically altered in the other direction
it is rare when i encounter one of those can eat anything type people i know one he's actually
an employee at stanford he's on our media team at stanford and this guy when i take him to lunch it's
like the and he's in his early 70s and he can eat and he's incredibly lean he exercises a little
bit but he's one of these mutants that just can eat and eat and eat and he's like he's
lean and he's vital and he's it's wild um and he's an expensive lunch uh but those people are seem rare
and even those kids are now seem rare they're getting increasingly rare and and that that leads me
to think it may be epigenetic factors in the womb environment so that kids are actually coming out
predisposed to obesity well let me ask you about that because i had a note here to ask this later but
I'm going to interrupt you now in order to capture this moment. My understanding is that, well,
as everyone knows, we inherit DNA. We get genes from both of our parents. And they mix,
although there are incredible data from Catherine Doolock's lab at Harvard and other showing that
we actually have entire regions of our brain that carry neurons that are of purely of moms or
of dad's DNA, depending on the brain region. This is a wild finding, but it's accurate. And this has
actually been known about in terms of heritability of disease, et cetera.
Maternal DNA, DNA from mom, genes from our mother, not to place blame on mothers at all,
my understanding is that the mitochondrial DNA come exclusively through the maternal side.
Is that true?
So it's a great question, and I've been asked this before, and yeah, psychiatrists are known
for blaming mothers, and some might say that I'm, like, trying to redo that whole thing and blame
mothers again. The data or the data. I'm not trying to blame mothers here. Mothers play an essential
role in everything. But if it is true, that mitochondria are the linchpin of all this, and maternal
DNA is what determines the mitochondrial DNA. I think it's an important place to look.
It's an important question. And the answer is unequivocally, no. That's not the way it works.
Oh, well then. Vindication for anyone that was asserting that. And so let me explain it. So
mitochondria have 36 genes under them.
themselves. 13 of those genes code for some of the mitochondrial machinery of making ATP and the other
36 play roles in epigenetic regulation, play roles in whole body metabolism and other things.
So that is what you're inheriting from your mom, is the mitochondria and those 36 genes for the most part.
but the majority of proteins that make up mitochondria,
over I think 1,300 genes that make up mitochondria
are actually encoded in the nuclear DNA.
And so you inherit a copy from both your mother and your father.
So the majority of people who have mitochondrial defects
or rare mitochondrial diseases
actually could inherit them from either mom or dad
because it can be a defect in the nuclear genes that code for proteins that make up mitochondria.
The much bigger issue, so when I talk about mitochondrial dysfunction being a primary driver of mental illness,
metabolic illness, it's not that people inherit a defective mitochondria or mitochondria from,
mom and then that just ruins their life forever. That's actually not the way it works.
The beautiful thing about this theory is that it connects all of the risk factors that we already
know play a role in mental health, but also metabolic health. Sleep disruption impairs
mitochondria and mitochondrial function. Stress, high levels of stress and trauma impair mitochondrial
function, drug and alcohol use, alcohol, tobacco, definitely in terms of the smoke, and marijuana,
THC in particular, all impair mitochondrial function.
THC directly or the smoke?
THC directly.
Those studies have been done.
And they, so mitochondria actually have CB1 receptors right on them.
And various researchers, a couple of studies from nature actually documented this,
that the mitochondrial CB1 receptors are primary points of the influence of marijuana
on human behaviors and effects.
Because when they remove CB1 receptors and animal models, these two,
changes don't happen. So the CB1 receptors, you know, we've got some large studies of
adolescents who use a lot of marijuana. And the areas where the mitochondria have the greatest
number of CB1 receptors are areas of their brains that actually are atrophied or shrunk
compared to normal healthy controls. So that means their brain tissue is aging prematurely. It's
shrinking prematurely. But the C.
TB1 receptors on mitochondria also seem to play a role in the memory impairment that can be induced from THC.
And they also play a role in the kind of lack of motivation, the behavioral, a motivational state from THC.
Now again, for people who want to chillax, that's what they're looking for.
They don't want to remember anything.
They don't want to think.
they want to be spaced out, they want to relax.
That's great.
But it's important that they know that they're actually harming the mitochondria in their brain cells.
And that although there's always an opportunity to repair mitochondria
and always an opportunity to stimulate mitochondrial biogenesis, so you can get it back.
But if you keep doing it chronically, you're probably not helping your overall mental or metabolic health.
Yeah, I'm glad you brought up THC.
We did an episode on Canvas.
We also did one on alcohol.
Probably lost some friends from that one.
I mean, when you look at the data, it's very clear.
I mean, I'm not arguing that people dislike the effects of these compounds when they take them.
But it is clear that, at least to me, based on the data, that regardless of what people have read about red wine,
that not drinking any alcohol is going to be healthier than drinking alcohol.
And that the thresholds for alcohol ingestion before people start to negatively impact their health is about one or two.
week. And then THC, because of the very high concentrations of THC that are present in a lot of products now,
vaping and smoking THC and even edibles, that it can be problematic. You mentioned adolescence,
you know, predisposition of brain atrophy, psychosis, et cetera. In any case, because you mentioned
alcohol and because it is a commonly used substance, I heard you give a talk in which I think
I have this right in which alcohol can disrupt the way that the brain uses fuels of all kinds,
which may disrupt one's response to alcohol, make alcohol seem more rewarding to those that drink
alcohol. So drinking alcohol makes alcohol more rewarding to the brain's alcohol drinkers,
but that it also might alter glucose metabolism that basically alcohol is not good for our brains.
Do you have that correct?
You do have that correct.
Okay.
What happens if you take an alcoholic or somebody that just drinks, you know, two to four nights a week, a couple of drinks, which I think is pretty common out there.
And you put them on a ketogenic diet.
Has that experiment been done?
That experiment has been done.
And led by none other than a woman named Nora Volka,
who is one of the leading neuroscientists and addiction researchers in the world.
She is the director of the National Institute of Drug Abuse.
She's been hot on the trail of metabolic abnormalities in the brains of people with alcohol use disorder,
which I will just refer to as alcoholics because that's what everybody knows it as.
So she's been hot on this trail for many, many years.
And as you said, it turns out that the reward pathways in particular are metabolically compromised in alcoholics.
And the metabolic compromise essentially in a nutshell means they aren't getting enough fuel from glucose.
The interesting thing is that when people drink alcohol, your liver converts alcohol into a molecule called acetate.
that acetate travels up to the brain and fuels brain cells, in particular some of these reward
pathway cells more than others.
And so chronic alcoholics have this chronic deprivation of energy in these cells.
And so Nora Volka and other researchers that National Institutes of Health did a study in which
they set out to see if we can change this brain.
metabolic problem in alcoholics, will that affect clinical symptoms of alcoholism?
And will it do anything, you know, it's clinically useful?
And so they actually did a pilot randomized controlled trial, admitted alcoholics to a detox
unit, half of the patients got a ketogenic diet, the other half got the standard American diet,
and then everybody else, all of them got the same detox protocol.
The patients who got the ketogenic diet required fewer benzodiazepines for their detox.
Despite that, they had fewer withdrawal symptoms from the alcohol.
They reported fewer cravings for alcohol.
And the researchers did brain scans, which showed improved brain metabolism in these key areas that they were looking at.
and their brains showed reduced levels of neuroinflammation,
which was also something they were really interested in.
And so that one study says to us that even though most people would think alcoholism
has nothing to do with diet, alcohol is just drinking too much.
It's a matter of willpower.
Or it's somebody who's addictive.
They've got an addictive personality, and it's that simple.
You come out of the womb with an addictive personality, and those people are, you know, novelty seekers and they're impulsive, and they have no patience, they have no discipline.
They can't sustain, you know, any kind of rewarding experience.
Or childhood trauma.
There's a story there, which they're very well maybe, but.
And there may be.
And but what that research study strongly suggests, and again, yes.
maybe we need larger controlled trials,
but this is one of the leading neuroscientists in the world
who's hot on this trail.
This is what she believes,
and this is what I believe,
is that if we can correct the brain metabolic defects
from chronic alcohol use,
we might be able to help people be sober
and give them a fighting chance
or give them an edge up
or pull a lever that we can use in their favor
for their benefit.
There's one caution to all of them,
of this research that I really do want to highlight. And so now I'm going to get hate mail from all
the keto community. That's okay. I mean, anytime I admire you for talking about nutrition at all,
because anytime one talks about nutrition, you're going to get hate mail from somebody.
So the caveat to all of this is that as part of the research that those researchers were doing,
They actually wanted to see what will happen to alcohol levels if an animal consumes alcohol while on a ketogenic diet.
So they didn't do this in humans yet.
This is a fairly easy study to do.
So I'm hoping somebody will do this study soon.
But they instead put rats, half of them on a standard diet and half of them on a ketogenic diet.
And then they expose them to the exact same amount of alcohol.
The rats who were on the ketogenic diet had a five-fold increase in blood alcohol levels.
Five-fold increase.
Meaning they drank more or it was metabolized differently?
It was metabolized differently.
The rats all got the same amount of alcohol.
So for people out there who are ketogenic, I'm chuckling, but who are not alcoholics, please,
alcoholics, please do something about it because it's so detrimental.
But I guess does this mean that they can drink less in order to get the effective alcohols?
that most people are seeking.
Cheap dates.
Cheap date is what you call that.
You only need a half a drink instead of three drinks.
I would think the keto community would thank you for this,
unless they somehow have a stake in the alcohol industry.
The reason that I put it as a caution is that if anybody is struggling with alcoholism
and thinks, hey, I need an edge up.
I need a lever to pull because I'm really struggling to give this stuff up.
I just find myself going back.
and if you're telling me my brain metabolism is messed up,
and this might help it,
I'm all in favor of that,
and yes, that's what the researchers are pursuing,
and that's what I'm saying,
with the following caveat,
that if you relapse while on a ketogenic diet,
you better not drink the same amount of alcohol
that you think you can drink.
Could be deadly.
It could be deadly,
and or it could be really deadly to you or someone else,
because unfortunately a lot of times when people drink, they get behind the wheel,
and they think that they can handle two drinks safely.
And they think, well, you know, I can go out for dinner and have two glasses of wine
and drive home safely.
I know myself.
If you go to a ketogenic diet, please don't drive with the same two drinks because it
means your blood alcohol level, if it models anything that we found in the rat study,
your blood alcohol levels maybe five times.
higher than they would normally be. And that means you are really wasted and you're probably not
safe to be driving. Probably the same is true for drinking me on an empty stomach. Yeah. Yeah.
No, it's a very important point. And thank you for raising that. I mean, I hear this,
again, about mitochondria, about blood glucose. You mentioned astrocytes. And for those of you
for that earlier, astrocytes are a non-neuron cell type in the brain, a glial cell type.
that my postdoc advisor was known for popularizing the modern science of glia, which include
astrocytes. And I'd be remiss if I didn't say that they are considered the cells that hold
everything together in the brain and are kind of passive observers, but they do many things actively.
I think now people appreciate the astrocytes as at least as important as the neurons.
And certainly for disease, they are often implicated in warding off of disease, et cetera.
everything that you're telling me about the fact that the brain can regulate things that are happening in the body
metabolism etc organ health obesity etc to me as a neuroscientist that's not surprising all of it just screams
hypothalamus hypothalamus hypothalamus because here you're telling me it's regulating these
basal functions like metabolism it's regulating how much we crave things and of course hypothalamus is
involved in motivation and craving there are other areas too other areas the brain too of course but
I would imagine that someone ought to or has mapped out where the receptors for all this business are in the brain.
And I guess that raises the question of when one goes on a ketogenic or low blood glucose diet or fast.
Has anyone observed changes in the brain?
Has anyone had neuroimaging of humans and their brains under conditions of ingesting one diet or another,
whether or not they're suffering from a psychiatric disorder or not.
I would think that that's where the gold is.
We do have some of those studies.
So, and they've, you know, when you do a neuroimaging study,
you can measure a lot of different things.
So one thing, with a PET scan, you can measure glucose metabolism.
So a researcher, Stephen Kuhnian, is doing that research,
in particular in Alzheimer's disease patients and Alzheimer's disease models,
but in humans.
And that's because we know that, again, a common finding in patients with Alzheimer's disease
is this glucose hypometabolism.
Some people are attributing it to insulin signaling impairment, and so some people are calling
it type 3 diabetes.
The end of the day, I think the clearest signal that we have is that cells aren't getting
enough energy from glucose as a few.
source. That is something that I think I can confidently say that's backed by numerous research
studies. There's debate in the research field about whether that's a primary driver of the
illness. I happen to believe it is. And if you ask the question, well, why would cells not be
getting enough fuel from glucose? You have to focus on mitochondria because they're the ones
producing the fuel from that glucose. So somehow you have to implicate mitochondria in that process
one way or another.
Others will say, no, that's just a side effect of whatever is causing Alzheimer's disease.
So Stephen Kuhnaen has done studies where he even gives ketone supplements.
These are liquid ketone esters.
So, yeah, ketone esters or ketone salts.
And it has actually found that these brain metabolism deficits can be corrected, at least short term, by giving a ketone supplement.
Is this in the context of people also ingesting some carbohydrate?
Because I confess, I've tried the ketogenic diet.
I probably did it wrong.
This was years ago and then the cyclic ketogenic diet.
But in the last year or so, I've started using liquid ketone esters.
And I do eat some carbohydrates each day, usually in proportion to how much high-intensity exercise I'm doing.
Those liquid ketone esters, for me, at least subdued.
I feel like greatly increase my energy levels and my ability to focus mentally.
And they improve my sleep.
This is my observation tracking some data, but just, again, subjectively.
So in this example, are you talking about people taking ketone esters or ketone salts
on a backdrop of a ketogenic diet or on the backdrop of a more typical diet?
So he's done both.
So he's done studies where patients aren't doing anything special with a diet.
So they're eating whatever they normally eat, absolutely non-ketogenic, giving them a ketone salt or ester,
and then noticing immediate and direct changes in the metabolism of these metabolically compromised brain cells,
as measured by pet imaging.
These are not household pets, by the way.
Sorry, we have to peach your positron emission tomography, not pets, although I'm sure that there are people out there who have their dogs or cats.
or whatever, or they're pet kangaroos, whatever you might own, on ketogenic diets.
Okay.
Absolutely.
Right.
So he's actually moved further.
He's done a pilot trial in a nursing home, actually, where he did not put the patients
on a ketogenic diet.
He simply reduced carbohydrate consumption at breakfast and lunch.
They still got the same dinner as everyone else.
And simply reducing carbohydrate consumption at breakfast and lunch resulted in cognitive.
improvement in a statistically significant way in some of those subjects.
I love that result. I'm sorry, I just have to highlight this. I'm a huge believer in directing
carbohydrates to specific portions of the day when one needs to be less focused and alert
and yet can replenish glycogen. Limiting carbohydrates most of the time during the day for me
has been a game changer in terms of maintaining alertness, et cetera. I'm not aware that I have
you know, age-related cognitive decline, but then again, I would, people around me may argue.
Let me, let me say, you are Andrew Huberman. There is no way you have cognitive impairment.
Although you didn't know me as a six-year-old. If you have cognitive impairment, we're all screwed.
Well, I have plenty of flaws in impairments. I'm well over 3,000 documented by people very
close to me. So, but this is very interesting, I think, in the context of everything we've been
talking about, because could it be that supplementing with liquid ketones?
or prescribing liquid ketones to people who are challenged with mood disorders or things of that
sort could be beneficial even if they are not willing or able to adhere to a ketogenic diet.
That is the million dollar question right now.
And we don't have good trial data to say yes or no.
My speculation, my hunch, having tried that clinically with you.
patients is it doesn't seem to work. It's not the same thing. The bigger reason for my
feeling confident in saying that is that we've had ketone salts and esters available for over a
decade now. We have tens of thousands of children and adolescents who are following a strict,
ridiculously strict ketogenic diet to control their epilepsy.
Those kids would love to be off the ketogenic diet.
Their parents would love to have them off the ketogenic diet.
Yeah, no birthday cake, no ice cream.
There is not one case report of any child controlling his or her seizures using exogenous ketones
without also doing the ketogenic diet.
I just find it hard to believe that at least some of those people haven't tried it out to see.
I do know some patients with bipolar disorder and even schizophrenia who are doing extraordinarily well on a ketogenic diet.
They have tried to switch off the ketogenic diet using exogenous ketones.
Their symptoms came back.
And so they found that it just wasn't effective.
Again, those are anecdotes.
My scientific speculation about why is because the ketogenic diet is actually not necessarily about ketones themselves.
Ketones are one of a multifaceted story there.
And so when people do a ketogenic diet, they're also improving, they're lowering glucose levels.
They're improving insulin signaling.
They're ramping up mitochondrial biogenesis, in particular in the liver.
Because mitochondria actually make ketones.
That's where they're made, and they're primarily made in the liver mitochondria.
So when somebody's in a fasting state or on a ketogenic diet, their liver mitochondria go through the roof.
Because they're being called to action.
It's like, hey, bodies in starvation mode get to work.
And so the mitochondria, the cell senses, we need more mitochondria to process fat, to turn it into ketones so that those ketones can get up to the brain and keep the brain fueled.
Because fatty acids can't fuel the brain.
Only ketones can.
Now, so my sense is that, and the gut microbiome changes and everything, the changes in hormones.
So if you're eating a lot of donuts and drinking a bottle of ketones, the donuts are going to prevent your body from lowering glucose levels.
You're still going to have the high glucose levels from the donuts.
You're still going to probably have the impaired insulin signaling.
You're probably still going to possibly have some inflammation from the inflammatory effects of that food.
and so just drinking ketones alone won't be enough.
I think for people who are metabolically healthy, I'll include you in that,
I think ketones can play a really beneficial role, no doubt.
I think exogenous ketones may in fact prove invaluable in clinical use
for patients who maybe can't follow a super strict ketogenic diet,
but maybe could do a low-carb diet.
And then given the research that's happening with alcohol use disorder,
I could imagine a situation,
here's the million-dollar like, you know, a tip to whoever wants to go out
and get this if it actually turns out to be true.
I could imagine a scenario where we use exogenous ketones with alcoholics
and that every time they have a severe craving for alcohol,
they drink ketones instead.
Which sort of tastes like alcohol?
The ketone esters, when I take them, they, I drink them straight.
Sometimes I'll put them in seltzer.
And I'm not a big drinker.
As I mentioned, I might have an alcohol drink every once in a while.
I just don't ever crave it.
I just do it every maybe, I think, I think 2020 was the last time I had a drink of alcohol.
And so obviously I'm not a good representative example.
But the ketones taste good to me.
And they obviously don't get you drunk.
They just, they do seem to flick on my alertness pretty quickly.
And my understanding is that they are the brain's preferred fuel source, meaning they are going to be the first fuels used by the brain when there's a buffet of fuels available.
If there's glucose in my bloodstream, there's circulating liquid ketones, that ketones would be used first or preferentially. Is that true?
I think it's a complex question.
I mean, some research that we have suggests that there are brain areas or brain cells that require glucose and cannot use ketones.
So 100% of the brain cannot be fueled with ketones as far as we can tell.
So there are some areas that require glucose, and that's probably the reason we have gluconeogenesis is to keep the body going and keep the brain going no matter what.
but when ketones are available, especially if ketones are high,
the way I think about it is not that ketones are like the preferred fuel source
and glucose goes to the wayside.
But the way I think about it is that you have a range of cells
with varying degrees of metabolic health.
And some of those cells are going to be extraordinarily healthy
with appropriate, healthy, abundant mitochondria.
And those cells are probably going to continue to use glucose as a fuel source.
But if ketones happen to be there, sure, they'll use that too.
Like, why not?
But the real money is metabolically compromised tissues,
whether it's brain cells or other tissues.
But we're talking about the brain.
So if you've got metabolically compromised brain cells,
because it's not across the board.
with Alzheimer's brain scans, there are specific regions that are more metabolically compromised
than others. And that's why we see patterns of atrophy in specific brain regions is because
those regions are dysfunctional metabolically for whatever reason. And we can get into why that might be.
But my sense is that if you've got a metabolically compromised cell, that cell is sending out a distress
signal. That cell is calling resources from the body, like feed me, give me something. And if it can't
use glucose effectively, it is going to suck up those ketones and then start running on all cylinders
or closer to it. And that process is so critical because what it means is that if that cell was
barely getting by on 60% of its real ATP requirement.
It means that it doesn't have enough energy for maintenance and repair functions.
As soon as you give that cell 100% energy or close to it,
even if you get it up to 90% of its preferred energy amount,
it can start to repair itself.
I mean, that's the beauty of the human body.
living organisms is that they have a priority list of what they're going to do. And if they,
if that cell senses that there are defective molecules, defective proteins in this cell that
need to be replaced, once it gets enough fuel, it will start repairing itself and doing that work.
That makes sense. Thank you for that clarification. I'd like to talk about Alzheimer's and
age-related cognitive decline generally. I know many people out there are just terrified of losing
their memory for the obvious reasons. Memory sets context, et cetera. And many people have relatives
that suffer from Alzheimer's or other forms of dementia. I've heard that the ketogenic diet and
diets like it can be very effective for helping to offset some of the symptoms of Alzheimer's and age-related.
cognitive decline. In fact, I even have a friend I won't out in by institution who's the chair
of cardiology who contacted me of all people asking whether or not I was aware of any studies or
whether or not I knew of anybody who had benefited from ketogenic diet for Alzheimer's. And I thought,
well, why don't you ask one of your colleagues in neurology? But his response was really interesting.
He said, there's, there are many books out there for the general public. There are a lot of online
discussions about this. There are a lot of assertions about this and some animal studies.
But again, these are his words. There are very few, if any, controlled clinical trials
exploring the role of the ketogenic diet for the treatment or reversal of Alzheimer's in
age-related cognitive decline. I'm hoping that statement was incorrect or soon will be incorrect
because those trials are ongoing. But he said, yeah, you know, the people are most popular for,
telling us about the important role and positive role of being in ketosis for Alzheimer's,
for some reason they just won't do a clinical trial.
And that's been frustrating to the community.
So this is a very educated, very accomplished person who's a physician of heart medicine
as opposed to something else relate to the brain.
But what is the story there?
And for goodness sake, why aren't there clinical trials?
on ketogenic diet and Alzheimer's.
I don't expect you to have the, to be responsible for that fact.
But goodness, I would think this would be like the obvious thing for NIH.
I'm on study section, you know, but not for these sorts of experiments.
Why isn't money just avalancheing into this area based on all the anecdotal evidence
that people are talking about?
So we've got a couple of small pilot clinical trials.
The best one was a randomized controlled trial.
I think it only included 26 subjects, something like that.
Randomized to 12 weeks of a low-fat diet,
10-week washout, 12 weeks of ketogenic diet.
Some of the participants got keto first and then low-fat,
other participants got low-fat, then keto.
And that trial actually found that when patients,
were in ketosis.
They had statistically significant improvement
in activities of daily living
and quality of life.
And they did have improvement in cognitive function,
but it didn't reach statistical significance.
That improvement did not.
We've got other trials.
We've got several animal models
showing that the ketogenic diet
can improve biomarkers of Alzheimer's disease in Alzheimer's models.
So it can reduce plaques and tangles.
It can even improve cognitive impairment in animal models.
We've got a couple of other small pilot trials of ketogenic diet in humans
showing that it improves biomarkers compared to, say, the low-fat diet
or the American Heart Association diet.
So we've got those.
I think one of the biggest challenges that I'll just share openly,
you know, and this is, I'm somebody who's pretty passionate about this research,
and I believe it has a lot of potential.
But, you know, Johns Hopkins researchers attempted to do exactly this kind of a study.
Alzheimer's patients, ketogenic diet versus the, I think, American Academy of Aging or something like that,
diet is the controlled diet.
which presumably has starches in there.
I think that's the key variable.
Probably lots of, yeah, lots of whole grains.
Lots of whole grains.
Yeah, some potatoes.
And they spent, I believe, over three years,
they screened over 1,300 participants,
1,300 people who expressed interest.
At the end of the day,
I think they only got 27 people to enroll
and only 14 of those people completed the study.
Wow.
Despite that, what they found was that the subjects who achieved ketosis had cognitive improvement.
But people on study section are going to look at a study like that and say,
even if the science is there, if you can't get people to do this diet,
why would we spend money on researchers trying to get people to do this diet?
I should mention study section is this closed door panels of 40 or so people.
There are many of these panels.
Different divisions in the National Institutes of Health use different panels.
And then grants are evaluated and a very small, because of the size of the federal budget for research,
A very small percentage, usually about 10% of these studies are funded.
The rest generally don't end up happening.
That is very informative.
What you just described is very informative because now it makes sense to me.
There's no conspiracy.
It's not like big pharma, I don't think, is trying to suppress trials of ketogenic diets
on Alzheimer's because I would imagine the first thing that,
that Farmer would want to do is to see that study done.
So they didn't have to.
And then the moment it was done,
if it showed a positive effect,
they'd probably wanna isolate the molecule
and wrap it up in something that people would take, right?
So I don't think there's any active suppression by pharma.
I think the farmer would probably be cheering from the sidelines
because they could capitalize on it
because ultimately the studies are done by scientists,
but the treatments are generally doled out
by pharmaceutical companies and we're physicians.
So I don't believe there's a conspiracy there.
That is very interesting and it's kind of amazing,
given our discussion of earlier, which is that you had a patient that was having schizophrenic
symptoms who managed to stay on this diet. So is there something special about Alzheimer's
patients and people with age-related cognitive decline? Presumably they're very dependent on others
to cook for them and shop for them. I think that this is a almost perfect controlled
environment for getting this study done. I think that is the key issue. So again,
I get patients with bipolar disorder, schizophrenia, extraordinarily impaired people to do this
diet and stay with it.
But it's because I'm providing like a weekly session for them.
And I imagine this study did not provide that kind of intensive support.
So I think, you know, in the pilot trial that I described to you, they actually got, I think,
over 90% compliance with the different dietary interventions.
So some of it is going to be dependent on the research group,
and does the research group understand that this is not,
it's not like prescribing a pill here.
Take this pill and take it every day and come back in three weeks.
And even then, we don't know for sure that the patient took the pill every day.
We just assume they took the pill every day,
and studies say they probably didn't.
But so I think when we think about a dietary intervention, we need to think about more intensive support in education.
And that support could be a health and wellness coach.
It could be a dietitian.
It could be education of the family.
It might even be providing them with dietary, like meals, that maybe for six months, we actually provide them with ketogenic meals.
once a week, put them in your freezer,
you know, microwave them when needed,
to make this diet as easy and doable as possible.
Because if we can get people to do the diet,
if we can get them through the first couple of months,
most people can learn how to do this diet.
More importantly, I didn't mention this before,
but the number one reason I am so successful
at getting patients to stop,
on this diet for years is because of the consequences to them when they go off of it.
That is the reason I can get schizophrenic patients and bipolar patients to do this diet,
whereas other people can't get an everyday human being to do it for weight loss.
Because the weight loss patient doesn't experience devastating, tormenting symptoms when they break the diet.
oftentimes they are rewarded.
They eat something they really enjoy
and they get a little bit of a dopamine rush from it
and they're off to the races.
They're like, I'm going to, oh, I've already cheated.
I'll cheat again.
I'll get back on it someday.
And they never get around to it.
My patients, when they go off the diet,
they start hallucinating within 24, 48 hours.
And they quickly realized that was a really stupid thing to do.
That piece of cake was
not at all worth the torment that I'm experiencing now. So they get back on the diet. I suspect with
Alzheimer's disease, we might notice something similar. These people, some of these people have very
mild symptoms, so maybe they won't have that kind of a reinforcement, negative reinforcing kind of
experience. But I think some of them will. Some of them recognize that they are impaired,
and if this diet could help them remember better, if this diet could help them function better.
And again, that's what the pilot trial showed, is activities of daily living.
That means these people are able to go to the bathroom on their own.
You're able to get themselves dressed, whereas they needed help with those things before.
Those are actually really important things to both the patient and the caregiver.
And if they go off the diet and then quickly revert into a more symptomatic state, that might be
reinforcing enough for them to figure out a way to do the diet on their own.
And if we think about, you know, if this really is an effective intervention, and yes, we need
longer trials, larger trials, all of that, because there are plenty of stories in the medical
field where pilot trials looked really spectacular and promising and then larger trials just failed
to show the benefits. I believe based on all the science of metabolism, mitochondria, glucose
hypometabolism, all of that, I believe the science makes this an obvious treatment that has real
potential. So, you know, people will call me bias. That's fine. I've got my bias.
No, based on clinical observation and extensive clinical observation at that.
I think biases that are simply because we want to feel a certain way or believe something
are worth are worth critiquing, but bias based on observation.
Here, I should mention that, you know, most of what we know about human memory was sparked
by one patient, a famous H.M., who I think was living in Harvard Medical.
in one of the hospitals around there, many hospitals on Longwood campus, but one patient.
I mean, the reason we associate the hippocampus with memory is because we knew that HM's hippocampus
was damaged, intentionally damaged for epilepsy treatment, right?
So this idea that everything has to be a randomized clinical trial to me is crazy.
I mean, of course, that's a gold standard and it's essential, but there's so much information in textbooks,
medical textbooks in particular that are gleaned from single patient case studies or from
three patient neurostimulation in the brain or something of that sort. So to me, I'm still
perplexed as to, you know, why there's this insistence on only one form of evidence. Clearly, what you're
doing, the important work that you're doing clinically and in the research side and in public
communication is assisting this. I have a question about, or more of a statement slash question about
the ketogenic diet. Based on everything that we've talked about, seems to me that the ketogenic
diet for weight loss is a very interesting aspect of the diet, as is intermittent fasting for
weight loss, even though it might just be by way of caloric restriction that occurs with fasting.
but then in some ways the effects of the ketogenic diet on weight loss are a bit of a decoy for most people.
That's where their mind goes.
This person lost X amount of weight.
Maybe that made them feel better.
Maybe that actually made them underweight.
I think you've talked about it for some people that can actually bring them underweight.
But I'm glad that we got the chance to dive into the description of ketogenic diet for epilepsy
because it really is a medical intervention that has a side effect of weight loss or could be used.
to treat obesity and induce weight loss. But it's really about far more than that. And that raises
a question for me, which is, you know, we've been talking about the ketogenic diet as one thing.
But I've heard you discuss this before where, you know, just as a physician will prescribe different
dose, dosage ranges of a given drug, you can prescribe different dosage ranges of a nutritional
plant, a diet. It's not one thing. It's not zesion.
necessarily zero carbohydrates or 100 grams or 50 grams.
It depends on the patient and a lot of other factors.
I've heard you list off various things.
Classic keto.
Maybe you could just briefly tell us what that typically is.
Because I think most people think it means eating a lot of meat and not carbohydrates,
but might not be that.
Fasting.
And then some of the other,
you mentioned Atkins earlier.
We don't have to go into each of these in detail.
And I know in your book you talk about not just the science and clinical background,
but also some actionable steps that people could consider so they can refer there for more detail.
But for somebody who, let's say, is depressed.
They've had some rounds of depression.
Maybe they're on intrepressants, maybe not.
And they want to try something like this.
Obviously, this has to be done in concert with a physician observing all this.
But what is the typical thing that you probe with first?
Just like with a drug, you might probe with 20 milligrams of a drug.
what's your typical pro initial dietary intervention probe terrible languaging I realize and I'm
criticizing myself for that but I think people get the idea the the real answer is that I don't
have a one-size-fits-all recommendation for any person so the first thing that I'm going to assess
with the patient is what symptoms are they having what is their current diet like and what are
they willing to do I try to meet them where they're at so um if somebody
And I want to point out, like you mentioned the all-meat version of this diet, which is often referred to as the carnivore diet.
A very controversial diet.
There is no doubt. That exists.
And for some people, some people swear by it.
They swear that they've tried other versions of ketogenic diets.
And only when they went to a carnivore diet did they get benefits.
But there are vegetarian and vegan versions of the ketogenic diet.
So in my mind, this is not at all about the diet wars of animal-sourced versus plant-sourced foods.
It's about inducing a state of ketosis, which is mimicking the fasting state.
That is what it's about.
And you can do that by not eating anything by fasting or intermittent fasting, and you get your
results.
So no diet is a ketogenic diet.
So it's not about the foods or the types of foods that you're eating.
It's about inducing a state of ketosis.
The first variable I'm going to look at when I recommend this or prescribe this is the person's
current weight. If somebody's obese versus somebody who's thin, I'm going to use different dietary
strategies for those two situations. In the obese patient, they have tons of fat stores on their
body already. Usually it is a goal of theirs to tap into some of those, and they'd like to lose
some weight if they're going to try a ketogenic diet for brain health anyway. And so I'm going to
Use that.
So that person, really the diet is carbohydrate restriction.
And that usually is a sufficient intervention.
Both simple carbohydrates, meaning sugars, and fructose also.
Fruitose definitely.
So no added sugars, essentially.
You can have added natural sweeteners like stevia or monk fruit.
You might use artificial sweeteners.
I'd probably years after doing this,
I'd probably recommend steer away from them if you can
because I think they tend to stimulate cravings
for high-carb foods.
So if you can kind of get through a couple of weeks
without sweet things,
your cravings for those will go down
and it'll make the diet easier and a little more sustainable.
But let's say you can have your artificial sweeteners
if that's what you really want.
So I'm going to say less than 20 grams a day for those people.
They can have all the protein.
they want, they can have vegetables and they can have all the fat they want, but I'm not going to push
fat on those people. I'm not going to tell them eat a lot of fat at the same time because I want to
use the fat on their body as the fat source, at least early on. Are you encouraging healthy fats like
mono and saturate fats like olive oil or are you encouraging people to eat a little less butter,
etc.
I tend to encourage, again, a wide range of fats, and it's going to depend on the person.
A lot of times people come to me with very specific ideas.
But I'm going to tend to encourage olive oil, avocados, nuts, which are usually considered
even by the American Heart Association, healthy sources of fat.
The more controversial thing are things like coconut oil or coconut cream.
which the American Heart Association might say is not a healthy fat.
I kind of disagree with that and don't think it's unhealthy at all, actually.
And when you look at the epidemiological studies of saturated fat causing heart disease
or causing adverse outcomes at best, maybe increases your risk 10 to 15 percent, at best.
How much coconut oil can people ingest anyway before they either develop diarrhea, no joke,
or just sort of get tired of coconut oil.
But anyway, your point is taken.
But they can eat meat if they like meat or they can eat eggs.
Or if they don't like meat and eggs, they could eat sardines or things of that sort.
I mean, I personally can't.
I can't even stomach the, I don't even like the word sardine.
I have nothing against the actual fish, but that's just me.
But obviously people have, I say this because people have different preferences, right?
Yes.
I'll eat a steak, but I'm not going to eat a sardine.
And I'm going to go with that.
And again, there are vegan sources.
of protein that people can eat tempe and, you know, other things.
So that's the obese person.
It's carb restriction is the primary initial phase.
The thin person is going to need to eat a lot of fat
because they don't have a lot of fat stores on their body.
And if I want them in ketosis, clinical ketosis,
I'm going to have to feed them fat.
So that's the person that I'm going to say,
make sure you get in avocados, olive oil, butter, maybe a cream, heavy cream.
So heavy cream is delicious.
It's a delicious way to get your fats in and have one patient who just drinks it straight
to just try to get it in.
I get it.
I've never had an appetite for sweets.
I absolutely love savory fatty food.
When I was in high school, I was thin, so I was able to do this.
but I used to drink half and half.
Sometimes I wake up in the middle of the night and drink it just because it tastes so good.
It does taste good.
So if they're on a ketogenic diet, I'm going to push them away from half and half
and toward heavy whipping cream.
And so you can whip that up.
You can freeze it.
It turns into ice cream.
You can add vanilla.
You can add cocoa powder.
You can add all sorts of things.
And you're off to the races with shakes and ice cream and moose and all sorts of things
that you can have.
with any of these patients, the beauty of this diet is I have objective biomarkers.
I'm going to have them measuring ketones, and I'm going to adjust the diet based on their state of ketosis
and or the clinical benefits that I'm looking for.
If it's an average person who is not currently under psychiatric care, not taking prescription medicines,
but is saying, I'm burned out, I'm exhausted.
I want some of that brain energy that Andrew Huberman's talking about.
He talks about feeling good.
I want some of that.
I'm probably actually going to recommend the protocol you describe,
which is let's see if we can just carb restrict for a while
and see if that produces clinical benefit.
I have one, he's not even a patient,
just somebody who read my book.
I didn't tell him anything.
and he came away from it saying he was ready to start an antidepressant for his anxiety
had chronic anxiety, he was trying meditation, was trying all sorts of things.
Nothing, those things weren't enough.
He was ready to go on prescription medicine.
He read an early copy of the book.
He took it upon himself without consulting with me to restrict carbohydrates alone.
He did not go ketogenic.
He is a vegetarian.
He restricted carbs.
Within three weeks said, I don't need prescription medicine.
I can't believe how much better I feel.
And all I did was cut out some of the high-carb foods in my diet.
So I think for some people, it can be that simple.
For people with serious mental disorders, if they are chronically depressed, if they're on lots of prescription meds,
if they're disabled by their symptoms.
And certainly if you're bipolar or have schizophrenia or something,
those are the people I really do want them to work with a medical professional
because meds may need to be adjusted.
They really need a real shot at this diet.
It's not like weight loss.
Weight loss, everybody wings it.
And either you're successful or you aren't.
You look on the internet or you read a book or you do, you know,
even the colleague that you mentioned, he's probably just reading.
Who knows whether it's credible information or not?
and just winging it and seeing whether it works or not.
For people with serious mental disorders,
I want you to treat it like you have epilepsy.
Because you do have a serious brain disorder.
It's impairing your ability to function in the world.
It's impairing your health and happiness.
You deserve a competent medical treatment.
And we have that.
We have a hundred-year evidence-based.
We've got dietitians who know this, like the back of their hand, they can monitor your level of ketosis.
They can help look for vitamin and nutrient deficiencies that can be a consequence of the diet and make sure that you're not developing those.
They can help tweak the diet if needed.
They can give you ideas if you're getting bored with eggs every morning.
They can give you ideas for what else you might have.
and, you know, if you're using it to treat a serious disorder, I think you need serious help.
A couple of questions, a little more detailed, but I think a lot of people will have this on their mind.
Is it ever the case that you'll prescribe somebody, the ketogenic diet in conjunction with intermittent fasting?
So eat keto, but eat between the hours of 11 a.m. and 8 p.m. or something like that.
That's the first question.
Absolutely.
So, and I have one patient with type 2 diabetes and chronic depression, and he will try to
follow the ketogenic diet, and sometimes his blood sugars are still very high.
And sometimes I will ask him to do either intermittent fasting or even a three or four day
water fast.
And it is shocking.
When he does a three or four day water fast, you know, the first day or two, he feels like
crap. I'll just stay up front. Don't do it if you've got an important meeting or business trip or
any, like, don't be. So this is just consuming water? This is just consuming water. No black coffee.
I usually tell him he can have plain black coffee or tea. But you have mercy after.
I have a tiny ounce of mercy. But when he does it, his blood sugars plummet in a good way.
his blood sugars are normalizing.
But the last time he did it,
he actually got to seven days at one point.
And he said,
I feel great.
I want to keep going.
I can't believe that I'm not hungry,
but I am not hungry at all.
I don't miss food at all.
And at seven days,
I kind of cut the core.
I was like, no, no, we're done.
You got to eat.
Well, I find it really interesting
that the intermittent fasting,
of course, controversial at some level,
but as to whether or not it's,
just beneficial by way of caloric restriction because it is one way to achieve
caloric restriction, whether or not it has additional benefits. But I'm very interested in the
neural side of it. And it does seem that the fasted state can start to take on its own rewarding
properties where people get dopamine release, not from eating, as most everyone does, but from
abstaining from food. Now, this can be pathologic in the sort of example of anorexia neurosa,
which is we both know as the most deadly psychiatric illness.
But for non-anorexics, I think it's interesting to note that eventually not eating can have its own rewarding properties to it that aren't just related to weight loss.
But in the short term, feeling, in other words, feeling really good by way of abstaining from eating.
Yes.
Well, and that's actually, it raises an important risk that I haven't mentioned yet, but at least in psychiatric patients, but even in some patients who just, you know,
use the keto diet for weight loss.
I have seen definite hypomania.
So these are people that aren't sleeping very much.
Are they also getting kind of delusional thinking?
They're going to run for president.
No.
So the distinction between hypomania and mania,
so mania, you might become psychotic and delusional.
Mania, by definition, is problematic.
It's causing a problem in some way or another.
And if you have psychotic symptoms,
it's definitely called mania.
blown mania. Hypomania, for better or worse, is something every human being probably craves.
So it is feeling extraordinarily good. It's getting by on less sleep, but you don't need
to sleep. Who needs sleep? I've got things to do. My brain is running on all cylinders.
I feel so creative. There have been lots of famous people through the ages who have
have been bipolar, probably bipolar, and some of their most productive periods of time, whether it's
art or creating scientific models or what have you, we're probably during hypomanic episodes.
So what do you do in that case? I mean, I'm obsessed with getting sufficient quality sleep.
It's a kind of a repeating theme in our podcast and many of my social media posts.
and I always recommend behavioral tools first, then exercise, viewing sunlight, et cetera, the appropriate
times, avoiding late night artificial light exposure, et cetera.
And occasionally for people who are doing all that and still struggle with sleep supplementation,
one of the things that I've seen some data on is that for people who are following a low carbohydrate diet,
that enositol in particular can be helpful for getting into sleep,
probably because it has a bit of an anti-anxiety effect.
But presumably there are other things out there too.
The magnesiums will generally do that.
A hot bath will do that too for that matter.
But what you're talking about is people who are going, what, a day and a half without sleep?
Or they're just, you know, two hours of sleep a night?
I have.
So the worst case I saw was actually a mental health professional who didn't recognize it initially.
He went six months with two to four hours of sleep every night.
Because they were on a ketogenic diet.
He was on a ketogenic diet.
was getting by on two to four hours of sleep every night,
did not initially recognize that this was a problem.
He was feeling great.
He was feeling that keto high.
And he was actually waking up and like at 4 a.m. going for 10 to 20 mile runs most days.
He finally stopped the ketogenic diet after about six months because he said,
I can't maintain my weight.
I'm losing too much weight.
Sorry, I was just thinking there's some social media personalities that associated with nutrition that might be hypomanic.
I'll let you do the clinical evaluation.
So what does somebody do in that case?
So I don't know that I've ever been hypomanic, but as I mentioned earlier, unless I've done a very high intensity workout early in the day and I need to replenish carbohydrates, I typically eat meat, fruit and vegetables throughout the day, minimum amounts of fruit.
but some. And then at night, I switch over to mainly carbohydrate. It really helps me sleep. It replenishes
glycogen stores. I sleep really well. Wake up the next morning, repeat. And of course, this goes
against a lot of the dogma that, oh, you're not supposed to eat carbohydrates late in the day.
And this is what works for me. And so I do it. For somebody like this mental health professional
who was hypomanic, would going off the ketogenic diet entirely be the best idea? Or could it
be that adjusting when they eat their carbohydrates would be advantageous in order to make sure that
they felt alert and great during the day, maybe not hypomanic, but then, you know, we could have
a four to eight hour night's sleep as opposed to a two to four hours night, which is really
very little sleep. Yeah, it can't be healthy. It's not healthy. Even if you can do it and feel great,
I imagine that the brain is suffering. It is. And the body is suffering. And your friends and family
the body is repairing itself with sleep. And so, yeah, it's, you know, if it's somebody who's
not a patient, they're not a mental health patient. They're not using the ketogenic diet as a
mental health treatment. They're simply doing it for whatever. I actually start with everything
you've just outlined. Let's start with behavioral measures first. And the first intervention is
education. You need at least six hours of sleep a night, period. End of story. That's non-negotiable.
If you're not getting at least six hours of sleep a night, we need to consider this a problem.
So figure out a way to get six hours of sleep. For some people, that's enough. Just the education,
they don't get out of bed at 3 a.m. It might take them an hour to fall back to sleep.
They fall back to sleep. For most people, if you can get three,
nights of decent sleep in a row, the hypomania goes away. That is the way to extinguish it. And
then they still go on feeling a high from it. They feel great. Their brain feels good in terms of
memory concentration, motivation, all of those things. But they're not hypomanic anymore.
And then I might use supplements, melatonin, others that you mentioned.
magnesium is a big one.
And for some, I will recommend exactly what you're doing.
Eat some carbohydrates in the evening before you're going to bed.
Either have them at dinner and then wait a few hours before you're going to go to bed
or have them right before you're going to go to bed,
just to try to calm your body down and get it going.
For when I'm using this as a clinical intervention,
especially with patients with serious mental illness,
I actually want them in a state of ketosis long term, so I'm not going to do the carbohydrate intervention.
I'm going to try all the other ones.
But if they still can't sleep, even with supplements, over-the-counter supplements,
then I'm probably going to go with prescription sleeping medicines as a temporary stopgap
to try to get them three to seven days of decent sleep that usually breaks the hypomanic cycle.
and then they stay on the ketogenic diet because it ends up resulting in all of these other improvements that I've described.
Their illness can sometimes go into full remission.
Is it low-dose tracidone as a first-line prescription?
I would not use tracodone.
I would actually specifically avoid tracodone because it's an antidepressant and they're already hypomanic,
and I certainly don't want to push that further.
So as long as it's somebody without a history of addiction, I'm going to use a benzodiazepine
or either commonly called the Z medicines for sleep, Zopadem or Ambien or something like that.
Those tap into the opioid pathway. Gabba, Gabba. So I'm probably, I usually start with something like
Ativan or Clonopin or something like that, probably Ativan because it's shorter acting.
And again, I'm only looking to use it short term. I let
them know that up front. We're looking for three to seven days of decent sleep, and then we're
going to try to get them off that medicine. And usually people are off to the races and can
sustain it well. A question about hormones. Many of the Huber and Lab podcast listeners will
ask, anytime we're talking about something like exercise or drug treatment or behavioral treatment,
people will say, what about the menstrual cycle? How is that impacted by this? And how does this
impact, how does the menstrual cycle impact its efficacy, etc. Carbohydrates and caloric restriction
have been implicated in different interaction, are known to interact with the endocrine system.
So what do you do if you have a patient who is depressed or could have psychotic symptoms,
but let's go with depression because that's probably a bit more familiar to most people?
and then they're on a low carbohydrate or full ketogenic diet, but their menstrual cycles cease.
How do you deal with those adjustments?
And I guess we could expand this conversation and say, what about male fertility also?
Because subchaloric diets seem to improve, my understanding is that sub-maintenance
caloric diets, weight loss diets, will improve testosterone and estrogen,
ratios in males that are obese, but for someone that's not obese to go on a subcholaric diet,
that it can start to impair testosterone levels and probably not render them infertile,
but certainly adjust that whole axis. So what about interactions between ketosis,
diets, et cetera, and the endocrine system? The real answer is I don't think anybody knows,
and there's not a one-size-fits-all answer. Because I've seen,
I've seen examples and I'm aware of science to back up polar opposite conclusions.
So the first general observation that I'll make, I know so many couples, husbands and wives,
boyfriends and girlfriends, heterosexual couples who have tried the ketogenic diet to lose weight
together.
And end up with a baby.
No, almost universally, the men have a much easier time with it than the women.
It's not across the board, but I know so many examples where the women say,
I couldn't tolerate that diet.
It did not make me feel better.
It actually made me feel worse.
And I think in those cases, it probably does relate to hormones.
I'm aware of animal models of, you know, mice and,
particular ketogenic diet in mouse models. One researcher shared with me, the thing that was
striking is that the female mice never got pregnant on the ketogenic diet, whereas the mice
on the standard diet were just having babies right and laugh, and it was just shocking the difference.
On the surface, it makes sense. The ketogenic diet is mimicking the fasting state.
Women who are trying to reproduce should not be fasting.
If your body is in a fasting state, it probably does not want to expend resources,
metabolic resources, calories, nutrients, and other things to creating a baby
because your very life is being threatened by quote unquote fasting or starvation.
that even though the ketogenic diet is a sustainable non-starvation diet,
we're really using that diet to trick the body into thinking that it is in a fasting or starvation state.
And so just from a kind of evolutionary stance,
it makes sense that women's bodies may actually have significant changes in hormonal status
to prevent pregnancy because a woman should not be having a baby.
baby when she's starving to death.
I know of examples of women who are the opposite, though, who have benefited dramatically and
tremendously from the ketogenic diet, have put schizophrenia, bipolar disorder into full
remission.
And I do actually know of one case, at least one case.
A woman infertile, she and her husband had been trying for three years, no pregnancy,
she went keto within four months she was pregnant.
How do I make sense of that? I don't know.
And unfortunately, I don't think we really have good controlled data
on what does the ketogenic diet do to male hormonal systems.
What does the ketogenic diet do to female hormonal systems?
But, you know, clearly I think changes are happening.
And I don't have a way to predict it, at least.
If somebody else has great insights, I welcome them.
But I haven't seen them published.
It's a terrific answer because when things are all over the place and bidirectional,
depending on one circumstance or the other,
I think it screams for controlled studies and more descriptions of case studies
and anecdotal data too.
So I think it's an excellent answer.
It also calls to mind the important public service announcement
that because of these bidirectional effects that you describe, please don't use fasting or the
ketogenic diet as a reliable form of contraception. Yes, please don't. I have a final question,
which relates to something that is very much starting to get buzz now and maybe more so for people
that hang out in the Twitter space or the nutrition space. But there's a new class of drugs
that I think initially were developed to treat diabetes, but are now being evaluated for their
efficacy to treat obesity. And these are the semaglutide drugs that are involved in, they tap into
these glucagon-related PEP-G-LP-1 pathways. And as is a story that we've talked about a little
bit on the podcast before, but many people I imagine probably haven't heard that conversation.
I would simply like to know what you think about these drugs.
They obviously adjust the way that glucose and insulin are managing energy,
both in the body and the brain, and can produce weight loss.
So that to me, when I look at the data, you know, it's impressive,
but a good, you know, a good logical shift in diet and exercise could achieve similar weight loss,
but a lot of people just won't do that.
So the question I have is, what are your thoughts on semi-glutide?
and other GLP, I think I might have said GLT before, excuse me, GLP1 related compounds.
And do you ever prescribe these in conjunction with these dietary shifts?
Because it seems to me they would fall right in with the catalog of other approaches that you have available.
The real answer is I am not at all an expert on these medications.
But what are your thoughts about them?
I mean, they seem to be weight loss drugs, not unlike the,
Fenn-Fen drugs of the 90s that then were banned because a few people didn't handle them well.
They are. And, you know, we had Fenn-Fenn-Fenn, and even before that, in the 1950s and 60s and
70s, dexedrine.
Amphetamine.
Amphetamine.
Mother's little helper.
Was, yes, was the treatment of choice for women across the United States to keep their slim figures.
and we created addicts and all sorts of problems,
but they were widely used in probably millions of women
because they work.
Because they kill appetite.
They kill appetite.
My overall thoughts are this.
There is zero doubt in my mind
that the obesity epidemic
is a threat to human health
and potentially the human space.
If it keeps going at the rate it's going, it is a threat to our species.
We have to figure out what on earth is happening and what can we do about it.
These medications in early studies are highly effective over a year or two.
That's promising.
I am worried, though, that we're not attacking the root cause of obesity.
and if we're not a if the root cause of obesity ends up being some kind of poisoning of the metabolic machinery in the brain or body
and i would argue that probably relates to mitochondrial health and mitochondrial function
i have every reason to believe that taking a medication that helps you lose weight may not
be addressing that problem and therefore may not be addressing all of the negative health consequences
of what we call obesity. I actually, so obesity in and of itself, we know that excess fat
can become inflammatory and can cause problems in and of itself, but I actually see obesity as a
symptom. I see obesity as a symptom of metabolic derangement in the body or brain.
And that is why people become obese. And that if we're really going to get anywhere,
we need to identify what is causing that metabolic derangement.
Using a symptomatic treatment like a GLP1 medication, to the best of my knowledge, is not a
addressing that core problem and we're just ignoring it.
Maybe I'll be wrong and maybe these will be the wonder drug
that saved the human species and everybody will be thin
and healthy forever and ever.
I'm not hopeful because we've never,
we've had so many promising drugs come along,
fen, dexogen, other things.
We've had so many promising drugs.
And at the end of the day, when you try to muck with human metabolism using a single processed molecule man-made,
I can't think of even one example where it's been great for large numbers of people.
I mean, certainly manufacturing insulin is life-saving for people with type 1 diabetes.
So that would be an example.
But giving massive doses of insulin to people with people with.
type 2 diabetes actually is a downward spiral. I would much rather see people with type 2 diabetes
control their diabetes through diet and lifestyle. And that might be a ketogenic diet or a low carb
diet or exercise or good sleep or all of the other thing, all of it. I'd much rather see that
because when people try to control their type 2 diabetes with a molecule, even though it's a natural
molecule insulin, we know that that results in really poor health consequences.
results in higher rates of cardiovascular disease,
higher rates of mental disorders,
higher rates of premature mortality.
Do I think GLP1, you know, molecules are going to be different?
No, I don't have any reason to think they are going to be.
So that would be buying two cents,
but we'll see.
Time will tell.
Time will tell.
Meanwhile, I want to thank you for doing what is,
without question, pioneering work.
I mean, I'm, again, I'm not a clinician, but I've been around this space long enough to know that, indeed, there are no wonder drugs.
There are drugs that certainly can help alleviate symptoms in some individuals, but that lifestyle and in case of your work in particular in the discussion today, diet and the ketogenic diet in particular, it's clear can have incredible effects, miraculous effects.
effects in some individuals and positive effects in others that might not be of the same magnitude,
but nonetheless are extremely important. So I, on behalf of myself and the listeners and
certainly just on behalf of everybody out there, because everyone does need to be concerned
about mental health issues, whether or not they have them and in their family themselves
or otherwise because they impact everybody. It's really want to thank you for doing the
work that you're doing because it really is pioneering and its brain.
and I can see now based on our discussion why it would work.
You've given us a lot of hints into the underlying mechanisms that suggest as to why it would
work and you've given us examples as to how it has worked in patients that you've worked with.
And this field is expanding fast.
I think this is an area of psychiatry and medicine in general,
meaning behavioral and nutritional interventions that is expanding very fast.
So thank you for being brave and for taking this on and doing it in such a structured way
and for communicating it here today and with the general public through your book and your online presence.
We will certainly point people in the direction of those valuable resources.
Thanks so much.
I really appreciate it.
Thank you, Andrew, for being brave and having me on your show.
It's been a pleasure.
And for a great conversation.
Thank you for joining me for my discussion with Dr. Chris Palmer.
I hope you found it to be as informative.
actionable and exciting in terms of the various treatments
that we can now think about
when considering treatments for psychiatric disorders.
Once again, if you're interested in his work
or his new book, Brain Energy,
I encourage you to go to his website.
That's Chris Palmer MD.com.
You can also find the book Brain Energy
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