The Dr. Hyman Show - How Supplementing With NMN Can Increase NAD levels, Energy, Reduce Inflammation, And Improve Insulin Resistance with Dr. Andrew Salzman
Episode Date: June 28, 2023This episode is brought to you by Rupa Health, BiOptimizers, Mitopure, and AquaTru. NAD has been popping up everywhere, and for good reason. It’s a fundamental driver of our health and longevi...ty, and we’re now learning how boosting NAD levels might offset and improve the effects of aging. On today’s episode, I’m excited to talk to Dr. Andrew Salzman all about NAD—how it is a key component involved in mitochondrial production, and is a critical substrate for several enzymes, including sirtuins, which play key roles in healthy aging, weight management, metabolic syndrome, and metabolism. Dr. Salzman is a physician, inventor, professor, and biomedical entrepreneur. Dr. Salzman received his medical degree from Harvard University and has spent decades in drug discovery and development, raising over $165M in NIH grants for research. In addition to 50 patents, Dr. Salzman is credited with a breakthrough discovery in cellular DNA repair, which led to the world's first clinical application for successfully treating breast cancer caused by mutations in BRCA1 and BRCA2 genes. Millions of patients are benefiting from discoveries by Dr. Salzman in areas including mitochondrial health, gastrointestinal microbiota, damage caused by inflammation and oxidative stress to human cells and DNA, autoimmune disease, and cancer. This episode is brought to you by Rupa Health, BiOptimizers, Mitopure, and AquaTru. Rupa Health is a place where Functional Medicine practitioners can access more than 3,000 specialty lab tests from over 35 labs. You can check out a free, live demo with a Q&A or create an account a RupaHealth.com. BiOptimizers is offering my listeners 10% off Sleep Breakthrough. If you buy two or more you’ll get a free bottle of Magnesium Breakthrough. This is a limited-time offer. Go to sleepbreakthrough.com/hyman and use the code hyman10. Get 10% off Mitopure at timelinenutrition.com/drhyman and use code DRHYMAN10 at checkout. Right now, my podcast listeners can access the AquaTru water filter for as low as $249. That’s $100 off the normal price. All you have to do is go to drhyman.com/filter, and you can get this special, exclusive price. Here are more details from our interview (audio version / Apple Subscriber version): How NAD helps us produce energy (5:00 / 3:04) The science behind how NAD impacts health and longevity (10:08 / 8:15) The role NAD plays in maintaining health (16:27 / 13:26) NAD’s multiple functions (23:46 / 21:18) Preserving NAD levels (30:34 / 27:47) Where NAD is made in the body (34:53 / 30:35) How NAD benefits sleep (41:17 / 37:04) Do NMN and NAD cause cancer? (47:12 / 42:57) Research on NMN in humans (50:23 / 46:07) The difference between NMN and NR (1:00:54 / 51:55) Learn more about Wonderfeel Youngr NMN.
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Coming up on this episode of The Doctor's Pharmacy.
There are inflammatory changes that are chronic or subacute where NAD is actually regulating the amount of inflammation in the cell
and that has a whole effect on the development of injury to our tissues, cancer development, a lack of healing.
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And now let's get back to this week's episode of The Doctor's Pharmacy.
Welcome to The Doctor's Pharmacy. I'm Dr. Mark Hyman. That's pharmacy with an F,
a place for conversations that matter.
And if you are curious about longevity, which I imagine many of you listening are, and you may have heard about something called NAD or NMN or NR or sirtuins or supplements you can take to potentially extend your life and improve your health. You're going to love this podcast because we have an expert today, Dr. Andrew Salzman, who's a physician and inventor, professor. He's a biomedical entrepreneur.
He lives in Israel right now. He's received his medical degree from Harvard University and spent
decades in drug discovery and development. He's raised over $165 million in the NIH grants for
research, which is astounding.
That's a lot of money.
It doesn't give away that much.
In addition to 50 patents, Dr. Salzman is credited with a breakthrough discovery in how cells repair their DNA, which led to the first clinical application in the world for
successfully treating breast cancer caused by mutations in BRCA1 and BRCA2 genes.
So he's benefited so many
people, millions of people have benefited from his discoveries in areas including mitochondrial
health, gastrointestinal microbiome, the damage caused by inflammation and oxidative stress to
human cells and DNA, autoimmune disease and cancer, all the things we like to talk about
on The Doctor's Pharmacy. So welcome, Dr. Salzman. Welcome. Thank you. Thank you very much for having me here today.
Well, I'm really excited to talk to you because, you know, as many of you listening today know,
I wrote a book called Young Forever about how do we enhance our health span, increase the time
we're healthy in our life, and potentially expand our lifespan. And there's been so much research
on this lately that has really gone really deep into the understanding of the mechanisms of aging, what we call the hallmarks of aging.
And in those hallmarks, there's a lot of data and information there.
But there is something that's really important, which is how we regulate energy in our mitochondria, which is really the key energy-produ producing units of our body. When we eat and
we breathe, we produce energy called ATP. And in the mitochondria, that's where we do it. And it
has to be functioning well, they have to be actually efficient, effective. And as we age,
they decline in their number and their function, their efficiency. And that's kind of why we get
old and slow and tired. So there's been an amazing compound that's been the subject of intense research, you might have heard about
called NAD, or nicotinamide and nucleonide dibriboside or something like that. It's a big
fancy word. And it's the driver of our health longevity in many ways. So can you tell us what
is NAD? Why is it so key as a driver of our health longevity? And just give people sort of a high level background about what we're going to be talking about today, which is mostly about NAD. And ultimately, that fuel, that food that we ingest is changed and modulated until ultimately it provides molecules of energy that the cells can use throughout the body.
And NAD and the mitochondria are absolutely central to that process.
When the sugar or protein or whatever we eat enters the cell, it enters into various pathways. And in
these pathways, the foodstuff, which typically as an example might be glucose, is then modified
and cut and shaped. And NAD plays a critical role in this process. There are three separate
sequential processes in the cell which produce the ATP.
And in each one of these, NAD is generated to a certain extent.
And without that NAD, we ultimately cannot finish this sequence, this cycle, which leads to ATP.
So NAD is sort of the transfer agent that goes from the food to the final product, which is ATP, which we can use.
In the absence of NAD, you can't make ATP.
So NAD is an essential part of life.
As we age and as we have various processes that reduce NAD,
we're putting a number of factors in this process.
For example, we can't make ATP as well.
So when you're 20 years old and you're running down the field with a football, you've got a lot of NAD and a lot of ATP.
When you're 60 years old, you start to notice quite a difference, of course.
And look at the muscle of a 60-year-old or of an 80-year-old, because when we're 80,
we're still doing a lot of stuff today. But what you're going to see is there are fewer
mitochondria,
these powerhouses of energy.
There are fewer of them.
That's a problem.
But within each individual one, they're not making enough NAD.
And of course, they're not making enough ATP.
Now, if you're a couch potato, you're sitting there and you're watching the 7 o'clock news,
you're probably not going to notice that.
But if you try to run up the stairs,
carrying some groceries, or God forbid, run down the football field at the age of 70 or 80,
you don't have the capacity to ramp up and generate the NAD and ATP that would be required
to be competitive with a youngster. So we start to feel it as we get older. Now, in the overall
picture, this NAD deficiency is much more than
just energy. Although energy, let's start with that discussion because that's the key point.
But there are other things that I will come to which show the broad effect of having lower NAD.
So it's not just energy. But focusing on energy, we now know in humans that with time, with age,
every year, it's a little less NAD available to us.
We know in animal models, if we artificially suppress the amount of NAD, those animals can't perform as well.
And we have even more data which show that if we supplement and restore and bring back the levels of NAD to where they were when we were younger, we can do a lot more.
So NAD is a they were when we were younger, we can do a lot more. So NAD is a
critical factor in our energy. Now, what's interesting recently is that this whole story
of NAD has been tied into other mechanisms and other pathways in the cell that we didn't realize.
For example, we now know that NAD is involved in inflammation. It's involved in pain. And as we get older,
we're all feeling a little bit more painful, and we're also having loads of inflammation. We have
more inflammatory diseases. So this deficit of NAD as we age is really causing a broad
effect on our health. Yeah, it's so important because, you know, I think as we're sort of
unpacking the science of aging and longevity, which really has been neglected for way too long in medicine,
we're understanding that there are underlying pathways that are in the body that are designed
to repair, regenerate, renew, heal, and optimize our health. We just screw them up by how we live,
what we eat, how we don't move, stress we're under, environmental toxins, all mess up these ancient survival pathways.
And there's thousands of genes that regulate the process of actually healing, repair, rejuvenation, renewal.
And we see these decline as we age.
But at any age, it's possible to actually activate these pathways and reverse that process.
So NAD seems to be really a key part of the story.
And one of the hallmarks of aging
that I talked about in the book, and it's really an important one, I think probably the most
important is that deregulated nutrient sensing, in which there are four key pathways that are
sensing your nutrient environment, mTOR, AMPK, sirtuins, and insulin signaling pathways. And NAD
works specifically on the sirtuins to stimulate
sirtuins when there's low energy states, right? So can you explain what NAD does in the process of
helping us to regulate the sirtuins, what the sirtuins do, and why that's so important in
longevity and aging? Because I think people need to understand the science behind why everybody's
talking about NAD and NMN and NR and all these compounds that sort of have nice alphabet soup,
but what the hell do they do and how do they work in the body on these ancient preserved
pathways that can be activated to optimize our health?
Well, there are a number of different pathways that are both immediate, intermediate, and then long-term.
And NAD seems to be playing an important role in all three of them.
So in the most acute situation where you have an acute stress, where you've lost function or you've lost blood flow,
like in a myocardial ischemia where you have a heart condition or in a stroke where you've suddenly lost blood flow to your brain. These are instantaneous problems. These are immediate problems.
And those settings, NAD plays the dominating role because it is regulating the ability of the cell
to survive in an environment where oxygen has been suddenly removed. So we can classify a whole
bunch of conditions that are instantaneous that
we have to deal with. And that involves PARP, which we'll come back to later. But there are
pathways that NAD is regulating or is a substrate for, which we must have for an acute problem. So
those are the acute instant problems. There are inflammatory changes that are chronic or subacute
where NAD is actually regulating the amount of
inflammation in the cell and that has a whole effect on the development of injury to our tissues
cancer development a lot of a lack of healing so when we look at processes like diabetes metabolic
disease liver disease um and there where there's colitis, where there's chronic
inflammation as we age, that is also very important with NAD. As we get into the longer term changes,
we're talking about genetic changes or regulation of genes, and I think this is where you were
coming at. And then, ____ and PARP are presently are known to regulate a lot of the different upregulated or downregulated expression
of key genes. So in the case of sirtuins, for example, NAD is a necessary cofactor.
They don't function without the presence of NAD or they function a lot less. They modulate
genetic transcription so they can upregulate and depress various genetic changes
which become important in aging and disease. In the case of PARP, our own research showed
that this- Can you just define what PARP is? Because I think most people have never heard
of that before. Yeah, PARP is actually the most abundant protein in our nucleus. It is a protein
that sits within the nucleus, which is the
center of the cell where all the genetic material is housed. And there, it is responsible for
ensuring that the DNA is in good health. So DNA is a very long, long molecule, and it can be
influenced or impacted by oxidants. We're always exposed to oxygen. We're in an oxygen-breathing environment,
and we have defenses against those oxidants, but some of them slip through.
And when they do so, they can go right into the nucleus of our cell, and they can actually alter
our DNA. So our genes can actually be damaged after we're born by some kind of oxidant stress. And they're damaged in very different ways.
But one of the most important ways is called a nick,
where the oxidant into the cell,
then actually cuts like a scissors.
One, two DNA strands.
We have two strands, double helix.
But if you cut one of them, it's called a single strand break.
And this is a very damaging effect on the cell.
If it accumulates, it can cause cancer.
So we have all kinds of mechanisms in the cell to make sure that when we have damage to our genetic material,
it's rapidly repaired.
And PARP is the key enzyme that does that.
It's a key enzyme.
And that's mediated through NAD. Well, when ARP recognizes, when the enzyme is recognizing that there's a break, it grabs onto
that break and holds on for dear life. And then it pulls an NAD around it and makes a long chain
of that NAD, which helps do the repair. So you a good thing because you want to keep your DNA repaired.
And if you have enough NAD, you can affect the repair and your cells stay in good shape. You're
not allowing the DNA to be damaged. So having NAD around chronically is very good. We know that
animals that are deficient in PARP, we can actually make
animals now that don't have the enzyme. These are genetic mites, and they are much more prone to
cancer. So having a constant way to repair your DNA as you get older is absolutely essential,
and PARP is the that takes care of that. So NAD is absolutely essential to having healthy PARP, having
sirtuins operate at the right level, and causing the upregulation and downregulation of various
genes so that we stay balanced. And as we lose NAD, this balance falls apart, and we start to see
dysfunctional gene expression, we start to see injury to various
tissues, which can kind of cascade as we age. So NAD plays the critical role and maintaining that
NAD level all the time becomes more and more of a challenge as we get old because we're starting at
a lower point. Yeah. So NAD levels decline with age. But what's really interesting about what
you're saying is that the body gets maybe 100,000 little nicks to its DNA every day, right, by 1,000 cuts.
But the body has its own built-in repair system, like a repair truck that goes out.
And this PARP is a key part of this repair system.
And the NAD is also involved in actually activating the sirtuins, which are part of this repair system.
Is that fair to say?
I think most people don't recognize that to be in health, it's not just a matter of the body doing a lot of good things to keep itself.
It's the defense.
The body is on defense, like a football team.
And in the case of defending ourselves against oxidant stress and injury, the body has a host of mechanisms.
And all of those are important.
It's like losing, you know, somebody in the front of the tackle or something in a football team.
If you don't have a good defense, you don't need a lot of offense to win, to get in trouble.
So what are the defenses in the cell?
How does the cell protect itself all the time?
Well, first of all, we have
evolved mechanisms to take care of these oxidants directly. We have antioxidant enzymes actually
sitting throughout the cell, around the nucleus, and inside the nucleus. And those enzymes, when
they see an oxidant, they come right in on it and they remove it. But in order for them to do that, they have to have ammunition,
if you will, to diffuse the oxidant. And what is that ammunition? It's a special molecule
called glutathione to neutralize and take out this oxidant stress. So glutathione, it's the
weapon they're using. Well, where does glutathione come from? It comes from a process in the cell,
which is completely dependent on NAD. So if you have NAD in the cell, cannot produce glutathione,
and the enzymes, they may be there, but they can't work. So NAD is applicable to protecting
ourselves from the oxidants, the very oxidants themselves. Okay, so we have antioxidants. That's the first line of defense.
It's immediate, very fast, very effective most of the time.
So that's fascinating that NAD actually boosts the enzymes in the cell
that actually can make glutathione, right?
Every cell in the body has to make glutathione or it perishes.
And within the cell, there is a special donor, electron donor called
NADPH, which builds the glutathione. And this molecule NADPH is absolutely essential to us,
and it comes from NAD. So without NAD being around, we cannot defend ourselves from immediate
threats in the oxidative sphere. Beyond that, if one of these oxidants slips through the line,
it's, you know, running towards the quarterback.
Okay, so the front line failed.
There has to be a defense, right?
Something there to protect that quarterback.
And in that case, the next line of defense would be this repair mechanism.
So the injuries happen, the quarterback got hit,
but he has to get back up again fast and keep working. The cell has mechanisms built within it
to repair the damage that's occurred. And PARP would be a classic example of that. So NAD is at
every stage. It's the initial stage on the front line, preventing the rusher coming in, and then
it's back farther. If there's injury that's happened,
it's there to heal. When NAD levels fall, none of these things are there, and the whole cell starts to run into trouble. And eventually, if it spirals out of control and it cannot recover,
that's when the cell dies or perishes. For example, I'll give you a classic example.
Someone has chest pain, and they find out they're having a
heart attack. So they're not getting enough blood flow into their heart. The muscle of the heart is
suffering. It's ischemic. So that is an immediate threat to the viability of the heart itself,
right? There's all these oxidants flooding in right now. So glutathione is right there.
NAD is doing everything it can to get there.
But if the NAD levels are not sufficient, the glutathione levels fall,
and now the injury goes one step further right to the DNA.
You get the X, then PARP is activated.
NAD rushes in, tries to help there.
Well, all of these things are good,
and they can keep you from having a full-blown heart attack.
But if at any point the NAD levels go too low, that's it.
And at that point, the ATP cannot be produced, the glutathione is not made, and you have
cell death.
That is an infarction where the tissue has actually died.
It's necrotic and it won't recover.
And this is the most severe situation.
So NAD is playing a role at every level trying
to protect us from that chronic stress and then acute stress is like stroke and heart attack
yeah i mean what you point out is so important because so many of the diseases of aging like
heart disease cancer diabetes dementia those are just way downstream from all these mechanisms that
go wrong that we can influence and that's's what scientists are now talking about. If we address the underlying root causes of aging, the hallmarks
of aging, which NAD in part does a lot of, we can actually do a huge job in preventing and even
reversing some of these diseases. And that's what's so exciting to me. I think we are reaching
a turning point in healthcare and medicine where we're understanding the root causes.
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What's really interesting, I sort of
want to unpack this a little bit because you basically said that we need NAD, which helps us
create energy in the cell, but also is involved in regulating antioxidant status. It's involved
in DNA repair and our epigenetic programming, but it also has all these cross-purpose actions.
When you activate sirtuins, which NAD does,
it's one of the main actions of NAD is to activate the family of sirtuins.
These signaling proteins, they work on many of the other pathways that relate to aging,
like, for example, mTOR, which is regulating your protein synthesis
and inhibiting and regulating autophagy.
So it helps inhibiting mTOR and helps stimulate the self-cleaning and repair recycling called autophagy. So it helps inhibiting mTOR and helps stimulate the cell for cleaning and repair recycling called autophagy. It reduces inflammation by inhibiting a big transcription factor that
turns on all the cytokines in your cells called NF-kappa-B. It activates FOXO, which is another
regulator of antioxidants in your cells. It helps to reduce oxidative stress by the mechanisms you
mentioned of increasing glutathione, but it also activates another family of transcription factors called FOXO, which increases antioxidant enzymes that
are built into our system. It can help reduce cancer by activating the tumor suppressor gene
called P53. It helps your mitochondria make new mitochondria and improves the efficiency.
It helps improve insulin sensitivity. It activates AMPK. It regulates our circadian rhythms and clock. So it's such a multifunctional substance. You think
you take a drug for one pathway. I'm taking a cholesterol drug for lowering my cholesterol,
blood pressure drug for lowering my blood pressure. But the beauty of these natural
compounds that are our body's own medicines is that they work across the board on all the
different pathways. And there are many redundancies in the system,
so it's not the only thing that regulates these pathways.
But that's what I think makes NAD so powerful.
What are your thoughts on how all these things connect
and how NAD has its multiple functions?
I think 30 or 40 years ago when I was in medical school,
we went from class to class and we learned about different diseases.
Yeah, me too.
We had a rheumatoid class, we had a stroke class, and we were told that there are these
diseases that people just get, right?
I mean, suddenly a Parkinson's disease or suddenly a diabetes.
And so we would study these and this is sort of how the specialties develop, right? But I think it's come full circle because what we really understand is that there's
really one fundamental disease, which is called aging.
And then these other manifestations which we see, which we call diseases.
Oh, I have Parkinson's disease.
But no, you don't.
What you really have is a sequential accumulated process
of aging that has dysfunction across multiple pathways connected to each other. And then we
suddenly have what we, oh, you know, we're 65 and now we have diabetes. Well, where did that come
from? But it's not just like a hit or miss thing. It is a sequential process. And as you get older, and as this aging
process inevitably drives forward, all of these mechanisms are at risk. And eventually, one of
them, or more of them, you know, becomes a disease that we can categorize and call a disease. But
really, it's a generalized process. And NAD is at the epicenter of all this process. So one different way to think about
disease management, I mean, yes, we need diabetologists, we need all these good people
who do all these good things. But fundamentally, we need to slow and arrest or reverse this
overriding, inexorable aging process that is starting to degrade all of these different pathways together.
And so the search is on now for more broad spectrum or more fundamental approaches than
just disease-specific ones. And as we look at the NAD story, what better candidate could there be
than something that underlies energetics pain inflammation immune risk dna repair tissue
repair signaling and all of the i mean this is a fundamental currency right prevention yeah insulin
sensitivity all that right right right i mean like we have currency like we carry a dollar bill in
our pocket we can buy many many things but they all go back. You better have that dollar bill.
So NAD is a fundamental driver of all of these processes. And you just mentioned many mechanisms,
but there are many others that we don't even know about yet. I mean, over in our research,
we're looking at new pain pathways that are related to NAD. We didn't even know about this until recently.
There's a whole story of pain-related problems that have to do with NAD deficiency. Recently, there's been a whole lot of research on prostaglandins and inflammation from NAD deficiency.
We didn't know that. So all of these separate things that we talked about and that we see in
our patients, they're starting to come together to a final common or final initiating pathway. And we better understand that pathway and then learn how to
manipulate it, how to help it, how to restore it. And that's where my interest is in.
Well, I tell you, I'm barely able to sit in my chair right now and not jump up and down and
scream, hello, hooray, yay, finally somebody's getting it because I've been singing this
tune for a long time.
And when you start to look at systems biology and network medicine, what we call functional
medicine, it speaks to exactly what you're talking about.
The diseases are just leaves on the trees.
We need to go to the roots and the trunk of what's really going on with our biology.
And it has to do with exactly this thing that you're talking about, which is this dysregulated function
that accumulates over age
that we can actually intervene with and create health.
And then all these diseases either would prevent them
or they go away or get reversed.
So that's what's so beautiful
about our kind of understanding of longevity science now.
It's sort of peeling back the layers
and people are going, wait a minute,
aging is a disease.
These are processes we can treat.
There's a way to think about this differently. The diseases aren't all these
separate things. They're all connected by these common roots. And it has to do with everything
you're talking about. And so when you look at NAD, you know, the mechanism of action,
it does so many different things from DNA repair to the activation of sirtuins to increasing energy
production of the cell to lengthening our telomeres, which shortened to making new brain cells and making new brain connections, reducing inflammation, boosting mitochondrial function, improving insulin resistance and exercise performance.
It's really quite remarkable.
I remember David Zagler talking about like a study where they had a mouse treadmill that only goes to like, I don't know, one or two kilometers.
And they never saw anybody like mouse go longer than that and then when they gave them nmn they just kind of
broke the treadmill because it was like went three kilometers the secret now or the trick now
that once we've recognized this is how do we get nad levels back up how do we preserve them how do
we preserve people who are reasonably healthy and give them optimal performance and How do we preserve them? How do we preserve people who are reasonably healthy
and give them optimal performance? And how do we help people who have low NAD who are in trouble
and get them back to a reasonable level? So to do that requires, like any medicine,
it means giving something to somebody that they're missing. So there's several ways that initially people started giving NAD. It made sense. You have low NAD, give the person NAD.
The problem with that is that NAD is a chemical or a molecule that's made inside cells. And it's
so valuable and so important to the cell itself that the cell is very clever and it embeds within NAD,
it changes the molecule in such a way
that it can't leak out.
It's precious.
And so NAD has been designed to stay inside the cell.
And if you give a person NAD,
it won't fall out of the cell once it's there,
but the big problem is it won't get into the cell. So if you get a lot of NAD, it won't fall out of the cell once it's there. But the big problem is it won't get into
the cell. So if you use a lot of NAD, that's great. It's all floating around doing all this stuff.
But in order for it to work, it needs to be inside the cell. Now, getting NAD into a cell is no mean
feat because you've got a problem there. It's designed not to cross cell membranes. So what
do you do? so you see all
these health products out there you know take nad take this pill it's got a lot of nad but the
problem is yes you can get into the body but you can't get it where it needs to go which is inside
the cell interesting but created the interest in other ways to boost nad so what people did is they
said well where doesAD come from naturally?
How does the body make NAD? Well, it turns out that there are two steps along the way.
First, there's something called NMN, and then there's something called NR, and then there's
something called NAD. And so they thought, well, if we give the molecule before you get NAD,
that can cross the cell membrane more successfully. It can cross the
gut when you swallow it. There are all of these good things that could happen maybe if you took
a precursor, an earlier step. So you'll see all these products now that have something called
NR, right? So nicotinamide. There are studies and cell studies and human studies looking at NR,
and it seems to do good things.
First of all, it gets in a little bit better than NAD, but more importantly and significantly,
you can see the NAD levels go up in the cell when you take NR. So that was a good thing.
And then people went out to the ultimate step, which was to give NMN. And they asked,
is this a good way to deliver
NAD? Will this do it? First of all, when you swallow a pill with NMN, it crosses into the body
a lot better than NAD and NARB. And that's because the body has created a special shuttle
in the cell that recognizes NMN when it's outside and provides a
lovely tunnel, if you will, for it to spread through the membrane and end up on the inside
of the cell. So the body has neared a way for NMN to get in there. And of course, once it's in the
cell, that's great because then it can be sliced up and form NAD and all is good.
And that's been shown.
So we now believe that the most efficient way to deliver NAD is actually not NAD itself, but it's in the form of NMN.
And that's why our focus has been to use NMN to make these necessary changes to boost NAD.
Interesting. these necessary changes to boost nad interesting now just to kind of loop back for a minute before we want to get into the delivery forms and what does and so forth is is do you know why nad levels
decrease as we age is this inevitable is there a way to prevent it can we naturally increase them
is there any understanding about how that may work uh no there really isn't a lot understood
okay good because i thought i missed it but I thought maybe you knew because you're the expert. I'm like, let's just go. Let's talk
about where it's actually made. The first part is when you take sugar and again, glucose is a
good example, and that is broken down by glycolysis. And there you get something that's spun out. The next part is a cycle called the Krebs cycle. And in that, you take what comes out of glycolysis and you wh, of the cell. Mitochondria, the NAD,
is grabbed a hold of, and it is used to fuel the production of ATP, which is the ultimate thing
which comes out of the mitochondria. So those are the three different things. If I had to
guesstimate where the deficit lies, it's almost surely in the last one. So we don't think
that as you age, you lose glycolysis and you lose the Krebs cycle. We think the mitochondria
are really the point where with aging, we start to see this degradation. It's not just,
first of all, it's in the number of mitochondria. Let's take a professional basketball player.
And they run up and down the court for 60 minutes.
They're not even sweating.
How on earth would that be?
If you take the muscle out of someone like Michael Jordan, you will be astonished what you see under a microscope.
It's not normal at all.
The number of mitochondria means you can jump over the rim.
And I'd imagine the amount of mitochondria in that. So when he takes a quiet breath,
he's producing so much more energy than I could ever even imagine. That's why he can run up and
down the court for 60 minutes, because he's just loaded with these mitochondria bulging out everywhere in the muscle cell.
Then take the same guy, and he's now 75, and he's still working out, still doing his thing.
If you look at the number of mitochondria in his cell at that age, it's fewer.
Now, why is that?
Well, in the last five years, we've learned a lot about what controls the number
of mitochondria in your cell. There's actually a pathway that tells us, tells the body how to make
or when to make or how many to make of these mitochondria. So we now know that one of the
stimuli, for example, is low oxygen tension. So if you were to exercise,
you're using up your oxygen very quickly and the muscle is in a state where it doesn't have enough.
It's hungry. And that is a powerful stimulus to make new mitochondria. That's why a guy who's 75
who works out every day, he will actually create new mitochondria. Whereas someone who's 75 who works out every day he will actually create new mitochondria whereas someone who's a
couch potato he has no stimulus and so you won't see those mitochondria being formed so the aging
process diminishes our mitochondria and that's probably can't say for sure but this is probably
the prime reason nad levels fall with age it. Yeah, that makes sense. Additionally, you know, you look at some therapies that are used for longevity, for example.
They're like hypoxia therapies.
And so when you look at Velica Bamba in Ecuador, they live a long time because they live at 17,000 feet.
Maybe it's because of that.
Or maybe, you know, when you use this technology called the Cell Gym, which essentially takes you up to Mount Everest and then back down. It makes you hypoxic. It activates your mitochondrial production. Or when you use
these hypoxia masks that actual athletes do, or when they go to the altitude to go train for
running a marathon, they'll run it 7,000 feet when they're going to run it 1,000 during the race
because it actually helps them build more mitochondria. So it's really all about
little tricks and building
muscle through strength training, through the right amount of protein, through actually using
some of these compounds like NMN can actually help to maintain and actually activate mitochondrial
biogenesis, making new ones and mitochondrial bioenergetics, which is the efficiency through
which we make energy in ourselves, right? Is that fair to say? I think there's so many serious athletes
who exercise at elevated altitude for that reason.
And it provides them,
well, I mean, you'd get the same thing, I suppose,
if you're doing a lot of activity, even at sea level,
but being at an elevated altitude
forces you into this domain
where you're already stressing your system with hypoxia and
athletes who train at an elevated altitude and then come down are in far better shape, right?
So they have a lot more loading of mitochondrial, we call it mitochondrial biogenesis. And that's
just, we now know how the hypoxia is actually influencing the creation of new mitochondria.
We know the molecular pathway.
We know the molecules involved.
And those, they haven't yet, but those will become drug targets.
So useful hypoxia factor, things like that.
Hypoxia reduction factor, HIF, responds to low oxygen environment.
But what would happen if you had a drug that could turn that on?
I wonder if that's how blood restriction exercise works.
There's this kind of blood flow restriction where you put, let's say, a blood pressure type equivalent on your arms or legs, and then you weight train at much lower levels.
But you get far more exhaustion sooner, and it actually increases muscle synthesis better than regular strength training, which is really interesting.
Sure.
Yeah.
It's the same mechanism.
And I think that we can do that through being active, by exercising.
And ultimately, I think there will be nutrients that stimulate mitochondrial biogenesis.
There should be research going on both in the pharmaceutical space
but also in the natural health food space.
Yeah, for sure.
Things that we can eat on our own or drugs that we can take perhaps,
but we can change our lifestyle through what we eat
if we can identify diets that potentiate HIF
and other factors that turn on mitochond mitochondria and i think that's
a wonderful area of research you know amazing so we're going to we're going to go into the forms
of mitochondrial support with nmn and r and ad talk about the differences uh but before i do i
want to talk about a few other topics related to nad which has to do with um sleep it seems like
there's a benefit to sleep as well,
which I think I've never heard about. And there's a new study that came out that basically found
that people who were part of this study and took NAD had better sleep duration, better deep sleep,
better REM sleep, and reported better overall improvement in sleep quality. Can you kind of
comment on how that would work? I don't understand the mechanism.
Well, I think there are two aspects there. First of all, there's the control of sleep. We know that
sleep deficiency leads to a loss of energetics, loss of focus, a loss of peak performance.
So some of that has to do, of course, with the brain in terms of it going through the processes that it needs to.
But also we know that sleep is a systemic phenomenon, and it allows muscles, really all of our tissues, to recover during the day.
So NMN, and this is an early area of research, but if NMN can potentiate better sleep, that's going to translate in a better systemic response.
You're more rested, and you've had a better chance to recover. So there's that effect at the central level
with NMN on the sleep process. And some of that may have to do with regulation of sleep centers.
We know, for example, that sleep is highly regulated by metabolites that have to do with energy. The main drive
of sleep is adenosine. And adenosine is accumulating during the day as we,
and we're thinking and we're doing all of these things. Little by little, we're breaking down ATP
because the brain uses ATP in a way that no other organ does. The brain is consuming a vast quantity of ATP,
way out of proportion to everything, including our muscles.
The brain is an ATP consumer.
Huge amount of, I think 25% of the energy in your body is in your brain.
So that's a prime area where you can't keep up, and you can't.
By the end of the day, by 9 o'clock or 10 o'clock at night, it is well documented that you have not been able to regenerate all of the ATP you've used.
There's always a continuous deficit.
From the moment you wake up, you are not keeping up. At 9 or 10 or 11 o'clock at night,
you have wasted enough ATP that you cannot regenerate
that the end product of that, which is the adenosine,
the final breakdown product, has accumulated.
And adenosine is what causes drowsiness and ultimately sleep.
I mean, ultimately you...
So does NAD improve adenosine production?
Is that what you're saying?
The NAD is responsible for taking the adenosine
that's forming during the day
and driving it back and getting rid of it
and keeping it low by pushing it back to ATP.
Adenosine is used to make ATP. So when you have ATP,
it breaks down to ADP and then to AMP and then the AMP is broken down to adenosine.
Oh, adenosine. Oh gosh. I just, I can't believe I just got that. Adenosine monophosphate,
adenosine triphosphate. Yeah, that's ATP, AMP. Okay. Adenosine, right? Of course. Yeah.
Never put that together. If you looked at the brain at six in the morning,
what is there? It's ATP. Everything's fine. You wake up, you feel good. You can conquer the world
by four or five in the afternoon. You've already got adenosine there. Some people even take naps
as they get older, but I'm it's 10 or 11 o'clock at night, your, your ATP levels are low and your identity levels are super high.
And a dentist scene directly influences the,
it's a part of the brain in the mid brain,
which controls your arousal,
how awake you are.
And the identity directly causes you to feel sleepy.
When you're driving down the road in the morning and you can hardly
keep awake, your brain is flooded with adenosine, very dangerous to drive. And so what you need
is to do one of two things, either get rid of the adenosine, which is called sleep,
it's the best way to do that, or you can take a drug which blocks the adenosine from binding to its receptor. So even though you're
swimming in adenosine, you can block the adenosine from activating the adenosine receptor. And I
would say that 99% of the American public does this every day because it's called coffee.
Coffee. Coffee.
So some people even have a problem in the morning and get going to work.
You know, they get up and they drink two cups of coffee.
And it's really unnecessary, frankly, because you don't have much adenosine at six in the morning.
If you have a good night's sleep, that is.
Now, if you haven't had a good night's sleep, you haven't had time to remove all the adenosine.
And you need your coffee at six in the morning to block it.
The better thing to do is to get some good sleep.
But if you wanna stay awake and alert
and bright-eyed and bushy-tailed, people drink coffee.
It's a natural adenosine blocker.
So that is the whole adenosine story.
Now NAD is there in the brain to take adenosine,
and turn it back to ATP.
So if we had sufficient NAD around,
we would be able to go through the day with a whole lot more energy and a lack of sleep.
And then when we reduce sleep, it improves the quality of our sleep?
Yes, because it's helping us to get rid of the adenosine.
Sleep is about many things.
Fundamentally, we've got to get rid of the adenosine that accumulates during our day.
That's our job.
Interesting.
All right.
So, okay, next question has to do with a research paper that came out in mice.
It got a lot of play, which basically got everybody in a kerfuffle, which is that NMN, NAD causes cancer.
Can you speak to that study, the challenges with it,
what's true? Because you are an expert in cancer. A lot of your research has been on cancer.
You know this stuff inside out. So can you unpack this for us and help us either understand why there's a problem or why there's not a problem?
Well, look, it's one lab that's very focused on this. God bless them, but they're doing the
Lord's work looking at this. But still, it's one lab, and it hasn't disseminated to other labs
which have shown this.
Oh, okay, let's take this guy and give him all the credit in the world
that he's doing a good job.
But let's walk through those.
Okay, if you give NMN in cells,
you have the potential to actually stimulate tumorigenesis. Well, what he later shows,
and it wasn't discussed initially, but is that it's not the NAD levels that are causing the,
it's not the NMN that's causing the cancer per se. It's that he created artificially a very unusual metabolic scenario.
He dumped a bucket of NMN into the cells, and there was so much NMN that it overwhelmed the NAD.
So you had a ratio of NMN very, very high, and NAD was normal, but the ratio was crazy, crazily in favor of NMN,
and that can't happen. Later studies have shown that if you have very low NAD and very high NMN,
yes, that has the potential for causing tumorigenesis, But can that really happen? No. If you ingest NMN, it doesn't hang around and
mind its own business. It's converted to NAD. That's what happens to NMN. It's not just,
you know, saying, hello, I'm here. It is rapidly transformed because it's a precursor into NAD. So you don't get this one abnormal ratio
of high NMN, low NAD.
It's not gonna happen in nature.
Now, maybe he speculated there could be people
with a genetic defect where they can't convert NMN to NAD.
I don't know.
I mean, in theory, yes,
you could have someone with this condition,
but I haven't seen it identified yet. So under normal conditions where NMNs converted to NAD, I don't think that scenario
can ever play out. It was an interesting lab trick, if you will. It's good to learn new things.
Knowledge is power. Yeah. So what you're saying basically is he created conditions that would
never happen in the living organism in the test tube that actually could never be replicated.
It might potentially cause cancer. So in a mouse kind of we're so far away from this being actually a
viable scenario for humans that you don't know not right now now i think we should continue to
all do research and that's a good thing i'm in favor of research i'll vote for that not worried
right now about that no um now what was really also interesting on the positive side was it was
a really interesting clinical trial on nmn it was in humans because we've done a lot of research in animals and david
sinclair and those guys lenny guaranty did a lot of work on sirtuins and found respiratory
trough could extend the life by a third of rodents by taking this compound that stimulated sirtuins
which was when nad does but it uh but it turns out that uh humans are important to study too so need to
study not just yeast and mice and so forth and there was a clinical trial and a man that i
thought was pretty impressive that that i i thought would be talking about both the safety the efficacy
and what it did in people who were middle age it was a double uh blind randomized multi-center
placebo control doseent clinical trial,
which is the highest level of research you can do.
And can you tell us about that study, what it showed, what the take-homes were?
And I thought it was pretty impressive, actually.
Well, what they're looking at there is basically the energy capacity of people,
and in particular, the ability to walk, to go distances.
And they were able to show that there was a longer capacity to be
functional. So you had more energy. And they looked at energy balance, and they looked at
insulin sensitivity and other things. And all of these things seem to line up to tell a story
that it was working. So although it's a small study, I mean, it's not a giant study.
And we know- Sure know 80 people, right?
That's right.
Yeah, it wasn't 80 or 800 people.
And it was a small number.
And therefore, the differences that are identified, you can question statistically about if they're there to really write home about.
But I think, you know, being in the right direction is positive.
There have been a number of small studies like this. And there was the six minute walk test has been looked at,
and people can walk further, which is a holistic way of looking at the energy. Those are all
positive. But I would caution the audience that all of these studies are still somewhat small. And I don't think we're there yet where we can conclusively say that NMN is going to be, has been proven to engender more energy.
In animals, yes.
It would appear in humans.
We also have evidence in cardiac function in humans that the cardiac function is better, particularly in congestive heart failure.
So there have been some studies, but as I say, they're early, and we shouldn't jump to the conclusion that it's been proven.
I think the pace of research will definitely increase and the quality of research. One of the problems with NAD and NAD in terms of research
is that it has not been yet driven into the classic pharmaceutical space.
And these are very expensive, especially if they're... And right now, the motivation to
carry out a large randomized double-blinded placebo-controlled trial, which can cost
millions of dollars. Definitely. And it hasn't been there yet because the pharmaceutical companies
don't own NMN. So when you invest $5, $10, $50 million in a study, you better believe,
or you must believe that you've got something that you own so that at the end of that, your evidence,
your data leads to financial outcome, which means you can sell it exclusively. That won't happen.
Although there's one company in the U.S. that's trying exactly to do that, to patent its
exclusivity. Yeah, I saw that. But this is the reason that NAD and NR and NMN have not enjoyed the large-scale studies that you would need in order to exclusively – and it's a problem with all natural products.
And it was a promising study because I thought they reversed biological age.
They improved six-minute walking.
They helped improve what we call SF36, which is subjective quality of life.
And these were people who were taking – didn't know whether they were taking a placebo or the compound.
So it was really well designed.
But I think you're right.
It was a small study.
We needed to get more data.
I spent a lot of time in my life at the FDA.
We have all these fancy tests that people do, and the audience may be that.
But at the end of the day, and it's fascinating.
I was sitting there at the FDA, and I was telling them all about these biochemical advantages of this and that.
And the guy looks at me and says, I just have just a simple question.
Can Mrs. Jones carry a bag of groceries up the stairs better or not?
That's it.
Because if she can't, all of this doesn't count for much. And the six-minute walk is a test where they take a person and they're on a treadmill and they say walk.
And walk as much as you can for six minutes and we're going to keep track of how far you went.
So if you can walk 200 feet in six minutes, you're hurting. But if you can walk a mile, this means your health is great, right? Because everything is integrated, your cardiac function, your respiratory mile would be a run, not a walk. I was able to do that when I was very young.
But that's the point.
That six-minute walk is really critical, understanding the overall promise of a drug like NAD or NMN that can create and boost up the intracellular NAD levels.
And that's why in that study, of all the things that I was impressed with more than the others was the fact that they could.
Was the war.
You can't fake it.
That's great.
Well, now let's talk about the practical application because, you know, there are people who recommend NR.
There's companies that produce NR.
There's companies that are making NMN.
You can get NAD sublingually, like through liposomal forms.
You can get subcutaneous N intravenous nad um and i'd love
to sort of have you sort of take us through you know what's the pros and cons of each because
you know one of the things i sort of want to bring up was was triggered by what you said earlier is
that nad given as a compound can't get in the cells very well uh and i had one experience with
a patient i read this in other studies who had park Parkinson's, and we gave her IV NAD, and her tremor went away, not permanently, but for the short time,
she had more energy, and she perked up, was able to walk better. And I was like, holy cow,
this is impressive. But that would lead me to think that actually giving intravenous NAD can
get it in the cell. So can you talk about sort of these different forms and the pros and cons,
and whether I'm just making this up about this woman or if there's actually something to that?
Black and white. I don't want to say that giving NAD cannot enter cells, period.
That's that's not correct, but it is impeded.
It's not efficiently taken up.
Now, having said that, there are hundreds of different cell types, and it might be that
certain cells have such a quenching thirst for NAD that maybe they've evolved shuttle mechanisms
for NAD. You're talking about Parkinson's disease, and that's a disease which ultimately
is regulated by a very tiny but very important tissue. Mitochondria.
And who knows, maybe those cells in the basal ganglia have a better ability to suck in NAD than other cells.
So I don't know.
That's never been studied.
But it is a mitochondrial disease.
Parkinson's is a mitochondrial disease.
That's why I think it may be effective.
Well, Parkinson's is a mitochondrial disease,
and it's also probably a disease in which the oxidant stress within certain select cells, these basal ganglion cells, it has been increased. research at Parkinson's that I've seen is really implicating tangles and, what do you call it,
precipitates from proteins from misfolding, very analogous to Alzheimer's, which is some new work
that's come out with alpha-synuclein. And it's thought that these aggregates might impact the amount or way that oxidants are developed in cells.
The whole cell starts to become a factory of oxidants and it injures itself.
There are also Parkinson's patients who have fundamental deficits in handling oxidants.
And so to get NAD into the cells of a Parkinson's patient might be,
you know, it might be a very interesting way to look at that. We know that the model of
Parkinson's disease that are used today, the most important one being the rotenone model,
which is from Emory University, Georgia, that is created by actually blocking the first protein, the first enzyme in the mitochondria.
Mitochondria.
Yeah, in the transport chain.
So definitely Parkinson's is somehow related as an example of NAD failure because the cells are not generating.
There's a deficit in the mitochondria. And what your observation, if it's correct, suggests
that maybe in that particular disease, NAD might be good. But the advantages of NMN
are that it is known, at least in the intestine, that there is a specific shuttle,
or a shuttle is a protein that's present in the membrane of the intestinal cells,
and it literally carries the molecule from the outside to the inside of the cell in a way that would not happen if it weren't for that.
The NAD or NMMN without that shuttle,
they can't.
Yeah.
Can't get in.
Can't get in.
It's like a smooth pathway that,
that helps it across.
So that's a reason from an oral perspective to suggest that NMN might be
good.
And those shuttles are present within the body as well.
It's not just on the intestine.
Yeah.
But it's, it's hard to get NAD because you have to take it intravenously or subcutaneously. And
the beautiful thing about NMN and NR is that you can take them as supplements. So what's
in between NR and NMN and why should we be more focused on NMN, which seems to be
winning out the horse race here? The shuttle is specific for NMN.
So even though NR is closer to NAD,
and it's easier to get into the cell, it doesn't have the advantage of a built-in shuttle that God
designed to move that material from the outside to the inside. NMN is, first of all, NMN is a
natural molecule, by the way. It's not just something we make NMN. And so this shuttle is there for a
reason. It's to facilitate entry. And we're just leveraging that when we give it therapeutically.
But that path, that shuttle is a fundamental issue. It changes the whole question about how
do you get this stuff into the cells that heretofore, NAD just doesn't cut it. Now, I do research with NAD and NR
because there may be certain cells
that function differently that we haven't examined.
So we should continue that.
And if you look at the literature,
there's far more studies of NAD than NMN by many folks.
So that was what began and it made sense.
They knew NAD is important. Let's give it
and see what happens. But I think the tide has changed and you'll see a lot more loading studies
now where NMN loads the cell with NAD. And that's going to be, there'll be a bevy of studies like
that, clinical, animal, and even cellular. You'll start to see a lot of that.
So you're saying that NR doesn't have the same shuttle to get the medicine or the supplement
or the ingredient into the cell as NMN, which has a specifically designed shuttle.
Yes.
Right?
Yes.
Okay. Well, I want to talk about specifics and in dosing and how we take it. There's a product
called Wonderfeel Younger NMN or Younger NMN, which includes not just NMN, but a bunch of other
stuff. So I'd love to talk about
that product. I know you're involved with the company. I've been talking to them as well,
advising them. Tell me why you think this is unique and different and what's important to
know about it. We began with the premise that NMN is important. NMN by itself is probably not the whole story because there are mechanisms within the cell
that are very active as you age, as you have disease, and these are going to interfere
with the benefits of NAD.
We talked about that already, oxidant stress being the most important.
So when you add NMN to a cell and you get NAD in there, it's good.
It's going to increase the glutathione levels. It's going to amend all of the mechanisms,
the defense I talked about, but you have a lot of offense, particularly as you get older.
A lot going on in this, a lot of injury, a lot of oxidant stress. So we said to ourselves, well, let's build a front line,
a defensive line that's more than just one guy. Let's build a whole defensive line with backups
so that it's a team effort to suppress the damage of the aging cell. So we were not
castigating or denigrating NMN in any way. It is the basis. As I said,
it's the basis we're starting with, but we have supplemented that now with additional team players,
each of which has their unique role. And together as a team, working in concert with each other,
we think we will have a much more effective result. So we chose supplements
to fill in the gaps, if you will, to make that front line, that defensive line.
The first one was ergothionine, again, natural molecule as something that we ingest in our food
stuffs. And that has very powerful and quite specialized antioxidant features that have effects on inflammation and on cell survival, on antioxidants specifically.
And so we put it, and it's very well tolerated.
I mean, another principle in this concoction was do no harm. So we did not want to create a model system where we had some
good things in there, but carrying some toxicity risk. We wanted this to be very, very safe based
on natural products. And that's something that could, you know, rear its ugly head with some
toxicity we hadn't thought about. Ergothioneine is like in oyster mushrooms and black beans and liver and stuff, right?
So it's found naturally in plants and animals.
Yes, we don't produce it.
You don't make ergothionine.
You obtain that from your environment
by eating various foodstuffs.
So that's a good thing.
It's almost like a longevity vitamin, basically, right?
Yes, and there are companies out there
that are marketing, not many, but they're marketing ergothymine as a standalone.
And it makes sense that it would have benefit and that it could help with aging and help diminish a lot of the oxidant stress that we're prey to.
Then we added resveratrol, which is a polyphenol. It's a simple molecule, actually. It's present in
grapes, present in red wine, for example, well-known. And it is also sold on the market.
You'll see lots of instances where people are out there advocating the use of resveratrol alone.
It's a weak, relatively weak antioxidant. It's not anywhere near as potent as the natural antioxidant mechanisms we have within the cell, but it is adjunctive and it's helpful.
I wouldn't recommend it much as a standalone because it's not that potent, but in concert,
it has specific types of antioxidant defense, particularly in the cell membrane and lipids and
various places in the cell.
And people who drink red wine a lot.
You have to drink a lot.
You know, it's known that the French, for example, are very enamored with red wine.
And in fact, that they're eating pastries and they have a lot of things that they shouldn't
be eating so much of their cardiac consequences are less than you would predict.
And one of the hypotheses that they're also drinking every meal with a big glass.
Yes, plural.
Maybe true.
But I wouldn't recommend drinking alcohol as a health strategy.
That's what the French are doing, you know.
So they're drinking a lot of red wine.
So that's resveratrol, a very interesting molecule, easy to purify and to add to the
supplements and moderately affect it. And then the last one, I think it's the most interesting one,
which is hydroxytyrosol.
And this came to me because, you know, I'm living in Israel right now
and we're not too far from Greece and we have a climate here.
And everywhere in Israel and in Greece, you know,
it's just covered covered covered with uh with
olive trees everywhere you look that the population that indulges in uh using uh special types of
olive oil which i'll come back to uh has a lower incidence of a host of different diseases including
alzheimer's disease and yeah and so there is quite a lot of research in Athens, especially by some friends of mine there, some professors at the University of Athens, and they've identified the elements within the olive that are most effective in creating this antioxidant and anti-inflammatory effect. And there are different molecules, but most of these are polyphenols.
And the most important one is this, this olipurine. And when you take people who are using a lot of
olives in their diet, they tend to have the benefits from that. And what we now know, we know a couple of things from this man's research there.
All olive trees are the same, which I didn't know.
So every orchard of olives is actually quite different.
They're the same?
They're not the same.
There are over a thousand.
No, they're not the same, right.
But he studied.
And when you do analysis in the olive from a cultivar to cultivar, orchard to orchard, there are vast differences.
Second thing, and so his research has identified orchards in Greece that are incredibly high, have incredibly high levels of these particular polyphenols. Second thing is that how you treat the olive has a
dramatic effect on the survivability. Make an American factory that's processing millions of
olives every day and all of that. And olive oil, you go to the shop and you buy olive oil, unfortunately, the processes used there to get there have decimated
the very most important molecules, these polyphenols, it's oxidized them and they're
not active. So in order to receive this benefit, you have to treat, you have to use virgin olive
oil and from these special orchards and on
and on and on. Now, most people can't find that olive oil in the store, but we know that the
hydroxytyrosol is very special in creating this effect. So what we've done is take pure hydroxytyrosol,
not olive oil, but the part of the olive oil that we care about. And that is what we've added together with the resveratrol, ergothionine, and the NMN.
Yeah, actually, I'm in Sardinia right now where I'm teaching a longevity retreat.
And there's olive trees everywhere.
And it's interesting, they have like wild olives sometimes.
They actually handpick them and drop them to the ground.
They press them right
away to make sure that the and i went to this olive oil tasting and you can hear it you can
taste the different qualities of olive oil and when you you can actually taste that that kind
of polyphenol content because it's a little bit of acidic and bitter in the back of your tongue
so you're you're uh you're absolutely right these are powerful molecules and olives and olive oil
and i think that combination is great. So I think any last
thoughts? So we're looking now in models where we explore these combinations to better tease out
how the juxtaposition of these different players has an effect on these outcome endpoints and to
try to understand how they're interacting with each other and supporting each other.
But it's definitely a team effort approach.
That was the concept biologically to bring a team,
an offensive line or defensive line,
and then to put them together in the right fashion.
Well, it's like olive oil, red wine, and mushrooms.
And you kind of add that with NMN and you get, you've got this product.
It's a younger NMN, which I love.
And what's interesting about this product also is the dose is high.
A lot of the doses of NMN or NR out there are low.
They're like 250 or if you take two, it's 500.
But actually, clinically, it seems like the dose needs to be much more like 900 or 1,000
to get the most benefit.
And this is actually done at a lower cost.
I'm sort of surprised. A lot of these products are really expensive,
but this is actually a reasonable cost for that higher dose.
Well, there are reasons for the dose selection, two reasons.
First, let me begin by saying always do no harm, right?
So that's the place you begin at where you do not want to use a dose of a material
that has the potential to harm. But the safety profile has
been so unremarkable with NMN to date from people's experience and in animals, although
there haven't been large formal toxicology studies. But the data out there suggests
that this is a well-tolerated ingredient. So therefore, it makes sense to use more of it if there's...
Why would there be a benefit?
Because we know that certain pathways, particularly on inflammation,
are very tightly related to the amount of NAD that will be there.
So a small amount of NAD doesn't cut it. There's a very special pathway in the cell regulating inflammation.
This is a pathway.
It's a fancy name called NF-kappa-B, but it's basically a pathway in there which turns up all our inflammatory genes at once, like a symphony.
Yeah, that's what I was talking about before.
Yeah, it's like the direct conductor lifting the baton, and the whole orchestra plays at once. And so that's NF-kappa-B,
that's the symphony conductor. And when you turn that on, you get what's known as a cytokine
release. And in an extreme example, you get a cytokine storm. And we now all know that word
because of the last few years with COVID.
That's why COVID patients die, because this pathway is turned on incredibly all at once,
and you get this massive release of problem. get there. So we specifically gave a high dose
of NMN so we could suppress that pathway and so that we could be sure that the mitochondria was
enjoying a full benefit. So there was a very careful decision about elevating the amount of NMN to do that.
That's great. Any other thoughts you have in conclusion about NMN, what should we be doing,
how much we should be taking? I mean, basically the dose you're recommending is about 900 a day,
right?
That's what's in there. Yes, that's right. I mean, I recommend further research. I recommend
research on how frequently to take it. We wanted to have a once a day,
if possible. People don't have time to take things, but we need to better understand the
pharmacokinetics to understand how long these things last, not just in the blood, but actually
in the cell where they're going. That's the important thing, whether they go to all the
right tissues, how long they're there. We need to look at specific inflammatory and oxidant-related conditions like Parkinson's and diabetes and arthritis and colitis
to elucidate which clinical problem might be best served.
We need to do more studies on aging, which is a very long, long study, but we need to do that.
I know I've started to take it and I think I've
committed to it as part of my longevity enrichment. Well, Dr. Salzman, thank you so much for being on
the Doctors Pharmacy podcast and teaching us all about NMN. I think it's a really important topic.
I think people just don't understand it well enough. You've done a great job of getting in
the weeds and helping us understand why it's important, how it's critical to our health and
aging itself. If anybody wants to learn more about it, you can read Dr. Salzman's work online.
Also, you can learn about this product he was talking about by going to getwonderfield.com.
That's G-E-T-Wonderfield, F-E-E-L.com, and learn more about it and reach out to science as well.
It's a great product and i think
your work is really important and i want to keep you going so we can learn more about how all this
stuff works for us and and actually advance uh the treatment of aging itself which is what we're
talking about um if all of you have enjoyed this podcast please share with your friends and family
on social media we're sure they'd like it i'm sure they'd love to hear about this and learn more.
I think I love this podcast.
I've learned so much.
Leave a comment.
Maybe you tried to take NAD or NMN or NRM.
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How have you felt?
We'd love to hear from you.
Subscribe wherever you get your podcasts.
And we'll see you next week on The Doctor's Pharmacy.
Hey, everybody.
It's Dr. Hyman. Thanks for tuning into The Doctor's Pharmacy. I hope
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