Exercise, Heat, Cold & Other Stressors for Longevity | Episode 3
71m 18s
In this episode, David Sinclair and Matthew Lapland discuss how iron levels and adversity mimetics impact aging. Sinclair explains that while iron is essential for oxygen transport, excess iron—especially from supplements or high meat intake—generates free radicals (superoxide, hydrogen peroxide, hydroxyl radicals) that damage DNA, proteins, and lipids, leading to senescent cells and accelerated aging. He recommends measuring blood iron and avoiding unnecessary supplements, particularly for those with the HFE gene linked to hemochromatosis. The conversation then shifts to "adversity mimetics," a term they coin for practices that trick the body into a survival state. Sinclair traces this to 1990s research on the DAF-2 gene in worms, which showed that a single mutation could double lifespan by mimicking starvation. The body’s protective circuits—mTOR (sensing amino acids), AMPK (sensing energy), and sirtuins (sensing NAD)—are activated by perceived adversity like hunger, cold, or exercise. Modern comfort suppresses these defenses, so intentional strategies are crucial: intermittent fasting (skipping meals), standing desks, and regular exercise. Even moderate activity—50 minutes weekly—reduces cancer risk by 23% and cardiovascular disease by 30%. Sinclair emphasizes that exercise not only improves fitness but directly slows disease by inducing hypoxic stress, which triggers cellular repair and longevity pathways. The key is to consistently challenge the body’s comfort zone to maintain healthspan.
I'm David Sinclair. I'm a professor of genetics at Harvard Medical School and co-director of the Paul F. Glenn Center for Biology of Aging Research. I'm joined by my lovely co-author and co-host Matthew Lapland. Welcome Matt. I love that you call me lovely. I think you are lovely. You're nice. You're nice. You can be nice sometimes. Hey, today in our episode we're going to be talking about exercise and other what you call adversity mimetics. But before we get to that today, right after we stopped taping in the last episode, you went, "Oh my God, iron." And then we had a really great conversation about iron. And so I wanted to bring us back there before we could move forward today. Is that all right? That'd be great. So the last episode, if anybody missed it, was about the foods that we can eat or not eat. Or not eat, right? To live a long time. And it was remiss of me not to bring up a pernicious element called iron. Pernicious. Yeah. It's one of the elements that is turning out to be quite a dangerous element to having too much of in your body. Increasingly, we see that people who have high levels of iron have accelerated aging. Okay, yeah, but iron is essential, right? We all need iron. In fact, people supplement with iron a lot of times. Right. Well, we need iron. It's a major component of hemoglobin, which carries oxygen, which we need. But the levels don't need to be as high as we once thought. In fact, people who live a long time and have these diets that are recommended, I typically say they have lower levels of iron and lower levels of hemoglobin. And this is not necessarily a bad thing. Conversely, people who have very high levels, either genetically hemacromatosis or take a supplement and end up with high levels of iron, might be predisposing themselves to accelerated aging. Okay, so what about just. I mean, this plays into your idea about why people should limit their meat intake, though, because meat intake meat is high in iron, especially red meats, especially in higher-notch. That's one aspect. But typically, if people are taking multivitamin with high levels of iron, this could be a really bad thing. It'll accumulate in tissues. And we know now that particularly ferrous iron leads to the production of free radicals, the damaged tissues in the body. And even worse, it leads to the accumulation of these zombie cells, which we call senescent cells. And those drive the aging process. In part, large part because they leach these inflammatory molecules that cause other cells in the vicinity to become inflamed to age to senescent even cause cancer. Let's back up for a second year, because I think we're going to talk more about senescent cells in a coming episode. But we have mentioned free radicals before, and I think that's a word that gets thrown around a lot. And maybe not everybody understands free radicals. Right. And we're not just talking about people in Portland, Oregon, or Eugene, or Berkeley. Yeah. So these are free radicals that these have been around for millions of years, of course. And we've known about them for at least the last 70. These are three main types of free radicals. There's the superoxide molecule, which is quite damaging and can lead to what are called advanced glycation end products, which are basically proteins that are damaged. It's one of the reasons you want to fast, sometimes during the day, to get rid of these damaged proteins. There's a superoxide anion, it's called, which creates most of the oxidative stress in the body. And then there's a third one hydrogen peroxide, which you can buy a bottle of and dye your hair blonde or orange as my hair went during the pandemic. Those three things are really bad. You dyed your hair during the pandemic. I got bored. I just dyed it. How did it look? Horrible. It really went orange. I've been dying it ever since just to cover it up, but it's almost gone. Thank goodness. But this is where iron comes in. When you have a superoxide molecule, it'll be turned into peroxide by an enzyme called superoxide dismutase, which is extremely important to get rid of that superoxide, which is going to damage the cell. But then you get hydrogen peroxide, and we know how bad that is. Look at my hair. You don't want that circulating. So then what happens is there's a molecule called glutathione, which will turn that into water. But if you have too much iron around, there won't be enough chance to detoxify it, and it'll be turned into this hydroxyl radical. And that's a really damaging molecule that goes on to damage your DNA, your RNA lipids, proteins, and drive aging and senescence. So you want to have iron enough not to feel a thargic, to have enough oxygen transported, but not super high levels that'll cause accelerated aging. And this is going to be different for different people. 10% of the population in the United States has the HFE gene, which makes them more susceptible to hemacromatosis, which means they have to be even more concerned. You can't know this without knowing if you carry this gene though, right? Right. You need to measure things. I, myself, and I recommend people measure their blood by a chemistry and determine whether it's free iron, which is the worst type, or even the bound iron, or out of whack. And you can correct for that. In the case of a normal person, I would say don't take an iron supplement necessarily, although women may need it, certain times of the month. But people who have hemacromatosis, they're particularly susceptible to aging. And their recommendation, typically, of a doctor is, don't ape blood if you can. Okay. So just to like go over what we talked about last time really quickly, you advocate for a plant-based diet. You advocate for low iron levels. What am I missing? Well, we're going to talk about that today. What type of exercise works best? I was just talking about how we should eat, but yeah. Well, we eat less often. Even less often. Yeah. So what I've gone from not eating breakfast now to not eating lunch as well, and just focus on dinner, and giving my body a rest from food overnight and through the middle of the day, so that it turns on our defensive genes against aging. Those three buckets, the mTOR, which senses amino acids, or lack thereof, the AMPK, which senses energy, which is glucose mainly. And the serotones, which I work on, that sense all of those things, including exercise. And those three protective mechanisms we can turn on by eating the right things, eating less often, and exercising. And this leads in really well, actually, to what we're talking about today, because what we're talking about is bringing your body into a state of perceived adversity as a way to turn on these genes. Before we can do that, we've got some business to take care of. We do, because this podcast comes to everybody for free. We should definitely mention the sponsors that make that possible. Our first sponsor is Athletic Greens. Athletic Greens is a Greens powder developed from a complex blend of 75 vitamins, minerals, and whole foods sourced ingredients. It's filled with adeptogens for recovery, probiotics, and digestive enzymes for gut health. They also have vitamin C and zinc citrate for immune support. I've been drinking Athletic Greens for a number of years now. I do that not just because it tastes good, but because I travel, and I often don't eat perfectly. And by having it every morning, I rest assured that I'm getting all of the vitamins and minerals that I need for optimal health. If you'd like to try Athletic Greens, you can go to AthleticGreens.com/Sinclair to claim a special offer. They're giving five free travel packs plus a year's supply of vitamin D3 for immune support. And K2, which will keep the calcium out of your arteries and put it into your bones. Again, go to AthleticGreens.com/Sinclair to claim this special offer. Today's podcast is also brought to us by Levels. Levels is an app that syncs with a continuous glucose monitor or a CGM, which they provide, and that interprets your glucose data for you. I've been so impressed with Levels that I've recently joined them as an advisor. Monitoring your blood glucose levels allows you to run experiments to see how different foods impact you. I did this myself a number of years ago, and I continue to do it. I've learned a lot about what kind of foods I should avoid and which ones are okay to eat. If you'd like to try levels, you can skip the 150,000-person wait list and join today by going to levels.link/Sinclair. That's levels.link/Sinclair. Today's podcast is also brought to us by InsideTracker. InsideTracker is a personalized nutrition platform that analyzes data from your blood and your DNA to help you better understand your body and reach your health goals. I've been using InsideTracker for over a decade. Over that time, I've been able to optimize my health and even potentially get younger than my actual age. They make it really easy. You can have somebody come to your house like I have or you can go to a local lab. The data is easily uploaded by them and you can see a dashboard on your body that also gives you personalized recommendations for exercise and nutrition. If you'd like to try InsideTracker, you can visit insideTracker.com/Sinclair and you'll get 25% of any InsideTracker plan. Use the code "Sinclair" my last name at the checkout. Let's get into this. In this episode, we're talking about some of the things that people can do to create and mimic in their lives the biological adversity that's more conducive to better life spans and health spans that people can use. We call these adversity mimetics. We call these that. When you say we call these that, it's like you and I call them that because I know we call them that but is that a term that scientists use that people actually use right now? We just made it up. You're just making it up. But it's a good word, right? We'll use it. So the reason why adversity is important ties back to. this idea that you've proposed of a survival circuit. So before we move forward on this, let's talk about the survival circuit. We don't have to go way, way back in history. - Not four billion years. We'll come forward in time a little bit. - Yeah, you can go back four billion years and that's in the book. But we're gonna start in the 1990s with Cindy Akeñan and her work on C.E.L.I.N.S. - That's a good starting point. So in the 1980s, it was all about just free radicals. We didn't know that aging could actually be controlled by any genes. It was certainly not single genes. And Cynthia came along as a young graduate student and looked for worms that would live longer. And she mutated them and found a strain of worm, a mutant worm that was living twice as long. So instead of living for 15 days, 30 days. And that was a remarkable finding because when she dissected the worms, bred them out, found that it was due to a single gene mutation. And when she cloned the gene and found out where it was, it was in a gene that sensed insulin. It was the insulin receptor gene called DAF2. That was remarkable because it had nothing to do with free radicals, it had nothing to do with DNA damage. It was a signaling molecule. And that was the start of a revolution in understanding how to control aging by using genes and supplements and drugs that turn on the body's defenses. - And this was the first so-called longevity gene. - Yeah, I would say that was the first. It came very close to the work that we were doing at MIT. We were maybe a year later than her. But we-- - You seem a little annoyed by that. - No, so much me. I'm careful because my supervisor, Lenny Garenti, used to get really annoyed when he was told that he was slightly behind. He thought his work was being done at the same time. So those two used to be the, I guess, maybe still are the, at the forefront of this field. - Certainly the grandparents, if nothing else. And they both showed, so Cynthia and Worms and then Lenny and Yeast, where I was at MIT, made the finding that a single gene alteration can have a huge impact on an organism's lifespan. - And these genes, there's a few of them now that we've identified. And all of them seem to work on a very similar circuit that all starts with adversity. - That's right. These signaling proteins, like the Daph-2-1, and Cynthia discovered, and the serotones that we work on. We didn't know what they were doing at first. This is crazy. It's got nothing to do with DNA repair and free radicals. But then when we tracked what they were actually doing, it turns out they're speaking to the rest of the cell to keep the cell healthy and alive. So in the case of that Worm, those Worms won't just longer live. The program to survive was activated. Those Worms are stress resistant. You can hit them with heat. You can hit them with cold. You can starve them or just put them in happy conditions. They live longer. The paradigm is that normally a Worm response to its environment, if it's starved, it'll hunker down, it'll survive. But here we had a Worm that was mimicking starvation and was able to have the benefits without having to starve itself. - How do these genes, for lack of a better word, no. How do they know that the conditions are adverse and they need to turn on? - Well, there are various sensors. And so the three main pathways that control this, we've talked about MTOR, which is sensing the levels of amino acids in the cell, lower levels of certain amino acids, branch, shanemino acids are good for the cell because they down-regulate MTOR activity. That's one way. The AMPK senses energy, glucose, and then the Certune sense NAD, which is a molecule that goes up with exercise and hunger. Together, those are the sensors. Now, how does a cell communicate with other cells? Well, there's insulin. We know when we eat a meal, insulin goes from our pancreas into our bloodstream and tells the rest of the body, hey, you've got sugar already, suck it in, use it. That's a signaling protein. And what Cynthia's Worms ended up when they were mutated, is that that signal to bring in the glucose was mutated. And this insulin signal was absent. And we don't have the insulin signaling in your worm, it means you're hungry, and you get the benefits of being hungry without having to starve. So our body is this always active monitoring system where perceiving the world around us and the world around us is constantly throwing different stressors at us, or at least it was in human history, right? We've always been a little cold or a little hungry or a little scared or having to run from the animal or that animal that wanted to eat us. This is the environment that our species evolved in. It all species evolved in, right? Is this constant state of adversity? - Right, and that adversity we've evolved to fight back. And so in the past, our bodies were constantly fighting disease and deterioration throughout life, even before birth, we're fighting against entropy, things are falling apart. The aging clock that we can now measure begins at conception. But if you fast forward to now, our society is built on comfort. We've got, most countries have enough food and shelter. We can sit down, we don't have to run away from predators very often. And this is a real problem because these longevity defences that normally would be activated by being cold and hungry and running are lethargic. The body doesn't expand energy to defend itself unless there's a need for it. And modern society is the worst thing. - We take away those needs. - Yeah, we love comfort. It feels good. But that's the worst thing for long term health. We need to trick the body into getting out of its comfort zone by doing these things. We've talked about eating the right foods, including foods that are stressed, eating less often. - Which puts stress on us, which causes our body to feel like it needs to protect itself because if we're not filling it with all of the nutrients and calories we want, it perceives a need, it perceives adversity and it turns out these genes. - Right, and as long as we have adequate nutrition, that's what we call it, intimate and fasting without adequate nutrition or I fan. This is another term we just coined in this podcast. That allows the body to turn on these defenses without suffering long term negative consequences. What's interesting I find is that even though we know the fridge is probably full with food, our bodies are not that smart. Our bodies don't get that message. And we can trick it, trick the body into thinking, oh my goodness, the fridge is running out of food or the field or the forest is lacking in food, we better get to hunger down and survive. What are those things? You burn fat, you increase your metabolism, so you've got more energy to run around and find food, you become more alert because you've got to go find more food and you defend your body against insults, whether it's incoming infections or diseases from within. And that's cool that we can trick our bodies and it's not that hard. We just need to do the things we're talking about on this podcast. And when we're talking, we've already talked about the real key effects that come from eating less often to basically turn on this adversity, the medic effect. There's another really easy way to do this though. - Right, and that's, get off your butt. - Just get off your butt. - Yeah, it's not that hard, as we say, sitting here doing this podcast, but one way I do it is I have a standing desk. So my butt actually atrophied when we were writing this book, Life's Ben, I ended up with a cramp in my piriformis muscle, which is the one that-- - Wait, you're what? - Yeah, yeah, it's a small muscle. - Where is it? - Size doesn't matter. It's right in your hip, it goes through that hole in your pelvis and it's essential for standing and it was cramped out. - I was wondering what that hole was for. - Yeah. It's-- - There's a muscle that goes through it? - Yes. - Okay. - All right, and then so the butt was cramped up on my left hand side. So I was limping for about nine months after we wrote the book and I thought, "Great, I'm writing about health and longevity and I've now crippled myself." I eventually got it to go away with a combination of exercise, physio and an injection of NAD in my butt, which we'll get to in probably the next episode. But the point here is that sitting down is bad for us. You atrophy, you have less muscle, which means your hormone levels, particularly testosterone will go down and you become in pain, that's not a good thing. But ultimately, if you have not a lot of muscle in your hips, particularly, you can break your bones when you fall over, when you're older. And all of that means you need to get off your butt, stand up, even better, go for a walk, even better, go for a run or cycle to get what we call a hypoxic state going. Your body needs to suck in my oxygen and that has remarkable health benefits. - And we really have to work hard at this, 'cause I mean, you're saying this as we're sitting in these chairs, right? A couple of days after I sat down and then share for a long time an airplane to get here, right? We've got a nice comfy couch over there that we've been working on. Like, we actually have to actively pursue opportunities to do this, to get exercise to promote this adversity mimetic effect because our lives are built around comfort and sedentaryness. - Yes, that's true. And what I think most people don't appreciate is that exercise isn't just beneficial for your fitness and for your vitality. It actually can stop diseases in their tracks. Exercise can slow down cancer, in fact, it can prevent up to 23% of all cancers from occurring. That's true for cardiovascular disease. In fact, it has an even bigger effect on that, 30% reduction just by doing moderate exercise every week. 50 minutes is sufficient.
or three times a week with 10 minutes, all cause mortality, right? So we have all cause mortality, basically, is basically slowing down aging. That's a 27% reduction in the rate of aging, just by exercising. The thing you just said, I love this idea of connecting the idea of all-cause mortality with aging, because as we've presented here, as you've been arguing for quite some time, most diseases, which bring us toward the end of our lives, are really just an accumulation of the symptoms of aging. And so if you bring down the disease rate, across various diseases, which is bringing down all cause mortality, you're really just. It's just another way of saying we're bringing down aging. We must be. Exactly. And we can also now measure that with the biological clock, the so-called Horvath clock, named after my good friend Steve Horvath, that is now a measure of the process that leads to all of these diseases that kill us. And one way that we know for a fact to slow down the ticking of that biological clock is exercise. And any kind of exercise is good. This is why the 10,000 steps a day goal is popular, generally speaking, it's good. It's not a magic number. I think there's. Somebody came up with 10,000 and actually some studies have shown health benefits that are existed four to 6,000 kind of Peter out from there. But the basic idea here is that when we move, we bring calories, we're putting our bodies into at least a low state of adversity. So try to get 4,000 in, 10,000 seems to be even better. It's a greekle. It's a round number. It's fine. Get off your ass. That's what we're saying. That's all it takes. It's not that hard. Walk around the block a few times. And particularly after a meal, as we spoke about last time, walking after a meal gets your glucose levels to be more level, which is what you want. Which relates to this, we were talking about this old Chinese proverb, like 99 steps after a meal. No, 1,000 steps after a meal, you'll live to 99, but walk after you eat. Right. Because. Well, it'll stimulate the uptake of glucose, but also it'll get your muscles moving and stimulate the production of new blood vessels, make sure that you don't run out of oxygen later. But mostly what happens when you move. The first thing that happens is a really important reaction that involves one of these longevity pathways, the middle one that I refer to called AMPK. And we can. We can turn on AMPK just with a low level of exercise. Just start that adversity. Yeah, so AMPK registers energy in the cell, which is chemical energy, called ATP. And when you have low levels of ATP, AMPK gets a lot of energy. And it stands for AMP activated kinase. And AMP is what you get a lot of when you don't have enough of this fuel ATP. Long story short, when you have high levels of AMPK activity, you will make more mitochondria, which gives you long-lasting benefits. So after you've exercised, your body will be making more power, more of these organelles we call them, that will actually give you long-term health benefits beyond the period of time. And your long-term health benefits beyond the period of exercise. We know that low-level exercise alone is good. It's a good start. We also know that it's really not enough. You need to also be getting a pretty consistent dose of vigorous exercise too. It doesn't have to be a lot of these studies show, you know, 10 minutes a day, 15 minutes a day. Even 15 minutes a week if you're getting started, it's going to have health benefits. But vigorous exercise, the easiest way to think about it is, your breathing rate goes up, and your heart rate goes up, right? Right. And there's a reason why vigorous exercise is so important beyond just walking and standing. It's that you have hypoxia. Low levels of oxygen are undoubtedly good for you, even though they may not feel good. And you know your hypoxic when you're panting so much, you cannot carry out a conversation. That's what you're aiming for. For at least 10 minutes, a few times a week. So why is being out of breath important? Very rarely people ask that. Well, the main reason. Because it doesn't seem to make sense on a state like you need oxygen. Right. So again, it's this hormisus idea, a little bit of what doesn't kill you makes you stronger. So what's happening is when your hypoxic is you're turning on what's called hyphwan alpha, hypoxia, inducible factor. And that pathway turns on a bunch of really helpful genes. That control in your blood vessel growth and mitochondria. My good friend and colleague over at Harvard won the Nobel Prize in 2019 for discovering hyphwan alpha. And it's role in biology. Now, the other thing that happens in that, there's two things. So one is the hyphwan alpha that turns on a genetic program that's good. But what also happens is you get free radicals generated. Because when you don't have enough oxygen, those electrons that should normally be used by what's called the electron transport chain in mitochondria, which generates ATP, they fly out and they become a superoxide radical. Can we talk about that electron? Yeah, because it's really fascinating how this thing works. And it is a little circuit around. Yeah, it's a little battery made of proteins. And there's a string of proteins that come together in the membrane. And they pass along an electron, like a hot potato. They don't want to hold onto it. They shove it along. Get rid of it, get rid of it. And in doing so, they're pumping protons, which are hydrogen atoms, into the inner membrane space. Because there's two membranes that surround the mitochondria. And in that little space, the goal is to make it really acidic by putting in these protons into there. And this electron transport chain does that. But you need oxygen because at the end, when you get to the end, you got to get rid of this electron and they give it to oxygen. And then that's called respiration. It's a reason we need to breathe so hard when we run. And why we need oxygen in the first place. Now, if you don't have enough oxygen, then that'll lead to these free radicals being produced. And it'll damage the cell. So you might say, well, that makes no sense. If you're running and you're damaging the cell, it's going to be bad, right? But remember, a little bit of damage can be good. So what happens is it stimulates what's called mito-hormesis, mitochondrial hormesis. And that has a whole variety of benefits as well, including the manufacturer of more mitochondria that gives you energy. But I want to mention something that's really interesting, I think, about this electron transport chain. Remember how I said those protons, those hydrogens, get pumped into that little space to make it acidic. So now you've got what's called a gradient. You've got more of them in that space than inside the mitochondria in a bubble. They have to, they want to get out. If they got too much somewhere, they should equilibrate. And what the cell does is it puts little holes that the protons can escape through. It's called the ATPase. And what happens is, as those protons shoot through, it's like a hydroelectric dam turbine. And as they shoot through, it literally spins like a turbine. There's a little wheel at the bottom of this tube that spins super fast, many times per second. And that spinning allows it to make ATP or chemical energy, which then you use, then to burn to make the muscle work. And so what's really interesting is that the more mitochondria you have, if you've been exercising for a few weeks, allows you to make more chemical energy and you don't feel puffed as much as you did before. And the other thing that's happened besides having more mitochondria is that you've built more blood vessels in your body. And so your oxygen gets transported to the tissues. Now both of those things go awry as we get older. And we'll talk later in tomorrow about how you can circumvent that and reverse your age to be able to regain that ability. With drugs and molecules and supplements. Besides what we're talking about today, exercise itself. Yeah. We keep going back to this idea of a little bit of adversity. It's good for you. Like a lot of it's going to, like a lot of anything is going to kill you. And a little bit of a lot of these things that might in big doses kill you is really good for us. Because it puts our bodies into the state of adversity. Let's talk about this in terms of another effect of exercise. Increase glucose sensitivity. Right. So that as you get older, our muscles and our brain become less sensitive to the insulin, the pancreas is putting out increasingly more and more trying to cope with this insensitivity that happens. Now that's largely we think now because of this aging biological clock that the genes that are required for a muscle cell to function or a brain cell to function are getting switched on and off in the wrong way. We call this ex differentiation. And if you didn't see episode one, you might want to go back and hear more about that. Basically cells are losing their identity as they get older and not putting out a particular protein called glute four, which is a glucose transporter on the outside of the cell. So the muscles are not bringing in the glucose. That's two problems. First of all, you don't have your energy to burn in the mitochondria to make energy. The other problem is that that sugar that glucose that circulates in your bloodstream and doesn't get taken up into your muscle and your brain starts to damage the lining of the blood vessels. And we know that is type two diabetes and cardiovascular disease. And that's where veg f comes in. So veg f is a little protein that signals the formation of new blood vessels. When you exercise, the capital V E G F. Okay, so if people want to look this up, then yeah. Okay, all right. So veg f is made by muscles after you exercise. You go on for your run or even your walk, but running is even better. And there's a gene called PGC1 alpha that is what's called a transcription factor. It'll be made.
It'll bind to the upstream side of the Vegev gene and make more of this Vegev protein. Now Vegev will be secreted out of the muscle and diffuse or just leak out into the lining of the blood vessels. Now the lining of the blood vessels is made of cells called endothelial cells, which pick up the signal. They have little receptors that sense Vegev. And when they get that signal, that says, "Oh, wow, we're being chased by a sebitruth tiger for the last week. We better build more blood vessels." And they do that. Normally, if you have a tube, which is a capillary, almost microscopic blood vessels, what happens is the endothelial cells will start to branch out to the side and make a new blood vessel. And that's what you get with exercise. Conversely, if you sit around all day, you won't build new blood vessels. You'll actually have fewer and fewer and your muscle and your brain start to get starved of oxygen. Now, one of the big problems we discovered is during aging, that signaling pathway, that signaling mechanism is defective. And even though you're exercising as you get older, you're not getting the benefits of it. You don't get the new blood vessels. And you can see this in amounts. I mean, when you take, when you pull the mouse apart, not to be too graphic, but you can actually see these thing. We don't even need to hurt the mouse to see this. We can use imaging to see the blood flow in a mouse without hurting it. And we can see the bright red areas where the blood's flowing nicely. And in an old mouse, you don't get that, even with exercise. But we found a way to restore the youth of the muscle and restore the ability of that VEDGF to trigger new blood vessel formation. And the trick was to turn on the production of NAD, which is the fuel for the SIR2 and survival circuit. Which can be turned on by exercise, because exercise upregulates NAMPT. Also known as NAMPT. NAMPT. Some people call it that. But yeah, this is the relative of that ancient yeast gene that we talked about in the first episode that extends lifespan of yeast cells. So let's add one more piece to this. And that is how exercise impacts the epigenome. Yeah, the epigenome. If you missed episode one, I encourage you to go listen to that and watch that, because we covered what the epigenome is and how it affects the aging process. But the summary is that the epigenome is the regulator of the DNA. It tells the genes, whether to be on and off. And that goes wrong during aging. And may actually be the reason we age. And one of the reasons we believe that is that you can measure biological age now in people. I could take one of your cells, Matt, back to my lab. Well, actually I have to take a chunk of your cells or a cheek swab. And we can measure the rate of your aging. It's called the Horvath Clock or DNA methylation clock. And when you look at people that have lived a healthy lifestyle, say they've been exercising for the last 30 years, they are much younger epigenetically, according to this clock, than someone who hasn't. So that tells us that very likely that exercise is not just protecting you against cardiovascular disease, it's slowing down your overall rate of aging. There are other clocks as well. One of our-- There are many, actually. Yeah, so one of our researchers, Dave Johnson, was involved in the study that used the proteomic clock, which was similarly. Let's talk about that really quick, because it's another way to measure biological aging. Right. So we measure proteins in the blood, which change predictably over time. There's a protein called GDF15, which is circulated. It's now a really great biomarker for aging. In fact, GDF15 is one of those genes that was used in that study we were referred to last episode, where the Mediterranean diet slowed the aging process. They found that GDF15, the methylation on that clock marker, was also slowed down. The point here being that these proteomic clocks and the epigenetic clocks and some others like an immunoclock can be used now to understand what slows down aging, but importantly, how do you reverse it with various treatments? And we've gone from a field where we had no idea what was going on in aging. Really, we had to look at tens of thousands of people on metformin to see if it helped health to a point where we can take 100 people, treat them with something two months later, see if they've gotten younger or not. And those experiments are being done right now. And one of the things we can treat them with is exercise. Exercise in the study we're just talking about, they looked at a robically active people versus sedentary people. And the robically active people were five and a half years younger on average according to this proteomic biological clock. Presumably, we'd see the same thing if we used a whorebath clock or an immunoclock. Yeah, and that's true, actually. It's been done on excised people, and they are also epigenetically young. And what's important about this clock to realize is that it doesn't just tell you your biological age. You can actually predict when you're going to die, or when someone's going to die. And when I say that, some people-- It's a little more people-- --that I don't want to know this. Well, consider this, that 80% of your future health is in your own hands. It's modifiable. 20% is genetic, which you can't do much about yet. That's powerful. If you have the tools to change your rate of aging, first of all, you have to measure it to know if it's working. So I recommend that. And we'll talk about ways to do that practically. But if, once you have that number, then work with me. We can tell you here in the podcast, how to actually slow and reverse that process. Well, we use car analogies a lot, you and I. I think a lot of people do these. But it bears mentioning, like, you know that your car is not going to last forever. There's a shelf life for a new car. You get to choose based on how you treat the car over time, whether or not the car is going to last 100,000 miles or 200,000 miles or three or 400,000 miles. Right. Take it to the body shop repair and the mechanics more often. That's what we're talking about for our bodies. And that's why I think it's important. Well, you need to measure it. You need to know when the car needs a service. You need to know if you're tweaking that knob, whether you're doing harm or good. And to that end, one of the really cool and exciting developments happening right now is there's this sort of race for these clocks to become available widely for people to use. So much so that the price point is predicted to be, well, like, a buck. Well, it's coming down for the whole time for a Horgoth test. Right. So right now, if you want to check your biological age, you can go to Inside Tracker, one of our kind sponsors. That's a blood test. Or you can also have a DNA test, which is available for a few hundred dollars from various vendors. A student in my lab, Patrick Griffin, we've posted recently a paper, which can be accessed on bioarchive.org, that describes a way to pool, put together thousands of people samples and run them all together, bringing the cost of that test down to less than a dollar, which means that very shortly in the future, when we bring out this product and we are bringing it out soon, you should be able to do this test routinely and see whether you try and you diet or supplement or just meditation, whether you're actually benefiting from that. A lot of people hear all of this and they go, okay, I get it. I have to exercise. But, and I hear this a lot, but I hate to run. Like, everybody thinks of like, that's the only thing they're allowed to do. And I think doctors make a drift, physicians make contribute to this a little bit, by saying, okay, well, I need to get you running and jogging or whatever. It's not just running, right? What's the best kind of exercise? Well, there isn't one exercise you're going to do. It's what you love doing and it can be a sport. It could be wind surfing, it could be sailing, but just move. That's the main thing. There's even sex, which is, we actually look this up. We did look this up. We were really hopeful when we looked this up, but it burns like four calories a minute or something. It's not as good as. Well, I'm sure it depends on the individual, right? I mean, you can make sex more aerobic. You can make it part of your exercise regimen, but you have to have a partner, a consenting willing partner who also wants to make it part of their exercise regimen. It's only 4.2 calories per minute, which, and we also looked up the average length of sex, and it's about five minutes. Right, so you've got to burn 20 calories if you're an average person. I'll burn 10. So instead of that, you probably need to go for a longer walk afterwards to really burn off those calories and get your blood flowing. And however you get your exercise, be it running or sailing apparently or sex, both the World Health Organization, the Mayo Clinic, recommend at least 75 minutes of vigorous exercise a week. So that's 15 minutes a day. 10 minutes. And it's better if you spread it out over the week. Right, yeah, you don't do it all at once, but that's the starting point. And most people can do that. You can be the busiest person in the world. You can be the most unhealthy person in the world. You can get your heart rate and your breathing up for 10 minutes a day. Sure you can. And the benefits will be huge. You'll feel better. You'll look better. And you'll also have a better resting heart rate. That's one of the best measures of your fitness. If you're less than 50 for a resting heart rate, that's really good for someone my age in my 50s. Mine's usually around mid 40s. That's a good indication of how well you're doing. And if you've got a high heart rate, it's you're either too stressed or you're unfit, try to bring that down again. You can measure your heart rate pretty easily. Just put your hand on your arm, but you could also either wear a ring or a new fitness. These fitness. And there's all kinds of wearables now that are going to help you do this. Yeah, and I'm a big proponent of measuring things, right? Because otherwise you're flying blind. That's why we're. a ring, I wear a wrist watch. Sometimes wearing right now. I am. This is also a major sleep, which we'll get to in another episode. But I also, there were some advanced biomonitors. We're also going to cover, there's one that I stick on my chest for two weeks that measures my body a thousand times a second for various parameters, including my heart function. And in the future, these will be used by people to predict heart attacks as well as the flu and all sorts of issues like depression. In the future, we're not going to be flying blind. We're going to be monitored a thousand times a second, as opposed to now where you go to the doctor once a year. And they spend 15 minutes asking you, how do you feel, which is a joke? Right. Right. Because in addition to the fact that it's a single, it's a single assessment of a single time, it's highly subjective, it's self-reported. This just crap data. Yeah, this is a bit of an aside, but it's worth noting here that I've been measuring myself for over 10 years using inside tracker. And that data is wonderful. It's graphed and you can see when things go wrong, I've corrected it, corrected it. They do an inner-age study. There's a measure called inner-age 2.0, which tells you how you're doing compared to others, your age, and you try to keep that low. And based on that calculation, I've been getting younger for the last 10 years, which is great to talk about. But it also means that I'm optimizing my body every time when I do something. And if something doesn't work, then I won't do it. And we are going to get into this, but I've got a friend named Price who helps people do this, the Institute for System Biology, and they help people create these charts that they can then bring in to show their doctors. And he was only about this woman who brought her chart into the doctor, and the doctor was at first dismissive, and she said, "Well, won't you at least look at it?" And the doctor looked at it and went, "Oh, wow, this is really helpful." That's exactly the response of my doctor to. My doctor said, "Well, how do you feel?" And I said, "I'm good. I'm sleeping well." And he said, "Okay, see you next time." And I said, "No, hang on. Let's do some more. I've got some data." And I showed you. And I showed him the inside tracker data on Zoom. And he said, "This is wonderful. I wish all my patients had this data." Of course, he cannot order 43 biomarkers every time. That's a health insurance. One pay for it. But individuals, if they want to spend their money instead of coffee, they can put it into a blood test, doctors actually do respect those data because they're actually produced by the same companies that the doctors would use anyway. And to bring this all back to size, it's all back to exercise and these other adversity mimetics, which we're going to get to, having this data. I'm a big soccer fan. The first time I saw a soccer player try coffee shirt and he was wearing a bra on. I thought, "What the heck is going on?" But it's actually holding these trackers that are measuring things in the middle of games and the middle of practices. The world's best athletes are doing this right now. And it's becoming more and more available for other people to track as well. And once you have this data, you can start to act on this data. You can start to arrange your exercise routine so that you're getting the most out of it. Exactly. And they can be fun too. You can use GPS to see where you're going. You can compare it with your colleagues, your friends. I'm running more than you. Let's move along here because we've got a lot more to talk about. But before we get away from exercise and start talking about these other adversity mimetics, there's another form of exercise that I know you enjoy, that I enjoy. A lot of people enjoy, but maybe doesn't get as much attention as aerobic exercises weight training. I'm glad you said that. All right. So weight training. Yeah, I do that fairly often, I would say at least every other day, if not every day. The way I do that is I have a gym in my bedroom. I also have weights next to my desk. You also have them in the trunk of your car right now, I thought. I do. Because I travel a lot. So I'm taking weights with me. But the reason that I do weight lifting is that it's going to maintain my hormone levels. It's going to maintain my ability to walk well and stay upright and have good posture. It makes me look better. Well, you may say that's debatable. But also as I get older, you're a really good looking guy, David. Thanks. You're a lovely Matthew. Thank you. The other thing is that is often not appreciated is it's harder to build muscle as you get older. And you want to maintain that muscle mass. I'm losing about 1% of my muscle mass every year unless I maintain it or build it up. As you get older, you're going to fall over, right? Everyone falls over, especially as they get older. And if you break your hip, that's close to a death sentence. A lot of people, well, 19 people every minute fall over and break their hip in the United States, which is a major cause of mortality in the mortality rate. And the mortality rate after a hip break just like skyrocket. Well, it's equivalent to having metastatic cancer. That's how bad it is. But if you've got muscles and you're flexible, you do, say, pilates in your older age and stretch, build up the muscles, particularly around your waist, then you're much less likely to break a bone when you fall. Yeah. Building muscle mass also helps maintain youthful hormone levels. Right. So I had trouble maintaining testosterone levels like most men, my age. Now there are two ways to go about it generally. The main one is that your doctor will give you an injection of testosterone to apply at home or a cream that you can rub on your forearm. Those are the two ways you can do it. There are others. But the other way, which I prefer, is to naturally boost it by maintaining large muscles, exercising my thighs, my butt, my back. And I've compared the two. I have tried cream on my arm for testosterone. It worked okay. My levels went up maybe by 20%. Wasn't great. I really maxed out my testosterone levels by doing leg exercises and back exercises. I'm talking about things like leg extensions, leg curls, as well as hip hinge, which is bending at the hip and lifting weights. And I also do dead lifts, which is standing up with lifting a really heavy weight with a straight back. There's another way that we know that exercise is impacting aging. And we talked about sentencing cells in terms of what iron may be doing to cause cells to go sentencing. But let's talk about that as one of the key aging, what is called the aging hallmarks. Exercise prevents senescence. It turns back sentencing. What exercise doing in terms of these zombie cells? Well, you let's start with what a senescent cell is. So when the epigenome becomes too dysregulated and this ex differentiation process happens, cells can either die. They can become a cancer. But what the body tries to do is to prevent that by shutting these cells down and make them more like zombies. They are alive, but they're not dividing and they're causing havoc. You're greeting all these chemicals and the bloodstream. They are. It's called the SASP. The senescence associated secretory phenotype. And these proteins cause inflammation. They also cause cancer. So the fewer sentencing cells you have in your body, the better. And we're starting to find that their lifestyle and supplementation and some drugs can slow their formation. Remember, keep the iron levels low. But also we can kill them off. And there's this study, the one you're referring to, which took 34 individuals for a 12 week exercise program and looked at the amount of senescent cells circulating in their immune system and it was dramatically lower in the exercise people, arguing that you can actually kill off or reverse that process. 12 weeks. Just 12 weeks. Because these 12 weeks to like destroy some sentencing cells seems like a pretty good deal. Yeah, it's one of the best ways to kill off senescence cells. That's the study that was just out this year in aging cell, England, at all. We will link to that in the show notes. Let's put a wrap on exercise. But let's have a few takeaways here. And there's really there's there's three big ones. The first is a low level of exercise. And and this is just steps, right? Get off your butt. Get off your butt and take. Yeah. Standing desk or a desk with a treadmill walk around the block after dinner or lunch. Those are the simple things. And you don't have to hit 10,000 steps but shoot for four. Four. Four is great. Okay. All right. And then that's the low intensity exercise that everybody should be getting throughout the week. Every single day, you should also get high intensity exercise. For sure. A few times a week 10 or 15 minutes lose your breath. It can be the form of hit high intensity interval training or running on a treadmill. That will get your blood vessels flowing and your mitochondria amplifying 10 to 15 minutes a day. Yeah. That's only five minutes a week. Yeah. That's what all the experts recommend. Okay. All right. And then muscle building. Yeah. Wait. That's just as important. So maintain that muscle mass for your hormones testosterone, particularly for men and women exercise the big muscles, particularly. Don't forget about those. Don't just work on your upper arms. So you look good. But it's pretty simple. You don't need to gym in your bedroom like I do. You can do push ups, sit ups, or just have some weights lying around. That's sufficient. Okay. And all of this is the goal is it's not just we want to look good. We want to write all of this is aimed toward the goal of longevity through putting your longevity genes into or learning your genes yourselves to a state of adversity. Yeah. The adversity mimetics. The diversity mimetics. I really do like this word. I think this is going to catch on. Yeah. We trademarked that one. Okay. So let's but this is not the exercise is not the only adversity mimetic. There are others. We're going to talk now about a few other categories. We're going to talk about cold temperatures. We're going to talk about heat. But there's a really exciting one right now. And it is related in some ways to exercise or the effects, the genetic effects, the cellular effects that we get from exercise. And
And it's really fast moving. The latest studies are only out in the last couple of years, and this is hyperbaric oxygen treatment. Right. Or H-B-O-T. Yeah, this is really fascinating because for a while we knew that wounds repair or heal faster when you give them a oxygen. Because why? Well, it's not clear. It could be hormisus. Free radical generation could be that the more oxygen in the tissues allows them to grow better. Those are all theories. But we know that it works. But then people started putting themselves in hyperbaric chambers. The military, certainly the Navy have been doing this for a long time to prevent the bends. But it's found to be quite therapeutic, particularly for neurological disorders, but increasingly for aging itself. And we should say what a hyperbaric chamber is. Right. The hyperbaric chamber is a room or sometimes just a little tube where the pressure is increased. And when the pressure is increased, the amount of oxygen that you get when you breathe is increased. Right. You can go up a couple of atmospheres or more and you supplement that with oxygen. You breathe in a bit more oxygen or pure oxygen. And so I recently tried this actually. I went out to LA. Fortunately, unlike you, I'm not claustrophobic. I'm so glad I can't do this. I cannot do this. You probably can't. But it's a glass cylinder, so you don't feel it. And I just watched Shits Creek for a while. It was pretty cool, especially when I was high on oxygen. You said it was funnier when you. It certainly was funnier, but it might just be because every time I watch it, it gets funnier. But it's really relaxing. I believe I was in there for about an hour and it was, you know, it can meditate in there or you can fall asleep or watch TV. It's really a great experience. But that aside, what the science says is that it actually can reverse an aspect of aging, which is telomere shortening. The ends of the chromosomes, many of us, of your will, have heard of this. Like the ends of the shoelaces, the egglets they're called. If they wear out, it actually leads to cellulose in essence, these ombicells. And this happens over time as we get older. And what we've been looking for, we scientists for many years, is a molecular treatment that makes them grow back again, because that should help slow down aging and give us longer life. And that's what was reported last year from a group in Israel who I know well, I've been over there and checked out their giant chamber. And you actually got a wind of this before, while they were working on it and you went to kind of like peek in on what they were doing. Yeah, I mean, this is one of the fortunate things about my job is that I get to hear about things before their public and I get a sneak preview. And I went over there and sat in their giant chamber, which looks like the inside of a bus and with a mouse you put on. And they showed me their data. It actually looks like a control room from Star Trek. It's really high tech. And but the data that they showed me in mice and in humans was really compelling. It looked like at least in the mice that those plaques and tangles in the brain of mice that were given Alzheimer's went away. Do you have a little miniature hyperbaric chambers for the mice? We're building one, because I'm going to use one in my lab. But they're not ready yet. But also what they were finding was that the humans that were put in there that had dementia or Parkinson's were dramatically improved after a few sessions of this. And it's become a real craze throughout the US. People are reporting remarkable benefits. Now what we need are more studies like the one in Israel to actually measure things. And if possible do a placebo control as well. But at least what we have right now are some studies, most of them fairly small scale, but human studies, memory, improvements, telomeres, T-helper cells. Right, they go up as well. And cognitive performance, there was six L-delepation suffering from memory loss. And in 2020 on this new study came out and they all improved. And the really cool thing about this treatment, even though not everybody has access to a hyperbaric chamber, obviously, but it is a pretty easy intervention. And it's easy to treat people this way. It's easy to test people in this way. So now we have the clocks. We can test if aging actually goes backwards. That would be a good experiment is to take people who have done seven or eight, ten bouts of this treatment before and after and see if they're biological age went backwards. So still early, it seems like these things are working across a variety of ways that we can measure aging and the problems of aging if this is working. Why is it working? Yeah. Well, we don't know for sure. But one of the theories is that it's working similar to exercise. So hypoxia, the low oxygen when you go for a run, what it's doing is turning on this HIF1 alpha protein that I talked about earlier. And that helps promote health in the body. The other thing that happens with exercise is the free radical generation that gives you a little bit of mydo-horomesis. It looks very much like hyperoxia, hyperbaric chamber treatment. Because the very similar thing, you get a production of these free radicals. And that stimulates also a mydo-horomesis response that gives you very similar benefits to low oxygen. There's one theory that I have is that when you come down from the high levels of oxygen, it stimulates hypoxia, like you're running as you come down from high levels to low levels. So it's not so much the oxygen, the explosion of oxygen that you're getting, but it's like once you temporarily get used to that, then you come off of it. It's the differential. And that fits with the new findings, which is going up once and coming down once, is not as good as going up and down and up and down within a treatment. Before we move away from hyperbaric oxygen treatment, I know you're most familiar with this Israeli study. Let's talk about the protocol in that one. Yeah, they took 30 people and put them in their large chamber, the one that I visited. And they did 60 daily sessions of 90 minutes, five of those per week, and had a look at the number of senescent cells in the bloodstream before and after and telomere length. And what they found remarkably was that those aspects of aging were reversed. These are impacts on senescent cells too. They did. They looked at the immune system, looking at these immune cells, you can measure senescence, you can stain them blue, which is bright blue when you get older. And they found that there was a dramatic reduction in the number of those senescent cytotoxic t cells as they're called. Okay, so 60 sessions, 90 minutes, this is not something anybody. Most people can do every day right now. This is not going to be a common part of people's longevity regimens anytime soon. Well there are a number of centers that are run by doctors in major cities. It'll become more popular. It's growing rapidly. But I think it's a great way in the future for people to mimic exercise. I wouldn't say don't exercise, right? But it's an interesting idea that you can lie down, watch TV, go to sleep, and get your run in by mimicking hypoxia, but in this case with high levels of oxygen in your body for a short period of time. It's really cool. Let's shift now to talking about cold therapy, which is another thing that a lot of people experimenting with now, another thing that there are centers for all over the place, but that the research is still sort of catching up to the excitement. So we're not, we're sort of on the edge here of our understanding, but we do know some things about what cold does to the human body and actually what cold does to organisms across the spectrum. Yeah, in fact, when we wrote lifespan, there was almost no data on this. And now we know actually that one of the huge benefits you get from being cold is the production of brown fat. So what is brown fat? Brown fat, or often called beige fat, is found in babies. It's typically to allow them to stay warm because they don't shiver until they're about one year of age. And what was discovered about 10 years ago at Harvard by Bruce Beagleman and Ron Kahn, a couple of my colleagues, is that adults also have some brown fat, and they discovered this with pet scanning. And they found it mostly exists on your back, in your shoulder blades. And when you get cold, it revs up. You get more of this brown fat. And this is a good thing because brown fat is extremely healthy. It revs up metabolism. It burns white fat. And we think that there are these factors, little chemicals, little proteins that get secreted out of brown fat that make the rest of the body healthy as well. One of the reasons we know that is because there's a gene that makes brown fat, makes cells turn brown from white to beige to brown. And it's called PRDM16. And mice that lack this gene, they don't have brown fat, but they also develop type 2 diabetes and cardiovascular disease as a result. Cold impacts, not just humans, it impacts all the organisms. We've seen this in model organisms too, these effects, right? There's the studies in worms, there's been studies in mice. You've got a couple of favorites I know. Do you like talking about the mice that got this spoon together? Oh yeah. So that one is a bit of a disappointment in the field that we had these dwarf mice, that Mike Bunkowski, who was working in my lab, he was the guy that generated the longest live mouse, he called it Yoda. And it was very long lived because it had a mutation in a gene for the growth hormone receptor, which means there were small and dwarfs. And these little small dwarf mice would live up to three times longer than a normal mouse. It was quite an amazing thing. And the field was rejoicing. Wow, we figured out how to make mammals live that much longer. And then it was noticed that they were shivering, little cold mice. And so the researchers thought, we'll just give them friends. So you give them? They were shivering because the lab was cold, they were shivering because. They didn't have a companion. You know, mice like to live not solitary, but with other mice. And so they gave them a buddy, each of these dwarfs had a buddy, and then the majority of the lifespan extension went away. - When they got their buddy. - Yeah. - Which is super disappointing, right? But what it told us was that a large effect of longevity was due to them being cold. - And why is that happening? When we go back to like thinking about the survival circuit, what's happening? - Yeah, well, the trick is, let's go back to the brown fat. What brown fat has a lot of is mitochondria. And within those mitochondria, they're actually quite different. They have high levels of proteins called UCPs or uncoupling proteins, which insert into the membrane of the mitochondria and allow those protons that were built up to leak through, instead of going through that pump that makes the energy, they leak through. Why is that interesting? Well, first of all, that generates heat that helps the animal and we survive cold. But also, you get fewer free radicals produced when you uncouple mitochondria with these proteins. And consistent with that, if you make an animal, let's say it's a worm or a fly or even a mouse that has high levels of these UCP genes, they actually live longer. So uncoupling and reducing that free radical load, and you can do this with cold therapy, we think, is beneficial to health. - And cold therapy, people call it cryotherapy, is this short term acute, super intense? You've done this before, right? You did this with Rogan, didn't you? - Yeah, Joe said, let's go do that after the show, which I did. It was pretty chilly. I had to strip down into my underwear and put gloves on and socks and whatever. But you get to play music at least. I got to choose help by the Beatles, which was quite appropriate because by the end of those three minutes, - You wanted out. - Well, the first two minutes, I'm like, what's the problem? This isn't cold, but that last minute, I really thought I was gonna get hypothermia and my ears might break off. - You're chattering and she's-- - Yeah, you really start to shiver, which is your body's way of generating heat by moving your muscles. But it was really enjoyable. I found afterwards I felt stimulated, I felt lucky to be alive. And I felt good for a number of days afterwards, which is probably because my mitochondria were revved up and I was building more brown fat. The one thing I think it's worth pausing here to talk about is why would you do this now? Why don't you wait till you're old to do cold therapy? And what's been found at least in mice is that old mice don't make brown fat as well as young mice. So what you wanna do is middle age do these treatments and so that you're ready for old age when it becomes harder. - Just like right now we need to be doing vigorous exercise. We can't wait until we're old to do vigorous exercise. - Though it's never too late, we do find that things work in elderly mice and elderly people, but it doesn't work as well if you start middle life or even older. - Okay, and maybe that's like the cryotherapy stuff is sort of a can do vigorous exercise, but you still have to have that low level of perceived adversity just like we have to get lots and lots of steps in every day. But we live in these environments, these temperature controlled environments, where it's like 68 to 72, that's not how our ancestors lived at all. - No, we were shivering probably most of the time during the ice age for sure. And our bodies recognize that. We've got those genes that respond and they keep us healthy as we've talked about. So there are a number of ways you can, if you don't have a cryotherapy center near you, what do you do? Well, you can take cold showers, some people do that. I don't, I find that unpleasant, but you can do that. It's very cheap to do that. Or you can do something that I do actually do, which is sleep with very few covers on my bed and lower down my body temperature. And that's also being shown to activate these uncoppling proteins and build brown fat. - The opposite side of this is heat, which is also something that throughout our evolutionary history we've had to deal with. We didn't always live in temperature controlled buildings. And we've got some emerging research on that as well. - Right, taking your body out of its comfort zone. And so all of these things are about taking your body out of its comfort zone. - They are, right? - Yeah. - And some of them are really enjoyable. I think sauna bathing is called in Europe, is super enjoyable. And it also is good for your skin. You get to sweat and get those pores unclogged. But this is one of the most ancient therapies for longevity. Even before Roman times, they were bathing in these sauna's, though the Romans would use fires under the floor. But this is something that Europeans still carry on as a tradition, particularly in Finland and other Scandinavian countries, where these studies are typically performed on men for some reason. But the data that I've looked at, which we'll put the show notes, is that there's absolutely no doubt that men who partake in sauna bathing a few times a week, often at home, because they build this into their houses, have a dramatic reduction up to 20% in the rate of cardiovascular disease and mortality caused by heart attacks. - This isn't happening for the same reason as cold therapy work. This has nothing to do with brown fats. There's another thing that's going on here, right? - It's different in this case. What we think goes on in a sauna is you're activating HSPs. And these heat shock proteins are helping to fold proteins correctly and also stimulate pathways that are beneficial such as building new blood vessels, making more mitochondria. And one of the reasons that I believe it's true is that in model organisms, if you take a worm, if you turn up his shock proteins, either by giving them a lot of heat or genetically modifying them, they also live longer. - We don't quite know what dosing is right for sauna baths at this point or like how much, how hot, not a ton of research in this area. - No, but it doesn't seem like you can overdo it. I haven't seen any evidence that it's negative. And I used to, before the pandemic, I used to go at least once a week and do multiple bouts of the heat shock in the sauna for about 15 minutes and then jump in an ice bath, which was nearby for four minutes and then cycle that. - You should probably consult your doctor before you do that. - I would definitely and I did. But yeah, it can put some stress on the body, certainly on the heart. But yeah, the idea though is to shock the body, heat cold, heat cold. And that way, I think you get the maximum benefit from these adversity mimetics. - And again, you don't necessarily need to have access to a sauna to do this. I mean, some people can build them into their home, some people have them in their gyms. That's kind of a point of privilege. Most people have a bath. - Or shower. - Or shower. I just certainly do that. I like to turn the heat way up. There are a variety of different sonas. There's the old-fashioned type, which is the cedar planks sitting in there and you just throw water on hot rocks. That's traditional. New ones such as infrared sonas. And the infrared light actually penetrates the skin and is thought, and there's some evidence, a real believable evidence, that they're also in the skin layer can reverse aspects of aging as well. And including improved hair growth. - There is, for some obvious reasons, there's a lot of questions I want to ask about hair growth. We're going to be discussing hair growth, skin care, all these like sort of like cosmetic aspects of aging things in a future episode. - One of the commonalities that I'm kind of sensing in all of these things, right? You do vigorous exercise and you get what, we term a runner's high. And you talked about doing the cryotherapy and you felt like, what did you say? Like, blessed to be alive? Or I've done sweats and sweat lodges and you come out of those things and it's just like, it's the best drug in the world. What do you think, why are these things so similar? - This happens in the hyperbaric chamber too. - Yeah, yeah, that's one of the nice side effects. That's when you know that you're doing a good longevity protocol 'cause what's happening at the cellular level is those three main defense pathways get turned on. But at the physiological level, the neurological level, you're getting endorphins as well. And that's when you know you've actually done the right thing. - So let's talk about a basic protocol with the caveat that we always make, which is everybody's going to be a little bit different. But if we're trying to get sort of like exercise, cold heat and hyperbaric, what's a good way to do that? We've already talked about the exercise protocol. Actually, I don't think we need to reiterate that. You need to exercise, get off your butt, cold heat and hyperbaric. - Yeah, well, as I mentioned, I used to do, and I will do again, the cycling of the heat in the cold about five times during one day of the week. This was on a Sunday with my son Benjamin. But I would say more is better. There's no evidence that you can overdo this. You could even do it every day. If you don't have access to a gym, you can always use your house. You can turn down the temperature, or you can use your shower. And that will work almost as well as is dunking yourself into a cold bathtub. Or you could do what Gabby recently had Hamilton do, which is shove us into an ice bath with literally with ice in it. I think that you don't need to do that every day. - It didn't you almost drown? - I did, but that was different. That was hyper-hypoxia. What they do is they make you do exercise with weights at the bottom of a pool below your height. So you're underwater, and you have to jump up with those weights to get a breath in there. - We're not recommending that at this time. - I think everybody should go knock on their front door and do it with them. - No, it's, but you can get hypoxia from exercise. It's very similar. So we've talked about hot and cold. The hyper-barric is more of an issue, I think. - That's a challenge. - There's not a lot of these centers around, and it's expensive. It's hundreds of dollars per treatment. But that's in the future. I think that that, well, I wanted to mention that because it's really interesting how it's so similar to exercise and hypoxia at the molecular level. But for most people right now, that's out of reach. - But that's not the only thing in the future. There's a lot of really cool things coming down the path.
right now that are going to be a fundamental part of people's lives pretty soon. We're going to be talking about a lot of those in upcoming episodes. We are and it actually I think a lot of people will be excited that we can mimic this adversity with molecules, with pills, with injections. And we're going to talk about that in the next episode. In the next episode. Yeah. So next episode, molecules, supplements, longevity, that's, that's going to be a lot. Yeah, I'm excited about this one because I get questions every day about it. And I think it's going to be one of the most downloaded episodes. Yeah, I think a lot of people are going to want to excited to dig in. Yeah. Okay, cool. Thanks for joining us this episode on exercise and other forms of acute stress. If you're learning from and enjoying this podcast, please subscribe to it on YouTube, Apple Podcasts and Spotify. On Apple, you have the opportunity to leave up to a five-star review. If you'd like to support us, please check out the sponsors we mentioned at the start. We've partnered with companies we truly believe in and they make this show possible. We also have a Patreon. That's patreon.com/DavidSinclair. There you can support the show at any level that you like. Thanks again and we'll be back next week to discuss supplements and molecules like NMN, NR, Resveratrol and how these impact longevity.
Podcast Summary
Key Points:
High iron levels accelerate aging by producing free radicals and promoting senescent ("zombie") cells; low iron levels are associated with longevity.
A plant-based diet, intermittent fasting (skipping breakfast and lunch), and regular exercise activate protective genes (mTOR, AMPK, sirtuins) that mimic adversity and enhance longevity.
Exercise reduces cancer risk by up to 23% and cardiovascular disease risk by 30%, with as little as 50 minutes per week of moderate activity.
The survival circuit, discovered through worm studies (DAF-2 gene), shows that mimicking adversity (e.g., hunger, cold, stress) turns on cellular defenses that slow aging.
Modern comfort (constant food, sedentary lifestyle) deactivates these defenses; intentional practices like standing desks, walking, and hypoxic exercise are needed to trick the body into a protective state.
Summary:
In this episode, David Sinclair and Matthew Lapland discuss how iron levels and adversity mimetics impact aging. Sinclair explains that while iron is essential for oxygen transport, excess iron—especially from supplements or high meat intake—generates free radicals (superoxide, hydrogen peroxide, hydroxyl radicals) that damage DNA, proteins, and lipids, leading to senescent cells and accelerated aging. He recommends measuring blood iron and avoiding unnecessary supplements, particularly for those with the HFE gene linked to hemochromatosis.
The conversation then shifts to "adversity mimetics," a term they coin for practices that trick the body into a survival state. Sinclair traces this to 1990s research on the DAF-2 gene in worms, which showed that a single mutation could double lifespan by mimicking starvation. The body’s protective circuits—mTOR (sensing amino acids), AMPK (sensing energy), and sirtuins (sensing NAD)—are activated by perceived adversity like hunger, cold, or exercise.
Modern comfort suppresses these defenses, so intentional strategies are crucial: intermittent fasting (skipping meals), standing desks, and regular exercise. Even moderate activity—50 minutes weekly—reduces cancer risk by 23% and cardiovascular disease by 30%. Sinclair emphasizes that exercise not only improves fitness but directly slows disease by inducing hypoxic stress, which triggers cellular repair and longevity pathways.
The key is to consistently challenge the body’s comfort zone to maintain healthspan.
FAQs
High iron levels can accelerate aging by producing free radicals and promoting senescent cells, though iron is essential for oxygen transport. Sinclair recommends measuring iron levels and avoiding unnecessary supplements.
Free radicals like superoxide and hydrogen peroxide cause oxidative stress, damaging DNA, proteins, and lipids. Excess iron can convert them into harmful hydroxyl radicals that drive aging.
Adversity mimetics are practices that trick the body into perceiving stress, activating longevity genes. Examples include fasting and exercise, which mimic ancient survival conditions.
Exercise activates protective genes and reduces disease risk, such as up to 23% of cancers and 30% of cardiovascular disease. Even 50 minutes of moderate exercise weekly lowers all-cause mortality.
The survival circuit involves genes like DAF-2 that control aging by sensing adversity. It was discovered in worms where a single gene mutation doubled lifespan, showing aging is regulated by signaling pathways.
mTOR senses low amino acids, AMPK senses low glucose, and sirtuins sense NAD levels. These sensors turn on defenses when the body perceives stress like hunger or exercise.
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