#51 Is Resveratrol a Longevity Compound?
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In this episode, Rhonda gives a summary of the science of resveratrol including its effects in animals and humans, the mechanisms behind how it works, and the bottom line on resveratrol supplementation and safety.
A few key moments...
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Resveratrol improves cardiovascular biomarkers in clinical trials
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Anti-inflammatory effects of resveratrol
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Improved cognition and memory in clinical studies
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Resveratrol improved healthspan, but not lifespan, in animals
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Induction of longevity genes via xenohormesis
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Contradictory effects on exercise-associated benefits
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Various factors that affect resveratrol bioavailability
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Unintentional effects on drug metabolism
For a more in-depth timeline, as well as references for this episode, click the timeline tab.
Learn more about resveratrol on our overview page
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Initial study at Cornell that suggested resveratrol was responsible for cardiovascular benefits of drinking red wine. Study.
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Overview of what resveratrol is and where it is found.
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Clinical effects of resveratrol in humans.
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How 150 mg/day resveratrol supplementation promoted caloric restriction-like effects in obese individuals. Participants had a significant decrease in blood pressure, blood glucose, and triglyceride levels. Study.
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How 10 mg/day of resveratrol in patients with a history of heart attack decreased LDL, and improved left ventricular diastolic function and endothelial function. Study.
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How 40 mg/day of resveratrol lowered reactive oxygen species, TNF-alpha and IL-6. Study.
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How 480 mg/day of resveratrol completely reversed arterial stiffness in monkeys fed an obesogenic diet. Study.
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How 200 mg/day of resveratrol improved memory in healthy individuals. Study.
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How 500-2000 mg/day of resveratrol improved mental status exam, spinal fluid amyloid beta levels, and spinal fluid levels of matrix metalloproteinase 9 in patients with Alzheimer’s disease. Study.
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The mechanism by which resveratrol is able to extend lifespan is through sirtuin activation, similar to caloric restriction.
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Resveratrol negated the negative effects of an obesogenic diet in mice by mimicking caloric restriction. Study.
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Resveratrol increased genes that are also activated by caloric restriction and reduced osteoporosis, cataracts incidence, vascular dysfunction and declines in motor skills in mice fed a normal diet. Study.
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Resveratrol induces autophagy- the adaptive response mechanism to remove unnecessary or dysfunctional cellular debris. Study.
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Resveratrol also induces longevity genes also known as stress response genes via xenohormesis.
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An evolutionary explanation of why our body responds to resveratrol the way it does. Hypothesis on origins of xenohormesis.
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How 250 mg/day of resveratrol blunted the positive effects of exercise in elderly men who exercised by engaging in cycling and crossfit 3 times a week. Study.
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How 150 mg/day of resveratrol blunted the positive effects of exercise in young men who performed high-intensity interval training 3 times a week. Study.
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How 500 mg/day of resveratrol increased mitochondrial density, muscle fiber and maximal oxygen consumption in elderly men and women who did resistance and aerobic exercises 3 times a week. Study.
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How resveratrol can be a mild direct antioxidant and what the difference between direct and indirect antioxidants are.
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Resveratrol bioavailability is increased with a moderate fat breakfast compared to a high fat breakfast. Study.
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Resveratrol is insoluble in water, but studies have shown that if it is enclosed in a nanocapsule – a shell that encapsulates an inner core – its stability and bioavailability are increased. Study.
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When consumed with black pepper derived piperine, the bioavailability of resveratrol increases over 14-fold in mice. Study.
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In humans, piperine consumption did not improve the bioavailability of resveratrol but it did improve cerebral blood flow. Study.
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How a glass of wine only contains a very small (arguably clinically irrelevant) amount of resveratrol.
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How 2 grams/day of resveratrol supplementation was shown to be safe in obese elderly individuals. Study.
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A word of caution about resveratrols effects on drug metabolism.
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Resveratrol causes 33% inhibition in CYP3A4 and 171% inhibition CYP2C9- two enzymes responsible for the metabolism of many commonly taken drugs. Study.
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Men with prostate cancer given 1 gram/day of resveratrol for 4 months had lower levels of androgen precursors but no effect on testosterone itself. Study.
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Conclusion
Hello friends. Today is another special episode. Today I'm gonna talk about resveratrol, probably one of the most studied plant compounds around. It first showed up on the nutritional radar in the early 1990s when a couple of scientists at Cornell University suggested that resveratrol might be responsible for the cardiovascular benefits then thought to be associated with drinking red wine, which contains resveratrol. Since then, a ton of research and maybe even more hype has emerged about the health benefits of resveratrol. For this round, we'll skip right past the hype and get down to the nitty-gritty of the scientific evidence, resveratrol effects on animals and humans, both good and bad, the mechanisms behind how it works, and the bottom line on resveratrol supplementation and safety.
Before we kick this thing off, a quick mention about this episode. It's actually been out for a few days already. This is one of the new elements of the engine that keeps FoundMyFitness not only running, but thriving. By offering a few solid concrete perks for supporting members, I'm able to keep this podcast free, grow my team, and actually make free FoundMyFitness better than ever before. Premium members now get a pretty sweet list of benefits including a members-only early access feed that also gives periodic exclusive content, free updates on genetic reports when they come out, a PowerPoint presentation with all of the videos, on-screen graphical figures, studies and on-screen notes. You also get a FoundMyFitness t-shirt fulfilled automatically by our print-on-demand distributor.
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Alternatively, you can avail yourself of the whole story behind my new premium offering, the how, what, and why, or just get signed up for $15 a month by heading over to foundmyfitness.com/premium. That's foundmyfitness.com/premium. Premium. Really folks, this is so much better than ads and it affords me the opportunity to continue making FoundMyFitness into the best, mostly free resource that it can be. Without further ado, let's get started. Resveratrol. Resveratrol is a natural compound found in the stems, leaves, roots, fruits, and seeds of a variety of plants. The primary purpose of resveratrol in plants is to protect them from their stressors, such as a fungal attack or effects of ultraviolet radiation.
Resveratrol is found mostly in the skin of red grapes, And of course, it's found in red wine in minute amounts. Also peanuts, blueberries, and the root of a plant called Japanese knotweed. Although resveratrol was first recognized for its cardiovascular benefits, multiple studies now show that resveratrol improves metabolic and neurological health, extends lifespan in unhealthy animals, and might even have anti-cancer properties. Since resveratrol was first considered for its cardioprotective effects, Let's start there.
Some of the major risk factors for cardiovascular disease include high blood pressure and abnormal blood lipids, but metabolic dysfunction and cardiovascular disease also go hand in hand with having type 2 diabetes, being overweight or obese, or having non-alcoholic fatty liver disease. They significantly increase the risk too. Resveratrol has been shown to have beneficial effects on all of these risk factors. For example, multiple studies in people who have type 2 diabetes have demonstrated that resveratrol treatment of 1 gram per day significantly reduces blood pressure, fasting blood glucose, and circulating insulin while increasing HDL levels.
In a small clinical trial involving 11 obese people, 150 milligrams of resveratrol treatment for 30 days promoted caloric restriction-like effects, which I'll come back to later. The study participants' blood pressure went down and they experienced improved blood glucose, insulin, and triglyceride levels compared to when they took a placebo. This study design used a crossover design so that each participant served as their own control, and they only showed improvements on the resveratrol, not on placebo. When people with non-alcoholic fatty liver disease took a resveratrol supplement of either 300 or 500 milligrams per day for 3 months, their serum LDL levels, liver fat concentrations, and inflammatory biomarkers such as NF-kappaB all decreased while their insulin sensitivity increased.
In a study involving 75 people who were taking a statin, those who also took a 350 milligram resveratrol-enriched grape extract daily for 6 months saw a decrease in multiple cardiovascular risk markers. LDL decreased by 4.5%. Oxidized LDL decreased by 20%, and apolipoprotein B decreased by 9.8%. After the 6-month treatment period, the people received double the original dose for another 6 months, which resulted in a decrease in inflammatory markers such as TNF-alpha and IL-6, while increasing the anti-inflammatory marker IL-10. Those are some pretty impressive results. When it comes to resveratrol and statins, however, there may be some more nuance to this because resveratrol, at least at high doses, may also slow drug metabolism, a factor we'll dig into a little bit more later.
While all of these studies focused on people who were at risk for cardiovascular disease, in a study in which people who already experienced a heart attack were given a very low dose of 10 milligrams of resveratrol every day for 3 months, the participants showed significant decreases in LDL and improved left ventricle diastolic function and endothelial function, both which are overall measures of heart health. You might have noticed a common theme in many of these studies, an improvement in markers of inflammation, a key player in the development of chronic diseases, including cardiovascular disease. Some studies have focused specifically on the anti-inflammatory properties of resveratrol.
In a study in which healthy people were given a 6-week course of Japanese knotweed extract containing 40 milligrams of resveratrol, the study participants had lower levels of reactive oxygen species and suppressed expression of pro-inflammatory cytokines, TNF-alpha, and IL-6. Studies in animals show similar beneficial effects. When monkeys were fed an obesogenic diet, they had a 40% increase in arterial stiffness and inflammation. But when those monkeys also were given a daily resveratrol supplement for 2 years, 80 milligrams per day for the first year, and then 480 milligrams per day for the second year, they had decreased inflammation due to diminished levels of NF-kappaB, decreased adipocyte size, and improved insulin sensitivity in their visceral adipose tissue.
They also had completely reversed the arterial wall stiffness and inflammation induced by the obesogenic diet. Resveratrol also appears to promote neurological health. It counters neuronal inflammation and improves cognitive performance by mitigating reactive oxygen species, inhibiting pro-inflammatory molecules such as COX-1, and inhibiting beta amyloid plaque formation and aggregation, a hallmark of Alzheimer's disease. In a study of healthy adults aged 50 to 75 years old, 200 milligrams of resveratrol taken daily for 26 weeks improved the participants' ability to complete memory tasks. Resveratrol also showed promise in a phase 2 clinical trial for the treatment of Alzheimer's disease.
The trial involved 56 patients diagnosed with Alzheimer's who were treated with 500 milligrams of resveratrol once daily with a dose escalation by 500 milligram increments every 13 weeks, ending with 1,000 milligrams twice daily. The patients saw improvements in mental examination status scores, improved cerebral spinal fluid amyloid beta levels, and lowered cerebral spinal fluid levels of an enzyme called matrix metalloproteinase-9, a mediator of neuroinflammation. These findings that resveratrol treatment may improve parameters associated with Alzheimer's disease are encouraging, but larger and longer studies are needed to determine whether resveratrol can promote cognitive and functional improvement either more broadly or definitively in the case of Alzheimer's disease.
Let's talk about cancer. Some rodent studies have shown the potential of resveratrol for the treatment of various types of cancer, including pancreatic, prostate, colorectal, liver, and breast cancer. But there simply isn't enough evidence to suggest that resveratrol is a viable option for cancer therapy in humans. The good news is, is that resveratrol might be effective as a chemoprotective agent to prevent cancer. 2 clinical studies in which healthy people received varying doses of resveratrol found that 1 gram or 2.5 grams reduced IGF-1, which is associated with tumor proliferation and metastasis.
Resveratrol treatment also increased carcinogen detoxifying enzymes, such as glutathione S-transferase and others, an effect also elicited by other useful compounds like sulforaphane, which isn't surprising since many plant compounds do act on partially overlapping genetic pathways. So that's just a sampling of the research showing resveratrol's beneficial effects. Let's talk a little bit about the physiological responses to resveratrol and the mechanisms that drive these responses. Probably one of the most well-known mechanisms by which resveratrol works is through sirtuin activation. Sirtuins have been shown to play a role in healthspan and longevity in multiple organisms.
They are linked to the regulation of a whole slew of metabolic processes, including insulin release, lipid mobilization, stress responses, and lifespan modulation. They respond to physiological changes in energy levels and mediate many of the beneficial effects seen with calorie restriction. Caloric restriction has widely been shown to increase healthspan across a wide range of organisms, from bacteria to primates. Resveratrol is thought to be a caloric restriction mimetic. A study in which mice were fed an obesogenic diet and treated with resveratrol found that the animals not only lived longer compared to mice that didn't receive, receive resveratrol, but they experienced physiological changes typically seen with caloric restriction, such as reduced IGF-1 and increased AMP kinase activity.
In a study in which healthy mice were fed a standard chow diet to test resveratrol's ability to mimic caloric restriction, resveratrol supplementation did not increase lifespan in the mice, but did exhibit changes in gene expression that mimicked caloric restriction. The mice also improved overall health as reflected by lower incidence of osteoporosis, cataracts, vascular dysfunction, and declines in motor skills, all signs of aging. As a calorie restriction mimetic, resveratrol promotes the induction of autophagy. Autophagy is an adaptive response mechanism that is activated upon cellular energy stress to remove unnecessary or dysfunctional cellular components, And to mobilize stored energy reserves. Resveratrol promotes autophagy through its activation of sirtuins.
It also induces autophagy independent of sirtuins by inhibiting the activity of mTOR, a key regulator of autophagy. Resveratrol's autophagy-inducing capacity likely has implications for both aging and cancer. More research is needed. One of the most intriguing mechanisms by which resveratrol, a plant compound, elicits its beneficial effects in humans is is via activation of cytoprotective responses that turn on genes that promote resilience against stress, sometimes called stress response genes or longevity genes. Let's talk about this a bit. Humans are able to eat a wide range of plants during both normal development and under conditions of stress. These plants produce a variety of compounds broadly referred to as phytochemicals. Examples include flavonols, anthocyanins, and resveratrol.
In plants, these compounds attract pollinators or serve as antioxidants, or in some cases act as antifeedants, substances that adversely affect or deter insects. In humans, phytochemicals can activate cellular stress response pathways, which confer long-lasting protective effects. This biological phenomenon known as xenohormesis Switches on protective mechanisms that not only protect ourselves from the phytochemicals themselves, but also provide protection against the potential deterioration of our environment, as well as the presence of damaging factors that we are exposed to on a daily basis. Things like air pollution or overexposure to UV radiation.
The scientific community has speculated about why animals, including humans, should respond with a stress response to compounds with otherwise Very low systemic toxicity. One school of thought suggests that humans and animals interpret signals of plant stress, the primary inducer of phytochemical synthesis, as indications that their environment may be demanding enhanced levels of biological fitness as a type of interspecies hormesis or communication. According to this theory, some ancient common ancestors of both animals and plants synthesize polyphenols.
Even though humans and animals lost the ability to produce these chemicals entirely, selective pressure helped us maintain the genetic machinery necessary to not only interpret the signals associated with their synthesis in plants, but also to produce enzymes and receptors with binding pockets that allow the modulation of these molecules and their metabolites. Thus, we kept the advantage of being able to continue to usefully interpret signals of a harsher environment before the degradation of the environment becomes too severe. And more importantly, allowing ourselves to turn on the necessary genetic programs while conditions are still somewhat favorable. This, however, is a hypothesis.
Regardless of whether it's true, the observation still stands that certain plant phytochemicals, such as polyphenols, are able to create a profound cellular response mediated by the interactions with enzymes that seem to be the sort of key-meets-lock interactions that you would expect from biological systems formed under selective pressure, rather than just coincidental interactions. Resveratrol, which is produced in response to stress in some plants like grapes, activates a variety of cellular stress response pathways in humans. Such as the activation of SIRT1, which is linked to anti-inflammatory activity, metabolic adaptations, and neurological protections.
AMP-activated protein kinase, a fuel-sensing enzyme that activates numerous pathways involved in catabolism and inhibits mTOR, leading to the downregulation of cellular growth pathways, and cyclic AMP phosphodiesterase, an intracellular signaling molecule that increases cellular NAD levels. The activation of these cellular stress response pathways may in part mediate some of the beneficial effects also seen with caloric restriction. The effects of resveratrol and exercise training are contradictory, however.
For example, a study involving 27 men between the ages of 60 and 72 years who participated in an 8-week training program with 2 days of cycling and 1 day of CrossFit showed that a low dose of resveratrol 250 milligrams daily, blunted the positive effects of exercise training on blood pressure, blood cholesterol, and maximal oxygen uptake. Another study in which 22-year-old men engaged in 4 weeks of high-intensity interval training 3 days a week and supplemented with 150 milligrams of resveratrol per day did not demonstrate increases in the men's aerobic or anaerobic capacity exercise substrate utilization, or muscle fiber-specific adaptations.
But a study involving 30 men and women between the ages of 65 and 80 years who participated in a 12-week resistance and aerobic training plan 3 days a week and took 500 milligrams of resveratrol daily showed that participants experienced increases in mitochondrial density, muscle fibers, And maximal oxygen consumption compared to exercise training alone. So as you can tell, these are contradictory results. The exercise adaptation blunting effects also contradict some animal research where a high dose of resveratrol actually reduced fatigue, suppressed age-associated decline in performance, improved aerobic performance during endurance exercise, and increased mitochondrial biogenesis and function. So how do we reconcile these facts?
Potential factors may include the type of exercise being investigated, the intensity and dose of resveratrol. All of these things may contribute to these contradictory results. Of particular interest is the dose of resveratrol used. Both of the human studies mentioned a moment ago that showed resveratrol had blunted some of the exercise-induced benefits used a low dose of resveratrol, either 150 milligrams or 250 milligrams per day. Whereas researchers observed positive effects with 500 milligrams of resveratrol per day. At a low dose, resveratrol can be a mild direct antioxidant, but at a higher dose, it acts as an indirect antioxidant. There is a difference between direct and indirect antioxidants. Direct antioxidants can bind to and sequester damaging reactive oxygen species.
Examples include vitamin C and E. High-dose supplemental vitamin C and E have also been shown to blunt some exercise-induced adaptations. That is because the reactive oxygen species that are generated during exercise are important for the exercise-induced cardiorespiratory adaptations. Indirect antioxidants can activate the body's own cytoprotective proteins like the NRF2 pathway, which subsequently activate a wide array of genetic pathways, including endogenous antioxidant systems like glutathione, for example.
The benefits of indirect antioxidants are much more longer lasting and in general seem to not run the same risk as direct antioxidants when it comes to blunting the effects or beneficial adaptations from exercise that seem to actually depend on the short bursts of oxidative stress acting as a signal that we generate from exercise. The bottom line is that more studies, particularly dose-dependent studies, are definitely needed to determine How resveratrol supplementation affects exercise-associated adaptations. Now let's talk about bioavailability. Resveratrol exists in 2 different molecular arrangements, trans and cis. Trans-resveratrol is the most predominant and stable of the 2 forms and elicits the major health benefits.
Trans-resveratrol should be protected from light because it converts to the less active cis-resveratrol form after just a few hours of solar or UV exposure. The majority of resveratrol supplements sold in the US contain the trans form of resveratrol according to their labeling. Resveratrol is only about 25% bioavailable due to rapid metabolism and excretion. Its metabolism varies in a circadian fashion with higher bioavailability occurring in the morning. It is also more bioavailable if taken with food. A study in healthy, healthy human volunteers found that resveratrol bioavailability is increased when taken with a moderate fat breakfast, Versus a very high-fat breakfast.
Resveratrol is insoluble in water, but studies have shown that if it is enclosed in a nanocapsule, a shell that encapsulates the inner core, its stability and bioavailability are increased. Other studies have shown that when resveratrol is given with piperine, a natural compound found in black pepper, its bioavailability and efficacy may be enhanced because piperine inhibits enzymes involved in the metabolism of resveratrol. When mice were given a single dose of resveratrol at 100 milligrams per kilogram of body weight, along with piperine at 10 milligrams per kilogram of body weight, there was an over 14-fold increase in serum concentration of resveratrol compared to mice that received resveratrol alone.
However, a study in which 23 adults took 250 milligrams of trans-resveratrol with 20 milligrams of piperine found that piperine didn't improve bioavailability, but it did improve efficacy in regard to improved cerebral blood flow, which may benefit cognitive function. Dose matters. People often talk about the beneficial effects of red wine due to its resveratrol content. It's important to note that a 5-ounce glass of red wine contains approximately 1.8 milligrams of resveratrol, while therapeutic doses typically range from approximately 100 milligrams to 1 gram. Dr. David Sinclair, one of the world's leading experts on the beneficial effects of resveratrol, recently tweeted, people often ask, how much red wine should I drink to get enough resveratrol?
To get the same as our mice, you'd have to drink a barrel a day, which I definitely don't recommend, however tempting. Human trials of resveratrol supplementation have demonstrated that doses up to 5 grams of resveratrol daily Don't cause toxicity or serious side effects. A repeat dose study for 29 days in healthy volunteers showed that resveratrol supplementation of up to 5 grams was not toxic, but doses above 2.5 grams were associated with mild to moderate GI distress, such as nausea, gas, abdominal discomfort, and diarrhea. Another study in which overweight adults who were 70 years of age or older Took 2 grams of resveratrol for 90 days. Resveratrol was well tolerated.
Despite resveratrol's beneficial effects, resveratrol supplementation should still be considered with at least a little caution. Long-term toxicology studies in humans longer than 1 year have not been performed. Studies have also shown that resveratrol supplementation may interfere with the way in which the body metabolizes other drugs. In particular, Resveratrol inhibits cytochrome P450 enzymes, which are involved with the metabolism of many drugs, such as statins, antiarrhythmic drugs, and antihistamines. This inhibition could reduce the metabolic clearance of these drugs and lead to increased bioavailability and risk of toxicity.
Specifically, in a clinical study where participants were given 1 gram of, of resveratrol per day for 1 month, it changed the activity of several cytochrome P450 enzymes in the liver. For example, resveratrol caused a 33% inhibition of CYP3A4, which is involved in the metabolism of the vast majority of drugs, including cholesterol-lowering statin drugs, chemotherapeutics, immunosuppressive drugs for transplant patients, and HIV protease inhibitors. Inhibition of this enzyme could result in elevation of the systemic blood levels of these drugs metabolized by this isozyme, Which could lead to increased drug toxicity. It also caused a 171% inhibition in CYP2C9, which is the second most abundant CYP in the liver and small intestine.
It is involved in the metabolic clearance of a wide variety of drugs, including many nonsteroidal anti-inflammatory drugs, COX-2 inhibitors, oral anticoagulants, and oral hypoglycemic drugs. Again, this raises the question of whether resveratrol would decrease the clearance of these drugs and lead to toxicity. Maybe it's not a problem, but it is certainly something worth being aware of otherwise. Another study I would like to mention is a pilot randomized placebo-controlled study, which found that men with prostate cancer that were given 1 gram of resveratrol per day for 4 months had lower serum levels of some androgen precursors like DHEA. Which was decreased by 41%, but had no effect on testosterone, dihydrotestosterone, PSA levels, or prostate volume.
DHEA is made from the adrenal gland. And while it is difficult to know the exact mechanism by which resveratrol lowered DHEA, the authors of this study suggest that resveratrol may reduce the concentration of androgen precursors by inhibiting their production in the adrenal gland or by increasing urinary excretion of the androgen precursors or a combination of both. It is also difficult to know if this is clinically relevant, particularly since there was no effect on testosterone levels, but it is one of those things that I still think it is important to mention. A quick wrap-up. Resveratrol elicits a broad range of physiological responses, such as activating anti-inflammatory and antioxidant response pathways and promoting the activation of sirtuins.
These responses have translated to functional health improvements when used to treat people diagnosed with various metabolic diseases, such as type 2 diabetes, but also in neurological disorders such as Alzheimer's disease. The jury is still out with regard to resveratrol's effects on exercise, and questions still remain about the appropriate dose for humans. Given resveratrol's ability to activate cellular protective mechanisms and act as a calorie restriction mimetic, In my opinion, it does seem to have the potential to be used as a preventative supplement. That's it for today's episode. Thank you so much for listening. If you would like to learn more about the topics I discussed today, check out the resveratrol topic page my team and I put together.
You can find that at foundmyfitness.com/topics/resveratrol, or just go to my website and click topics in the menu and get it from there. Remember earlier at the start of this podcast about my commitment to make FoundMyFitness better than ever before? This is one great example. Now available on my website are deep dive overviews we call topic pages. If you have questions about anything you heard in today's podcast, aside from asking me the question directly as a part of my monthly Q&A, if you happen to be a premium member, you can also just look them up on the topic pages. And there's a really good chance your question might be answered right there. The topic pages are a free resource with illustrations, dozens of citations, and more.
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A neurodegenerative disorder characterized by progressive memory loss, spatial disorientation, cognitive dysfunction, and behavioral changes. The pathological hallmarks of Alzheimer's disease include amyloid-beta plaques, tau tangles, and reduced brain glucose uptake. Most cases of Alzheimer's disease do not run in families and are described as "sporadic." The primary risk factor for sporadic Alzheimer's disease is aging, with prevalence roughly doubling every five years after age 65. Roughly one-third of people aged 85 and older have Alzheimer's. The major genetic risk factor for Alzheimer's is a variant in the apolipoprotein E (APOE) gene called APOE4.
An enzyme that plays multiple roles in cellular energy homeostasis. AMP kinase activation stimulates hepatic fatty acid oxidation, ketogenesis, skeletal muscle fatty acid oxidation, and glucose uptake; inhibits cholesterol synthesis, lipogenesis, triglyceride synthesis, adipocyte lipolysis, and lipogenesis; and modulates insulin secretion by pancreatic beta-cells.
A toxic 42 amino acid peptide that aggregates and forms plaques in the brain with age. Amyloid-beta is associated with Alzheimer's disease, a progressive neurodegenerative disease that can occur in middle or old age and is the most common cause of dementia. Heat shock proteins have been shown to inhibit the early aggregation of amyloid beta 42 and reduce amyloid beta plaque toxicity [1].
A molecule that inhibits oxidative damage to DNA, proteins, and lipids in cells. Oxidative damage plays a role in the aging process, cancer, and neurodegeneration. Many vitamins and plant-based compounds are antioxidants.
An intracellular degradation system involved in the disassembly and recycling of unnecessary or dysfunctional cellular components. Autophagy participates in cell death, a process known as autophagic dell death. Prolonged fasting is a robust initiator of autophagy and may help protect against cancer and even aging by reducing the burden of abnormal cells.
The relationship between autophagy and cancer is complex, however. Autophagy may prevent the survival of pre-malignant cells, but can also be hijacked as a malignant adaptation by cancer, providing a useful means to scavenge resources needed for further growth.
The extent and rate at which drugs or other substances, such as plant-based dietary compounds, enter the body’s circulation. Bioavailability is influenced by a variety of factors, including dose, the presence of other foods or substances, and interindividual differences in metabolism due to gut absorptive surface and commensal microbial populations.
The practice of long-term restriction of dietary intake, typically characterized by a 20 to 50 percent reduction in energy intake below habitual levels. Caloric restriction has been shown to extend lifespan and delay the onset of age-related chronic diseases in a variety of species, including rats, mice, fish, flies, worms, and yeast.
Compounds that induce a similar biochemical milieu in the cell as starvation or nutrient deprivation, including the reductions in cytosolic acetyl CoA and increases in protein deacetylation that serve as a trigger for the cellular autophagic machinery. Popular examples of compounds that exhibit this type of effect include: hydroxycitrate (inhibits ATP citrate lyase), spermidine (inhibits Ep300, a protein acetyltransferase), and resveratrol (activates deacetylases called sirtuins).
The body’s 24-hour cycles of biological, hormonal, and behavioral patterns. Circadian rhythms modulate a wide array of physiological processes, including the body’s production of hormones that regulate sleep, hunger, metabolism, and others, ultimately influencing body weight, performance, and susceptibility to disease. As much as 80 percent of gene expression in mammals is under circadian control, including genes in the brain, liver, and muscle.[1] Consequently, circadian rhythmicity may have profound implications for human healthspan.
- ^ Dkhissi-Benyahya, Ouria; Chang, Max; Mure, Ludovic S; Benegiamo, Giorgia; Panda, Satchidananda; Le, Hiep D., et al. (2018). Diurnal Transcriptome Atlas Of A Primate Across Major Neural And Peripheral Tissues Science 359, 6381.
A broad category of small proteins (~5-20 kDa) that are important in cell signaling. Cytokines are short-lived proteins that are released by cells to regulate the function of other cells. Sources of cytokines include macrophages, B lymphocytes, mast cells, endothelial cells, fibroblasts, and various stromal cells. Types of cytokines include chemokines, interferons, interleukins, lymphokines, and tumor necrosis factor.
The single layer of cells that lines the interior of the blood and lymphatic vessels. The endothelium participates in blood flow, platelet aggregation, and vascular tone. It also regulates inflammation, immune function, and angiogenesis. Endothelial dysfunction is a systemic pathological condition broadly defined as an imbalance between vasodilating and vasoconstricting substances produced by (or acting on) the endothelium. It is a robust predictor of heart attack and stroke risk.
Flavonoid are widely distributed in plants, fulfilling many functions. Flavonoids have been shown to have a wide range of biological and pharmacological activities in animal, human, and in-vitro studies. Examples include anti-allergic, anti-inflammatory, antioxidant, antimicrobial, anti-cancer, and anti-diarrheal activities.
An antioxidant compound produced by the body’s cells. Glutathione helps prevent damage from oxidative stress caused by the production of reactive oxygen species.
The years of a person’s life spent free of disease.
A critical element of the body’s immune response. Inflammation occurs when the body is exposed to harmful stimuli, such as pathogens, damaged cells, or irritants. It is a protective response that involves immune cells, cell-signaling proteins, and pro-inflammatory factors. Acute inflammation occurs after minor injuries or infections and is characterized by local redness, swelling, or fever. Chronic inflammation occurs on the cellular level in response to toxins or other stressors and is often “invisible.” It plays a key role in the development of many chronic diseases, including cancer, cardiovascular disease, and diabetes.
A peptide hormone secreted by the beta cells of the pancreatic islets cells. Insulin maintains normal blood glucose levels by facilitating the uptake of glucose into cells; regulating carbohydrate, lipid, and protein metabolism; and promoting cell division and growth. Insulin resistance, a characteristic of type 2 diabetes, is a condition in which normal insulin levels do not produce a biological response, which can lead to high blood glucose levels.
One of the most potent natural activators of the AKT signaling pathway. IGF-1 stimulates cell growth and proliferation, inhibits programmed cell death, mediates the effects of growth hormone, and may contribute to aging and enhancing the growth of cancer after it has been initiated. Similar in molecular structure to insulin, IGF-1 plays a role in growth during childhood and continues later in life to have anabolic, as well as neurotrophic effects. Protein intake increases IGF-1 levels in humans, independent of total caloric consumption.
A pro-inflammatory cytokine that plays an important role as a mediator of fever and the acute-phase response. IL-6 is rapidly induced in the context of infection, autoimmunity, or cancer and is produced by almost all stromal and immune cells. Many central homeostatic processes and immunological processes are influenced by IL-6, including the acute-phase response, glucose metabolism, hematopoiesis, regulation of the neuroendocrine system, hyperthermia, fatigue, and loss of appetite. IL-6 also plays a role as an anti-inflammatory cytokine through inhibition of TNF-alpha and IL-1 and activation of IL-1ra and IL-10.
An enzyme that participates in genetic pathways that sense amino acid concentrations and regulate cell growth, cell proliferation, cell motility, cell survival, protein synthesis, autophagy, and transcription. mTOR integrates other pathways including insulin, growth factors (such as IGF-1), and amino acids. It plays key roles in mammalian metabolism and physiology, with important roles in the function of tissues including liver, muscle, white and brown adipose tissue, and the brain. It is dysregulated in many human diseases, such as diabetes, obesity, depression, and certain cancers. mTOR has two subunits, mTORC1 and mTORC2. Also referred to as “mammalian” target of rapamycin.
Rapamycin, the drug for which this pathway is named (and the anti-aging properties of which are the subject of many studies), was discovered in the 1970s and is used as an immunosuppressant in organ donor recipients.
Tiny organelles inside cells that produce energy in the presence of oxygen. Mitochondria are referred to as the "powerhouses of the cell" because of their role in the production of ATP (adenosine triphosphate). Mitochondria are continuously undergoing a process of self-renewal known as mitophagy in order to repair damage that occurs during their energy-generating activities.
The process by which new mitochondria are made inside cells. Many factors can activate mitochondrial biogenesis including exercise, cold shock, heat shock, fasting, and ketones. Mitochondrial biogenesis is regulated by the transcription factor peroxisome proliferator-activated receptor gamma coactivator 1-alpha, or PGC-1α.
A coenzyme that is required for the production of energy in cells. NAD+ is synthesized from three major precursors: tryptophan, nicotinic acid (vitamin B3), and nicotinamide. It regulates the activity of several key enzymes including those involved in metabolism and repairing DNA damage. NAD+ levels rise during a fasted state. A group of enzymes called sirtuins, which are a type of histone deacetylase, use NAD+ to remove acetyl groups from proteins and are important mediators for the effects of fasting, caloric restriction, and the effects of the plant compound resveratrol, a so-called caloric restriction mimetic.
Fat is deposited in the liver due to causes other than excessive alcohol use such as diet, genetics, and long-term medication use. NAFLD is related to insulin resistance and the metabolic syndrome and may respond to treatments originally developed for other insulin-resistant states.
A protein typically present in the cytoplasm of mammalian cells. Nrf2 can relocate to the nucleus where it regulates the expression of hundreds of antioxidant and stress response proteins that protect against oxidative damage triggered by injury and inflammation. One of the most well-known naturally-occurring inducers of Nrf2 is sulforaphane, a compound derived from cruciferous vegetables such as broccoli.
A class of chemical compounds produced in plants in response to stressors. Polyphenols contribute to the bitterness, astringency, color, flavor, and fragrance of many fruits and vegetables. They often serve as deterrents to insect or herbivore consumption. When consumed in the human diet, polyphenols exert many health benefits and may offer protection against development of cancers, cardiovascular diseases, diabetes, osteoporosis, and neurodegenerative diseases. Dietary sources of polyphenols include grapes, apples, pears, cherries, and berries, which provide as much as 200 to 300 mg polyphenols per 100 grams fresh weight.
Oxygen-containing chemically-reactive molecules generated by oxidative phosphorylation and immune activation. ROS can damage cellular components, including lipids, proteins, mitochondria, and DNA. Examples of ROS include: peroxides, superoxide, hydroxyl radical, and singlet oxygen.
A related byproduct, reactive nitrogen species, is also produced naturally by the immune system. Examples of RNS include nitric oxide, peroxynitrite, and nitrogen dioxide.
The two species are often collectively referred to as ROS/RNS. Preventing and efficiently repairing damage from ROS (oxidative stress) and RNS (nitrosative stress) are among the key challenges our cells face in their fight against diseases of aging, including cancer.
A polyphenolic compound produced in plants in response to injury or pathogenic attack from bacteria or fungi. Resveratrol exerts a diverse array of biological effects, including antitumor, antioxidant, antiviral, and hormonal activities. It activates sirtuin 1 (SIRT1), an enzyme that deacetylates proteins and contributes to cellular regulation (including autophagy). Dietary sources of resveratrol include grapes, blueberries, raspberries, and mulberries.
Resveratrol Autophagy ↑ Deacetylases (especially SIRT1) → ↓ Protein Acetylation → Autophagy
Environmental factors which may reduce reproductive success in a population and thus contribute to evolutionary change or extinction through the process of natural selection.
A member of the sirtuin protein family. SIRT1 is an enzyme that deacetylates proteins that contribute to cellular regulation (reaction to stressors, longevity). It is activated by the phytochemical resveratrol as well as fasting.
A class of enzymes that influence that influence aging and longevity through multiple molecular pathways. Sirtuins regulate a variety of metabolic processes, including release of insulin, mobilization of lipids, response to stress, and modulation of lifespan. They also influence circadian clocks and mitochondrial biogenesis. Sirtuins are activated when NAD+ levels rise. The dependence of sirtuins on NAD+ links their enzymatic activity directly to the energy status of the cell via the cellular NAD+:NADH ratio, the absolute levels of NAD+, NADH or nicotinamide or a combination of these variables. There are seven known sirtuins, designated as Sirt1 to Sirt7.
A class of drugs that lower blood cholesterol levels by blocking the production of an enzyme in the liver called hydroxy-methylglutaryl-coenzyme A reductase (HMG-CoA reductase). Taking statins may reduce the risk of cardiovascular disease in some people. Although statins are generally well tolerated, as many as 10 – 20 percent of people taking the drugs experience complications, including myopathy (muscle damage), liver damage, and cognitive problems, including issues with forgetfulness, memory loss, and confusion.
An isothiocyanate compound derived from cruciferous vegetables such as broccoli, cauliflower, and mustard. Sulforaphane is produced when the plant is damaged when attacked by insects or eaten by humans. It activates cytoprotective mechanisms within cells in a hormetic-type response. Sulforaphane has demonstrated beneficial effects against several chronic health conditions, including autism, cancer, cardiovascular disease, diabetes, and others.
The primary male sex hormone. Testosterone is critical to the maintenance of fertility and secondary sexual characteristics in males. Low testosterone levels may increase risk of developing Alzheimer’s disease.
A molecule composed of a glycerol molecule bound to three fatty acids. Triglycerides are the primary component of very-low-density lipoproteins (VLDL). They serve as a source of energy. Triglycerides are metabolized in the intestine, absorbed by intestinal cells, and combined with cholesterol and proteins to form chylomicrons, which are transported in lymph to the bloodstream.
A proinflammatory cytokine. TNF-alpha is produced by a wide range of cells, including macrophages, lymphocytes, glial cells, and others. TNF-alpha signaling inhibits tumorigenesis, prevents viral replication, and induces fever and apoptosis. Dysregulation of the TNF-alpha signaling pathway has been implicated in a variety of disorders including cancer, autoimmune diseases, Alzheimer’s disease, and depression.
A metabolic disorder characterized by high blood sugar and insulin resistance. Type 2 diabetes is a progressive condition and is typically associated with overweight and low physical activity. Common symptoms include increased thirst, frequent urination, unexplained weight loss, increased hunger, fatigue, and impaired healing. Long-term complications from poorly controlled type 2 diabetes include heart disease, stroke, diabetic retinopathy (and subsequent blindness), kidney failure, and diminished peripheral blood flow which may lead to amputations.
An excess of visceral fat, also known as central obesity or abdominal obesity. Visceral fat, in contrast to subcutaneous fat, plays a special role involved in the interrelationship between obesity and systemic inflammation through its secretion of adipokines, which are cytokines (including inflammatory cytokines) that are secreted by adipose tissue. The accumulation of visceral fat is linked to type 2 diabetes, insulin resistance, inflammatory diseases, certain types of cancer, cardiovascular disease, and other obesity-related diseases.[1]
- ^ Fontana, Luigi; Eagon, J. Christopher; Trujillo, Maria E.; Scherer, Philipp E.; Klein, Samuel (2007). Visceral Fat Adipokine Secretion Is Associated With Systemic Inflammation In Obese Humans Diabetes 56, 4.
A potent water-soluble antioxidant found in citrus fruits. Vitamin C is an essential nutrient involved in tissue repair, neurotransmission, and immune system function. Also known as ascorbic acid.
A fat-soluble vitamin. Vitamin E is the collective name for a group of eight fat-soluble compounds (alpha-, beta-, gamma-, & delta-tocopherol and alpha-, beta-, gamma-, & delta-tocotrienol) with distinctive antioxidant activities. Of these eight, only alpha- (α-) tocopherol meets human requirements. Vitamin E serves as an antioxidant that breaks the chain reaction formation of reactive free radicals. In doing so it becomes oxidized and loses its antioxidant capacity. Vitamin E also protects LDL from oxidation and maintains the integrity of cell membranes throughout the body. Dietary sources of vitamin E include nuts, seeds, eggs, and fatty fish, such as salmon.
An adaptive physiological response in which bioactive compounds, produced by environmentally stressed plants, induce beneficial stress response pathways in animals, including humans. Xenohormetic responses ultimately confer stress resistance and longevity and may explain some of the beneficial effects of plant-based foods. The term xenohormesis stems from two terms: xeno (stranger) and hormesis (a protective physiological response induced by mild stressors). Polyphenols, isothiocyanates, and other plant compounds are thought to exhibit some of their beneficial properties by inducing a type of xenohormesis.
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Resveratrol News
- Green tea catechins, resveratrol, curcumin and metformin reduced amyloid plaque formation in herpes-induced Alzheimer's disease tissue models. (2022)
- Chronic estradiol exposure led to hypertension in rats by promoting excessive superoxide levels in a blood pressure regulating brain area. (2011)
- Reservatrol strengthens tight-junction proteins in the blood-brain barrier and protects against oxidized LDL
- Resveratrol reinforces the blood-brain barrier and reverses dysfunction due to diabetes
- Resveratrol and exercise improve quality of life for older adults.