This episode will make a great companion for a long drive.
A blueprint for choosing the right fish oil supplement — filled with specific recommendations, guidelines for interpreting testing data, and dosage protocols.
Low energy levels, such as those that would occur during exercising, fasting, or caloric restriction, stress the cell. In turn, cellular levels of nicotinamide adenine dinucleotide, or NAD+, a coenzyme that participates in the production of cellular energy, rise, switching on energy-generating pathways and activating enzymes such as sirtuins. Levels of NAD+ vary according to nutrient intake, activity, and even time of day. In fact, the body's circadian rhythms are subject to NAD+ levels, which drive the body's master "clock." Altered NAD+ levels may be the root cause of jet lag and the overall loss of energy we experience as we age. Modulating NAD+ levels and the pathways in which it plays a role may be the key to extending healthspan and lifespan. In this clip, Dr. David Sinclair describes the role of NAD+ in the regulation of the body's circadian clock and sirtuin production.
Rhonda: Something that comes to mind when you... So you're talking about, really, this important role that calorie restriction or intermittent fasting plays in activating this sirtuin pathway and also deactivating things like the insulin signaling pathway and IGF-1 pathway, it is the fact that the sirtuins are regulated by something called NAD, nicotinamide adenine dinucleotide plus. But that is something that actually, those levels rise during a fasted state.
David: They sure do... Right. And in response to exercise as well. And so the reason NAD is so exciting compared to the 1980s when we thought it was just a housekeeping molecule for reactions, is that the levels of NAD go up and down depending on not just what you eat, but whether you're exercising and even what time of day it is. So, during the day, your NAD levels will rise and then you eat a big meal and they'll go down again. And it's... We think it's one of the reasons you also get jet lag, is your NAD cycles are out of whack.
Rhonda: Is it on a circadian rhythm? Is it completely regulated by meal intake?
David: It's a combination. It will be going up and down with circadian rhythms, mostly, but you can adjust it within the...
Rhonda: What about macronutrient composition? Like if you eat more high fat versus carbohydrate?
David: Yeah, no one knows. That would be a good experiment. The circadian field hasn't looked at nutrition as far as I'm aware. But what I can tell you anecdotally is that if I raise my NAD levels when I'm traveling, I feel a lot better if I have a shot of an NAD booster in the morning when I get to Australia, which I travel to pretty often. And so I don't know if it's truly working, we need more than one person in a clinical trial. But it fits with the mouse studies, which is that you can use NAD to reset your clock. What's interesting about this is that NAD isn't being driven by the clock, the clock is being driven by NAD.
Rhonda: Okay. Yeah. So for people that are viewing or listening, the clock, meaning what's regulating circadian rhythm?
David: Yeah. How your organs coordinate what time of day it is. And when you're jetlagged, your brain might realize that it's morning because your eyesight, you know, sees sunlight, but your liver still thinks it's the middle of the night, so you feel queasy. And that's the feeling.
Rhonda: And the reason why NAD is... I mean, NAD is really important for a variety of metabolic... I mean, it's required for metabolism, for metabolizing glucose, metabolizing fatty acids, your mitochondria need it. But it's also important for a variety of other tissues as well, activating sirtuins and then DNA repair enzyme, PARP.
David: Yeah. Right. You could argue that NAD is the most important molecule in the body, maybe with the exception of ATP, but without either of them, you're dead in about 30 seconds. So NAD and ATP were probably the first two molecules that life on this planet used to survive. And it's, to me... And amino acids as well. And so isn't it interesting that the amino acid levels, ATP, and NAD are the three main molecules in our bodies that are sensed as to what our environment is like and whether we need to hunker down and survive or go forth and multiply? And those are the three main pathways. There's the sirtuins, there's AMP kinase, which is the metformin pathway. And then there's mTOR, which is rapamycin, which I'm sure you and many of your listeners are aware. But we're tapping into very early aspects of life that's found all over the planet and that's why I think we're having such big effects in the animals. Often, people say it's too good to be true. You know, you tweak one pathway and all this good stuff happens. Well, these are pathways that have existed for going back probably more than 3 billion years. And we're only just learning how easy and seemingly safe it is to tweak them.
An energy-carrying molecule present in all cells. ATP fuels cellular processes, including biosynthetic reactions, motility, and cell division by transferring one or more of its phosphate groups to another molecule (a process called phosphorylation).
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.
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.
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.
Any of a group of complex proteins or conjugated proteins that are produced by living cells and act as catalyst in specific biochemical reactions.
A molecule composed of carboxylic acid with a long hydrocarbon chain that is either saturated or unsaturated. Fatty acids are important components of cell membranes and are key sources of fuel because they yield large quantities of ATP when metabolized. Most cells can use either glucose or fatty acids for this purpose.
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.
A broad term that describes periods of voluntary abstention from food and (non-water) drinks, lasting several hours to days. Depending on the length of the fasting period and a variety of other factors, intermittent fasting may promote certain beneficial metabolic processes, such as the increased production of ketones due to the use of stored fat as an energy source. The phrase “intermittent fasting” may refer to any of the following:
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.
The thousands of biochemical processes that run all of the various cellular processes that produce energy. Since energy generation is so fundamental to all other processes, in some cases the word metabolism may refer more broadly to the sum of all chemical reactions in the cell.
A drug commonly used for the treatment of type 2 diabetes. Metformin is in a class of antihyperglycemic drugs called biguanides. It works by decreasing gluconeogenesis in the liver, reducing the amount of sugar absorbed in the gut, and increasing insulin sensitivity. A growing body of evidence indicates that metformin modulates the aging processes to improve healthspan and extend lifespan. Furthermore, metformin may prevent genomic instability by scavenging reactive oxygen species, increasing the activities of antioxidant enzymes, inhibiting macrophage recruitment and inflammatory responses, and stimulating DNA damage responses and DNA repair.[1]
[1] Najafi, Masoud, et al. "Metformin: Prevention of genomic instability and cancer: A review." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 827 (2018): 1-8.
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.
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.
One of four nitrogen-containing molecules that comprise DNA. A nucleotide consists of one of four chemicals, called a “base,” plus one molecule of sugar and one molecule of phosphoric acid. Nucleotides are typically identified by the first letter of their base names: adenine (A), cytosine (C), guanine (G), and thymine (T). They form specific pairs (A with T, and G with C), and their bonds provide the helical structure of the DNA strand.
A family of proteins involved in a number of cellular processes such as DNA repair, genomic stability, and programmed cell death (apoptosis). PARP's primary role is to detect and initiate an immediate cellular response to metabolic, chemical, or radiation-induced single-strand DNA breaks by signaling the enzymatic machinery involved in repair. NAD+ is required as substrate for generating ADP-ribose monomers. Evidence suggests that overactivation of PARP may deplete cellular stores of NAD+.
A compound initially developed as an antifungal agent. This use was abandoned, however, when it was discovered to have potent immunosuppressive and antiproliferative properties due to its ability to inhibit one of the complexes of mTOR (mTORC1). Rapamycin has since shown interesting lifespan extension properties in animals.
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.
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