This episode I discuss how hormones from our gut, liver, pancreas and
brain control our appetite-- and the specific tools we can use to
adjust those hormones in order to achieve specific goals. I explain
the brain areas that control our desire to eat, and our desire to stop
eating. I discuss a hormone we all can make that is regulated by UV-
rays from sunlight that reduces our appetite. I also explain that when
we eat controls our appetite and not the other way around (and how to
leverage that fact). I describe how we are basically always eating
until we reach a threshold level of fatty acids and amino acids in our
gut and the factors that can alter that signaling and make us eat far
more than we need. I also explain how insulin, glucose and glucagon
work, why cholesterol is so key for ovary, adrenal, liver and testes
function and how the ketogenic diet impacts glucose and thyroid
levels. As always, I describe many tools: specific supplements,
prescription compounds, specific types (and timing) of exercise to
regulate hormones, specific timing and types of eating, ways to reduce
sugar cravings by triggering the release of the hormone CCK, and more.
- Introduction
- Hunger: Neural & Hormonal Control
- Chewing & Hunger
- Siamese Rats Reveal the Importance of Hormones In Hunger
- Neurons That Powerfully Control Hunger by Releasing Specific Hormones
- Anorexia & Extreme Overeating
- Why Sunlight Suppresses Hunger: a-Melanocyte Stimulating Hormone (a -MSH)
- Blue-blockers, Injecting a-MSH: Instant Tan & Priapism
- Ghrelin: A Hormone That Determines When You Get Hungry, & That You Can Control
- Meal Timing Determines Hunger, Not the Other Way Around
- Satchin Panda, Circadian Eating & Intermittent(ish) Fasting
- How To Rationally Adjust Meal Schedules: The 45min Per Day Rule
- CCK (Cholecystokinin): A Hormone In Your Gut That Says “No Mas!”
- Eating For Amino Acids, Fatty Acids & Sugar
- L-Glutamine: Stimulates the Immune System & Reduces Sugar Cravings
- Things To Avoid: Emulsifiers; Alter Gut Mucosa & Nutrient Sensing
- “A Calorie Is NOT A Calorie” After All
- Insulin & Glucose: Hyperglycemia, Euglycemia, & Hypogylcemia
- The Order Your Eat Foods Matters: Managing Your Blood Glucose & Glucagon
- Movement, Exercise & GLUT-4
- Why Sugar Stimulates Your Appetite
- Keeping Blood Sugar Stable With Specific Exercises, The Power Of Insulin Sensitivity
- High-Intensity Exercise, Glycogen & Metabolism
- Cholesterol, HDL, LDL & Glucose Management: Ovaries, Testes, Liver, Adrenals
- Prescription Compounds That Reduce Blood Glucose: Metformin
- Berberine: A Potent Glucose Buffer That Also Adjusts Cholesterol Levels, Canker Sores
- Chromium, L-Carnitine, Ginseng, Caffeine, Magnesium, Stevia, Vitamin B3, & Zinc
- Acids: Vinegar, Lemons & Limes & False Alkalinity
- Ketogenic Diets (In Brief): Effects On Blood Glucose, Thyroid Hormones
- Diabetes, Filtering Blood, Sweet Urine
- The Power of GLP-1 & Yerba Mate For Controlling Appetite, Electrolytes
- Summary & Notes About Thyroid, Estrogen, Testosterone
- Zero Cost & Sponsor-Based Ways To Support The Huberman Lab Podcast
- HubermanLab #Hunger #Hormones
-- Welcome to the Huberman Lab Podcast, where we discuss science and
science-based tools for everyday life. [gentle music] I'm Andrew
Huberman, and I'm a professor of Neurobiology and Ophthalmology at
Stanford School of Medicine. This podcast is separate from my teaching
and research roles at Stanford. It is however, part of my desire and
effort to bring zero cost to consumer information about science and
science-related tools to the general public. In keeping with that
theme, I'd like to thank the sponsors of today's podcast. Our first
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understand your body and help you reach your health goals. I've long
been a fan of getting blood work done. And the simple reason for that,
is that most of the things that you want to know about your health,
such as hormones, metabolic factors, blood sugar levels, et cetera,
can only be analyzed from blood. And nowadays there are also excellent
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Athletic Greens, the vitamin D3K2, and that's a year supply plus the
five free travel packs. Today's episode is also brought to us by Munk
Pack. Munk Pack is a company that makes keto-friendly snacks that
taste incredible but have just one gram of sugar or less. And indeed
they taste incredible. In fact, my production team here at the
Huberman Lab Podcast teases me because I actually have to keep the
boxes of Munk Pack bars in my basement 'cause otherwise I'll tear
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Which is why I keep them in my basement. As I mentioned previously on
this podcast, I'm neither keto nor carbo. I don't really follow a
particular diet in that sense. I eat in a way that maximizes my
alertness and my levels of focus during the day when I want to work,
and that maximize my transition to sleep at night. So, I basically eat
low carb keto-ish during the day. And I know the ketonistas will say
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main idea, is I keep my carbohydrates low during the day. And then at
night I do eat carbohydrates. So for me, the Munk Pack bars are a
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purchase. This month, we're talking all about hormones. Hormones are
incredible and they control so many processes in the brain and body.
Last episode, we talked about the role of estrogen and testosterone.
Today we're going to talk about how hormones impact feeding and
hunger, as well as satiety, the feeling that you don't want to eat or
that you've eaten enough. Now, it's important to understand that
hormones don't work alone in this context. Today I'm going to describe
some hormones that have powerful effects on whether or not you want to
eat more or less or stop eating altogether. But they don't do that on
their own, they do that in cooperation with the nervous system. So
today, I would say as much or perhaps even more than any other
episodes, we're going to hear a lot of biology but there are multiple
what I'm going to call entry points for tools that you can apply in
order to regulate your levels of hunger, your meal timing, your levels
of satiety of not wanting to eat more. And many of this is actionable
with behaviors, but of course, we're also going to talk about
supplements and we're actually going to talk about a little bit of
brain machine interface devices that can actually be involved in
manipulating these incredible things that we think of as hunger and
appetite and satiety. So, the first thing that you need to know about
the nervous system side, the neural control, over-feeding and hunger,
is that there's an area of your brain called the hypothalamus.
It's in the forebrain, which tells you it's in the front of your
brain, and it's at the base of the forebrain. Now, the hypothalamus
contains lots of different kinds of neurons doing lots of different
kinds of things. There are neurons in your hypothalamus controlling
sexual behavior, controlling body temperature, controlling circadian
rhythms, the desire to sleep or be awake. Even neurons controlling
rage. There are actually neurons that if we were to stimulate them
would send you or anyone into a rage. They're just powerful control
centers for the brain and body. There's a particular area of the
hypothalamus called the ventromedial hypothalamus. And it's one that
researchers have been interested for a long time now, in terms of its
relationship to hunger and feeding. And the reason is, it creates
these paradoxical effects. What do I mean by that? What they found was
that sometimes lesioning, or disrupting the neurons in the
ventromedial hypothalamus would make animals or people hyperphasia,
they would want to eat crazy. And other lesions in other individuals
or animals would make them anorexic, it would make them not want to
eat at all. It would make food aversive. So that means that the
ventromedial hypothalamus is definitely an interesting control station
for hunger and feeding and satiety, but it doesn't really tell you
what's going on at a deeper level. In fact, it's a little bit
confusing or paradoxical. It turns out that there are multiple
populations of neurons in there, we're going to talk about those. Some
are promoting feeding, and some are promoting not feeding or not
eating.
Now, the other neural component of all this that you need to know
about, actually has to do with your mouth. So there's an area of your
cortex, so that's a little bit further up in your brain, called the
insular cortex. And it processes a lot of different kinds of
information. Mostly information about what's going on inside you, so
called the interoception. The insular cortex has neurons that get
input from your mouth, from the touch receptors in your mouth. And
insular cortex has powerful control over whether or not you're
enjoying what you're eating, whether or not you want to avoid what
you're eating, whether or not you had enough, or whether or not you
want to continue eating more. And that has to do, believe it or not,
with the touch or sensation of eating. I'm very familiar with this.
I'm one of these people, I love eating so much, that I just like the
mere act of chewing. You know, I like celery sticks enough. I'm not
crazy about them, but you know they taste fine to me and I like
chewing on celery sticks, but I actually just like chewing on them. I
could eat all day long except that it's not healthy to do that. But
the mere act of chewing for me is very pleasurable. People who chew
gum feel this way as well. And just as a point about gum or chewing,
if you choose something like celery or cucumber slices or chew gum,
provided it doesn't have any sugar or caloric content, it's not going
to drive increased hunger. That generally isn't the case. But if you
eat something with sugar, as we'll find out, it has a very specific
action in the insular cortex and in other areas of your nervous system
that promotes the desire to eat more. But the key point right now is
to know you've got these two brain areas, the ventromedial
hypothalamus, that's involved in hunger and lack of hunger, sort of an
accelerator and a brake on feeding. And you have this insular cortex
that gets input from your mouth, and cares about chewing and the
consistency of foods and all sorts of interesting things that are just
very tactile. And I think most people think about the touch receptors
on, excuse me, the taste receptors on the tongue. But we often don't
think about the touch or tactile essence of food. And the thing that
comes to mind just now is I've gone to sushi several times, and some
people really like the urchin. I don't like the urchin. There's
something about it that kind of creeps me out about the consistency,
other people love it. So it's highly individual and it's probably
learned, and there's some probably cultural background to this if you
were raised eating urchin. Some people love that consistency or that
touch. So touch has a lot to do with whether or not you want to eat or
not. Now, let's get back to the ventromedial hypothalamus. Sometimes
it makes animals or people want to eat more, sometimes less, so what's
going on there? There's a classic experiment that was done in which
researchers took two rats, and so-called parabiosed them to each
other.
What that meant is that they did a little surgery and they linked
their blood supply so that they were forever physically linked to one
another and could exchange factors in the blood, but their brains were
separate, their mouths were separate, and they essentially did
everything separately except that they were linked to one another. So
they had to walk together and go to the same places in order to do it.
This parabiosis experiment revealed something really important. When
they lesioned the ventromedial hypothalamus in one of the rats that
was connected to the other rat, that rat got very, very fat, just
really obese, huge rat, super rat, jumbo rat. The other one however,
got very thin, it actually lost weight, despite consuming the same
amount of food that it had prior to the other one getting the lesion.
So what does this tell us? This tells us that there's something in the
blood that's being exchanged between the two animals, because it was
their blood supply that was linked. And that tells us that there's
hormone or endocrine signals that are involved in the desire to eat,
and hunger and appetite. And so next, we're going to talk about what
those endocrine signals are, and then I'm going to immediately point
to some entry points that you can use. And you can use these even if
you're not parabiosed to anything. And that can allow you to time your
meal frequency, and predict when you're going to be hungry or not. As
well as a drive up appetite. Believe it or not, there are people out
there who are trying to eat more. Although I think far many more
people are trying to eat less because nowadays, the data just point to
the fact that there is essentially an epidemic of diabetes, type II
diabetes and obesity. And most everyone agrees now, that maintaining a
healthy body weight and body weight composition, is one of the best
paths to longevity and to just feeling very good and actually being
able to think. Cognitive functioning is actually linked to levels of
adipose tissue and so forth. So, let's talk about the endocrine
factors that regulate feeding, hunger and satiety. One of the really
exciting things to emerge in the science of feeding and appetite in
the last 20 years, is the discovery of another brain area.
And not just the ventromedial hypothalamus, but it's an area of the
brain called the arcuate nucleus. And the arcuate nucleus has some
really fascinating sets of neurons that release even more incredible
molecules and chemicals into the blood. And these chemicals act as
accelerators on feeding and appetite, or breaks. And the really cool
thing is that you can actually control these molecules through simple
behaviors. And once you understand what these molecules are, you'll
start to understand why that's the case. And the control points that
you have right now in order to control your appetite in either
direction, increase or decrease. So, first of all, there are set of
neurons in this arcuate nucleus called the PMOC neurons, okay? I don't
want to get into what the acronym stands for, but I'll do it anyway.
It's the Proopiomelanocortin system, okay? So these are PMOC neurons,
Proopiomelanocortin. And if you heard melano, that should tell you it
has something to do with pigmentation in skin cells or in hair cells,
pigmentation of some sort, because of melanin. Last episode, I talked
a little bit about the relationship between light dopamine and
melanin. So you should already be thinking, wait, melano means it
probably has something to do with that system, and indeed it does.
Now, the POMC neurons, make something called Alpha MSH. Melanocyte-
stimulating hormone, Alpha-Melanocyte-stimulating hormone. If you
don't want to remember any of the other acronyms and terms I've talked
about, this episode so far, do try and remember M-S-H, okay? Mouse,
Sam, Hamster, M-S-H, okay? MSH reduces appetite and it's a powerful
molecule, all right? So just put that on the shelf, MSH reduces
appetite. Now, there's another population of neurons in the arcuate
nucleus, called the AgRP neurons. And there I'm truly not going to
read you what that stands for 'cause it's related to the mouse strain
it was first identified in, but humans have these cells as well, but
AgRP neurons. The AgRP neurons stimulate eating. And anytime you are
approaching food, or you feel some excitement about food or anxiety,
because some people actually experience a kind of heightened anxiety.
Some people actually get a little bit of a resting tremor before they
eat, even if they don't have any sort of eating disorder. There's kind
of a ramping up of autonomic activity. That's largely due to the
activity of these AgRP neurons. So, the activity in these AgRP neurons
goes way up when animals or people are starved. And I don't mean
starved for long periods of time, but I mean when they haven't eaten
for a while. And the activity of MSH, the release of MSH goes up when
we've eaten. However, there are other things that will stimulate the
release of things like MSH. So, just briefly the experimental
evidence, if you kill AgRP neurons, animals and people stop eating.
There are people of lesions. They just stop eating, they become
anorexic. I know you're familiar with anorexia as a clinical term, but
that's actually a term that's used in the scientific literature about
a pattern of behavior, okay?
As well as a clinical term of course. If you were to stimulate the
AgRP neurons, animals or people eat like crazy. They will eat to the
point where they burst. Which just sounds horrible, but it just tells
you this is the accelerator on eating. And yes, it has relationship to
the ventromedial hypothalamus I talked about earlier, but I don't want
to go back there just yet, we will circle back. So Melanocyte-
stimulating hormone, such an interesting hormone.
This thing can shut down the desire to eat. The Melanocyte-stimulating
hormone, is released from the medial pituitary. We talked about the
pituitary last time. This is a gland that is very closely positioned
to the hypothalamus. Actually some of the hypothalamus neurons
actually project their neural connections directly into the pituitary,
to release things like gonadotropins and luteinizing hormones, stuff
we talked about last time in reference to testosterone and estrogen.
But MSH is released from the medial portion of the pituitary and it
stimulates the desire to not eat, to cease eating. What's really
interesting, is that Melanocyte-stimulating hormone is activated by
ultraviolet light. And it's not activated by ultraviolet light to the
skin or directly to pituitary, it's activated by ultraviolet light to
the eyes. Now, if you've been watching this podcast or listening to
this podcast for any period of time, or you've heard me on other
podcasts or you follow my Instagram, I am a big fan of this whole
thing of getting morning light in order to synchronize circadian
rhythms, et cetera, avoiding light in the middle of the night. This is
yet another reason why getting ample light, ideally sunlight, but it
could be other sources of UV light to the eyes, stimulates MSH, this
has been shown over and over again. And keeps the desire to eat or
appetite in check, in healthy ranges. This is also why in the spring
and summer months, animals and people eat less. Now, for hibernating
animals it's different, because they bear hibernate, actually. Ashley
bears don't truly hibernate technically, by a scientific criteria they
don't hibernate, but they go into a kind of torpor. The hibernating
animals they don't eat much because they're in boroughs or dens, or
they're just wrapped up in a little ball or whatever it is that
hibernating animals do. So they're of course going to eat far less in
the winter. But that's a unique scenario, we are not hibernating
animals. But humans generally have greater appetite in the cold winter
months. And it's not just because of the holidays and the abundance of
food that we're presenting ourselves with, but when we get a lot of
sun our appetite is reduced or at least it's easier to control. And
that is due in part, because if you're getting ample sunlight to the
eyes, it's converted into a signal for the MSH neurons, the neurons
that release MSH, excuse me these PMOC neurons release MSH. And then
MSH can bind its receptors, and can keep the break on appetite in
check. So the takeaway tool from this, is make sure you're getting
enough light not just in the morning, but throughout the day. And yes,
it has to be light to your eyes. And blasting your eyes with sunlight
or artificial light to the point where it's damaging or painful, won't
accelerate or improve this process. It's about getting photons,
ultraviolet light to the eyes consistently throughout the day. That's
best accomplished by not wearing sunglasses provided you can do that
safely. And if you don't have access to enough sunlight, then you can
do this with artificial light.
This also points again to our old friends, the blue blockers. Many
people know I'm not a huge fan of blue blockers especially not during
the daytime, because they block a lot of the UV and shorter wavelength
light that you want and need to create alertness, but also to create
release of MSH from the medial pituitary. Now there are people out
there, subcultures, that actually inject MSH. That are taking MSH or
things similar to it. I am not suggesting people do that. But there
are three main consequences of doing that. First of all, it reduces
appetite, no surprise there. And they're actually using it as a
dieting drug. This is kind of in the underground. I don't know what
the legal status is. And again, I'm not promoting that people do it.
Two, it makes them very, very tan, which makes sense, right?
Melanocyte-stimulating hormone. And the third is, it purportedly,
never tried it, purportedly sends libido through the roof, to the
point where it's actually distracting for other activities. It
actually can create priapism, which is a kind of chronic erection in
males to the point where it actually can be physically damaging to the
genitalia. So this is a drug, I don't know whether or not it's call it
a drug. It's a substance that one can regulate with healthy levels,
with sunlight and perhaps artificial UV light. I have not heard much
about treatments for obesity involving getting ample sunlight or
getting ample UV light, but to me, the logic is just very clear. And
so if you're pursuing those avenues, you certainly should talk to your
physician but you might want to think about how some of those logic
hangs together. Absolutely fascinating hormone, I think most people
aren't aware of it. And the subcultures that are aware of it are using
it for two very particular end points, and they're using it at super
physiological levels. That's enough about that 'cause I really don't
know. I've talked to a few people in research. Believe it or not for
this podcast, I reached out to a few people and asked whether or not
the these are side effects in air quotes. I've heard about are true,
and indeed they're true. But again, that's super physiological,
controlling MSH, it's actually Alpha MSH levels through viewing
ultraviolet light seems like an interesting and mechanistically
logical thing to do, if your goal is to keep appetite in check. So MSH
inhibits hunger.
Next, let's talk about a hormone peptide that activates hunger. And
this is a really interesting one because it relates to when you get
hungry, in addition to the fact that you get hungry at all. And it's
called ghrelin, it's spelled G-H-R-E-L-I-N. Ghrelin is released
actually from the GI tract. And its main role is to increase your
desire to eat. And it does that through a variety of mechanisms. Part
of that is to stimulate some of the brain areas, the actual neurons,
that make you want to eat. In addition, it creates food anticipatory
signals within your nervous systems. So you start thinking about the
things that you happen to like to eat at that particular time of day.
And this is fascinating. Ghrelin is sort of like a clock, a hormonal
clock that makes you want to eat at particular times. Now, the signal
for ghrelin is reduced glucose levels in the blood. We're going to
talk a lot today about glucose and insulin, ways to manage glucose and
insulin. But for now the simple version of this, is you normally want
your glucose to be in a kind of modest range, and I'll explain what
range is in a little bit. But if it drops too low, ghrelin is secreted
from your gut. It activates neurons in your brain at various locations
including the PMOC neurons, and the other neurons of the wingin' it.
It also activates the VMH in particular ways. And it might even
activate some of these neurons that are in the periphery in your mouth
that actually make you salivate and want to eat, right? Now, we all
know about the famous Pavlovian, experiments of Pavlov's dogs. You
know, they start salivating to the bell. After the bell was presented
with food, you remove the food, and then just the bell can stimulate
the salivation. We become Pavlovian at times. But rarely is it ever
discussed what the neural pathways for that are. And it turns out that
these hormones that are secreted from the gut can stimulate the
neurons to create a sensation and a desire for certain foods at
certain times of day. You've done this experiment.
If you are somebody who eats breakfast at more or less the same time
each day, let's say 8:00 AM plus or minus 20 minutes. And then you eat
lunch 12:30 plus or minus 20 minutes. Or let's say you're somebody
like me who typically skips breakfast, and just eats lunch usually
around 11:30 or 12 or something like that. Your ghrelin secretion will
start to match when you typically eat. And it does that. And it's able
to override the low levels of glucose in your bloodstream, because the
ghrelin system also gets input from a clock in your liver that is
linked to the clock in your hypothalamus, in your brain. And what this
means is, if you eat at regular meal times, you'll start to get hungry
a few minutes before those meals times. If you've ever wondered why
your stomach kind of starts to growl because it's a particular time of
day, and you're like, Oh I must want to eat, well, that's ghrelin. And
for those of you that don't know why your stomach growls, I'll also
tell you that today. It's actually really interesting. It not at all
what you expect, and it's not just the gurgling of liquids in your
stomach. That's not what it is. It's actually a muscular phenomenon.
So, ghrelin is secreted as a food anticipatory signal, to get you
motivated to go eat at regular times. So, nowadays there's a lot of
interest in intermittent fasting. There's also a lot of interest in
just what meal plans and schedules and what to eat in general, in
order to maximize one's health and wellbeing. And people have all
sorts of cosmetic reasons and brain reasons and metabolic reasons for
wanting to control this kind of stuff. So let's make it really simple
by first looking at the extremes. Some people need to eat every two or
three hours. They feel this, "I need to eat every two or three hours,"
or else their blood sugar drops. In general, blood sugar doesn't drop
so low, that they truly need to eat in order to alleviate a blood
sugar issue. Although sometimes that can happen. Some people are truly
hypoglycemic, low blood sugar. But most people as the blood sugar
starts to head down towards the low-ish ranges, ghrelin is secreted.
And so for those people not eating on the clock, it's very disruptive
to them because it activates these neurons in the brain. For people
who eat once a day or twice a day, or tend to shift their meals, you
know, and they might eat a lot but during a limited so-called feeding
window, it's kind of interesting humans now eat and talk about foods
in ways that for years I used to hear about in classes, in courses,
and research lectures about feeding animals, you know, restricted
feeding windows. And we owe a great deal of gratitude to Satchin
Panda, who was a colleague of mine when my lab was in San Diego at the
Salk Institute, who really is one of the pioneers of this restricted
feeding window work and has done a beautiful work.
He has a book that's excellent called 'The Circadian Code' that I
highly recommend. And he's done a lot of important work on neurons in
the retina, that control circadian timing, but also the relationship
between feeding windows and health. And he's sort of among the major
proponents I should say, of circadian eating, that means eating during
the daytime, not at night or intermittent fasting, restricting feeding
windows to anywhere from four to six to eight hours. I'll use myself
as an example of the transition from regular feeding schedule to a
more intermittent-ish fasting, although I don't really fall into true
intermittent fasting. So I was one of these people that just got so
accustomed to waking up and eating about an hour after I woke up. That
to go from eating every three or four hours to eating twice a day,
lunch and dinner, maybe a couple of snacks in the afternoon or
something. At first it was excruciating. I remember thinking like,
this is really brutal pushing out feeding. I didn't think I could
exercise unless I had eaten first. We now know that during most all
forms of exercise unless you're really focused on optimal performance
like you've got to hit key lifts or you have to sprint at your maximum
speed. And maybe even then that you can exercise faster just fine,
because you're mainly relying on sources like glycogen from the liver,
some undigested food sometimes, as gross as that may seem it's true,
as well as body fat if the exercise about is extremely long. But what
that means is that if you suddenly go from eating on a very regular
schedule to skipping a meal, or pushing your meal timing out or
shifting at all, you're going to have ghrelin in your system. And that
ghrelin is going to stimulate the desire to eat by acting at the level
of your brain. And it is indeed at that point, just mental. When we
hear about just mental, just physical, it's really kind of the same
thing 'cause it's all chemicals, brain and body. But it's the
stimulation of neurons that anticipate feeding. You're stimulating the
arcuate nucleus neurons that make you want to eat those AgRP neurons.
So ghrelin stimulates the AgRP neurons, which makes you want to eat.
So what can you do with this? What this means is, if you want to start
shifting your feeding schedule to one where you're not eating quite as
frequently, and there are some advantages to that that aren't just in
the biochemistry and health related, you know, cellar health related
things.
But some of them include not having to think about or buy food, right?
You actually don't have to think about food all day if you're not
eating so often. The other is, it gives you a far more social
flexibility, right? You can go to a noon meeting if you have to or you
can go out to dinner at a particular time. And you know, I guess it
makes it kind of tough if you want to meet somebody for breakfast,
'cause then you're the dork who's just like sipping black coffee and
like refusing everything. But anyway, I've been that dork. So it's one
of those things you just kind of work with. But the fact of the matter
is, ghrelin secretion, because of its relationship to the nervous
system, can be shifted by about 45 minutes per day. Now, it's going to
vary. Some of you have more so-called willpower, you know. But if you
really want to just start pushing that first meal out or shifting in
any direction, some people might want to eat in the early part of the
day and not in the evening. Trying to shift the mealtimes out the
spacing by about 45 minutes, is what the neural circuits that link the
ghrelin system to the neural circuits that control feeding, really can
handle because it's a form of neuroplasticity. And so what this would
look like is, if you normally you eat breakfast at eight o'clock plus
or minus 20 minutes, and you want to start eating your first meal at
noon you would take maybe four or five days and just start pushing the
meal out by about 45 minutes to an hour each day. So it's not quite as
painful. Or you can just take the plunge and just do it all at once. I
have a colleague who was a neurosurgeon at Stanford, came up through
my lab, he's now at Neuralink, and he has a great practice. He keeps
his ghrelin system at random. What he does is he skips one meal per
day and he makes his external schedule dictate that. So, sometimes he
skips breakfast, sometimes he skips lunch, sometimes he skips dinner,
he just skips one of the three major meals per day. And in doing that,
the ghrelin system has always kind of kept off kilter. And it probably
also allows him to have a lot of neural flexibility, what we call top-
down control. Just the knowledge, Oh, you know the hunger I'm feeling
isn't necessarily hypoglycemia. And in his case, it's almost certainly
not. And therefore what I'm feeling here is an activation of these
AgRP neurons, and therefore I can push my meal schedule around however
I want. Now, I should mention that top-down mechanisms are powerful.
Belief, motivation, these things can really shift neural circuits.
We're going to talk more about that a little bit later. But there are
also people who are genuinely hypoglycemic and they need to take
really good control of their blood sugar levels and try and keep them
stable. And so of course, you want to do what's medically safe for
you. I'm not at all recommending that people that suffer from
hypoglycemia suddenly disrupt their blood sugar patterns in any
direction, that wouldn't be healthy. But for most people out there who
have reasonable blood glucose levels, it's kind of interesting and
kind of fun to play with these parameters in order to optimize what
you want to do. And sometimes that might change across the year with
schedules. Many find great benefit in having flexibility over when
they eat. Regularity of eating equals regularity of ghrelin secretion
equals regularity of activity of these AgRP neurons, meaning you'll be
hungry at very regular intervals. So that's something that you can
work with, it's grounded in deep mechanism of hormone and neural
systems, and there's a lot of modern research to support what I just
said.
So, if MSH inhibits feeding, makes us want to eat less and ghrelin
makes us want to eat more, there's another hormone called CCK,
Cholecystokinin, that is potent in reducing our levels of hunger. Now,
I learned about CCK back when I was an undergraduate. So, well over 20
years ago, when it was first discovered. And there was a lot of
excitement about CCK at that point as a diet drug. You know, anytime
there's a molecule or a chemical discovered in the brain or body that
can suppress feeding, the diet industry just goes wild and they think,
this is going to be the thing that's going to allow people to move
from being obese to losing all sorts of unhealthy weight, et cetera. A
similar phenomenon was observed with leptin. Leptin is a hormone
that's made by body fat that signals to the brain when there's a lot
of body fat, and in animals injections of leptin can make fat animals
thin. They lose a lot of adipose or fat. In humans, it didn't work out
that way. It just the studies were done and leptin was successful in
treating a certain rare form of diabetes, but it really wasn't very
potent as an anti-obesity drug. Similarly, CCK has been looked at as
an obesity drug, something to reduce obesity. But it had some pretty
unhappy side effects actually caused some pretty serious side effects.
Now that's as drug. However, CCK when released at normal levels by
your gut has a powerful effect in suppressing appetite for a period of
time. And there are healthy and direct ways to activate CCK. Now, CCK
is in the GI tract, it's released from the GI tract. And it's release
is governed by two things.
One is a subset of very specialized neurons that detect what's in the
gut, the specific contents of the gut. And by certain elements of the
mucosa, of the mucus lining of the gut and the gut microbiome. So
what's really interesting, is that CCK is stimulated by fatty acids
and particular fatty acids that we'll talk about. Amino acids, and
particular amino acids that we'll talk about, as well as by sugar.
Now, let's put sugar on the shelf for a moment. We're going to talk a
lot about sugar because if CCK inhibits appetite and reduces feeding,
and it can be triggered by fatty acids, amino acids, or sugars, then
you might say, well, then in eating a lot of sugars should make us not
want to eat more, but we all know that eating sugar makes us want to
eat far more. That's the role of a lot of sugars. And that has to do
with a separate mechanism we'll talk about today. So, which fatty
acids in the gut stimulate the release of CCK? It turns out it's the
omega-3 fatty acids, the ones that come from algae or krill or fish
oil. I talked about this in the episode on nutrition and some of the
things related to the gut microbiome. And I'm going to revisit that
now. Omega-3 fatty acids and Conjugated linoleic acid, CLA, either
from food or from supplements, stimulate the release of CCK which then
reduces, or at least blunts appetite. And I'm not talking about
blunting appetite to anorexic levels where you don't want to eat at
all. I'm talking about regulating appetite to the point where animals
and people don't over-consume. So it's keeping appetite at a healthy
level. The other thing that stimulates CCK that I mentioned, are amino
acids. So when we eat, we have the ability to break down different
macronutrients, you know, carbohydrates, fats or proteins, into sugars
and glucose, that then we can convert to ATP and all that stuff from a
Krebs cycle from high school. We're not going to go into that today,
that's for a future episode. But amino acids are one of the things
that we are eating for. Amino acids both can be used as energy through
a process called gluconeogenesis, of converting proteins into energy.
Or those amino acids can be broken down and then rebuilt into things
like preparing, excuse me, repairing muscle tissue as well as other
forms of cellar repair. They're involved in all sorts of things
related to protein synthesis. What does this mean? If we eat the
proper amino acids at the proper levels, if we ingest omega-3's and
CLA's, Conjugated linoleic acids at the proper levels, or get them
from supplements, there's a blunting of appetite. Appetite is kept
clamped and we don't become hyperphagic. We don't overeat. We tend to
eat within healthy or normal ranges. So this is very important,
because most people don't understand that when we're eating, we are
basically fat foraging and amino acid foraging. And there are several
studies now have shown, that people and animals will essentially eat
until they feel they've consumed enough omega-3's, omega-6's, CLA's,
and certain amino acids. In other words, even if it's not conscious,
we are eating until we trigger the activation of CCK. Now, there are
other reasons why we shut down eating too. Are literally, the volume
of food in our gut can be large, and we can feel very distended.
That's the physical reason obviously. There are other reasons, maybe
we just have top-down control. We have knowledge that this is the end
of the meal and we stop 'cause we have to go back to work or to a
meeting, or we tell ourselves we've had enough. But at a subconscious
level, the gut is informing the brain via CCK and other mechanisms
when we've ingested enough of what we need. And these omega-3's and
CLA's and certain amino acids are vital for sending out that signal
that we've had enough. Now, which amino acids is actually really
interesting? We have essential amino acids and we have non-essential
amino acids.
Among the essential amino acids, there's one in particular that can
trigger the release of CCK very potently, and that's glutamine.
Glutamine is a very interesting amino acid. First of all, it's been
shown in a few studies to play a role in bolstering the immune system.
It can increase the number of killer cells in the immune system. It is
consumed but in supplement form. You know, people can take it. You
know, a teaspoon of glutamine or some people take glutamine throughout
the day, if they're really into it or for whatever reason, they think
they're battling off an infection or something of that sort. Glutamine
can also of course be derived from foods. And you can just put into
the Internet, do an Internet search and find out what foods are rich
with glutamine. Some of the ones that I'm aware of off the top of my
head are like cottage cheese, and things of that sort. But other foods
have glutamine as well. Once a threshold level of glutamine and other
essential amino acids are reached, once the threshold level of these
Alpha-3, excuse me, Omega-3 fatty acids and CLA's are reached, CCK is
released, and it helps reduce the activity of those AgRP neurons that
promote feeding. So as you can see, feeding is an interplay between
brain and body. And it's some of the micronutrients and even the
breakdown of particular nutrients, that's putting the accelerator or
the brake on the feeding process. It's not just one thing. So from an
actionable standpoint, you, we should probably all be trying to get
our omega-3, Omega-6 ratios correct anyway, because they are
antidepressant. I talked about the peer reviewed studies on that. They
are healthy for the gut microbiome, and we should be seeking
sufficient glutamine. Now, whether or not you decide to supplement
with glutamine or not, is up to you. One of the reasons why one might
want to do that, and again, you should always check with a doctor,
especially if you have any predisposition to cancers or you have
cancer, many cancers and tumors like glutamine, so that's something to
note. But one reason why you might want to supplement with glutamine
or consider eating foods that are rich in glutamine, isn't just to
keep your appetite in healthy ranges, but as well, glutamine can
actually reduce sugar cravings. So this is very interesting. I have a
friend, he's an absolute chocolate, sweets addict. He's a grown adult,
but he eats candy and chocolate as if he was like a 14 year old kid
hanging out at the local convenience store. It's really incredible.
And he has probably a sugar addiction, but he's very aware of this and
he's managed to kick all other addictions. So, for whatever reason, it
stimulates his brain and body in the ways that make him want more, but
he hates this. It's actually quite frustrating for him. He's somebody
who cares a lot about his health. He took the approach that I know
many other people have who know about this role of glutamine, of
taking a teaspoon or a couple of teaspoons of glutamine several times
throughout the day or anytime he craves sugar. And indeed, glutamine,
well, reduced sugar cravings. Some people who are really on the kind
of ketogenic front, will mix it with a little bit of half and half and
down that, and because I guess it makes it taste better, it's a little
bit chalky. So, glutamine has some very interesting properties. But I
think for most people that aren't suffering from adverse levels of
craving, making sure you're getting the right omega-3's that can come
from a variety of sources, check out the episode we did on nutrition
if you want to learn more about that. And CLA's, and making sure that
you're getting enough glutamine is going to be important for making
sure that the CCK signal gets through. The one thing I do want to
mention about glutamine, it's a minor effect, but it alone can have a
small increase, excuse me, it alone can increase blood sugar. It's not
a huge increase in blood glucose. But because the gut takes proteins
and breaks them down into these amino acids, and essentially looking
for glutamine and things like it, other essential amino acids as well.
When you ingest glutamine or branch chain amino acids, there is a
small but real increase in blood glucose. And that's because they are
essentially food. And there I'm talking about the supplemental
version. So, just know glutamine can increase blood sugar slightly,
especially diabetics should know that. It can reduce sugar cravings.
And just know that what your gut is doing at a core level is it's
forging, it's waiting, and it's trying to assess levels of omega-3
fatty acid, conjugated linoleic acid, and glutamine, and other
essential amino acids. You are essentially trying to eat to get these
nutrients and then a signal can be deployed up to your brain, that
you're not really interested in eating that much more.
Whenever preparing an episode for this podcast I'm always faced with a
particular challenge, which is, how many tools should I offer that
involve doing something new? You know, a new behavior, a new exercise,
supplement, something, things of that sort. And how many should be
related to not doing things, avoiding things. It's never really fun to
talk about all the things that we're supposed to avoid, but some of
them are so powerful in light of the mechanisms of a given topic that
I'd be remiss if I didn't mention them. So now you understand how
hormones, and peptides like CCK and ghrelin impact appetite. There's
one particular aspect of food that can powerfully impact CCK. And I
think most people, I'm guessing 99.9% of people out there are not
aware of this. And it has to do with highly processed foods. There's a
lot of reasons why one would want to avoid highly processed foods. In
fact, if you're interested in that topic and the history of whole
foods, transitioning to highly processed foods in this country, I
highly recommend you listen to a YouTube video by Dr. Robert Lustig,
he's at university of California, San Francisco. It's very easy to
find, put Stanford, Robert Lustig, it was a talk hosted by Stanford.
Gives a a beautiful description of the history of this, and why the
food industry started packing in additional sugars and salts, and
turning foods into commodities, it's really fascinating. It has no
conspiracy theory is just all scientific facts. It's really a
wonderful lecture. It has millions of views, it should be very easy to
find. We can provide a link to that, and we will. There's another
reason to avoid highly processed foods however, and that has to do
with what's called emulsifiers. Now, many of you are familiar with
emulsifiers, even though you don't know it. When you put detergent in
the laundry that contains emulsifiers, the goal of that detergent is
to bring together fatty molecules with water molecules and be able to
dissociate them and break them up to get the stains out of clothes and
things of that sort. There are a lot of emulsifiers put into processed
foods. And those emulsifiers allow certain chemical reactions to occur
that extends the shelf life of those foods. So it's like candy bars
and cereals, and all sorts of things that are in processed foods. The
worst of which are the typical kind of pastries that you see at the
convenience store. But this extends into chips of various kinds and
even some meats of various kinds, they pack this stuff into meats.
They have names like soy lecithin and other things. Why are
emulsifiers bad? Okay, there are a lot of reasons why they're bad, but
the reason why they're bad for the mechanisms that we've been talking
about today, is that when you ingest those foods, you're bringing
those emulsifiers into your gut. And those emulsifiers strip away the
mucosal lining of the gut, and they actually cause the neurons that
innervate the gut, that extend those little processes we call axons
into the gut, to retract deeper into the gut. And as a consequence,
you're ingesting a bunch of food and the signals like CCK never get
deployed. The signals that actually shut down hunger are never
actually triggered. And so, as a consequence you want to eat far more
of these highly processed foods. In addition, if you then go from
eating a highly processed food to non highly processed foods, you're
not able to measure the amounts of amino acids, sugars, and fatty
acids in those foods as accurately. You've actually done structural
damage at a micro level, but structural level damage, excuse me, to
the mucosal lining of the gut. Now, this can all be repaired if you
stay away from highly processed foods for some period of time. But the
negative effects of these emulsifiers are quite real. So, to make it
really clean and simple, emulsifiers from highly processed foods are
limiting your guts ability to detect what's in the foods you eat and
therefore to deploy the satiety signals, the signals that shut down
hunger. In addition to that, there's a parallel mechanism at play,
that I talked about in a previous episode but I'll remind you again,
that you have neurons in your gut that are sensing sugar, and are
sending a subconscious signal up to the brain via the vagus nerve. And
those neurons trigger the release of dopamine, which makes you crave
more of that food. So now you've got parallel signals making you want
to eat more sugar, making you unaware of how much sugar you've eaten,
and that are disrupting the inputs to the nervous system that signal
to the rest of your brain and body that you've obtained enough fatty
acids and you've obtained enough amino acids. So these highly
processed foods are really terrible. And you know, I'm not out here to
say, you know, never enjoy a processed food of any kind, I'd be a
hypocrite 'cause I do eat processed foods from time to time. Although
the ones that I tend to eat, I try and make of the healthier variety.
But eating whole foods has tremendous value and eating highly
processed food has tremendous negative impact on the gut and on the
gut brain axis. And so, recently there was a paper that came out in
Cell, Cell Press journal, it's kind of the apex of Cell journals,
which is a phenomenal. This paper showed that, ingesting highly
processed food leads to more intake of not just highly processed foods
but other types of food in general. There was kind of an overeating
compensation generally across foods for people that consume these
highly processed foods. And there are a lot of other reasons to avoid
highly processed foods. So again, I don't like to focus too much on
the do nots, I like to arm you with tools to do. But I think this
visual of certain foods and these emulsifiers actually stripping away
some of the critical lining of your gut and disrupting the hormone
signaling to the brain controlling feeding, is important enough and
cryptic enough, meaning it hasn't been talked about, it works at a
subconscious level, and that it's important that people are aware of
it so they can make decisions about what they do want to eat or not
want to eat for themselves. Before moving on, I just want to say one
more thing about highly processed foods.
There was an absolutely beautiful study done by my colleague, Chris
Gardner at Stanford, exploring whether or not certain diets were
better than others. They looked at vegan, vegetarian, omnivore, I
don't know if they looked at all meat or not, but they looked at the
different forms of diets, intermittent fasting, et cetera. And they
essentially found that, whichever diet people adhered to, whichever
one they followed, was equivalent to the others. Provided that they
followed it, they lost the equivalent amount of weight. There really
wasn't a strong effect of the food type or the pattern of eating, et
cetera. However, in a study like that, adherence is very high because
people are a part of a study. And for many people, the ability to
adhere to a certain eating plan is one of the most, if not the most
powerful determinants of whether or not a given diet meaning
nutritional plan works. Now, this thing about highly processed foods
however, is really diabolical. Because it truly says, and I think the
recent data in cell metabolism and other journals really proves that,
a calorie is not a calorie. That's absolutely absurd because of these
emulsifiers and the contents of these highly processed foods. In fact,
the data in humans points to this. So what they did is they took in-
patient adults, so they had total control over their food intake. And
they received either ultra processed or unprocessed diets for 14 days,
as a short study. The diets were matched for calories, sugar, fat,
fiber, and macronutrients. So everything else was matched. Just
processed or non-processed is the major variable. And basically what
they found, is that the people who are eating the processed food diet
happened to eat much more, right? This was after this period of
putting them on either diet and clamping for all other variables. Then
they would eat much more, and the body weight changes were much more.
And those body weight changes, were such that they couldn't be
accounted for by just increased calories. So, the bottom line is that
highly processed foods are just bad for you. They increase weight
gain. They disrupt the lining of your gut in a way that disrupts
things like CCK and proper satiety signals. And they contain a bunch
of things, in particular sugars, but other things as well, that
disrupt not just the hormonal systems but also the neural systems that
control the desire to eat after the diet is done. So there's just so
many reasons why these highly processed foods are terrible, and they
can explain a lot of the ill health effects that we've seen in the
last 50 years not just in the United States, but all over the world.
That enormous increase in diabetes, juvenile diabetes. It's just
remarkable how far down the path of diet we've gone. And it's clear,
it's almost a smoking gun what the cause of this is. If you'd like to
learn more about that please refer to the Lustig lecture. He also
spells out why non-processed foods is far more economical in terms of
just at the level of the household or individual as well as at the
societal level. Really interesting stuff, I highly recommend you check
it out.
So now let's move on to some other hormones that regulate hunger and
satiety, in particular insulin. Now, you've probably heard of insulin
before. Insulin is the thing that's lacking in type I diabetics,
that's why they have to inject insulin whenever they eat. The reason
they have to do that, is because when they eat their foods are broken
down into glucose. And in order to shuttle glucose to the appropriate
tissues in the body, and also to keep glucose levels in check, you
need insulin. So the simplest way to think about insulin and glucose
is that when you eat, that food is broken down into sugars, that's
true whether or not it's fats or it's sugars, or eventually if it's
proteins, they are oxidized into fuels as we say. And those fuels can
be used as the name fuel implies into energy, they're eventually made
into ATP. There's a bunch of biochemical steps there we're not going
to go into today, but that's essentially how it works. You break down
food into glucose. Now, if you're ketogenic, we'll talk about that in
a little bit. But in general, you eat, food is turned into glucose.
Your blood sugar needs to be kept in a particular range. Hypoglycemic
means too low, hyperglycemic means too high. And what they called
euglycemic E-U, glycemic, is the healthy range. Now, what those
healthy ranges are, in general the healthy range, the euglycemic
range, is about 70 to a hundred nanograms per deciliter. But most of
you aren't walking around with a glucose monitor. Some of you are, but
most of you are not. The more important question for us to address
right now, is why is it important that glucose be kept at a particular
level? Once you understand that, keeping glucose in check starts to
have a rationale behind it and the ways to do that start to make a lot
more sense. So the reason is, if glucose levels get too high because
of the way that our cells in particular neurons, interact with
glucose, high levels of glucose can damage neurons. It can actually
kill them. You can start getting what are called peripheral, excuse
me, neuropathies. One of the symptoms of some forms of diabetes is
that people start losing the sensation of touch in their fingers or
their hands or their feet, and they can start going blind. There's
diabetic retinopathies. So it's very important, that insulin manage
your glucose levels. Now, there's also type II diabetes where there's
insulin secreted from the pancreas, but people are insulin
insensitive. There's a disruption in the receptors and insulin
insensitivity isn't quite the same as having no insulin at all, but it
parallels some of the same mechanisms. Now, type I diabetes is often
picked up because someone has a sudden weight loss, because they're
not processing blood sugar the same way they were before. Type II
diabetes is often, although not always associated with being
overweight and with obesity. Both of them are challenging conditions.
Type II diabetes almost always can be managed by managing one's
weight. And of course there are prescription drugs and supplements
that can help manage those. We're going to talk about all of that. But
for most people that don't have diabetes, the important thing is to
manage glucose, to keep it in that euglycemic range. And there are a
number of different ways to do that. Some of them are behavioral, some
of them are diet based, and some of them are based on supplements or
prescription drugs. So let's talk about those now.
So if you eat, and in particular if you eat carbohydrates, blood
glucose goes up. If you eat fats, blood glucose goes up to a far less
degree. And if you eat proteins, depending on the protein, it will
eventually be broken down for fuel or assembled into amino acid chains
for protein synthesis and repair of other tissues and bodily
functions. But glucose goes up and then is kept in range. When you are
hungry, you secrete a different hormone and that's called glucagon.
And glucagon's main role, is to pull stores of energy out of the liver
and the muscles. And once those are depleted, you'll eventually tap
into body fat, okay? So, and this is for people that have a typical
blood glucose range, so that 70 to 100 euglycemic range. So, the two
kind of push and pull systems that we're going to think about now to
keep this simple, is that you have the insulin system managing
glucose, and you've got the glucagon system pulling energy out of your
liver and muscles for immediate fuel. And eventually you'll pull fuel
out of body fat if you've been active for a very long time and all
your glycogen stores are depleted or close to depleted. So what does
this all mean? There's a lot of important biochemistry and a lot of
important cellar processes involved in whether or not your anabolic or
catabolic. Whether or not you're breaking things down or building
things up. Let's talk about feeding in a simpler way, however. And
let's weave the tools to manage blood glucose, to keep it in check, as
we do that. So, let's say you had a meal and that meal consisted of
rice, a carbohydrate, some meat or fish, let's say a piece of salmon,
and some vegetable, some fibrous vegetable like asparagus or cabbage
or something like that. If you were to eat all of that at once, you
know, you take a bite of one, a bite of the other, you're going to mix
it up. You know, one of these, it all ends up in the same place kind
of people, mix it all up. Then you'll experience an increase in
insulin and increase in blood glucose that's moderately fast. It's
going to increase pretty quickly. What's remarkable, is that the order
that you consume each macro-nutrient has a pretty profound influence
on the rate of insulin and glucose secretion into the blood and how
quickly those levels rise. So if you will make it really simple. If
you were to eat the rice first, your glucose would rise in a sharp
spike, especially if it doesn't contain any fats to slow the
absorption. Now, that might be good if you're very hungry and you want
to get an increase in glucose. In fact, this is the reason why you're
often served bread before meals, because it is... And sometimes it's
bread and butter, or chips before meals or appetizers, are designed to
get your blood glucose going up high because big steep increases in
blood glucose tend to promote the desire to consume more glucose. And
this also relates to the dopamine system and the way that something
tasty in the mouth and sugar in the gut and fats and sugars in the
mouth, trigger the activation of a lot of systems in the brain and
body to consume more of whatever you have or whatever is available to
you. So, the basic idea is that eating carbohydrates and/or fats early
in a meal will give a steep rise in blood glucose. However, if you
were to eat the fibrous thing first, so a lot of chewing, but not a
big rise in blood glucose because in general there's... Unless it's
laid in with sugar. Or something we're just talking about some
vegetable, fibrous vegetable, that will actually blunt the release of
glucose until you eat the fish and the rice. But believe it or not it
will actually blunt the glucose increase that the rice would cause.
Now, I'm not talking about neurotically eating each macro-nutrient
separately in sequence. I'm just trying to give you a picture of
what's happening ordinarily. So what this means is, if you feel a lot
of food related anxiety, or you feel you're one of these people that
you can kind of sense like your blood sugar increasing very quickly, a
lot of people can sense this, some people can't, has a lot to do with
how well they manage their blood sugar as well as some of the
psychological factors. And yes, their family and historical reasons,
you know, I've got friends who had a lot of siblings, and when they
sit down to eat they have to really suppress the desire to not beat up
everyone else at the table and take all the food. It's sort of like
not... It's hard for them to understand that there's plenty to go
around, because of their upbringing. So there are psychological top-
down effects. A lot of the psychology around food is geared towards
getting people to be relaxed when they eat and these sorts of things.
But these blood sugar effects are real just cellar and basic
biochemistry of how the body manages sugars ingested into the blood.
So what does this all mean? It means that if you want a steep increase
in glucose, you are very, very hungry, then you should eat the
carbohydrate laid in food first, or you should eat a bunch of
macronutrients combined. So that would be like the hamburger or the
sandwich, the bread, the whatever's in that sandwich altogether,
usually that's protein and vegetables as well. If you want to have a
more modest increase in glucose or you want to blunt the increase in
glucose, then have the, at least some of the fibrous thing first, and
then the protein and then the carbohydrate. You will notice that your
blood glucose will rise more steadily, and that you'll achieve satiety
earlier in the meal. Or at least you won't get this huge peak at sort
of the Thanksgiving meal effect. Some of you are international, so if
you don't celebrate Thanksgiving is a time of year where... It used to
be the one-time a year or two times a year where Americans would give
themselves permission to eat enormous meals. Now that seems to happen
a lot more often. But there is this effect of you're full and yet
you're hungry for more, that's because your blood glucose has gone
through the roof and it's triggered a number of other mechanisms.
There's also usually a lot of alcohol consumption, and alcohol itself
because it's a sugar will increase blood glucose very, very sharply.
It depends on the alcohol, some alcohols have more sugar than others.
But basically what you're trying to avoid are steep increases in blood
sugar. And the order that you eat foods has an enormous impact on
that. The other thing that has an enormous impact on how long and
shallow, or how steep that curve of glucose is, depends on on whether
or not you recently were moving, are moving or start moving after you
eat.
So it turns out that your blood glucose levels can be modulated very,
very powerfully by movement. If you did any kind of intense exercise,
or even just walking or jogging, or cycling anything before you eat
your blood glucose levels will be dampened somewhat. And that has to
do with the release of something called, some people call it GLUT4,
which sounds like glutton. Other people call it GLUT4. These are
things that are involved in shuttling glucose to particular cells in
the body, namely toward muscle and glycogen stores and away from body
fat stores. It has to do with sequestering of glucose from the blood.
The point is that, if you're somebody who struggles with blood sugar
regulation, in addition to getting your body weight in a healthy
range, doing all the other sorts of things that you should be doing,
the key thing is to try and get some movement, sometime as circuit
meal. Now, very few people can actually eat and walk at the same time,
although I do it all the time. Not because I'm trying to regulate my
blood sugar but just 'cause I tend to be busy. I eat and drive,
[mumbles] busy. Busy if I'm not giving this podcast, or if sleeping,
I'm eating, but except the early part of the day when I fast. But the
bottom line here is that, if you, for instance take a 30 minute walk
after a meal, your blood glucose will be blunted in ways that are
beneficial. If you have exercised in the recent hours before a meal,
that can be beneficial. The order that you consume foods is
beneficial. And there are a few things that you can consume that can
also adjust blood glucose levels. So let's talk about those, but I
thought it was important to really tamp down that it's not just what
you eat, we talked about that before, but also the order that you eat
those things, believe it or not, whether or not you combine macro-
nutrients, carbohydrates, proteins and fats and fibrous vegetables.
And whether or not you've moved recently. The higher intensity the
movement, the greater the GLUT4 increase, and the more that the blood
glucose will be blunted and you'll shuttle more of that to glycogen
and muscle stores. And even just moving after a meal, even just a calm
easy walk, can really adjust the ways in which blood sugar regulated
for the better. I don't want to perseverate on this processed foods,
hidden sugars thing too much.
But understanding now a little bit about how insulin and glucose work,
you can probably imagine why hidden sugars are such an attractive
thing from the standpoint of processed food manufacturers. Because if
they can put sugar in that you can't even taste, that sugar is going
to amplify the amount of glucose, it's going to increase the rate of
glucose increase into your bloodstream and it's going to promote more
feeding. So in that case, you're really being tricked. It's not that
you're actually reaching for the additional appetizer and your blood
glucose is going up. The food that you ate is actually increasing your
appetite as you eat it. It's a positive feedback loop. So don't want
to demonize those any more than I already have, but you should be
aware that these things are happening at the level of your bloodstream
and brain.
The other thing I'd like to address for a moment, is this notion of
stable blood sugar versus lay bile blood sugar or unstable blood
sugar. Some people just have stable blood sugar. They can go long
periods of time without eating and feel fine. Other people get really
shaky, really jittery, and/or when they do eat, they feel really keyed
up. Sometimes they'll even sweat. Sometimes their vision will go
blurry. And some of that can actually be because they've become
hyperglycemic. And those effects that you experience when you are
hyperglycemic are the early warning signs of the kinds of things that
damage neurons and lead to the really terrible stuff they talked about
before like peripheral neuropathies. Now, it takes some time for those
things to occur, those neuropathies to occur. But whether or not your
blood sugar is all over the place or whether or not stable, can be
impacted by a number of things. One of those things is exercise. So
these days there's a lot of interest in what they call zone two
cardio, which is that kind of steady state cardio, where you can just
nasal breathe even at pretty high output, where you could maybe have a
conversation. Although I'm such a huge proponent of nasal breathing
during exercise, most forms of exercise especially zone two cardio,
that you probably shouldn't be talking while you're doing that cardio
unless it's absolutely essential. But periods of zone two cardio that
lasts anywhere from 30 minutes to an hour or sometimes more for your
endurance athletes, can create positive effects on blood sugar
regulation, such that you people can sit down and enjoy whatever it
is, the hot fudge sundae, or whatever the high sugar content food is.
And blood glucose management is so good. Your insulin sensitivity is
so high, which is a good thing, that you can manage that blood glucose
to the point where it doesn't really make you shaky, it doesn't
disrupt you. And you know, to say nothing of the weight-related issues
or the adipose fat gain, et cetera, that's a separate issue because
people vary there. But basically doing zone two cardio for 30 to 60
minutes, three to four times a week makes your blood sugar really
stable, and that's an attractive thing for a variety of reasons.
On the flip side, high intensity interval training or resistance
training AKA weight training, are very good at stimulating the various
molecules that promote repackaging of glycogen. So sprints, heavy
weight lifting, circuit type weightlifting provided there is some
reasonable degree of resistance, those are going to trigger are all
sorts of mechanisms that are going to encourage the body to shuttle
glucose back into glycogen, converting to glycogen, into muscle
tissue, restock the liver, et cetera. Depleting one's glycogen
actually takes some time. You know, if you do a couple sets of tricep
extensions and some crunches, you're not depleting your glycogen.
Glycogen depleting workouts are very high intensity. Generally they're
less than an hour or so, but those are the sort that are going to lead
to big increases in the kinds of enzymes and metabolic pathways that
are going to repack glycogen and shuttle most things towards restorage
of foods not into adipose tissue, not into fat, but taking glucose and
making it into fuels that you can access later for more of that high
intensity activity. And I should mention that one of the advantages of
high intensity interval training or weightlifting of various kinds, is
that it causes long standing increases in basal metabolic rate. I
don't want to go too far down this path because we're going to do an
entire month on human performance and athletic performance. But it's
not just the increases in muscle that increase metabolism, because
muscle burns more energy than other types of tissues, except your
brain, which truly burns the most energy. Anyway is the main reason
why your basal metabolic rate is what it is. Well, high-intensity
training. So it could be sprints, it could be high intensity interval
training of different kinds, it could be weight training, also has an
effect of increasing thermogenesis even long after you've completed
the exercise. So there's a long tail. There's a kind of post exercise
metabolic effect that's also beneficial. So it's not an either or,
it's really that high intensity interval training and resistance
training. And things of that sort are very good for one reason. And
the zone two cardio is very good for other reasons. And now you can
see why it's just a healthy thing and why most people should probably
be doing exercise most days of the week, if not every day of the week.
If your goal is to manage blood glucose and your goal is to manage
some of the metabolic factors that control repackaging of glycogen and
encouraging excess glucose to not get diverted into body fat stores.
We haven't talked a lot about lipids today, that's because most of
today's discussion is about hormones and insulin is the dominant
hormone in terms of mobilizing and managing glucose in the body, at
least for most people. But fats are very important. And there's just a
little anecdote about fats that I think will be useful in thinking
about why you want to manage what they call the LDL or HDL ratios. And
this is deserving an entire episode, many, perhaps even several
episodes. But some of you may be familiar with LDLs and HDLs, some of
you may not. The LDL is low density lipoprotein. This is the one that
you don't want it to be too high. Castillo's dreaming, he's barking.
He loves all forms of cholesterol but that's just Castillo dreaming.
So LDLs are the ones that you want to keep low. You don't want those
to go excessively high. HDLs, the high density lipoproteins are the
ones that are the so-called healthy lipoproteins. That's all fine and
good. But you might ask yourself, what are they doing? What is the
actual role of these things, and why would you want healthy levels of
HDL and not too much LDL? Well, one of the reasons is, that fats don't
like water, right? They are hydrophobic. And yet you need to move fats
in your bloodstream, all tissues in your body need fats. They need
cholesterols, they're... In last episode we talked about cholesterol
is a precursor to the sex steroid hormones, estrogen, and testosterone
and other hormones as well. Well, HDL and LDL, actually coat fats to
allow them to be transported through the bloodstream. They do a number
of other things as well. But HDL, is a key component of the delivery
system that brings those fats to the liver, ovaries, testes, and
adrenals. In other words, having adequate levels of HDL is good,
because it allows fats to be delivered to the tissues that
manufactured testosterone, estrogen, cortisol in healthy levels and
the liver. So this is why when LDLs are too high what's happening is
you're not getting fats to the correct tissues. And you can get
buildup of fats like fatty liver disease and some of these things can
happen. A high sugar content can even lead to some of these fatty
liver conditions that starting to happen is actually the first time in
human history perhaps that we're aware of anyway. That we're starting
to see liver conditions that normally were associated only with severe
alcoholism starting to come from sugar content. So what does this
mean? This means keep your LDL and HDL ratios proper. You want those
HDLs in order to deliver fatty molecules to the very tissues that use
cholesterol in order to manufacturer hormones. So how do you keep LDLs
and HDLs in their proper ratios? Well, a lot of people don't realize
this, but the debate about dietary cholesterol and its relationship to
LDL and HDL ratios, it is a barbed wire debate. I don't want to get
into it right now. There are still a lot of open questions as to how
much dietary cholesterol impacts LDL and HDL ratios. I don't want to
get into that now, I'm not taking a stance either way. But what is
very clear, is that having highly elevated glucose, consuming too much
sugar or not managing glucose in your body through some of the
mechanisms that we've been talking about up until now, can also
negatively impact LDL, HDL ratios. So managing glucose goes way beyond
just managing blood sugar, and making sure that you don't lay down too
much body fat, making sure your metabolism stays high and making sure
you're not getting jittery at meals. It also has to do with making
sure that you're creating enough of the molecules HDL and not too many
of the molecules LDL, that are going to disrupt the delivery of things
to the organs of your body that allow you to make healthy levels of
testosterone, estrogen, and so forth. If that wasn't clear, let me
make this ultra simple. You want healthy levels of HDL, and you want
low levels of LDL, because if you have ovaries it will allow the fats
that need to get to the ovary to produce estrogen, to get there. And
if you have testes, it will allow the fats and the cholesterol
molecules that you need in order to manufacture testosterone to get to
the testes. As well, in order to have proper adrenal function and
proper liver function, you want HDL and LDL in the healthy correct
levels. So now we've talked a lot about behavioral tools and the
underlying biological mechanisms that justify those tools in
particular circumstances.
Now, I'd like to turn to supplements and prescription drugs that
regulate the hormone systems, controlling feeding and satiety. There
are a huge number of these. Some have more powerful effects than
others. There are two that I want to describe because they've been
getting a lot of attention recently. First of all, there's a
prescription drug Metformin, which was developed as a treatment for
diabetes. And it works potently to reduce blood glucose. It has
dramatic effects in lowering blood glucose. Metformin involves changes
to mitochondrial action in the liver. That's its main way of depleting
or reducing blood glucose. And it does so through the so-called AMPK
pathway, and it increases insulin sensitivity overall. Metformin is a
powerful drug. In fact, I'm surprised that so many people have sought
it out, given that most of the people that I'm aware of that sought it
out are not diabetic. I think for diabetics it seems to be a useful
drug. For non-diabetics, it can also of course, lower blood glucose.
It also has the potential to make people hypoglycemic, genuinely
hypoglycemic. So, you really need to approach Metformin with caution.
I get a little concern when I hear about people blasting Metformin,
simply because fasted states or low blood sugar states are healthy.
Doing that pharmacologically can have long standing effects. You
really want to approach that with caution. Now, there's a comparable
drug, it really should be called a drug. But it's non-prescription,
that's also in fairly prominent use out there called berberine, B-E-R
B-E-R-I-N-E, berberine, correct.
So berberine is a really interesting compound. Its actions very much
mimic Metformin. So let's talk about berberine for a second. Berberine
actually comes from various plants and tree bark. It is sold in
supplement stores, it's sold online. It is, as far as I know
unregulated, it is powerful. If you're going to experiment with
berberine, you definitely want to talk to your doctor and you want to
approach it with caution. It also works to activate the so-called AMPK
pathway. AMPK by the way stands for Adenosine Monophosphate-activated
protein kinase, AMPK. And it inhibits a protein tyrosine phosphates 1B
pathway. I think that's enough nomenclature. It activates a certain
pathway that's associated with fasting and low blood glucose. The
effects of berberine are as far as I can tell, when looking at the
literature, are very similar if not identical to Metformin. Now, the
number of studies out there on this are many. So I'm just going to
review a few of them and their major effects. As always, I invite you
to check out examine.com. It's a wonderful website where you can put
in any supplement or compound or biological goal for that matter. And
it will list out the various effects in the human effect matrix. So
studies on humans, if they're available. And it will tell you whether
or not they're strong effects or weak effects or modest effects. And
it will point to the specific subject population, it's a wonderful
resource. So berberine, not surprisingly has very strong effects in
lowering blood glucose. There are four studies on this. In fact, they
say that berberine is one of the more if not the most effective
supplements for lowering blood glucose. It talks about dosages there.
Although I'll just mention that I've tried berberine, and the dosages
that are typical on the bottle of most supplements, is much higher
than I needed. So when I took berberine, two things happened, first of
all, I got a pretty splitting headache. It gave me pretty vicious
headache. So for me it was a no, almost immediately. The other thing
is, I became so hypoglycemic. That in order to get my blood sugar back
up, I think I ate something like 10 donuts and I didn't feel like I
had ingested all that much sugar. It was really kind of weird. I was
hyperphagic for sugar. I was craving sugar, craving sugar and I was
very thirsty as well. And so, I don't want to promote any bad
behavior, but I know that certain people use this when they've
overeaten sugars or they're doing their cheat days, something that I'm
personally just not a fan of. And they want to keep their blood sugar
in check or they know they're going to consume a huge meal. They'll
take berberine to keep blood glucose clamped. And it does do that. It
has very strong effects. Three peer reviewed studies on HbA1c levels.
HbA1c is something that can be measured in a blood test. That is sort
of an average readout of your blood sugar levels over the previous two
or three months, sometimes shorter period. But that's mostly what
HbA1c is about. So, it radically decreases your blood sugar levels. It
actually lowers cholesterol. It acts remember on the liver, and the
liver is involved in cholesterol metabolism. And remember it's both
sugars, blood glucose, and dietary fats. Perhaps it's still heavily
debated in terms of how your blood total cholesterol HDL and LDL are
regulated. So it seems to lower total cholesterol, and it seems like
it lowers HDL and LDL in parallel. So that's interesting. One study
showed a minor increase in HDL, the so-called good cholesterol.
Insulin levels dropped, not surprising. Another study showed a slight
decrease in LDL, though seem to be kind of minor. Here's a kind of
interesting one, just to help you remember berberine as of the fact
that it comes from tree bark, isn't trigger enough to remember it.
Direct contact of berberine on canker sores seems to eliminate canker
sores very quickly, which is kind of cool. I've not had canker sores
in a few years but when I dig down, they're extremely painful. I don't
like those. So that's kind of interesting, and there's some study
references there. I find it amazing that these compounds exist. You've
got this prescription drug Metformin, and then you've got berberine,
this stuff from tree bark, and they have effects that are essentially
equivalent to one another. So again, I'm not promoting their use or
even their exploration, but those compounds do exist, they're out
there. And check out examine.com if you'd like to learn more.
Certainly do your reading, do your homework, before you start just
popping the stuff. And if you have hypoglycemia or hyperglycemia, be
especially careful and also do understand that dosages and dose
requirements vary. So if you do go down this path, really approach
things carefully. Always start with the lowest amount that you could
get away with. For me, the headache thing just made it a no-go. I do
keep a bottle of it in a full disclosure, in the odd chance that I
feel like eating a ton of doughnuts. It's not so much about not
ingesting the calories, it's just that I don't like the feeling of
being hyperglycemic, the blurry vision, just feeling lousy, I do love
donuts. Other things that impact blood glucose in supplement form.
Chromium has been shown in 29 studies to have a minor, I want to
emphasize a minor effect on reducing blood glucose. Things like
L-carnitine, something we've talked about here on the podcast before
in terms of its relationship to power output in ATP production for
both aerobic and anaerobic exercise, as well as sperm quality and egg
quality. We talked about that long ago. Things like Panax ginseng can
have positive effects on, I should say, can have effects of reducing
blood glucose slightly. I don't want to give a valence to or judgment
to whether or not it's positive or negative. Here's something that's
interesting that you should know about. Caffeine has very reliably
been shown to increase blood glucose just a little bit, okay? So I
always thought that caffeine would drop blood glucose, but it actually
can increase blood glucose just slightly. Things like magnesium. We
talked about magnesium as a tool for enhancing the passage into sleep,
in particular magnesium threonate and bisglycinate. Magnesium can also
have a modest reduction in blood glucose. You're just trying to get
the impression, everything reduces blood glucose, but that's certainly
not the case. And then a couple episodes ago when we were discussing
nutrition we talked about artificial sweeteners, sucralose, aspartame,
NutraSweet. Some of those are generic names. Some of those might be
brand names and how they have negative effects on the gut microbiome
and that's supported by a number of studies. There's one artificial
sweetener, it's stevia, S-T-E-V-I-A, which seems to lower blood
glucose just slightly. And I still can't find data on whether or not
Stevia impacts the gut microbiome in either direction. Many of the
things that I consume do have small amounts of Stevia in them. So I'd
love to know if anyone out there is aware of quality peer reviewed
research, as to whether or not Stevia impacts the gut microbiome
similarly or differently from other artificial sweeteners. Please let
me know. Please send me the references. I'd really appreciate it if
put it in the comment section on YouTube or elsewhere. Comment section
on YouTube would be the best place. So Stevia seems to lower blood
glucose a little bit, which makes it kind of an attractive artificial
sweetener if one is going to use artificial sweeteners. But remember,
sweet taste itself stimulates the desire to eat, which will increase
more blood glucose. So I'm guessing that they probably cancel each
other out. So you have to think logically about these things.
Vitamin B3, so some of the B vitamins do indeed stimulate appetite by
triggering increases in blood glucose, vitamin B3 in particular. I
don't know if B6 does. Things like zinc seem to lower blood glucose.
And then there've been an enormous number of other things that have
been tested for their roles in blood glucose. Apple cider vinegar,
anything acidic. This is well-known now that any kind of acidity, so
it could be lemon juice or lime juice, or Apple cider vinegar, lowers
blood glucose slightly. Some of those can also have other effects that
we're not talking about today. So that's kind of interesting because
there's a movement now towards creating a sort of people talk about
becoming more alkaline, you know, what these... I hate to break it to
you but you don't really want your body to be too alkaline. You want
to stay in the right pH or else you're start... There are conditions
that make you more alkaline. You don't want to be too acidic or too
alkaline. If you see a beverage or something that purports that
ingesting that beverage is going to make you more alkaline, that is
absolutely false. There's no evidence for that, is impossible
biochemically. It's just marketing. But nonetheless ingesting foods
that are acidic can make some slight adjustments to the pH of the gut
in ways that can slow or alter the absorption of foods and can blunt
blood glucose. You can try this sometime if you want, if ever you're
feeling kind of over sugared out like you ate something with too much
sugar. You can drink a small amount of lemon juice mixed with water or
lime juice, and you'll notice that it will blunt that kind of
hyperglycemic effect just a little bit. Again, you don't want to use
this as a medical tool, but the effect is fairly potent. And then,
excuse me. And then there are a number of other things like capsaicin
and hot chili peppers that will lower blood glucose. The list goes on
and on, The most powerful one is absolutely berberine and Metformin,
but that's really heavy caliber stuff. And the other ones I mentioned
have more minor effects. I do want to mention because I'm sure some of
you out there are curious about the ketogenic diet.
I'm going to do an entire episode about ketosis and the brain and the
body, but the ketogenic diet has been shown in 22 studies to have a
notable decrease on blood glucose. And that is not surprising, because
the essence of the ketogenic diet is that you're consuming very little
or zero of the foods that promote big spikes in insulin and glucose.
If you consume enough protein, some of that protein can be converted
into glucose, of course, through gluconeogenesis. But the ketogenic
diet has a very strong support for its role in regulating blood sugar,
which is glucose. But the specific effects of the ketogenic diet, and
one particular effect that I'll address later but I'll mention now,
which is, the ability of the ketogenic diet to adjust thyroid hormone
levels in ways that make it such that if you return to eating
carbohydrates after being in ketosis for too long, you don't manage
fibroid and carbohydrates as well, that has been shown as well. So
we're going to dive deep into ketosis in a future episode. So for you
ketonistas does out there don't worry, I certainly have nothing
against ketogenic diet. I actually don't have anything for against any
particular nutrition plan. I know it works for me, at least at this
stage in my life. And I'll update it if I need to. I'm simply trying
to get you as much information as I possibly can, so that you can
navigate through that landscape in a way that's in keeping with your
particular goals. So now you understand a lot about blood sugar and
how it's managed, and the ways that you can manage it better depending
on your particular needs.
This is also a good opportunity for us to look back at some of the
medical literature, because it really points to just how far we've
come in terms of understanding these important mechanisms. And it
points us in the direction of some actionable protocols. So diabetes,
which is these huge increases in blood glucose, because there's no
insulin, was known about as early as 1500 BC, which is just
incredible. And the way physicians then understood that certain people
had high blood glucose without actually knowing what blood glucose
was, is that they would take the urine of particular patients, and
they'd find that ants preferably move toward and consume the urine of
certain patients and not others. And they understood that there was
something in that urine that was correlated with the weight loss and
some of the other probably very unfortunate health symptoms that these
people were experiencing. So they knew that there was something in
blood and urine. But you might be asking yourself, wait, that's urine.
But as I tell every kid that I meet, two things. I tell a kid, your
brain is here, I make them point to their head. And then I tell them,
do you know what? Do you know that your urine is actually filtered
blood? And they usually go, [grunts]. I get parental permission to do
this first. But most adults don't realize that your urine is actually
just filtered blood. And that's why if you see blood in your urine,
that's a problem. You want to filter the blood, but urine is filtered
blood. Now, this business of measuring blood sugar from the urine has
been something that lasted way beyond these early stages of 1500 BC.
It turns out that as late as 1674, physicians at Oxford university
were figuring out who had pathologically high levels of blood glucose
by analyzing their urine. And again, they were measuring the sweetness
of their urine, and this is medical fact. They would do this by taking
urine samples from different patients, and tasting them. And they
developed an intuitive sense of what excessively sweet urine was
relative to the other urines that they had tasted. So for those of you
that are in the medical profession or those of you that are seeking
out the medical profession, do you understand this is not done
anymore? And you can also just reflect on how far we've come in terms
of the medical profession itself. In our ability to measure things
from the blood and measure things from urine without having to ask
ants which urine is sweeter or ask oneself, which urine is sweeter. So
indeed we are making progress as a species.
Before we close out today I want to talk about one more tool that many
of you will probably find useful. I certainly have, I'm a big consumer
of caffeine, although I don't consume a ton of it, I consume it very
consistently. So I'm big on consuming Mate, which is a strong
caffeinated tea. And I generally do that early in the day. Although I
do delay about two hours after I wake up for reasons I've talked about
in previous episode, to maintain that nice arc of alertness and focus.
I do drink black coffee as well, mushroom coffee as well, I love that
stuff. But Mate, also called Yerba Mate, is an interesting compound
because unlike coffee, it has been shown to increase something called
glucagon like peptide GLP1. And increase leptin levels. Now, we didn't
talk a lot about glucagon today. Glucagon is really elevated in the
fasting state. I mentioned that it's sort of the opposite of insulin
in kind of rough terms that's one way to think about it. But GLP1, or
glucagon-like peptide one, is increased by ingesting Mate and it acts
as a pretty nice appetite suppressant. Now, I'm not trying to suppress
my appetite. I like to eat as I mentioned before. But it works really
well to stimulate the brain and to give you a level of alertness and
to do a lot of the things that coffee does. It also contains
electrolytes. So we meaning our neurons and our brain run on a variety
of factors, electrical activity and chemical transmission, et cetera,
but they require adequate levels of sodium potassium and magnesium.
So, if you were to learn the biology or the physiology of the action
potential, the firing of a neuron, something we teach every first year
neuroscience student, and I'd be happy to teach you if you're
interested. You'll hear about sodium rushing into cells and potassium
entering and leaving cells in order to allow neurons to communicate.
Electrolytes are critically important for the function of the nervous
system. And many things that act as diuretics, that promote excretion
of water, like caffeine, can also take electrolytes out along with in
particular sodium. And sometimes the lightheadedness or the brain fog
that people experience, isn't just because electrolytes are low but
because they're kind of out of balance. So I like Mate because it has
electrolytes, it has caffeine. It stimulates the release of this
glucagon-like peptide GLP1, and it's been a big help to me in
extending that early morning fasting window out to about noon or so
when I eat my first meal. It also just tastes really good. I don't
drink it out of the gourd even though I have Argentine lineage. The
gourd to me it's just kind of an inconvenience, I drink it out of a
mug. There's no promotion here. I have no relationship to any Yerba
Mate plantations or companies, I just happen to really like the stuff.
And the fact that glucagon-like peptide one is enriched or is released
more when you drink Mate. And the fact that GLP1 can regulate blood
sugar in ways that keep your blood sugar in that we called euglycemic,
not too high, not too low mode, is one reason why ingesting Mate is
attractive to me. If you go to South America, well, you'll see
especially among Oregonians, but also Argentines, is people actually
carry a thermos of this stuff with them around and bring it to meals
in restaurants. And it's just considered cultural convention, it's not
unusual to see that. So we don't see that so much here in the States
but I happen to really love this stuff. I brew my own, because that's
the most economical way to do it. And I really enjoy it. It can be a
little bitter for some people. The real key there if you want to know,
the Mate trick is to not use water that's really boiling hot. You go
just shy of boil and then it doesn't have that same kind of tobacco
like or really acidic flavor to it. It's just a little bit sweeter,
although not quite sweet. So, Yerba Meta GLP1, can manage in healthy
ways leptin levels, glucose levels, and glucagon levels in ways that
if it serves you, that you might want to try.
So once again, we covered an enormous amount of material, focused on
how hormones regulate feeding, hunger, and when one feels they don't
need to eat, so-called satiety, that you've had enough. As always, we
covered a lot, but I could not be exhaustive about all the information
related to this topic. It's just so vast. For instance, we did not
talk about thyroid hormone, an extremely important hormone and pathway
in the body and brain. We are going to do an episode related to
thyroid and tools to regulate thyroid, I promise. Having seen this
episode, you will be able to digest that material with far more ease.
We also didn't talk about the fact that testosterone and estrogen can
impact blood glucose in ways that are opposite to one another. That
when estrogen levels are high, appetite tends to be reduced. When
testosterone levels are high, appetite tends to increase. So there are
all sorts of interesting interplays between the various hormones. But
that's too much of a deep dive of now. Right now, we've just focused
today mainly on things like ghrelin, on things like, Melanocyte
simulating hormone, incredible powerful hormone that can suppress
appetite. On things like Cholecystokinin that comes from the gut and
can suppress appetite. On things like food emulsifiers. On the fact
that when you're eating you are amino acids seeking, even though you
might not realize it. That you are also seeking out particular fatty
acids in particular, the conjugated linoleic acids and Omega-3's. So
I've tried to give you a number of actionable tools. Many of them
behavioral. Some of them are based on supplements or even prescription
drugs. Again, always do what's best for your health, and do that in
company with a healthcare professional. I'm not a physician, I don't
prescribe anything. I'm a professor, I profess a lot of things. And I
try and share with you what I think to be the best high quality peer
reviewed literature. So that's what I've done today. Really appreciate
your time and intention.
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thank you for being with us. I hope you learned a lot. I hope you
explore some of the tools and that the mechanistic information that
you learned today will serve you well. If you know anyone that's
interested in this topic or you think that someone could benefit from
it, please suggest the podcast to them as well. And most of all, thank
you for your interest in science. [upbeat music]
Note: A future episode will cover Thyroid hormone. Also, I misspoke
when explaining POMC neurons. I said “P-M-O-C” but should have said
“POMC”. Apologies. The name I gave for what POMC is, however, was
correct: "proopiomelanocortin".
HubermanLab #Hunger #Hormones
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Links:
* Dr. Lustig’s Lecture - https://www.youtube.com/watch?v=nxyxcTZccsE
* Paper In Cell Metabolism On Processed Food Effects - https://doi.org/10.1016/j.cmet.2019.05.008
Please note that The Huberman Lab Podcast is distinct from Dr.
Huberman's teaching and research roles at Stanford University School
of Medicine. The information provided in this show is not medical
advice, nor should it be taken or applied as a replacement for medical
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assume no liability for the application of the information discussed.
[Title Card Photo Credit: Mike Blabac https://www.blabacphoto.com/]