The Peter Attia Drive - The impact of stress on our physical and emotional health | Robert Sapolsky, Ph.D. (#51 rebroadcast)
Episode Date: April 24, 2023View the Show Notes Page for This Episode Become a Member to Receive Exclusive Content Sign Up to Receive Peter’s Weekly Newsletter In this episode, Robert Sapolsky, Ph.D., discusses the widespre...ad impact of stress on our physical and emotional health as well as the mechanisms by which it can precipitate chronic illness, dementia, depression, and more. He also provides insight into the factors that contribute to the stress response (and our ability to handle it) such as social rank, personality, environment, and genetics. Lastly, we discuss how our behavior is altered in the face of stress and how that not only has a pervasive effect on a personal level, but also on society as a whole in how we interact with each other. We discuss: Background, interest in stress, and Robert’s time in Kenya studying baboons [2:45]; Physiology of a stress response, and why it’s ingrained in our DNA [9:45]; Individual variation in the response to stress, and how everyone has a different optimal level [19:45]; How social rank and personality differences affect our stress response [26:30]; What’s happening in the brain when faced with stressful situations? [35:00]; What makes the human brain different than all other species? [44:15]; Imprinting stress to your kids epigenetically [48:00]; The role of stress on memory and the consequences of hypercortisolemia [53:00]; The impact of subjective socioeconomic status and social media on stress levels and health [57:45]; Tips for managing stress in the modern world [1:13:15]; What Robert learned about himself studying the social behavior of baboons [1:25:30]; The multilayered factors behind every human behavior, the context of “good and bad”, and exploring the human capacity of the wild extremes of violence and altruism from moment to moment [1:30:15]; PMS: How two women with identical hormone levels can have completely different emotional experiences [1:34:45]; How much of a role do genes play in depression and other emotional states? [1:38:00]; Why is cortisol elevated under sleep deprivation? [1:46:00]; The impact of stress on cancer [1:50:30]; The impact of stress on atherosclerosis, dementia, addiction, and depression [1:57:00]; Impulsiveness, impaired judgment, and lack of empathy in times of stress [2:01:45]; What advice would Robert give his 25-year-old self? [2:08:45]; and More. Connect With Peter on Twitter, Instagram, Facebook and YouTube
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Now, without further delay, here's today's episode.
Welcome to another special episode of The Drive. For this week's episode, we're going to
re-broadcast my conversation with Robert Sapolsky, which was originally released back in April
of 2019, about four years ago.
Many of you may recognize that name because Robert has written some incredible books,
including the very popular, Why Zebras Don't Get Alcers, A Guide to Stress, Stress-Related
Disease, and Coping.
I had first seen Robert speak about a year and a half prior to my interview with him,
and I remember thinking during his talk, this is the first time I'm really
being convinced of the true pathology of stress.
You know, I think prior to that, I'd always heard the old adage that stress could kill you,
but I kind of dismissed it as, yeah, yeah, yeah, and we used to think that stress caused
ulcers, but then we found out it was H. Pylori, et cetera, et cetera.
But the way Robert spoke about it, I really began to pay more attention to it, which of
course led to me reading up on this more.
And at that point, I just decided I needed to meet Robert.
Robert's work, in particular, his presentation that day, got me to think about the molecular
and physiologic harm of hypercordisolemia in particular.
In my conversation with Robert, we spoke a great deal about that, but we also talked about
things outside of them.
We talked about the role of depression, what the impact is of stress on the developing brain, and also on the brain later in life.
And even on areas where the relationship between stress and disease is not that well understood yet,
that clearly came across in our discussion of cancer. Robert is a professor of biology,
of neurobiology, and of neurosurgery at Stanford. He's also a MacArthur fellow in 1987. He was
awarded the fellowship,
which some of you may recognize by its other name, the Genius Grant, something I consider
very appropriate for a man of Robert's talents. Overall, I found this discussion riveting,
and I hope to speak with Robert again, but for now, I hope you'll enjoy revisiting this discussion
as much as I did. So without further delay, please enjoy or re-enjoy my conversation with the
wonderful Robert Cipalski.
Robert, thank you so much for making the time to meet with me today on a lovely, rainy
San Francisco afternoon.
Sure, glad to be indoors here.
As I was saying earlier, we had met once before really briefly, so briefly that you would
not remember it, and of course, only I would.
Summer of 17, I believe you were giving a talk in Sun Valley and I was there and you gave a talk on stress.
Now, it was to a lay audience.
So you didn't really get to go into the depth.
And I remember sitting in the audience thinking, oh, you know, a lot of what he's saying is really starting to make sense to me.
And I can't wait to get a little deeper into this stuff because truthfully, and I'm just
going to open with sort of my meoculpa, you've always heard people say stress kills.
And I got to be honest with you.
I always thought that was sort of nonsense.
I was like, come on.
What do you mean stress kills?
Stress is good.
It builds resilience.
Oh, what is the mechanism by which stress, stress kills? Stress is good, it builds resilience, blah, blah, blah.
What is the mechanism by which stress quote unquote kills?
But of course, once you start to understand the endocrine system and of course training
is a surgeon and not an endocrinologist, I sort of missed out on that, you start to see
it.
And in that talk, you admittedly at a sort of high level for the audience really walked
through the danger of hypercordislemia.
And so in many ways, I guess a year and a half ago was really when I became a fan of your
work and then kind of said, you know what, there is something to this.
So anyway, with that, I appreciate you taking this time.
Sure.
And just to sort of back off a bit from that, I actually don't think stress kills you
out right very often, but it sure makes other things that kill you more effective at doing it.
Maybe it's semantic, but your right stress can amplify and accelerate the diseases of aging.
You grew up in New York, right? If I recall, you grew up in Brooklyn or in Brooklyn.
I remember reading that after college, you actually went straight off to Kenya first,
is that right? What prompted that? Well, I was one of those.
I've sort of spent my career oscillating between being a lab neuroscientist, studying
the effects of cortisol on the brain, punch line to decades of work, is you don't want
to have a whole lot of it marinating inside your head.
But also for more than 30 years, I've alternated spending my summers studying a population
of wild baboons in a national park in East Africa.
And it's the same animals I go back to each year.
These are animals I can dart to nest the tithes, get blood, do whole workups on them.
And essentially asking among them, what does your social rank have to do with patterns
of stress related disease? What does your personality, what does your patterns rank have to do with patterns of stress related disease?
What does your personality, what does your patterns of social affiliation?
So it's been sort of a counterbalance to the lab where, you know, we've been sticking
artificial genes into neurons and fairly reductive stuff like that.
So I was actually about eight years old when I decided I wanted to be a primatologist.
So I was kind of planning on that for a long time and lucked out.
I spent all of college brown, those in the right person who shipped me off to a field site
right after graduation and I wound up sort of inheriting that site.
And those have been my my baboons ever since.
Did you spend the whole time in Kenya?
I remember reading that you also were in Uganda and obviously there I think if my geography's
correct their neighbors so that's a pretty easy switch.
Where do the actual baboons like what is their scope of their residents?
How broadly?
Oh, there's spread actually all over Africa.
They're one of the most ubiquitous primates for a lot of the same reasons that we are, which is they'll eat anything
They're carnivores, but they're also perv or they're omnivores. They scavenge dead stuff. They eat insects
They'll they'll eat most anything so they can fill a lot of niches
So they're scattered everywhere, but my main work over the years has been this one troop in the Serengeti in Southwest Kenya,
you know, for about 25 years.
I camped under the same tree, so it's really, it's been continuity with the same population
of animals.
What is their natural predator besides man?
Leopards, lions, hyenas.
Nonetheless, if you were male baboon, the most likely thing to kill you violently is another male.
Yeah, exactly. Sort of like humans. Yes indeed. Did you say it's every summer or every other summer?
Well, it was initially for about 25 straight summers and then parenthood and all those complications
came in. So wound up being every other, and then our kids were old enough to go
with us one summer. But unfortunately, the field worked ended about eight years ago.
So why is that? My Kenyan field assistant of 30 years, we started together when we were
20. He died of AIDS, political issues there, some game park issues that made it harder and harder to get
researched on.
And that middle-aged realization, that I could find some new game park or new country or
something and start all over, but it was kind of time to pack it in instead.
So after you did your PhD, which you did in New York, right?
Yeah.
Rockefeller University.
Did you come straight out to Stanford for a postdoc or?
Postdoc to the Sock Institute at San Diego, spent a couple of years there with people
are sort of familiar with the hypothalamic hormone that runs the stress response, a hormone
CRH, CRF, corticotropin, releasing hormone.
I went and postdoc to this guy, Wiley Vale, who had discovered it in like two years before. So that was a pretty
exciting time to be there. So I spent a couple of years there. Stanford hired me.
And I've been there for 31 years.
That's kind of amazing. I keep coming back to people at Stanford that
you know, would have been there when I was there
in medical school, but if it wasn't in the medical school, like you just weren't paying as close
attention. I honestly don't recall if you ever gave us a lecture in med school. Do you remember
giving lectures in med school 20 plus years ago? I did, almost certainly, the students were paying
as little attention as I was. That's true, because that was about to say. It certainly seems like
something we should have been learning in medical school, And yet I feel ashamed to say, I don't
know if I recall it. It was not much of an emphasis and was sort of snuck in embarrassably.
Like a lunchtime seminar or something. Yeah, exactly. So that
thrived them with free food. That's an even still only about five people would stay past the cookies.
That's a much bigger issue we can come to.
So so you wrote a book.
Gosh, how many years ago was why Zebra's don't get ulcers?
That's that 20 years ago.
Let's see.
First edition was 94.
It's gone through three editions.
Now most recent one was 2004.
So at some point I got to do another one.
As we talk about that and you've written a book more recently that I want to talk about
as well, let's back up and explain something you touched on a second ago, which is sort
of the physiology of a stress response.
So walk us through the relationship between the hypothalamus, the pituitary, and the adrenal
glands.
So when we're under stress levels of 11-D different hormones change in our body. Most of them are relatively
minor players. The two workhorses overwhelmingly first one famously adrenaline, a British
term, epinephrine, sort of the North American term, output from the sympathetic nervous
system. It's on the scene in your bloodstream within one, two seconds or so after all hell breaks loose.
And I just want to explain what sympathetic means to the listener. We've had this discussion before.
It's not to say it's a nervous system that is kind. It just means it's one of the two branches of these so-called
autonomic or immediate, not under your conscious control, right? So the fight or flight.
Exactly. And the other half being parasympathetic, sympathetic
fight or flight, all hell breaking loose alarms going off parasympathetic, calm, vegetative function.
So not only do you turn on the sympathetic during stress, you very emphatically turn off the parasympathetic.
Second main workhorse, which is already been alluded to, the steroid hormone,
class of hormones called glucocorticoids, human version, cortisol, also known as
hydrochlorozoan, rat version, corticosterone, synthetic versions, prednisone,
dexamethasone and such. These come out of the adrenal glands, your brain, note
something stressful is happening within two seconds. Your hypothalamus is secreting
that CRH, which within about 10 seconds, is getting your pituitary to release a hormone called ACTH,
which within about 30 seconds has gotten to your adrenals and you are slowly starting the
glucocorticoid component of your stress response. And in lots of ways, the adrenaline,
the sympathetic response, the glucocorticoid response, they work on hand and hand, they synergize.
You want to metaphor adrenaline in two seconds as handing guns out of the gun locker,
to whatever it's going to defend you. Glucocorticoids are building the aircraft carriers that a year from
an hour are going to be essential.
It does some of the slower components of the stress response, stretching out over minutes
to hours.
Because I was just about to ask you, and I think your question basically answers it was,
why would we have evolved these two separate systems?
One can only speculate on such things, but it's basically that certainly nor epinephrine
epinephrine, they stick around for such a short period of time.
I mean, we don't even measure these things clinically.
I can't poke your arm and measure your nor epinephrine or epinephrine level.
The best I can do is collect its metabolites in your urine for evidence that it's been
around.
So I guess we have this hormone or pair of hormones that are on the scene in seconds, gone in seconds,
and really deal with the, I guess, from an evolutionary perspective, when the tiger is there,
this is what gets you to jump into the tree.
Is it doing much beyond that?
And is there some evidence of chronic low levels of those hormones, which come out of
a totally different part of the adrenal gland?
I mean, that's the other thing that's sort of interesting is you have two separate pieces
that cortex the medulla that secrete these hormones separately.
And embryologically, they're two very different tissues.
They start off separately.
It could have just as randomly wound up that your adrenaline comes from your big toe and
glucoticoids from your thumbs, why they wound up being in the same organ?
Um, is in fact somewhat just, I think, serendipitous probably because you're
more likely to have your toes and fingers lopped off.
And we wouldn't want to have an incidental adrenalectomy is happening.
You're right.
That's certainly why they didn't wind up out there in the
exactly lower species is one of these considered more primitive is the epinephrine
arm, something that began earlier and the cortisol
arm more recent?
Yep, nonetheless, the cortical arm is just ancient.
When you get stressed in your secreting glucoticoids, it's basically the exact same class of molecules,
as if you were a fish or bird or reptile, nonetheless, it's very ancient wiring, and that's
part of what winds up
getting us in trouble. It's a system that's been serving vertebrates, doing a lot of help for
them for an awful long time, and it's been a very recent modification, doing instead secrete them
in response to thinking about taxes. This basic dichotomy between the very human domains where we activate the stress
response and the more typical domains of animals.
So, if you and I were sitting here 10,000 years ago, I can think of lots of things that we
would want an adrenaline response for, you know, the tiger jumps out of the thing, whatever.
What are some of the things that would result in that cortisol response? Because, describe that it is building the aircraft carrier well, gosh, if the tiger's
there, either I'm dead or I'm not, but I don't need a stress response a day from now or the next day.
So what is it that cortisol was doing 10,000 years ago that was serving our interests? I want to
certainly talk about what it's not doing today. When you look at what it does, it actually makes perfect sense.
As long as you're being stressed like a normal mammal, running for your life, running after
a meal, where if you don't catch something, you're going to be dead by tomorrow, a short-term
physical crisis.
The first five seconds of doing that, which Epinephrine is critical for. That's great. If we're heading into a couple of minutes of
evading a predator, being vigilant, thinking there might be, if you're getting into the realm of
a couple of minutes worth of the stress response, cortisol-related glucose-quartiquant hormones
are absolutely essential. So the glucose that's coming rushing out of your liver pretty important
in that situation.
Exactly.
So it takes you about one second to decide you're going to use your thigh muscles and run like
mad.
You need energy for them.
And the main thing Glute corticoids are doing in the metabolic realm is collucocorticoids.
They're increasing glucose levels in your bloodstream.
They're going to storage sites throughout your body,
or liver, your muscle, and breaking stuff
that what they do is they go to the bank,
they empty out your savings accounts
and turn it into cash.
Glucose in the bloodstream to hand to whichever muscles
are good to save your neck.
What they also do makes better perfect sense
with where you were running for your life,
or running for a meal,
which is they increase cardiovascular tone.
And epinephrine is doing the first five seconds of it
by 30 seconds in glucocorticoids,
you're bolstering it as well.
And it's that same logic,
you're running like crazy,
you want to deliver that glucose to your thigh muscles
as quickly as possible,
you increase your heart rate, you increase your breathing rate, your blood pressure, you alter your vest
lecture so you're preferentially shunting to the exercising muscle.
So that makes perfect sense also.
Turns out some of the most interesting stuff glucose cordicoids do in those circumstances
is basically run a triage program.
They shut down everything that's not essential,
not essential to surviving the next five minutes of this massive physical challenge.
So digestion would be a major.
Exactly. You got better things to do than digest breakfast when you're trying to avoid
mean somebody's lunch. And you're sure not going to get any metabolic benefits of digestion during this five minute.
It's slow, expensive, the energy you're getting, you're getting from your liver, you're
getting from your fat cells.
It shuts down growth.
Obvious logic there, you know, grow antlers tomorrow, if you're still around to embalm
right now, shuts off reproduction.
Same logic there.
It shuts off all the long-term building projects
and just focuses your energies on what's immediately there.
And this makes perfect sense.
If you are running for your life, running after a meal,
and all you need to do is look at a couple of diseases
where people don't turn on the endocrine stress response,
had a sins disease, shideide Raker, Syndrome, whatever.
These were not diseases where somebody,
who now is more at risk for adult onset diabetes
eight months for now.
These were diseases where somebody goes running
after their commuter bus and they dropped
at from hypicalycemic shock.
JFK had this, didn't JFK have Addison's?
He had Addison's and that greatly constrained
the famed pictures of all those
Kennedy's playing touch football out.
And you know, Martha's vineyard or stuff were mostly for the benefit of the
photographers.
How did he survive World War II?
Because he had done some pretty heroic things in that war.
Although I've seen it's hard to tell if it's snarky revisionism as to how much
that was public relations stuff afterward sort of orchestrated. But just to get through basic
training even strikes me as an accomplishment because most people I guess who don't have a
medical background wouldn't appreciate this but the tan that seemed to be eternally on JFK
is the result of the Addison's disease because the hormone you alluded
to earlier that is released by the pituitary ACTH in someone who's not making cortisol
is going to be very, very high.
And ACTH stimulates the pigment producing cells in the skin, and that's what would give
someone with Addison's Digi's darker skin.
The fascinating thing with Kennedy is if it were this situation now, presumably his doctors
would be on the air somewhere 24-7.
There's remarkably little known about when his onset was, what the course of it was, how
severe it was.
It's not quite clear, but what little is known is it had a hell of an impact on his functioning.
You really do need a hormone if you,
like, glucorticoids,
if you were gonna be physically activated
in a moment of crisis.
This is sort of the amazing thing with hormones
like insulin and cortisol.
I'm always impressed by how tight the u-shape is
on those curves.
Thyroid hormone would be another example.
Certainly less so with something like testosterone.
You have just a much wider range that you can function in, and the benefit is largely
monotonically increasing.
Sometimes if my patients will tolerate me going on and on about this, I love to draw
the pictures of which of these hormones can you, you know, but to me, cortisol probably, if you thought of it as a drug,
it has the narrowest therapeutic index. To your point, too much of it will kill you eventually
and make you miserable as hell on the way, and too little of it will kill you quite quickly.
And what's most interesting about it is, okay, so there's an optimal level,
among other ways of translating that, That means we don't hate stress.
We hate the wrong amount of stress.
When it's the right amount, we love it.
We pay money to be stressed to get on a roller coaster, to go to a scary movie, when it's
the right amount, when it's the optimal amount, we call it stimulation.
Okay, so exactly as you say, it's a narrow range. So that's a tough biological problem
understanding a
hormonal system that's pretty damn essential and wear an awful lot of the time you're walking on an eye
Fidge where either side is bad news too much or too little
But when it comes to glucoric oids and what counts as good stress and stimulation
corticoids and what counts as good stress and stimulation, there's the added factor that there's incredible individual variation as to what counts as the optimal level in between.
And one person's like hair raising, autobahn, society, walk one Saturday morning looking
for birds while the other person goes and signs up to be a mercenary in Yemen, because that's
when they feel alive and awake and all of that, not only that it's a narrow range, but we differ
so much as to what each person's optimum is.
Now, I want to make sure I understand that point, Robert.
And this is probably overly simplistic, so feel free to correct this.
One of it would be the external scenario that is being perceived.
And I can see definitely how two people can have vastly different views on that.
I mean, it's the reason someone can voluntarily go and be a Navy seal and someone can say,
I feel much better not doing that, right?
There's clearly a different appetite and or capacity for distress.
Is that what you're referring to?
Or are you also referring to you and I could be sitting here
and have different levels of physiologic benefit
and harm at the same level of cortisol?
Both.
Nice.
Absolutely.
So I mean, the former, I think most people would acknowledge,
the latter is pretty new, right?
I mean, I shouldn't say pretty new.
That's not intuitive to me.
Because there's centuries of endocrinology saying, what's the most important thing about
hormones?
How much of the stuff there is in your bloodstream?
What the levels are, and if you and I are sitting here with the same circulating levels
of whatever, centuries of dogma was, that will translate into the same biological effects.
And then, I don't know, sort of endocrine revolution of 70s, 80s or so, turns out how loud someone
is yelling at you, counts what the hormone levels are, how sensitively you can hear them,
the levels of your receptors.
In target cells, turn out to be essential as well. And there's all sorts of
endocrine domains where in fact, scrui receptor levels are much more consequential and impactful
than our scrui levels of the hormone itself. And individual differences in levels of receptors,
what version you have, how well it works, how avatally it holds on to the
hormone, what it is then coupled with afterward downstream inside the cell. That whole world turns out
to be as central to understanding individual differences as are the levels of hormones themselves.
And as sensitive to all those things ranging from genes to prenatal environment to early
development to psychological factors and so on.
So yeah, that's a huge piece of the story now.
When I hear you say it like that, Robert, it seems pretty obvious because we would talk
about insulin in exactly that way.
You could have two people with the exact single level of insulin, completely different physiologic response because of
insulin sensitivity. When insulin hits its receptor, it leads to the phosphorylation
of AKT, and that's what leads to the Glute-4-Transporter coming up to the
surface, and different people with the same insulin can do that totally
differently, and different people will have a different insulin response to the
same food, the same meal. That's the reason we do glucose tolerance tests. So you could basically say,
someone is cortisol sensitive and cortisol resistant to make the analogy to insulin.
At the end product end, absolutely. If you're an obsessive with cortisol stuff,
in the 80s, there was briefly this deep puzzle in that it turned out new world monkeys,
monkeys in South America, marmosets, tamarins or whatever, when you compare them to traditional old world
monkeys, the Asian and the African ones, turns out they have like an order of
magnitude higher glucocorticoid levels. Oh my god, that's crazy what's that
about, all sorts of theorizing about how for some reason it's more stressful to
be a new world primate than an old world which didn't make a whole lot of sense.
And then there was this issue of these animals should have been falling out of trees from
there, their cushing's disease.
And finally, somebody found an explanation.
No, somewhere back when there was a mutation in the gene for the glucocorticoid receptor
in new world primates and it has roughly one-tenth the sensitivity.
So the system just equilibrated out at a different set point, but that's such a great example
of just natural variation, not only in how loudly you speak hormone, but how effectively
your cells listen to hormone.
Do you have a sense in the human population today? I mean, a
log-fold difference that you just described sounds extreme. But do you have a sense of what the
variability is in humans today? Is it a two-fold, three-fold delta on the receptor side?
Gut feeling and reflecting the fact that my world, the brain, you don't get to measure receptor
levels anywhere near as easily as in a white blood cell, well under an order of magnitude.
We just acknowledged, or you just pointed out, that when a zebra sees a lion, everything
that happens as far as the fast end, what I would call the acute and the subacute stress
response, is perfectly evolutionarily sound and completely in the best interest of
that zebra.
We could also come up with a countless examples of 10,000 years ago, or even today, when
the same thing is true in humans.
When did that transition occur in our species to where you started to see either something
in the civilization or society that was unhealthy?
So today, I could point to a thousand examples, social media, you name it.
I mean, it's an infinite number.
When did that start to crop up?
What does your research suggest is the arrival of that?
I think it predated us being humans.
And instead is a feature of smart social mammals. Because you see indices of stress-related stuff,
bad wounds, that's what I've spent my whole career on,
and other non-human primates, cetaceans, elephants, and such.
Okay, so why study bad wounds if you're trying
to understand human stress?
And it turns out they perfectly illustrate the point
you just brought up.
If you're a baboon
living in the Serengeti in East Africa, your life is pretty good. It's a fantastic ecosystem.
Baboons, they live in these big troops, 5,200 animals or so, so they really don't have to worry
about lions very often. The infant mortality rate is lower than among the neighboring maceye tribes people, and
probably most importantly, unless it's a once-generation drought.
If you're just a bad wound going about your everyday business, it takes you about three
hours a day to get your days calories.
And that has a critical implication, which is if you only need to spend three hours of sunlight each day, getting enough food to get by, you've got nine hours of free time every day to devote
to being miserable to some other baboon.
And that's the key thing.
They are well off enough in our westernized sense that they consider around and generate psychological stress
for each other.
Overwhelmingly, if you're a baboon in the Serengeti and you're miserable, it's because
another baboon has worked very hard to bring that state about.
They're wonderful models for westernized disease.
In that very few of us get hypertensive because tigers are chasing us.
Instead, it's psychosocial stuff that we invent and that we can wallow in for hours every
day.
And that's exactly what bagoons do through great models for Westernized stress.
Do we have evidence, I'm not sure it exists, but in the humans, I would just be willing to
bet that if you and I were subjected to the same external stressor, I would just be willing to bet that if you and I were subjected to the same external stressor,
I would probably internalize it more than you. That's my guess. So if we were both baboons and
there was a third baboon tormenting us, is it safe to say that you could be the baboon that would
roll with it more than me? Individual differences like that, absolutely. My guess is both of us would
respond to it by saying, I'm just going to get a longer, a longer CV and then you
just got to regret it someday, pushing me around. They'll be sorry when they see how many
degrees I have. But yeah, individual differences. One of the things that I focused on, you know,
I spent my first 10 years deciding rank and status, social status, everything.
If you're a baboon and you got a choice in the matter, you want to be high ranking because
on the average, you have lower glucorticoid levels, you're resting blood pressures, lower,
all sorts of stuff works better. But what took me some growing up out there to do
was to realize that yeah, social rank is important. Far more important
is the contextual meaning of your rank. Is that the same as your perception of your rank,
or is there there's more to it, right? Well, it's what the rank means in your particular troop.
You can be a low ranking guy in one of two different troops and one troop simply because of
its culture. And that's a perfectly
scientific world word to use for another species these days. In one troop being low ranking could be
a whole lot crappier than in another troop in terms of how often somebody in a bad mood
displaces aggression on you in terms of how often somebody actually grooms you and off in terms of how often you get to finish a meal
before somebody steals it from you kind of thing. So the same exact rank means different things in
different sort of baboon cultures. So I'll take an extreme example. In a prison, there's a clear
hierarchy starting with the warden, the guards, the inmates, and of course within the inmates, there's
a hierarchy, presumably I'm making this up, but certainly the pedophiles the guards, the inmates. And of course within the inmates, there's a hierarchy,
presuming I'm making this up,
but certainly the pedophiles would be at the bottom
of that list and a violent criminal
would probably be at the top of that list.
So within that hierarchy, there's probably a manner
in which you would be perceived as a function
of that unique environment,
which is so artificial in its own way,
but that wouldn't necessarily
be the same outside.
Absolutely.
And one of the most interesting things about us, us humans, when we talk about what across
all sorts of primates being low ranking in general is bad for your health or what about
humans we don't have ranking in the same system that sort of other primates
do in a strict linear kind of way. But the other thing about us is we belong to multiple
hierarchies at once, and we can have very different ranks in them.
So for example, family work sports team.
It's happy.
You've got some guy who's the mail room clerk in this giant corporation and you could not possibly
be lower status, but he's the captain of the company softball team this year. And you better
bet when you ask him what's important in his life, nine to five Monday to Friday is just
a stupid way to pay the rent and what really matters is when the weekend comes around,
you have somebody with a horrible,
low status job who's the deacon of their church. We belong to multiple hierarchies and
we are very good psychologically at deciding that whichever hierarchy we're highest in,
that's the one we define ourselves by.
Let's take another extreme example, which is you take people who are very successful in what they do, you know, whatever they're the most famous hedge fund manager or an entrepreneur that started some great company, you would argue.
Well, they seem to be pretty good on the food chain, but yet many of them would say or you could measure objectively their hypercordosolemia is problematic. So it seems like there's even more than just that ranking, right?
Isn't there something else?
Because they're at the top, if they were baboons, they're the alpha, but they're still
grossly stressed out.
In other words, thank God we're more subtle than baboons, but it turns out baboons are
even more subtle than just rank.
They have personality. And you can be a high-ranking baboon,
and personality differences. And again, this is a scientific word as this culture.
If you're a high-ranking baboon, and you're worst rival sneezing a hundred yards away,
as seen as a major provocation, you're going to have much higher,
good, corticoid levels, than if you're a highest ranking
baboon for whom that's no big deal. And in fact, often,
you may have higher glucoticoid cortisol levels than if
you're number 10 or number 20 on the hierarchy. There's lots
of psychological filter stuff. And I spent a ton of
time studying that baboons differ as to how readily they
see things as being provocative or not,
threatening or not.
You're sitting there and again, your worst rival shows up and takes a nap 100 yards away.
There can be two baboons of the same rank and one of them keeps doing exactly what he's
doing.
And the other one is interrupted from whatever nice social thing is happening. He's agitated and he's doing. And the other one is interrupted from whatever nice social thing is happening.
These agitated, these vigilantes got to look at the guy and lunge towards him a couple of times.
If we're going back, if you're worst rival taking a nap is as disruptive as the guy threatening you
in your face, you average about twice the cortisol levels in your bloodstream after controlling
for rank as a guy who can tell the difference between the big thing and the little thing.
Maybe this is too deep a question and the answer isn't known, but what is it that actually transmits that information
through the filter of your personality into the physiology that's very well understood. So I understand the book ends, right? I understand how the visual cortex takes the guy who's your enemy sleeping over there and transmits that to your cortex.
And then I understand how the sympathetic chain kicks off the response. Is there a link in between those the processing link?
Here's one of those filters. You take people and you're flashing up faces at
them, stick them in a brain scanner, and you're looking at how jumpy their amygdala is. Their amygdala
central to fear, anxiety, aggression, and such. And what you see is tremendous individual
differences in you show somebody a face with kind of a neutral expression, does this person look happy,
sad, angry, threatening, whatever, and lots of variability. And you look at the people who tend to
view neutral expressions as threatening. In other words, they see threats that most other people don't.
What is that correlate with a bigger amygdala? Physically larger amygdala.
A physically larger amygdala amygdala with a higher metabolic rate and amygdala that
is more electrophysiologically reactive than stuff.
Let's back up for a moment. I mean, tell people in case they don't know where the amygdala
sits, what part of the brain it evolved from and why it's sort of referred to as this
reptilian brain. I think everybody's heard of the amyg evolved from and why it's sort of referred to as this reptilian
brain.
I think everybody's heard of the amygdala, but I think you could explain this in a more
interesting and accurate way.
Okay.
Amygdala is like one of the anchors of what's called the limbic system in the brain.
Limbic system, it's the part of the brain that's all about emotion.
Not surprisingly, mammals have a whole lot more
limbic development than fish do.
Fish are not famous for their emotional lives.
Limpic systems, arousal, fear, anger, lust,
love, maternal, pair bonding, mother, infant bonding,
all of that, and it's a whole series of structures.
Not surprisingly, ancient in mammals, infant bonding, all of that. And it's a whole series of structures, not surprisingly,
ancient in mammals, not surprisingly, highly complex interconnected, not surprisingly sitting
underneath the cortex, the cortex that more recently evolved part of the brain that does your
taxes, all of that limbic system underneath there, all this subterranean emotion stuff.
And a migdala is one of the key limbic structures and it's involved in fear. It's
involved in anxiety, it's involved in aggression. You learn to be afraid of
something or somebody that didn't use to scare you. And you're
remigdled as the exact same sort of cellular basis of learning that goes on
another part of your brain when
you learn somebody's middle name and actually remember it.
Your amygdala learns to be afraid of new things.
And when you manage to stop being afraid of something, when you stop being afraid of
thems because it turns out, oh, they're actually more similar to use than you thought there
are some say, it's your amygdala that becomes less reactive to stimuli like that.
So your amygdala is absolutely central to some of our worst human moments.
It's so interesting because it's sandwiched between, you know, you can think of the human
brain as having sort of very grossly three parts, right?
This brain stem, this mid brain, which the amygdala, you could argue, is the mayor,
and then the cortex that you describe, it's not an oversimplification, I think, to say that as
the complexity of the organism evolved, so too, did that hierarchy, right? I mean, the brain stem basically
handles everything we don't have to think about ever, breathing, and all of those autonomic, and
sympathetic parasympathetic functions. And then you layer on this midbrain that does everything that you said, which is still
kind of happening beneath consciousness.
And then of course, there's where most of us live in our cortex where we think we live,
which is we're thinking these thoughts, but it seems we're maybe not as aware of how
influenced the cortex is by what lies beneath it.
Exactly. Which is incredibly important.
If you think of this kind of ancient reptilian brainstem part of the brain, what does it
do?
It keeps track.
It makes you breathe every now and then without having to think about a boring sort of stuff,
then on top of the emotional limbic system, then on top of that cerebral thinking, cognitive
cortex thing.
It's very easy to come up with a conceptualization that what's fancy about humans is, for example,
you're a lizard, and the only thing that's going to change the functioning of that ancient
brainstem stuff is if you're bleeding, if you're too hot, if you're too cold, just like
boring physiological states, once you layer a mammalian emotional
limbic system on top, suddenly you can do something no visitor on earth can do. You're
sitting there and you're some will to beast and some other scary will to be shows up and
is peeing on some tree in your territory and nothing regulatory has changed in your body, but your heart starts beating faster.
Aha, your emotional brain can alter sort of the basic regulatory stuff down on the basement.
Now you go one step higher and you lay where a cortex on top of it, and now you could do amazing
stuff. You sit there and you think about the fact that your heart's going to stop beating
someday. And you start breathing faster. And your brains, then the more ancient stuff has altered
as a result. And you've just done something not only that no reptile can do, you've just done
something that no warthog can do, which is think, think about something that's scary or arousing or remember the time
that you would, and suddenly something changes down below there.
So there's this easy picture of sort of top down complexity once you get to us and where
the cortex can regulate your emotional brain and that regulatory brain at the bottom,
your emotional limbic brain can regulate what's far more interesting or underappreciated.
This is exactly what you bring up, which is those lower levels can influence what's going
on up above.
One example of this, this is like this classic, great study and sort of physiological psychology, social
psych. You take people, and I think in the study, they would take male volunteers, heterosexual
male volunteers, and of course they were no doubt college freshmen taking psych 101. And
they had these guys walk across this really scary suspended bridge. And the deal was that either halfway across the bridge,
you were met by from the other side of researcher
who happened to be an attractive female.
And she would ask the volunteer some questions,
and what do you think of this bridge,
or how is it walking across this, or whatever,
the other half of the time you would not encounter
this person until you were safely out of the other end.
Then they would ask you to evaluate the attractiveness of the person.
Same person.
That same person.
Seeing her in the middle of the bridge or at the far end.
Exactly.
Say, hey, remember while you were doing that, there was this, you know, do you want to rate
her attractiveness?
Was she friendly?
Did she seem smart?
And what you would see is guys in the middle of the bridge with their hearts racing because
they're terrified would do some misinterpretation.
Why is my heart beating so much faster than if I was standing safely?
So they would rate her more attractively in the middle of the bridge?
Exactly.
And then the ceiling of detail is now you do the same experiment, and you give the person
a beta blocker so that they don't have the accelerate, and they don't rate the person
as attractive.
Is it the same with the beta blocker?
You would treat you.
You do nothing to their ratings of them as how smart they seem, how kind they seem, whatever
it's just this, okay, if my heart's racing it must be because
so that's a great example boring reptilian regulatory stuff down there is helping influence what
do you think your emotions are that reminds me of the 1995-ish movie speed with Kiano Reaves and
I'm blanking our name. Bullock.
That's right, center Bullock.
Yep.
We're at the end of that movie.
There's some cheesy line about how relationships that start under this much distress, you know,
it's dangerous.
But, but of course, the other read on that now is, yeah, if you're on a bus that's about
to blow up, like, I think you're going to think the chair is attractive, right?
Potentially.
Yes.
Wow.
I have a photo that moved me in years. Thanks.
I'm sorry.
That was so.
You can go home and I'm sure Netflix will stream that for a while.
Right.
So I've read something you wrote. I can't remember where it might have been in another interview
that, and I didn't know this. And this is a great example of why I just love doing this podcast
because there's never an exception to how much I'm learning. It's like drinking from a fire hose. And you'd
think I would have remembered this from medical school. The neuron of a human and the neuron
of some other organism, when you look at it at the single cell level, can't really differentiate
it. If I showed you two microsubsides and here's a human and here's a fish, huh?
So what is it about and this is maybe getting us a little off topic, but I also think it feeds into this broader
Issue of like the stew and the alchemy of how this stuff is put together But if we all have the same neurons what is is it the number of our neurons like what is it that enables us to have?
All of this additional torture? Yeah, it's incredibly interesting because I mean, there's there's three and a half people
on earth who have spent their entire careers being able to tell the difference between like a
tree-shroom neuron and a human neuron and could recognize it and their sleep. But yeah, for the
most part, we are not humans because we have invented brain
areas that you don't find in other mammals, or because we've invented neurotransmitters that
you don't find in other vertebrates, or types of neurons. Here's a couple of types of neurons
that people use to think we're specific to humans, and it turns out you find them in elephants,
and whales, also, and that's plenty interesting. But it's the same enzymes.
It's the same gene regulation.
It's the same, you know, we're sharing 98% of our DNA with a chimp or a binobo.
So you say we're going to humanists come from.
And I think it's exactly the issue you talk about.
We have the same signal, transduction pathways and neurons, as you see in a fruit fly.
And what's the key difference?
Isn't that a bit humbling when we just think we're that special?
And it's the where you can take one of their genes or one of our genes and stick it in
the other one and it functions just fine.
Or you could take it from a single cell organism, some genes related to program cell death, you can do that. So what's the big difference for every neuron
that a fruit fly has, we have a hundred million. And sort of the sound bite that
I think summarizes all of that is with enough quantity you invent quality. And
this is this whole world of emergent properties of complex systems.
You take one ant and you put it on a table and nothing that it does makes a huge amount of sense.
And you put 10 ants there and pretty much the same thing and you put on, I know, a thousand and maybe
they start making a trail or something. And you put 10,000 and they build a colony, and they farm mushrooms,
and they take aphids as slaves, and they could keep the temperature in the colony, plus or minus
two degrees, and they have specialization of labor. And no ant has any more rules than he had when
he was watering around on the table by himself. And you put enough of them together and complex adaptive stuff
emerges out of the very simple rules that each of those components has for dealing with
another component. It almost defies entropy, doesn't it? Like, why does that happen?
It's amazing that it does that. And that's what our brains are. We've got more ants that are
coming together in our heads than does a fruit fly and you get more
Complex emergent stuff happening. It blows my mind. So let's go back to some of this stuff
Maybe about a year ago I read something that really frightened me because the implications were so significant
If a mother is under great stress
There was this critical window in which her child could see something
in her eyes that would communicate that stress to her or maybe it wasn't in her eyes, maybe it
had been just through her entire face, but it would imprint epigenetically into the child
and alter many features about them as they would age, for example, their propensity to be depressed.
I mean, I remember reading this in sort of a lay press thing, so I don't even think
it got into the description of epigenetics, but that was the only assumption I could make
was that this must be modulated through that mechanism.
Do you see evidence of this in animals?
I mean, it's absolutely.
And it's one of the trendiest topics around, like, hooray science finally recognizes childhood matters.
Like what your child is like has a lot to do with what sort of adult you're
going to wind up being what do you know?
And like lots of childhood adversity versus childhood security and, you know,
very different trajectories.
And what's been the huge mechanistic challenge for the field is understanding,
so what is it about being in a scary neighborhood
or an unstable home or having a parent read to you?
Or what is it about this whole world
of developmental individual differences?
What are the nuts and bolts changes that occurs in a kid?
So that as an adult, they are now
30 fold more likely than the next person for this or that to happen to them.
And this whole trendy field of epigenetics, which is early experience doesn't change
your genes, doesn't change your DNA sequence with some like, you know, circus trick exceptions.
You've pretty much got
your DNA sequence forever.
What epigenetics is is early experience changing the regulation of your genes.
How easily you turn certain genes on, how easily you turn others off in different parts
of your body, different parts of your brain, and so on.
And that's exactly the sort of domain where you see the sort of stuff that you
outlined. So that, for example, if you're a fetal rat and you that rat
have made a terrible decision, you've picked the wrong room to be developing
in and you happen to be inside a mother who's highly stressed.
She's secreting a lot of
rat glucocorticoids, which get into the circulation through the placenta and to the fetal circulation
into the kid's brain. And one of the things that it does is it causes an epigenetic change
in the amygdala. So is that rat going to be born with a larger amygdala or is the phenotype
more complicated than just size?
It size in a bunch of other things as an adult, it's going to have a bigger amygdala and it's going to be more
excitable and it's going to be more prone towards interpreting a neutral situation as a threatening one
that's virtually the definition of rat anxiety disorder seeing menace that other people don't. And you see much the same evidence
in humans by now. Early experience. Forget early experience. What kind of kindergarten teacher
you had. This is fetal early experience. And this is exactly a domain where you get potentially
a lifelong epigenetic effect. Okay, so that turns out to have a hell of an
implication that's just the most exciting subfuel around there by now. Okay, so you were fetus
and got exposed to lots of mom's glucocorticoid levels. And as a result, as an adult,
you've gotten a large domicula, and you see threat all over the place that other rats don't.
And among other things, you secrete elevated levels of glucocorticoids, because the world is full of menace that only you are seeing.
So you get pregnant, and during your pregnancy, as a result, your fetus is exposed to elevated glucocorticoid
levels.
And to be clear, it's not because you have altered the germline genome.
It's that you have changed the expression of the gene, which has altered the phenotype,
and now that phenotype is being passed generation to generation through parallel expression. Exactly. Something term non-genetic transmission of traits non-mendelian.
And people have now shown some of those traits. You see that ripple. It gets
smaller each generation, but it's their half a dozen generations later. And the
exact equivalent of some of these have been found in humans. In other words, individual differences are arising not only from experience, but from
the multigenerational transmission of some of the consequences of experience, which is
just mind-boggling that that can work that way.
Let's go back a little bit to why this is problematic.
So at the outset, we alluded to this idea that it's a misnomer to say stress kills.
I'd love to hear if you have a particular definition of stress.
I probably butcher this stuff, but I sort of think of stress as the external thing, and
I think about it as it's anything that is sort of emotionally or physically either
chronically or acutely distressing.
I mean, that's sort of a dumb definition because it contains the word stress,
but I think people understand distress
a little more than they understand stress.
But of course, it's your response to that
physiologic response, right?
Which is so let we can quantify this stuff
in terms of what hormones are happening in the body
and how the hormones are moving the body.
It's your response to that that probably has a greater impact on your health.
So let's go through three things.
Help me understand how hypercordicellemia and or it's accompanying features will impact
the brain, especially well through any timeline you want.
I'm obviously interested in the aging brain, but I can't imagine this also doesn't impact the developing brain. This is basically what I've spent my whole
professional career thinking about. And historically, the first place where people sort of realized
something scary was happening was a brain region called the hippocampus. Hippocampus is all about
learning and memory. You want to have a hippocampus. It'socampus is all about learning and memory.
You want to have a hippocampus.
It's the main brain region that's damaged in Alzheimer's disease and it's vulnerable
in lots of other ways.
Turns out it's extremely sensitive to glucoricoids, translated more reductively.
It's got extremely high levels of receptors for glucoricoids by the standard to the rest
of the brain.
And what's the evolutionary basis for that? Is that to have a feedback loop?
There's two reasons. One is to have a feedback loop, but the other is, okay, so the hippocampus
remember stuff for you. You don't remember everything. You don't remember where you were on 9,
10 as opposed to 9, 11 kind of thing.
Your memory processes has to come with a filter saying, is this one important?
So you're saying the cortisol amplifies memory consolidation and that you use this to consolidate
stressful memories as a way of learning. Exactly. Along with epinephrine and neuroepinephrine
indirectly, they have some of the same effects. So cortisol crosses the blood brain barrier with no difficulty?
Exactly.
I assume epi and norepi do the same.
They have to work more indirectly heavily through the vagal nerve because they don't get
them as readily.
But some of it is also neuroepi being released within the brain during stress.
So it has some of its own memory enhancing effects.
Again, a great example of evolution's got this awesome system set up and it only gets out
of whack when the stimulus becomes too much.
You do want that imprint, but you don't want that happening full time.
Or stated another way, this is the reason why you don't get much out of a class if you're
semi-comatose and you had two hours of sleep last night. If you're like three-coordinate, your glucororoid levels are low, you're semi-comatose and you have two hours of sleep last night, you're, if you're
like three-coordinate, your glucoricoid levels are low, you're not consolidating stuff.
If you are out of your mind terrified because there's a lion sitting next to you, you're
not going to absorb much either.
Inverse, you optimal range, all of that.
So it turns out the optimal amount of glucocorticoids, something that is moderately stressful, in other words,
something stimulating, does great stuff to your hippocampus.
It increases blood delivery there, glucose, oxygen, it makes the synapses, the connections
between neurons more excitable in the hippocampus.
Does great stuff, a little bit of arousal alertness is a good thing for learning and memory.
Now instead, transition to your stressed 24-7 ever since you were like 10 years old kind of thing,
and you're in the range where glucose quarts do exactly the opposite. They decrease oxygen and glucose
delivery to the hippocampus. They make neurons less excitable. They disconnect
synapses. They cause the processes in neurons to shrivel. They block the birth of new neurons
there. They make other insults more damaging to neurons in the hippocampus. What do you
have there? That's the world in which, if you were stressed out of your mind, memory doesn't work so hot. And what we're increasingly
realizing is, if you're exposed to excessive glucoticoid levels, like on the scale of years to decades,
you're going to make this part of the brain get older faster. Which speaks to something that I know
you're quite passionate about, which is the differences in how socioeconomic status
can sort of affect generational changes in this manner
because you know, use the example of a 10 year old.
Well, I did my residency in Baltimore.
Let me tell you a 10 year old in inner city Baltimore
who's in the wrong house versus a 10 year old in Palo Alto
who's in quote unquote the right house.
And look, that's not to say that you could have a 10 year old in Baltimore that's got a great environment and 10 year old in Palo Alto, who's in quote unquote, the right house. And look, that's not to say that you could have a 10 year old in Baltimore that's got a
great environment in 10 year old in Palo Alto that's dealing with a whole bunch of other
different issues, which, you know, especially in the air of social media.
But all things considered, probably, realistically, that 10 year old in Baltimore is going
to have a much harder time given what you just said.
Or I don't know if stated the other way.
I have a friend who's a cardiologist who splits
his time between a hospital in Oakland and a private practice in San Francisco.
Some of the time what he's doing is dealing with eight-year-olds who are considering getting
a pacemaker because the ski season is coming and they are wondering if they're going to
be in shape and time for that and maybe and then back in Oakland he's dealing with 50-year-old elderly men who are having
heart disease. Yeah, socioeconomic disparities are I won't get on my soapbox now.
When you look at the source of variability and health among humans on this planet,
socioeconomic differences, differences in absolute levels,
differences in degrees of inequality within cultures
and within communities and so on,
as an enormous predictor of health.
You want to look at the most medically impacted,
low-ranking primates you could find on Earth,
look at poor humans. Because when
humans invented socioeconomic status, and the capacity to be poor, they invented a way
to subordinate the have-nots like no-chimp on earth could ever dream of doing.
As you've alluded to, there's something else to it. You know, recently I interviewed
an amazing physician named Tom Katena, who practices in the new Bammoutons in the south of Sudan.
He's the only physician to take care of one million people who, as you know, are being
killed by their own government.
Bashir is indiscriminately killing these people.
My discussion with Tom was one of the most riveting discussions I've ever had with a human
being.
It just happened to be in front of a microphone.
But one of the things that just as an afterthought we were discussing that surprised me
is we were going through all of the different things that people die of there.
They don't have vaccines.
You've got measles outbreaks that are killing people left right in the center
and the trauma, like, you know, the shrapnel blowing people apart.
Not surprisingly, they're just not getting the same chronic diseases, you know, and the cancers they get are not the cancers
we get, and they're not getting heart disease, and they're, you know, almost unheard of to
get type 2 diabetes. But what really surprised me is there was no suicide. And I found that
as the single most interesting thing I, yes, I learned from Tom, which was, we would look at their life and think, that is an abysmal existence that I couldn't tolerate for
one second.
And yet, I would have to guess that their level of cortisol might be lower than ours, even
though they're in a much worse environment.
So whether it's that sense of community that they have or the shared purpose, there's something about it. So in other words, my point is, even in the presence
of such great poverty, it seems that there's ways that this can be overcome, whether it's
through there's no comparison to anybody else because another point he made was most of
the folks there don't even know they're in Africa. Like they don't necessarily know that
Africa is the continent in which their country resides. So is the bigger issue there, you think that there's no disparity. So even though
that's complete poverty, there's no real perceived disparity. Or do you think it's the sense of community?
Like what would you hypothesize explains that health, that mental health?
All the above. There's a whole world of people who study happiness, along with more traditional
public health people who study things like longevity. You look at the quarter poorest places on earth
and indeed people there don't live very long and are miserable. But once you get past sort of the subsistence level, there's not a great relationship between the wealth
of a country, GDP per capita, anything, and levels of happiness or life expectancy. And you look
at the fact that you as a shorter life expectancy than Cuba and Lebanon and Costa Rica, and it's
like the shame of this country kind of thing. Once you get past mere subsistence
level, income is not a great predictor of any of this stuff. And that's instead where you get
into worlds of social capital and social support. And when you look at the whole literature,
and you look basically at every westernized country under earth and it's now seen as they become westernized.
And what you see is the health socioeconomic gradient.
The poorer you are, the worse your health on the average.
The more of a whole array of diseases, you get, not all of them,
but a huge number.
The more impactful they are.
And when you look in the West, the United States is the
poster child for that. We've got the steepest curve of any country on earth. the more impactful they are. And when you look in the West, the United States is the poster
child for that. We've got the steepest curve in any country on earth. And the westernized
world, the least steep ones are you bet. Of course, the Scandinavian countries, ever reliable,
sort of utopias. And then you begin to unpack why this relationship occurs. And like some
incredibly smart people have spent their careers looking at it most obvious one is
If you're not healthy, it's very hard to pull off being the CEO of a company poor health precedes and gives rise to poor socio-economic status
Okay, that's plausible that turns out to explain a tiny percentage of the variability and you could look at the status socioeconomic status of the home in which a child is raised and that
to predict or they're likely that of diabetes half a century later.
So absolutely the socioeconomic status comes first and explaining the vast percentage
of the variability.
Okay, so next thing maybe it's just that well everybody's kind of the variability. Okay, so next thing, maybe it's just that,
well, everybody's kind of equally healthy.
It's just that the really poor people are very unhealthy.
We have a step function.
No, you start with Jeff Bezos and Bill Gates
and every step down there and statistically,
the lower you go down every wrong of the way,
the poorer you are.
The poorer you are with respect to alcohol.
I'm sorry.
The poor your health.
Yes, yes, thanks.
So now you unpack that and what's the most obvious explanation?
And this is what people call a neomaterialist explanation, which is obvious.
The poor you are, you don't have healthcare access.
You don't have health insurance.
You can't go to the doctor as readily.
Your care is more lousy.
That's obviously
that explains everything that explains virtually none of the variability in the data because
you see the gradient nonetheless in countries with socialized medicine, universal healthcare,
you see it for diseases where it doesn't matter how often you get healthcare access, juvenile diabetes. So it shows an SES gradient kind of thing.
So it's not healthcare access. You then look cross culturally and you see wildly different
income levels and wildly different levels of healthcare access. And you see very similar
life spans across these countries and very similar gradients. So what people spent like the last 30
years doing is having this huge shift towards
it's got so little to do with the material aspects of
wealth or poverty. It's got to do with the psychological aspects.
It's got to do with the stress. First key
finding, somebody at UCSF named Nancy Adler who's
done wonderful research showing,
okay, your socioeconomic status, your wealth, your objective measure of wealth, is indeed
a predictor of your health. Turns out, at least as good of a predictor is your subjective
socioeconomic status. On the level when you look at people around you, how
do you, how are you doing compared to other people? Where would you place yourself on this
10 step ladder in terms of what's your absolute SES? What's your subjective one and by asking
it that way? You're asking the person to consider the community that's most pertinent to them.
Who's the comparison group? My next-door neighbors, Warren Buffett,
in-between, whatever. When you think of other people, how are you doing compared to them?
And it turns out your subjective SES is at least as good of a predictor of your health as is your
objective. In other words, if you took someone's income, which is quite objective, it would offer
no more prediction than asking that person in
the new but mountains. Where do you rack up in this tribe? And it's sort of like, you know,
sort of top two thirds. Yeah, exactly. Or another way of stating that is you look in some
bloated corporation, and there's some guy who's the assistant manager, the mail room, and that's
an incredibly status-filled position for that guy.
And there's some other guy who's number two in the company who was just passed over to
be number one, and the only pertinent thing in his mind is not the 99,000 employees that
he's higher ranking in, that there's still somebody ahead of me.
And you would see the same thing in baboons. In other words, it's not being poor, it's feeling poor.
The next critical piece in the story is work from this guy,
Richard Wilkinson in the UK, who shows what's the best,
most like effective way to make somebody feel poor,
independent of their absolute levels of income,
surround them by inequality,
surround them by reminders of all the people who are doing better than them.
I mean, this is where social media, it's the amplifier to all amplifiers of this, right?
You can't go 10 minutes if you're on it without looking at somebody who's obviously better
looking, obviously smarter, obviously richer,
obviously having more fun.
I think this has been pretty well documented, right?
Life style of the rich and famous, or you could be driving down a freeway and somebody
passes you in, I don't know what counts as a high status car these days, the cost of fortune,
but they come speeding past you and you can feel crappy and diminished and
like a less successful human. And you never even saw that person's face. This is unheard
of in the history of humans or a primate of being able to feel socially subordinated. And
you don't even interact with the person. Oh, there's people out there with, you know,
at least if the next door neighbor has more camels
than you, that's a very like tangible, real thing
in terms of like likelihood of surviving that extra,
income inequality explains the mediating effect
between objective socioeconomic status,
subjective socioeconomic status, and health outcome.
What I'm hearing you also say, though,
that's a more subtle spin on this,
is it's not necessarily global income inequality,
it's local income inequality, that is much bigger.
But what technology is allowed us to do
is to like what counts as low.
It makes the local counts as low.
That's right, that's exactly right.
It's expanded what local means.
You can sit there and watch, I don't know, lifestyles are the rich and famous. And back when you would never
have gotten into like the petty or fiftoms, castle or what. And now you can see all the crap they
have that you're never going to get and feel less loved as a result. It's so interesting to hear
you talk about this.
This is a topic that I think anybody listening to this is well aware of, especially if you're
a parent, because you also have to think about this through a developmental lens, which is
at least when you and I grew up, I didn't grow up with a lot, but you really had no idea
what was different, right?
Like you simply, everybody was the same. I mean, everybody's parents bought used cars, and instead of new cars, and everybody had
more or less the same sort of clothing that wasn't exactly the best and whatever.
So at least you could argue, well, were we at least spared some of this difficulty during
a critical window of development. And what happens now to a 10-year-old that's got a smartphone
and is subjected to this, because I remember that funny show,
Lifestyles of the Rich and Famous. I can still sort of hear the goofy cheesy theme song.
I think I even probably watched it once or twice as a kid.
But it's a lot easier when that's the one exposure you have to extreme
wealth or disparity, and either you can watch it for one hour or not, but it's quite a different
thing if not to pick on the Kardashians. I'm just, but if you're inundated with, oh my god,
look at how awesome the Kardashians are and what they're doing and how great their life is and
multiply that by three log orders. Do we have any data that suggests that we are
at a critical juncture? Because now I was having a discussion with a friend yesterday,
which is, is there evidence of any greater transition in technology in both a positive and
negative way than this generation to the last. Is this truly the greatest step forward?
I would assume so, but the things we worry about,
people have been worrying about for centuries.
Oh, my kids, they don't go outside, they don't play,
they don't have like meaningful relationships
because they spend all their time talking on the telephone.
They spend all their time listening to their transistor radio.
So maybe we're blowing this up.
Maybe this is just this generation's version.
I mean, I guess the one difference is
when you're talking on the telephone,
when you're listening to the transistor radio,
I don't know if it creates that global to local phenomenon
quite as easily or as quickly
or with less resistance as we see.
Maybe you're right.
Maybe this has always been one generation's struggle with the last.
But what you get is an amplifier now, because if you're an insecure, socially isolated,
periatal, lessened kid who's vulnerable in all sorts of ways.
And, you know, no matter what decade or century it was, you're the last one picked for the
game, you're the one who released popular or whatever, and that has all its corrosive effects.
Now if you really set your mind to it and you're that kid, you could spend 24, 7, just
wallowing toxically in evidence of a gazillion other people who are better looking than you
and more popular and invited to parties. You'll never be in for it amplifies further.
And the technology does absolutely that. What I think it does is it makes the vulnerable more damaged than in the past.
I think it's safe to say these amplifiers aren't going anywhere. So rather than wallow in
their harm, I guess the more relevant question is, what do we do if you're a parent today,
or not a parent today, and you're thinking about this through the lens of yourself
versus your kids, whatever, what are the steps that one can take to become less susceptible
to these forces that seem to drive this? Because I want to take a step back for a moment.
When I think about these areas that we've talked about before about the impact of nutrition
and sleep and exercise and stress or distress to make it more the term I use.
When I think about this personally, the one I'm most worried about is the last one.
I think I've got a pretty good handle on nutrition, and it's in many ways easier to control.
I feel like I'm more in control of what I eat, And when I make bad choices, I'm usually doing them consciously.
Like I've decided I'm going to eat this pizza versus I can't help myself. I'm going to eat this pizza.
Similarly with exercise, like, and again, I'm not saying this for anybody else, but this is just my personal thing.
And even with sleep, like once you commit to it, which is not something I did until probably seven or eight years ago,
that I sort of committed to, wow, this really matters.
And to forgo this thing, bad idea.
It's this last one that really drives me crazy, which of course doesn't help matters because
the fact that it drives you crazy makes it worse.
But I'll give you an example.
As a general rule, outside of the immediate post-prandial period of a high glucose meal, far and
away my highest blood glucose is always in the morning. Now I wear a 24 hour
glucose meter, kind of a weird guy. For almost four years I've been wearing a
glucose monitor all the time. So it measures my glucose 24-7 at one minute
increments. And out of say 365 days in a year, I'm easily wearing
at 330 days of the year. So I've got a lot of data. And without a question, when you look
at a 24 hour period, if you stripped away the x-axis of time, I could easily identify
mourning for you without exception. I'll give you an example. This is not something I'd plan to do.
I had breakfast yesterday, yesterday being Sunday, really early, because I woke up with my kids
made breakfast. I normally don't eat breakfast, but I did. So I had a breakfast 730 in the morning,
did a workout, had to catch a flight, didn't have time to eat after, had a very, very busy day,
didn't have time to eat after. It had a very, very busy day. Didn't eat a single thing, got to the hotel around 10, 30, or 11. Didn't want to eat, so didn't. Got up this morning.
It's been almost 24 hours since a meal, and I looked at my glucose meter, and it was like,
said 110 milligrams per day. I was like, there's no way that's right. Calibrated it,
sure enough, it was 110. Now, there is no way that's right. Calibrated it, sure enough it was 110.
Now, there is no earthly reason I should have had a glucose
of 110 milligrams per deciliter, 24 hours after my last meal,
which by the way, was bacon and eggs.
It's not like I was eating pancakes, right?
Well, I promise you if I could spot check my cortisol,
it was high.
And here's the thing, before I went to bed, my glucose was quite low.
You know, my glucose was probably 80 when I went to bed and it slowly rose.
And sure enough, as my day wore on, today the glucose went lower, lower, lower, lower,
lower.
It was about 78 before you walked in here.
I'm not alone, by the way.
So I've seen this a lot clinically with patients.
Once you start putting these 24 hour glucose sensors on people
which a lot of my patients are now doing,
you get this insight into this horrible thing
that's happening when we think we're sleeping
and nothing else is going on,
but we're ruminating or God knows what else.
And fits perfectly with morning awakening
is when you get your highest glucoit-quite levels,
which is probably one of the main driving forces on the increased blood glucose level.
And when you think about it from a circadian standpoint, what's the most challenging thing
you have to do each day in the absence of any major tumult?
Get up, start functioning, all of that.
It just seems like it's disproportionate.
Certainly, the dawn effect has been well-described.
It's more amplified in people with type two diabetes,
which is another interesting point, right?
Which is, why is it that someone who already has glucose
to this regulation would have an even higher cortisol response
in the morning, and you'll see enormous fluctuations
in glucose?
I guess my point here is, this seems like a harder problem to fix,
and certainly meditation is by far the best tool I have ever found to even
approximate getting this under control. But it's still hard because it's not like you have a pill.
If your blood pressure is high, well, I think it's probably best to fix it in any way possible,
but we also
have really great drugs that fix high blood pressure that can at least mask these things.
We don't have a pill to fix hypercordisolemia.
It's one of the most complicated endocrine situations, and yet as you've described eloquently,
it's also so innately wired into us, and we have this miserable midbrain that's just killing us.
First of all, I'd love to hear your thoughts on meditation, but then also other things
that given how much time you've spent thinking about this problem, I'd love to know how
you would suggest someone who doesn't have quite the zen mindset that I can tell you do.
Which is someone else be thinking?
Right off the bat, I'm delighted to see that I have a persona of us and I'm actually like one of the most type-based rest people you're ever going to
run across. I've spent 40 years professionally studying how bad the outcome is going to be of
all of these like bad lifestyle aspects without having anything insightful to say about how to actually fix it or
prevent it. And I certainly have learned personally absolutely nothing from my lifetime of work.
I'm like incredibly stressed. I'm mostly good at telling you what's going to happen if you don't
get stuff under control rather than how to get things under control. When I look at the stress
management literature, I don't do it very often because I tend to get sort of agitated at that point, but
broadly it works. It works as in you can lower blood pressure, you can lower cholesterol levels, you can lower subjective sense of health, you
objective measures as well, with all sorts of interventions.
objective measures as well, with all sorts of interventions.
What do you see when you look at the literature closely? First off is you can't do your stress management on the weekends kind of thing. It needs to be a regular sort of thing. You can't do it
while you're on hold on the phone for 30 seconds. You need to set time out for it. The benefits of
aerobic exercise, I don't know what the magic
number is. These days about 20 or 30 minute blocks is a minimum to start getting the cardiovascular
benefits. So it's got to be something like you stop things to do.
So that's important. Let's double click on that. What you're basically saying is, because
I think you're understating how much you know about this topic. Obviously it's something
you know a lot about as seriously as we would take nutrition.
And if you think about how many hours a week do you put into eating?
I mean, even if you're shoveling food down your throat, it still takes quite a bit of
time.
If you're going to exercise to the levels that have demonstrated benefit, we're talking
about hours a week, not minutes a week.
If you're going to make the difference between getting by on sleep versus getting
restorative sleep, I'm not talking about the absolute amount of sleep. I'm just talking
about the delta between those two. Think about how many hours that is. In fact, for the
average American, that would work out to be about an extra seven to eight hours a week
of sleep. And what you're basically saying is, if you want to combat this hypercord of salibia, dude, guess what? It ain't a 20 minute a week thing.
And in some ways, that taps into one of the 80, 20 rules of sort of mental health professionals.
Okay, so you have this crazy stressful lifestyle. And there's just a bazillion things you can't
say no to and you're just going 24, 7.
And if you've gotten to the point of saying,
this is crazy, this is not a quality life.
I want to live a healthy quality old age.
Well, I got to get this stuff under control.
I'm going to start doing something stress management-y.
And if you've gotten to the point
where in this lifestyle where there's a billion things you can't say no to each day
You're saying no to them enough that nonetheless 20 minutes every single day you are doing this
It almost doesn't matter what intervention you're doing you're 80% of the way they're already
If you're managing to do that and that's very similar to this sort of amazing classic finding. You get people who were clinically depressed. And finally, finally, finally, they're going to do something about it
and merely making a first appointment. Even before you've seen the person, people feel significantly
better because you are finally saying, I matter enough to do something about this or I'm activated enough or I'm optimistic enough to actually
go your halfway there at that point merely by doing something on a near daily basis.
So just on that logic, even though I don't know that this has been done, you would argue
that 10 minutes of deliberate mindful practice of meditation daily would probably be better
than one hour once a week.
Absolutely. In part because if nothing else, if you do a daily seven times a week,
you were sitting in the aftermath of having done that versus only one time a week,
and an awful lot of what's most interesting about physiology and its impact on sort of mental
health, things like that, is what's happening in
the recovery period after something like that. In the same way, one awful hour long stress
or a week versus punctuated episodes of it throughout the week without question, the latter is
worse because you've now got empty different times that you have to recover from having turned
on the stress response, and that's where a lot of the damage occurs. You've now got umpteen different times that you have to recover from having turned on
the stress response, and that's where a lot of the damage occurs.
You know, I learned something about myself that's, you know, sounds so stupid because it's
so obvious.
Although, I don't think it's true for everybody.
Email is a huge stress to me.
To be blunt, I hate it.
That would be the kindest thing I could say about email.
I really, a few months ago hit a true
nader in my response, and I'm like,
looking at these glucose levels going up,
and I'm looking at these morning glucose levels.
So even though my overall glucose level still look great,
I mean, this trend was upsetting to me.
I'm watching my resting heart rate in the morning go up
over the course of four months.
It had gone up like six beats per minute.
And if anything, I was in better shape, exercising more regular.
I made this observation one day, which is how many times in a day do I stop to look at
email, even if it's just a check one or two.
And the answer was like 50.
And every time I do it to your point, even if it's very brief, the after effect is not
that brief.
So I could look at an email and see two stressful things, but it might sit with me for 20 minutes.
So I tried this experiment, which is, I'm going to just check email twice a day,
two 30 minute blocks of email. And I would say within two weeks, I just really felt better.
It seems to me like we just have to figure out ways
to figure out what those triggers are for us individually.
There's probably some people
for whom email doesn't trigger them at all, right?
There's probably, you know, for me,
Twitter doesn't trigger anything
because, A, I have a very narrow window that I pay attention to and it doesn't
involve things that are aggravating like politics or religion or whatever.
It's just sort of, I'm only really following science.
So anytime I look at Twitter, I'm actually learning something kind of new and there, but
I'm sure there are many people listening to this who would say, oh my god, if I spend
an hour on Twitter, my blood pressure could be through the roof.
So it's like, everyone's got to kind of pick their thing.
You said your type A, which obviously you are.
I mean, you know what I didn't say
at the outset when we started speaking,
but you've won one of the most prestigious awards
imaginable, which is the MacArthur award.
And you won that about 30 years ago, right?
That's impressive.
They don't give that award out lightly.
So that's the one that's referred to as the genius award.
And I know you're probably, like, your skin is crawling
when I say that. My point being is you're an incredibly accomplished successful
guy. It's not surprising you would describe yourself as a type A. What have you learned
about yourself over the past 30 years or even longer going back to your first days in Kenya
about what those triggers are for you and what you can do to lower your cortisol levels. Not surprisingly, if you hang out with people who are field biologists of any sort,
and again, I've only been a part-time annual one over the decades, but nonetheless,
still think of myself as a field biologist. We're kind of a solitary tribe.
I mean, during my peak periods of doing field work,
I'm spending three, four months a year alone living
in a tent where 12 hours a day,
I wouldn't say a word to another person.
Temperamentally, this is kind of who I've been for a long time.
And there was always this ironic thing
because I was sitting there studying these baboons
because I'm a primate social behavior.
I'm interested in primates, social behavior, and there's big sort of piphony I had in my
work that, okay, you're a social rank as a bad wound, that's something to do with your
health, but much more importantly, as your patterns of socialization and social networks,
and how often do you groom, and how often do somebody groom you, and how often do you groom and how often do somebody groom you and how often do you sit
in contact with another bad boom or playing with an infant and then I you know finish the day's
work and go back to my tent. So there was something ironic that I was like studying the health
benefits of sociality, living alone and a tent large part of the year. Your wife is a scientist too
isn't she? She was, she kind of decided she was sick of it
and she now directs a musical theater program,
which is much more fulfilling for her.
But at one point, my wife came along.
Yeah, yeah, that's what I was gonna ask.
And eventually family and, you know, kind of realizing,
oh, I've missed out on an awful lot of what are really,
like the wonderful worth
living for moments in life out of the sociality stuff. And that is a refusional sanctuary
from the world's madness. And I could not have predicted as a 20 year old who had been
planning to be a field biologist for a dozen years at that point, I could not have predicted sort of how much of my equilibrium at this point turns out
to be due to interacting with the right two or three other primates, like being in love
with them and stuff. That one was kind of a revelation for me. I am not the social being that I would have guessed I would have been back when.
Which is interesting because having this discussion with you today, I can sense much more
of your introversion than the first time we met when you were giving an unbelievably charismatic
animated talk.
I don't know how many of us were there, maybe a hundred people, which is so interesting, right, because you would, I think anybody sitting in the
audience would look at this and say, oh, that's the life of the party. But it's
interesting that we can compartmentalize and separate those things, right? I mean,
you couldn't get up there and you can do what you need to do, and you're at your
happiest, I'm guessing, in the way you described it, versus in the aftermath of
that talk, when a hundred people run up to you to ask you four questions each.
Not to get too self-reflective or something, but I'm a fairly introverted person who does better with scripts and giving a lecture is a pretty structured script and having sort of an academic
persona or whatever is another version of it as well. What year did you become a full professor at Stanford?
33 or something early 90s. I mean you live in San Francisco, so you're not making that commute every day, I hope.
But I did for about a quarter century. Yeah, that'll hurt the court of salt levels, won't it?
I use the commuter train, counter train here. So you could read and...
I loved it.
This was much of it.
It was before cell phone.
So you'd take it up at fourth and king and you'd just go, yeah, I used to make that ride
all the...
I used to have a girlfriend that lived in San Francisco and I loved that train ride.
And then you'd get off on your bike at fourth and king and you could go anywhere in the city.
Yeah, exactly.
I wrote half my book writing was on the train there.
It's pretty weird when you realize that like one of your valid social communities are
the conductors on CalTrain, sort of as you're watching them grow up on you and things like
that.
But yeah, no, that was, I was a big fan of train commuting.
So speaking about books, let's talk about your more recent book.
It's about human behavior, which, you know, I mean,
I can see based on this discussion now,
how your interest would shift to that,
what was the impetus for that research?
Well, title is, behave the biology of humans
that are best and worst.
And sort of as we were talking about before, I closed my lab four years ago and stopped active research to sit for four years and write
this book. And it's basically trying to make sense of the biology of what is for me the
most puzzling thing about us as a behaving species, which is we are simultaneously the most
miserably violent species on earth, and the most altruistic and cooperative and empathic.
And any given human is capable, depending on the setting of incredible gyrations, as
to whether they are being wonderful or awful or in between
where behaviors aware whether that counts as good or bad is incredibly dependent on what
culture they happen to be doing it in. Just trying to make sense of the biology, I mean,
totally boring biology is to like how your brain makes you do something like pull a trigger, like which muscle groups have been told?
Like that's like studying cockroach neurobiology.
What's totally interesting is the fact that we're a species
where sometimes pulling a trigger can be one of the most awful things a human can do.
And sometimes it could be one of the most wondrous ones.
If you're suicidally drawing fire from innocent people and
you're sacrificing yourself or in one setting you put your hand on somebody else's and
that could be a moment of incredible compassion or in another moment you do the exact same
thing with your primate muscles and that's the first step of betraying a loved one of
just making sense of this contextual stuff about human behavior, which is hugely complicated.
And the song and dance that I go through and nearly 800 agonizing pages in the book is, you're going to understand nothing about that. If you've concluded, aha, we now know this is the part of the brain that explains everything.
Or this is the neurotransmitter, or the hormone, or the gene, or the child.
Instead, to make sense of human behavior, you got a factor in what your neurons did one second ago.
But you got a factor in the environmental triggers of that 30 seconds ago.
And you've got a factor in what your hormone levels
were like this morning.
And what neuroplasticity you've done over the last two seasons
and what your adolescence was like in your childhood,
in your fetal life, in your genes, and amazingly,
what sort of culture were your ancestors
inventing centuries ago,
because that influenced the way you were raised
within minutes of birth and what
things you value and what things your amygdala does or doesn't respond to and all the thing of that.
What sort of ecosystems produce different types of cultures and then finally evolution.
And why we're in some ways like chimps and in some ways like bonobos, but we're not chimps.
We're not bonobos.
We've solved our own special evolution.
Like, if you got to understand this stuff, it's everything from one second before to a
hundred million years before, and all these levels interact, and it's complicated to sell.
When people ask the question, which I'm sure you've heard this a hundred times, and you
hear people asking all the time, are we innately good or bad?
That question doesn't really permit the level of nuance you're describing.
The answer is yes.
Yes.
Exactly.
And what's most startling about us is most of us have the capacity to do
something that we would be stunned and sick and that we were capable of doing it.
And most of us are capable of in some circumstance of doing something that is so damn heroic.
And most of us spending most of our time doing things that are ambiguous and multi-layered
and full of ulterior motives and what's really going on there.
And you look at the worst of us and the best of us, and there's not a whole lot of really
reliable predictors
beforehand.
And how much of this, like, you know,
you wrote a little bit about PMS.
So when I think about PMS, I think about it purely
through the lens of the endocrine system, right?
I think of it purely through the lens of when a woman
is in her loodial phase, that progesterone level has to rise for the placenta,
and then of course, virtually every time,
it's a false alarm, you don't need it,
you shed that lining,
and that progesterone level comes crashing down.
And it's this crashing down a progesterone
that has always interested me, why two women could experience
the same we can measure progesterone levels
throughout the cycle.
And we could know that at day 22, two women could have the exact same progesterone.
And on the first day of their mencees, they could have the same progesterone.
So you know they had the same peak to valley.
And yet two women can experience that in two totally different ways.
Now I've thought about that through the lens of progesterone receptors, and the way we sort of talked
about the cortisol stuff, is there something else to that
that you layer on top of that that is even more subtle
about those differences?
Yeah, tons of this sort of additional insights.
Here's one example that comes completely out of left field,
and this was actually my wife's thesis research on baboons.
So your female baboon and you're coming up on your period
and we could frame it as you just did.
Here's two females who are both about to have their period
and they have the same exact progesterone levels
and as soon as they start menstruating,
progesterone drops in exact same way.
And one of them is a totally irritable, awful jerk
to all the other females around her for three days afterward.
And the other one is not.
The other one withdraws and becomes socially isolated.
Okay, what's the difference?
It sure can't be progesterone levels.
So it's probably not gonna be progesterone receptor levels.
It's one of them's high ranking.
She could afford to be a jerk to everybody else
and get away with it.
The other one's low ranking.
Oh, it's not just your hormone levels.
It's what sort of position in your society you have,
even if you're a baboon.
Or now you look at humans,
and depending on what sort of culture you're in, are you in an individualist
culture or a collectivist one, individualist, the United States, poster child of individualist,
thinking collectivist, 99% of the research has been done on East Asian cultures and how you somatisize your mood shifts
and your physical shifts during your period differs
in collectivist versus individualist cultures,
how irritable you become.
Not because there's a difference in how much
of negative affect your feeling during the time,
are you in a culture where it's culturally acceptable
to bitch and moan to all your best friends when you're not feeling well?
Or are you in a culture where when you're feeling lousy, what you're supposed to do is reach out affiliatively and reify your like social values?
And how much of that do you think is also genetic?
So for example, I mean, even though I'm not a gynecologist and therefore don't see a lot of this, I see
enough to realize that women will often say my sister and my mother either go through or
went through the same feelings.
And of course, as you describe, there are so many different variants.
The stereotypical one is the, you know, the sort of the nasty phenotype, but actually the
one that I think might be more prevalent is the sadder
phenotype, the more emotionally distraught, just emotionally labile, but in a non-aggressive
way. That's probably the phenotype I see more, easier to cry or something like that.
So how much of that do you think is heritable in the way that eye color or some other aspect
of body habit is, or even depression is quite
heritable.
Versus the ecosystem you're in purely environmental.
Well, the answer is you really can't choose one of the other blah, blah, but if you could
only manipulate one, which would be the first one, and I'm definitely of the school of
genes get overrated in terms of their impact.
And, you know, a gene affecting your eye color,
it's okay to use words like determine.
And it's probably not even 100% accurate.
But when you get to genetic influences
on all the interesting stuff and behavior
and our internal lives and all of that,
yeah, gene to important, but overwhelmingly, these are genes that modify
vulnerability, vulnerability to certain types of environments. Okay, so for example, you bring
up depression and catastrophic pandemic of that. And, you know, there's a whole shopping list
by now of genes that have been implicated.
And probably the single most important one, it's called the gene for the serotonin transporter
and serotonin SSRIs, pro-zacol, and those serotonin is just like right in the middle of what
we understand about the neurochemistry of depression. And it turns out this serotonin
transporter gene comes in a few different flavors, a few
different genetic variants, and a ton of basic research, rats, monkeys, etc. suggested
that if you had one particular variant, you were more at risk for major depression.
Okay, so this classic work, this guy had Duke, offshore on caspies, sort of a god in the field,
goes out and he follows like 17,000 people
from birth up to age 25,
or so he's got genetic information on them.
And he's able to ask this critical question,
okay, if you have the quote, bad version of this gene,
by age 25, are you more likely
to have a history of clinical depression?
And what's the prevalence of the gene approximately?
It depends on the population.
In his population?
His was a mixed one, but Westernized Western European populations, I think it's got about
a 20% incidence.
So the question then is of those 20% how many go on to get depressed, of the 80% how
many go on to get depressed?
The answer is very likely going to be it's not a one-to-one mapping. It might be an increase in risk by some factor.
And what they saw was overall there was no increase in risk having the bad variant. However,
if it was coupled with a lot of childhood stress, you had about a 20-fold increase in the risk.
So just to be clear, on aggregate, there was no difference.
The hazard ratio was one for with gene versus without.
Because of a ton of variability.
But if you wanted to amplify it, take that gene
and expose it to childhood stress or trauma
and you almost assure depression.
You get a massive boost in predictability.
Look at people without the
scaryant vulnerability variant and look at the same severity of childhood stressors and loss
and you got a moderate increase in incidence of depression. These folks massive order of magnitude
multiples of that more increase there. What that tells you is this is a gene whose variance alter how readily you deal with
experiential kicks in the ass is growing up. And it turns out these different variants
are regulated in different ways by glucocorticoids. Aha. So there's a stress angle, all of that.
The same way, there's another gene for the people who are interested in the genetics of aggression.
The same way, there's another gene to the people who are interested in the genetics of aggression.
This gene model would mean oxidase and it comes in variants and it's...
And there's a class of drugs that targets these perceptors.
Yeah.
Again, a ton of basic research had suggested, ooh, there's a scary variant of it, which if
you have it, you are going to be more predisposed towards violence.
And in fact, the same group working with the same population,
massive data set, winds up showing,
just having that variant doesn't get you
a higher risk of antisocial violent behavior by age 25.
If and only if it was coupled with abuse,
childhood abuse growing up.
Oh, if you didn't have the scary variant, childhood abuse,
a little bit of increased risk, have this variant with the abuse and it was virtually
the same figure as with the serotonin transporter gene, huge boost and very over and over the
genes that are interesting when it comes to this stuff. These are all genes about vulnerability and potentialities and tendencies that are
emerging only in certain environments and not in others. The factors are inseparable.
It makes me think of the apoe geneotype, which is linked to Alzheimer's disease. And
there we see that there is a difference. About 25% of the population carries at least one copy
of that gene, and they represent about two-thirds of the cases of Alzheimer's disease.
It's not a deterministic gene, but it does increase risk.
Now of course, you could argue that maybe in a decade or more, we will be able to say
something very similar about ApoE, which is it's
not remotely deterministic.
It only gets turned on when x, y, and z happen before this period of time or in absolute.
And of course, we don't know what those things are right now.
At least in the examples you gave, you could say, well, trauma or childhood, you know,
some event in childhood was the trigger.
And if you're seeing a 20-fold difference, it's pretty clear that you found the trigger.
Nonetheless, there's still variability to explain after that.
But yeah, it's pathetically that counts as virtually state of the art for understanding
the modifying factors.
And it's going to be that way. In any time you do these like GWAS massive fishing expeditions and you come out with 300 genes
are implicated in a trait that's as boring as height, 300 genes, which you put together all of
your knowledge of the variation in them and then you give individual, and you have like 4% predictability of their height.
You know, Christ, if you're talking about genes
for propensity towards feeling poignancy,
or genes for anything that's interesting, it's just not a chance.
Even if you just limit yourself to diseases,
you know, of the 20,000 genes in our body,
you can really only point to about a hundred that are directly
this mutation means this disease. And
they're all pretty esoteric, right? It's all like inborn errors of metabolism and certain things like that.
But when you start to talk about the complex diseases like Alzheimer's disease, even as predictive as the APA we for is
it's not even close
to being enough to understand it. And I think, yeah, it's funny. When you talk about it through
that lens, you realize the importance of environment, which is, you know, through a specific
statement, obviously, you said something a while ago that I made a note of because I wanted to come
back to it. You talked about the effective glucocorticoids on the hippocampus, and not only how harmful it was for memory consolidation,
but overall cognitive impairment.
And listening to you talk about that was exactly the way Matthew Walker, Berkeley, speaks
about sleep deprivation and its impact on the hippocampus, which then makes me wonder,
I assume it's been well studied that, you know, when people are sleep deprived, we see greater
elevations of cortisol.
Do you have a sense of what the evolutionary basis of that is?
Because it seems counterintuitive.
You would think even evolution would want that to be in the opposite direction.
I mean, the only explanation I can come up with is if you're sleep deprived, you're assuming
that there's a reason for it that's good, and therefore you want that.
Of course, not with any of the fact that higher cortisol will then prevent that. I think that's probably the best sort of piece of tealiology for that.
Yeah, if you're like a basic mammal, which means either you are emphatically diurnal or emphatically
nocturnal, and if instead you're wide awake eight hours into what should be the 12th, this does not
happen by chance. The odds are you
have something stressful going on. I think that's the logic of it. Turns out the stress,
sleep, sleep quality cortisol cluster of interactions, even more subtle, incredibly cool study. This
was a science paper some years back that, okay, so as we talked about the circadian
peak of glucoricoids around the time you wake up, what's interesting is about an hour
before you wake up, levels begin to rise, telling you something, a subtle point, which is
a lot of glucoricoid actions, are not for dealing with a stressor that has already commenced,
but can be preparatory. So the preparatory stressor is having to actually get up and get out of bed
and start functioning the stress, and an hour before people wake spontaneously,
glucoticoid levels are elevating. Now in the study, what you do is you take a whole bunch of volunteers,
you're sleeping, and you see the preparatory rise, all of that, what you do is you take a whole bunch of volunteers who are sleeping and you see the
preparatory rise all of that and you tell them tonight we're doing something different. I'm going to wake you up at four in the morning
And what you see is around three o'clock
Gluquaticoid levels start rising. Okay, now you do something even more interesting. You say
Okay, tonight I'm not going to tell when, but I'm going to wake you up
at some point during the night, and that's the end of your night's sleep. And the person is about
90 minutes into their sleep stage and all of that. And cortisol rises and stays high for the rest of
the night. You get one sleep cycle. And then the adrenal gland says, that's it. I'm on ready alert.
Yeah, exactly. So not only is it bad not to get enough sleep, not only is it bad if the
insufficient sleep is fragmented, but the worst is if it's fragmented unpredictably.
And that's like every medical resident in history.
It's the first thought I had actually when you said that which was every night of call you have this
pager and you're in this call room and you just want so desperately to sleep for an hour or two
hours, three hours. I remember as my residency went on, the degree of sleep deprivation got greater
and greater that the steps I had to take to ensure I wouldn't sleep through a page got greater
and greater and I'm not making this up. I don't think I've ever told the story before. It's so ridiculous. I used to use this really heavy paper tape and tape
the pager to my head, my forehead at full volume because you would get both the sound to your ear
and then you'd get the transmission, you know, through the bone. But imagine laying in bed with tape
wrapped around your head holding a pager on your forehead
in anticipation of what's coming, not knowing when it's coming. It could be in five minutes or it could be in two hours.
You know you're gonna wake up.
Yeah, I'm guessing that wasn't great sleep.
No, that's like wildly destructive. And what do you know? It turns out if you have elevated glucoticoid levels while you're asleep,
you have less delta sleep time, which is the restorative stuff. You make less adenosine
stores in your brain during. So even if you manage to go to sleep, if it's under the, I could be a sleep for two hours,
now or 30 seconds, the sleep quality is going to be horrible.
This interplay becomes more pronounced.
What about cancer?
What role do you think stress plays in cancer?
And do you think it's mostly medillated through the immune system?
I mean cortisol can be quite damaging.
Yeah, a hugely, hugely controversial subject.
There is a common perception that stress can play a very substantial role in the onset
of cancer in coming out of remission and rates of tumor growth and such, sufficiently so
that there's been all sorts of studies where you ask cancer patients, what do you think
is the cause of your cancer and stresses and variable way up there.
The actual evidence for a role of stress in causing cancer, bringing it out of remission,
accelerating tumor growth is very, very minimal.
There's been a remarkably small number of good prospective studies of humans that have
really, truly ruled out all the confounding factors.
When you look at the animal studies, what they typically involve
is you experimentally induce a tumor, you inject transform cells, you give a carcinogen
some such thing. My lab back when did some of that work under those circumstances, you
can accelerate the growth of a tumor, but those are circumstances of cancer acquisition
that are virtually irrelevant to human cancer.
And the other question is, can you do it without perturbing other things?
So for example, if you go ahead and stick the tumor into the mouse and apply a stress
to it, it seems that that by definition will alter some other parameter, what it eats,
how much it sleeps, the quality of it sleeps.
So it becomes difficult to disentangle cortisol.
I mean, I guess the only thing I can think of is what does the experiment look like where you take the mouse that
experimentally has the tumor and you just start injecting more glucocorticoid? So in other words,
you don't actually increase the stress level. You just increase the readout state of stress.
You accelerate the tumor growth. We did one study showing that as soon as cells become transformed, they
upregulate the glute-4 glucose transporter, and that's the one that's further upregulated
by glucoticoids and target cells. So you're just shoveling energy over those cells.
Yeah, but these are-
Which preferentially consumed glucose anyway, just given the number of them that fall
by the warberg effect. So to me, even though that's very mechanistic and artificial, that strikes me as pretty
reasonable evidence that cortisol can play a role in cancer.
I mean, I guess it's going to be much more difficult to disentangle that in the real
world.
Yep.
And again, these are types of cancers where this was virally induced transformation of cells that are then transplanted in very
artificial systems that turn out not to be terribly applicable to human cancers.
And what you wind up seeing then, okay, yes, gluc corticoids can be potently immune-suppressive.
Usually by the time you have a tumor growing, that's long past the point
where it's an immunological problem.
It's now, can you keep the tumor from growing a whole bunch of capillaries that will feed
it?
Can you keep it from stealing all sorts of energy?
Can you keep it from turning off cell death programs?
It's no longer in the immune realm.
So it seems that there'd be hard to make the case that acute bouts of stress can really
have any impact because, you know, yes, sure, you can acutely disrupt the immune system
and maybe get sick, right?
That, you know, I could explain why you might get a cold under a period of great stress,
but not necessarily cancer.
And what that wants, meaning is that should be a massive, massive take-home
message for anyone who is predisposed towards thinking, ooh, stress caused my
cancer. Too bad I didn't have better priorities in life. Now I know who's
faulted is. That sort of thing. And it certainly make you damn cautious if
there's some highly credentialed quack out there who is selling a stress management
will stop your tumor, will make a disappear entirely, and you'll watch your wallet at that point.
All that being said, there's been some wonderful work, and a lot of this was pioneered by a
Stanford colleague of mine, David Speagle, who showed that things like supportive group therapy among cancer patients
enhance a survival.
So what do you think is the mechanism of that?
Okay, this was when he first published this in the late 80s, this was front page news.
I remember this.
I mean, I don't remember it when it was published, but I remember learning about it in medical
school.
Massive finding.
And one is immediately tempted to release there's a biology type like me to come up
with a biological explanation along the lines
of what you proposed.
Okay, supportive group therapy, you're less stressed.
So you don't secrete as many glucoticoids
and therefore you're not having loose adverse effects
of it when your immune systems,
you're better able to fight the tumor,
you live longer, trull on this.
And lower glucose levels and lower glucose and lower insulin and lower IG.
If you could, you could come up with a complete biological.
And in general, those studies have shown that pathway does not occur, Spiegel and I did
some of those studies.
So what's actually going on, something which if you're a nuts and bolts reductive biotype
person is terribly disappointing, but is so interesting
and important. People, when they have supportive cancer therapy with other people going through
the same hell, they become more compliant when they're medical regimes. They're more likely to
go the extra round of chemo because everybody else is cheering them on saying,
I didn't want to do it either.
And they're more likely to take the meds that make them nauseous as hell.
Have you eaten today?
Me neither.
We're going to eat right after we're done with the group.
Have you taken your meds?
You're going to take them right now.
People become more compliant.
And that was very hard to demonstrate because what cancer patient
ever wants to admit to a researcher, actually, I skip about a third of my meds because they
make me feel so damn sick. They're saving your life, would it? It's in some ways a dark,
dirty secret in cancer therapeutics. How much people diverge from their optimal treatment regime,
because the treatment regimes are sheer utter hell. When you're surrounded by people who are going
through the same thing and understand, you're more likely to be compliant. I think that winds up
explaining an awful lot of that effect. So when you look at cancer, atherosclerosis, and
cancer, atherosclerosis, and neurodegenerative disease. It seems to me that the direct lines of evidence for the damage of hypercordisolemia and the accelerated stress response are probably
most demonstrated in cardiovascular disease and atherosclerosis, vis-a-vis several mechanisms,
not the least of which is hypertension, both macro and microvascular, but also through endothelial disruption.
Adhesion of cells and sludging and yeah, it's the best understood realm. Cancer is probably the
weakest realm. I would expect that it's playing a role in dementia, but again, this probably gets
to the layer of susceptibility, right? There's probably an isolation, maybe this wouldn't play a
role, but in combination with other factors, it would. And it seems that, for example, we know that
cortisol inhibits melatonin secretion. So even if you take two people who have the same amount of
blue light reduction, which should therefore stimulate melatonin, the one with hypercortisolemia
is going to, and we actually measure this, right?
We can measure overnight urinary cortisol and overnight urinary melatonin.
You can see this association quite strongly.
Well, melatonin, it's a pro-nerogenic molecule.
So having less of that is less restorative to the brain, even beyond its important role,
which is sort of removing the brakes on being awake.
So what other lines of evidence do you see beyond what you've already described at the
developmental stage now later in life?
Basically everything we talked about with the hippocampus applies in the adult brain as
well.
And it's the first place we tend to see changes.
And it was the first area of research, first evidence for stress
damaging the hippocampus and hippocampal dependent memory type
stuff, late 70s. I mean, that was really the first domain and
superb studies from a number of groups. And I had my two cents
and that would return also showing you could accelerate aspects
of hippocampal aging with lots of stress,
lots of glucoticoids, extensive neuron loss, extensive memory problem, extensive reactive
galeosis, etc., etc. Next big outpost that people began to appreciate in adult brains was
derivative of what we talked about before, which was the mictula. I was just about to say,
is there a direct correlation,
I guess, between the MIGDLA size and dementia?
What you see instead is the syndrome
where it's most demonstrated as PTSD.
You see expansion of the MIGDLA
and you see atrophy of the hippocampus
and glucocorticoids probably play the driving role in both.
So in the MIGDLA, like the hippocampal story is stressing, corticates, screw it up. Neurons don't work as well. Networks
don't work as well. The overall size decreases. You had atrophy. And the amygdala, it's
the exact opposite story. Neurons work better than they should. Neurons become more excitable
form denser networks. The amygdala gets bigger. What's that about?
The problem with chronic stress is your memory goes down the tubes, hip campuses, and working as
well as usual. The problem with chronic stress and the amygdala is it works better than it's supposed
to. And this is the link between stress and anxiety disorders, stress and fear, stress and all of that.
Next sort of outpost that people started looking at
was the dopamine system in the brain.
And dopamine neurotransmitter,
most famously associated with reward, pleasure,
cocaine works on the dopamine system,
a much more accurate subtle picture of it is dopamine
is actually more about the anticipation of pleasure
than it is about pleasure itself,
and about goal-directed behavior you're willing to do in anticipation of reward.
But then a whole literature showing what distress and glucoticoids do there, they mess with
the dopamine system. It's less clean of a story than a MIG-DLABOR hippocampus, but in
ways that predispose towards the two big psychiatric diseases
of screwed up dopamine systems, number one, addiction.
More vulnerability to addiction, harder to get off of addictive substances, number two,
depression.
Depression is a disease of on a certain level, dopamine depletion.
It's a disease of inability to feel pleasure
and hedonia. And that's the neurochemistry of the link between chronic stress and why
that increases the likelihood of the first three, four episodes of major depression.
What for me is the most exciting area is one where if I was starting over, you know, forget
the hippocampus who cares about
like how many digits you could remember backwards or whatever, the most interesting domain
is turning out to be what's directly glucoticoids to to the frontal cortex.
Judgment, impulse, control, executive function, long-term planning, strategizing, and it turns out virtually every bad thing
cellularly that's dressing glucoticoids doing the hippocampus, they're turning out to do
in the frontal cortex as well. And what does that begin to explain in this entire world
of why it is during moments of extreme emotional arous, so especially aversive ones, why we make terrible, terrible decisions
that seem brilliant at the time.
And you spend the rest of your life regretting it
because impulse control, you're a miktola
overpowers your frontal cortex at those times,
your amygdala has a lot more talking
to your motor systems than your frontal cortex does.
It's the reason why judgments and impulse control
become terrible when we're frazzled.
It's also looking like as a side story with that.
It's one of the reasons why when we're very stressed,
it's hard for the frontal cortex to do
one of its harder jobs,
which is to take the view of the world from somebody else's perspective.
Empathy.
Empathy, exactly.
Some research on animal models of empathy, and this was worked with this guy at McGill,
named Jeffrey Mogel, and we're collaborated with him, showing in both rats and humans,
you're less empathic towards strangers when they're in pain.
And if you block glucocorticoid release,
you don't get that effect anymore.
Glucocorticoid, the stressfulness of dealing with
scary novel humans or scary novel mice,
if you're a rodent,
glucocorticoids narrow your window
as to who counts as an us and whose pain
registers and things of that sort.
So for me, you know, it's incredibly interesting if you're stressed and suddenly your SAT scores
plummet, the fact that stress makes people crappier to each other and less empathic and
more parochial and more xenophobic and more impulsive with the worst of our impulses,
that's the stuff that really interests me these days.
Everything you just said, Robert,
is almost a call to action in criminal justice reform.
I've done a podcast on this topic
where it was very fortunate to go into a maximum security
prison with a program that is really there
to do incredible, rehabilitative work led by this woman named Catherine Hoek.
It's a humbling experience.
There's a game that we played about halfway through the day
called Step to the Line.
This is a game that's used to basically identify
the vast difference between those of us who are volunteers.
Like in other words, the role of luck in our lives
versus the gentleman who two-thirds
of these men are never going to get out of prison.
One man had even spent more than half his life in solitary confinement, his total life.
So it starts with these questions of step to the line if you grew up in a home that had
two parents and, you know, of the volunteers, you know, 60% step to the line of the inmates,
five step to the line, right? Step to the line if you grew up in a home where there were more than four books.
You can imagine the disparity.
Step to the line if you saw someone die with your own eyes before this age.
I mean, and it's a very emotional thing to go through because as this game is unfolding,
you're just, you're feeling more and more fortunate on the one hand
because you realize, if not for the grace of this luck. And at the same time, the empathy
you have for these men who have done the most heinous things grows. And you start to realize,
boy, there's a fine line between those of us on the inside, those of us on the outside, because everything
you said really resonated when I was thinking about some of the stories the men told us, about
the decisions that they made.
And there's this one part of the exercise that's incredibly emotional where you're partnered
with one guy.
So it's one volunteer, one inmate.
And you were each telling the other person the greatest regret of your life, the biggest mistake you've made.
And hearing some of these stories, it's not to justify anything that's been done, and
it's not to say that there shouldn't be consequences for it.
But a lot of these things that people have wound up in prison for are really impulsive, horrible decisions, as opposed to decades of sinister
planning.
It's one thing to look at what Hitler did.
It's hard to argue that anything that he did that was bad was impulsive.
It's quite another thing when you look at someone in a gang-related incident where this guy
gets shot and you're going to shoot this guy
back or this guy's about to shoot you and you shoot him.
And yet that type of drug-related violence is disproportionately represented in, certainly
in the US penal system.
And then to build on what you said, it's not clear that the environment in there is reducing
cortisol levels to the
level that would enable rehabilitation, which is really the thesis of, and a lot of people
I'm sure listening to this are thinking, why would you feel empathy for these folks that
are in there and why should society care about them?
But the reality of it is, if they're going to get out, you should care.
That says nothing of maybe the higher level that you should care, which is the injustice
of it.
But even if you took a purely selfish view, a non-trivial number of these men and women
are going to get out.
So wouldn't you rather they get out and function better?
And yet it's really tragic to see this.
And I know two people actually very well who spent a great deal of time in prison, one
of whom I interviewed on this podcast, his name is Corey McCarthy, and it really strikes me as the exception
and not the rule that people are able to emerge from that environment and go on to be successful
outside.
It's a system that is so, so broken.
Any study the last century and a half, some worth of neurobiology and genetics and
child development and all of that and the notion that we are free agents of our
action is so destructively misplaced. I'm sure you're familiar with the work of
Sam Harris. Sam has been one of the most interesting forces in my life at
getting me to really even question this notion of free will.
And once you realize that free will may not even be yours, it takes luck to a new level.
It's something I spent a lot of time thinking about now.
What advice would you offer somebody who is interested in the neurobiology of stress or behavior and who wants to be able to look back when
they're your age and be as, you know, maybe accomplished as the wrong word. I don't want
I know you sort of bristle at that, but to have made as many contributions as you've made.
I mean, what in retrospect was sort of the secret to being able to pursue your bliss and be
as successful as you've been and look frankly to be where you are and to still have the passion
that you have for what you're doing, which to me is really the marker of success.
It's that you're sitting here saying, there's this other problem. And I, you know, like I
could spend, you know, the next 20 years just thinking about that. How do you think about
how you've done that?
Just damn luck. Every bit of neurosis, every bit of affective instability. I've got every child to trauma, I've got tucked away.
I've titrated in just the right way that I've turned it into
more productivity and incredibly lucky in that regard.
My capacity to sublimate a motion into intellectual pursuit,
into really, really, really wanting to understand something, into
I've just been very lucky on that regard. I've gotten just the right levels of all sorts of
like tumult that have synergized most productively. In other words, just huge amounts of luck,
in other words, just huge amounts of luck, huge amounts of luck, and at least now coming later in life, and increasing capacity to more carefully try to analyze what cost each
type of ambition comes with.
Hmm, say more about that.
I don't know, I don't know. This had much to do with my closing
my lab four years ago. The big booming lab with lots of people and all sorts of labs around the
world. We were going to kick the asses of by getting the answer to this or that. And you know,
if you're raised in the right sort of rarefied ambitious world of biomedical research at age 25, you've
got a list down to the floor of the disease as you're going to vanquish and the problems
you're going to solve and all of that.
And you know, getting to that point in life where you're realizing it's not going to happen.
Is that what actually happened four years ago? Was it that much of a cerebral realization
or was it combined with other factors? You've described obviously having this network of people
around you who matter the most. I mean, it was part of it just thinking, I haven't spent
enough time with them at the expense of this or was it the this problem is enormous and when,
you know, a thousand years from now, whether I worked this much harder or this much less
It won't have altered the trajectory of x was like I mean how much of it is all of these?
Holy love yeah family
growing real fast as they tend to do
Realizing your best work was decades behind you realizing there's
This book you want to write
and where the only way you can do is to just sit for really long stretches,
Kenyan fieldwork having collapsed a few years before
body feeling older limits to how many 80 hours of work a week you can do,
all of them converging.
What did, I mean, it's such a cliche question. What advice would you give the 25-year-old Robert as he was just finishing that PhD at Rockefeller?
BLS ambitious.
Well, I think on that note, which by the way, I think is some of the greatest advice one
could ever get and receive.
Those of us who are still on the climbing ambition curve
should do everything to listen to it. I want to thank you so much for taking the time
to sit down with me. And more importantly, I think for just all of the work you've done
and you're continuing to do. Thank you so much.
No, thanks for having me on. This has been fun. It's the wrong word, but stimulating, good.
Glad we did this. Thank you for listening to this week's episode of the drive.
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This is a great way to catch up on previous episodes without having to go back and necessarily listen to everyone. Steep discounts on products that I believe in,
but for which I'm not getting paid to endorse.
And a whole bunch of other benefits
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If you wanna learn more and access these member-only benefits,
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