Files
gigachad-library/intelligence-and-metabolism.html
T

835 lines
52 KiB
HTML

<!DOCTYPE html>
<html lang="en">
<head>
<meta charset="UTF-8">
<meta name="viewport" content="width=device-width, initial-scale=1">
<title>Intelligence and metabolism — GigaChad</title>
<link rel="icon" href="/favicon.ico">
<link rel="stylesheet" href="/style.css?v=1">
<meta property="og:type" content="website">
<meta property="og:title" content="Intelligence and metabolism — GigaChad">
<meta property="og:description" content="The greatest website on the interwebz!">
<meta property="og:image" content="/icons/chads/chad.png">
</head>
<body>
<script>
const setTheme = () => {
const root = document.documentElement
const storage = localStorage.length > 0 ? localStorage : sessionStorage
for (let key in storage) {
if (storage.hasOwnProperty(key)) {
root.style.setProperty(key, storage.getItem(key))
}
}
}
setTheme()
document.addEventListener('visibilitychange', () => { if (!document.hidden) setTheme() })
</script>
<h1>Intelligence and metabolism</h1>
<div style="text-align: center;">
<a href="/"><img class="epic" src="/icons/chads/chad.png"></a>
</div>
<hr>
<p class="nav"><span class="nav-left">Listed under <a href="/ray-peat.html">Ray Peat</a>.</span><span class="nav-right"><a href="/theme.html">Theme</a></span></p>
<p>From the <a href="https://raypeat.com/articles/articles/intelligence.shtml" target="_blank">original article</a> in 2009. Author: <a href="https://raypeat.com/" target="_blank">Ray Peat</a>.</p>
<p><strong>Appropriate
stimulation is an essential part of the developmental process. Inappropriate
stimulation is a stress that deforms the process of growth. Mediators
of stress, such as serotonin, can cause persistent distortions of physiology
and behavior.</strong></p>
<p><strong>Education
can either activate or suppress mental energy. If it is mainly obedience
training, it suppresses energy. If it creates social dislocations, it
disturbs mental and emotional energy.</strong></p>
<p><strong>Stress
early in life can impair learning, cause aggressive or compulsive behavior,
learned helplessness, shyness, alcoholism, and other problems.</strong></p>
<p><strong>Serotonin
activates the glucocorticoid system, which can produce brain atrophy.
Antiserotonin agents protect against brain atrophy and many other effects
of stress. The brain-protecting neurosteroids, including pregnenolone
and progesterone, which are increased by some kinds of stimulation,
are decreased by isolation stress, and in their absence, serotonin and
the glucocorticoids are relatively unopposed. </strong></p>
<p><strong>Since
excess serotonin can cause thrombosis and vasospasms, and the excess
cortisol resulting from hyperserotonemia can weaken blood vessels and
the immune system, a person&#39;s longevity is likely to be shortened if
something doesn&#39;t intervene to alter the patterns induced by stress
early in life.</strong></p>
<p><strong>Baroness
Blatch: “My Lords, the levels of achievement are well above the national
average of our own state schools.” </strong></p>
<p><strong>“This
is a school which attained 75 per cent A to C passes in 1998, and 63.9
per cent in 1999. Those figures are well above national averages. There
is no truancy; and there is the highest possible level of parental satisfaction
with the school. When those parents are paying their money and know
what they are paying for, who are we to take a different view about
the philosophy of education in a private school?”</strong></p>
<p><strong>Comment
during debate in House of Lords, June 30, 1999, on Chief Inspector of
Schools Woodhead&#39;s threat to close Summerhill, a democratic school which
had been started in 1921. </strong></p>
<p><strong>In
1927, the government inspectors had recommended that &#39;all educationalists&#39;
should come to Summerhill to see its &#39;invaluable&#39; research, which demonstrated
that students&#39; development is better when they regulate themselves and
are not required to attend lessons.</strong></p>
<p>Having
written about animal intelligence, and the ways in which it is similar
to human intelligence, now I want those ideas to serve as a context
for thinking about human intelligence without many of the usual preconceptions.</p>
<p>Intelligence
is an interface between physiology and the environment, so it&#39;s necessary
to think about each aspect in relation to the other. Things, both biochemical
and social, that enhance intelligence enhance life itself, and vice
versa.</p>
<p>Psychologists
have tried to give their own definitions to words like idiot, imbecile,
moron, and genius, but they have just been refining the clichés of
the culture, in which “dummy” is one of the first words that kids
in the U.S. learn. Many psychologists have tried to create “culture-free”
tests of intelligence, making it clear that they believe in something
like innate animal intelligence, though they usually call it “genetic”
intelligence. Other psychometrists have transcended not only biology
but even rationality, and have catalogued the <strong><em>preferences</em></strong>
of people that they define as intelligent, and designed “I.Q. tests”
based on the selection of things that were preferred by “intelligent
people.” This behavior is remarkably similar to the “psychometry”
of the general culture, in which “smart” people are those who do
things the “right” way.</p>
<p>About
thirty years ago, someone found that the speed with which the iris contracts
in response to a flash of light corresponds very closely to the I.Q.
measured by a psychologist using a standard intelligence test. The devices
used to measure reaction time in drivers&#39; education courses also give
a good indication of a person&#39;s intelligence, but so does measuring
their heart rate, or taking their temperature. Colleges would probably
be embarrassed to admit students on the basis of their temperature (though
they commonly award scholarships on the basis of the ability to throw
a ball). Colleges, to the extent that they are serious about the business
of education, are interested in the student&#39;s ability to master the
culture. </p>
<p>The
way a person has learned during childhood can shape that person&#39;s manner
of grasping the culture. To simply accelerate the learning of a standard
curriculum will increase that person&#39;s “I.Q.” on a conventional
test, but the important issue is whether it is really intelligent to
learn and to value the things taught in those curricula. Some educators
say that their purpose is to socialize and indoctrinate the students
into their discipline, others believe their purpose is to help their
students to develop their minds. Both of these approaches may operate
within the idea that “the culture” is something like a museum, and
that students should become curators of the collection, or of some part
of it. If we see the culture metaphorically as a mixture of madhouse,
prison, factory, and theater, the idea of “developing the student&#39;s
mind” will suggest very different methods and different attitudes
toward “the curriculum”</p>
<p>Even
sophisticated people can fall into stereotyped thinking when they write
about issues of intelligence. For example, no one considers it a sign
of genius when a slum kid is fluent in both Spanish and English, but
when some of history&#39;s brightest people are discussed, the fact that
they learned classical Greek at an early age is always mentioned. No
one mentions whether they were competent in idiomatic Spanish.</p>
<p>One
of the old cultural stereotypes is that child prodigies always “burn
out,” as if they were consuming a fixed amount of mental energy at
an accelerated rate. (This idea of burn-out is isomorphic with the other
cultural stereotypes relating aging to the “rate of living,” for
example that people with slow heart beats will live longer.) Some of
the men who have been considered as the world&#39;s brightest have, in fact,
gone through a crisis of depression, and Terman&#39;s long-term study of
bright people found that “maladjustment” did increase with I.Q.,
especially among women. But the facts don&#39;t support the concept of “burn-out”
at all. I think the facts reveal instead a deep flaw in our ideas of
education and professional knowledge.</p>
<p>In a world
run by corporation executives, university presidents (“football is
central to the university&#39;s mission”), congressmen, bankers, oilmen,
and agency bureaucrats, people with the intelligence of an ant (a warm
ant) might seem outlandishly intelligent. This is because the benighted
self-interest of the self-appointed ruling class recognizes that objective
reality is always a threat to their interests. If people, for example,
realized that estrogen therapy and serotonin-active drugs and x-rays
and nuclear power and atomic bomb tests were beneficial only to those
whose wealth and power derive from them, the whole system would lose
stability. Feigned stupidity becomes real stupidity.</p>
<p>But apart from
ideologically institutionalized stupidity, there are real variations
in the ability to learn, to remember and to apply knowledge, and to
solve problems. These variations are generally metabolic differences,
and so will change according to circumstances that affect metabolism.
Everyday social experiences affect metabolism, stimulating and supporting
some kinds of brain activity, suppressing and punishing others. All
of the activities in the child&#39;s environment are educational, in one
way or another.</p>
<p>Some
of the famous prodigies of history illustrate the importance of ideology
in the development of intellect. Family ideology, passing on the philosophical
orientations of parents and their friends, shapes the way the children
are educated. </p>
<p>Some
of these family traditions can be traced by considering who the child&#39;s
godfather was. Jeremy Bentham was John Stuart Mill&#39;s godfather,
Mill was Bertrand Russell&#39;s; Ralph Waldo Emerson was William James&#39;
godfather, James was W. J. Sidis&#39;s. Willy Sidis was educated by his
parents to demonstrate their theory of education, which grew out of
the philosophies of Emerson and James. His father, Boris Sidis, was
a pioneer in the study of hypnosis, and he believed that suggestion
could mobilize the mind&#39;s “reserve energy.” Willy learned several
languages and advanced mathematics at an early age. After he graduated
from Harvard at the age of 16, he tried teaching math at Rice Institute,
but he was displeased by the attitudes of his students and of the newspaper
and magazine writers who made a profession of mocking him. He attended
law school at Harvard, and would have been imprisoned as a conscientious
objector if the war hadn&#39;t ended. </p>
<p>Antisemitism
probably played a role in his sense of isolation when he was at Harvard
and Rice. In 1912 Henry Goddard, a pioneer in intelligence testing (and
author of <strong><em>The Kallikak Family: A Study in the Heredity of Feeble-
Mindedness</em>)</strong>, administered intelligence tests to immigrants and
determined that 83 percent of Jews and 87 percent of Russians were “feeble-minded.”
By the standards of the time, it was highly inappropriate for the child
of extremely poor Jewish immigrants from eastern Europe to be so bright.</p>
<p>Sidis
hid from the press, and worked as a bookkeeper and clerk, while he studied
and wrote. During his years of obscurity, he wrote books on philosophy
and American history. Eventually, the journalists discovered him again,
and after prolonged lawsuits against the magazines for invasion of privacy
and slander, he died of a stroke at the age of 46.</p>
<p>Sidis
is probably the culture&#39;s favorite example of the child prodigy who
burns out, but people (Robert Persig, Buckminster Fuller) who have read
his books have said favorable things about them. The journalists&#39; emphasis
on the fact that Sidis never held a prestigious job nicely illustrates
their cliché mentality: “If you&#39;re so smart, why aren&#39;t you rich?”
But throughout history, intelligent nonconformists have supported themselves
as craft-workers or technicians--Socrates as a stone mason, Spinoza
as a lens grinder, Blake as an engraver, Einstein as a patent examiner,
for example. </p>
<p>In
conventional schools (as in conventional society) 10,000 questions go
unanswered, not only because a teacher with many students has no time
to answer them, but also because most teachers wouldn&#39;t know most of
the answers.</p>
<p>The
parents of W. J. Sidis and J. S. Mill were remarkably well educated
people who, because they dissented from society&#39;s ideology, chose to
spend much of their time educating their children. Whenever a question
about Euclidean geometry or Greek grammar occurred to the child, it
could be answered immediately. It was only natural that progress would
be fast, but there were more important differences.</p>
<p>When
questions are answered, curiosity is rewarded, and the person is enlivened.
In school, when following instructions and conforming to a routine is
the main business, many questions must go unanswered, and curiosity
is punished by the dulling emptiness of the routine.</p>
<p>Some
schools are worse than others. For example, slum children were given
I.Q. tests when they started school, and each subsequent year, and their
I.Q.s dropped with each year of school. In a stimulating environment,
the reverse can happen, the I.Q. can rise each year. Since the tests
aren&#39;t “culture free,” their scores reflected the material that
they were being taught, but they undoubtedly also reflected the increasing
boredom and despair of the children in a bad school, or the increasing
liveliness of the children in the stimulating environment.</p>
<p>I
have spoken with people in recent years who still held the idea of a
fixed genetic mental potential, who believe that poor children fall
behind because they are reaching their “genetic limit.” For them,
the I.Q. represents an index of intrinsic quality, and is as important
as distinguishing between caviar and frogs&#39; eggs. The rat research of
Marion Diamond and others at the University of California, however,
showed that the structure, weight, and biochemistry of a rat&#39;s brain
changes, according to the amount of environmental stimulation and opportunity
for exploration. This improvement of brain structure and function is
passed on to the next generation, giving it a head-start. It isn&#39;t likely
that rats are more disposed than humans to benefit from mental activity,
and in the years since Diamond&#39;s research there have been many discoveries
showing that brains of all sorts complexify structurally and functionally
in response to stimulation.</p>
<p>Rats
isolated in little boxes, generation after generation--the normal laboratory
rats--were the standard, but now it&#39;s known that isolation is a stress
that alters brain chemistry and function.</p>
<p>
Willy Sidis and John Stuart Mill were being stimulated and allowed to
develop in one direction, but they were being isolated from interaction
with their peers. When Mill was twenty he went into a depression, and
later he wrote that it was because he discovered that he was unable
to <strong><em>feel.</em></strong> He had developed only part of his personality.</p>
<p>Bertrand
Russell (1872-1970), orphaned at the age of four, went to live with
his grandmother, who chose not to send him to school, but provided tutors.
He didn&#39;t experience a sense of academic pressure, and was able to read
whatever he wanted in his late grandfather&#39;s library. He didn&#39;t realize
that he was unusually bright until he went to Cambridge. The unusual
freedom of his childhood must have contributed to his willingness to
hold unpopular opinions. In 1916 he was fined, and in 1918 imprisoned
for 6 months, for opposing the war.</p>
<p>In
1927, Russell and his wife, Dora Black, started a school. He later wrote
that, although the average student at the school was very bright, an
exceptionally bright student was likely to be ostracized by the less
bright students. He commented on the harm done to the brightest students
by their social isolation, probably thinking about his own education
in relative isolation. A psychologist (Leta Hollingworth, 1942) has
made similar observations about the isolation that can be produced by
a large difference of I.Q. She did a series of studies of very bright
children, beginning in 1916, including working with some of them in
a program she designed in a New York public school. Her empathy allowed
her to discover things that weren&#39;t apparent to her contemporaries. </p>
<p>During
this time Lewis Terman was studying bright children, and wanted to disprove
some of the popular stereotypes about intelligent people, and to support
his ideology of white racial superiority. In 1922 he got a large grant,
and sorted out about 1500 of the brightest children from a group of
250,000 in California. He and his associates then monitored them for
the rest of their lives (described in <strong><em>Genetic Studies of Genius</em></strong>).
His work contradicted the stereotype of bright people as being sickly
or frail, but, contrary to his expectation, there was an association
between maladjustment and higher I.Q.; the incidence of neurotic fatigue,
anxiety, and depression increased along with the I.Q. The least bright
of his group were more successful in many ways than the most bright.
He didn&#39;t really confront the implications of this, though it seriously
challenged his belief in a simple genetic racial superiority of physique,
intellect, and character.</p>
<p>I.Q.
testing originated in a historical setting in which its purpose was
often to establish a claim of racial superiority, or to justify sterilization
or “euthanasia,” or to exclude immigrants. More recently, the tests
have been used to assign students to certain career paths. Because of
their use by people in power to control others, the I.Q. tests have
helped to create misunderstanding of the nature of intelligence. A person&#39;s
“I.Q.” now has very strong associations with the ideology of schooling
as a road to financial success, rather than to enrichment of a shared
mental life.</p>
<p>If
a bad school resembles, on the intellectual level, a confining rat box,
the educational isolation of Mill, Russell, and Sidis was emotionally
limiting, almost like solitary confinement. Once when Willy Sidis was
arrested for marching in a May Day parade, his father was able to keep
him from going to prison, but Willy apparently would have preferred
the real prison to life with his parents.</p>
<p>None
of these three famous intellects was known for youthful playfulness,
though playfulness is a quality that&#39;s closely associated with intelligence
in mammals and birds. (Russell, however, in middle age developed many
new interests, such as writing short stories, and had many new loves
even in old age.) Stress early in life, such as isolation, reduces the
playfulness of experimental animals. Playfulness is contagious, but
so is the inability to play. </p>
<p>In
schools like Summerhill, which was founded in 1921 by A. S. Neill, students
aren&#39;t required to attend classes when they would rather do something
else, but at graduation they usually do better on their standardized
national examinations than students who have dutifully attended classes
for years. For students, as for rats, freedom and variety are good for
the brain, and tedious conformity is harmful. When a school is very
good, it can spread a contagion of playfulness along with an interest
in learning.</p>
<p>An
environment that fosters optimal intelligence will necessarily promote
the development of emotional health, and will almost certainly foster
good physical health and longevity, because no part of the physiological
system can thrive at the expense of another part. And within the boundaries
of life-enriching environments, there are infinite possibilities for
variety.</p>
<p>There
is a common belief in the rigidity of the adult nervous system, in analogy
with feral cats or dogs, that supposedly can&#39;t be tamed if they have
grown up without knowing humans. But people who have had the inclination
to understand wild animals have found that, even when the animals have
been captured as adults, they can become as sociable as if they had
grown up in domestication. The “horse whisperer” demonstrated this
sort of empathetic approach to animals. Sometimes, these people have
a similar ability to communicate with people who are retarded, or autistic,
or demented, but the professionalization of society has made it increasingly
unlikely that people with the need for intuitive help will encounter
someone who is able to give it. The closest psychology has come to professionally
recognizing the importance of empathy was in Carl Rogers&#39; work, e.g., <em>
Client-Centered Therapy.</em></p>
<p>Rogers
showed that a sense of solidarity must exist between therapist and client
for the therapy to be helpful. A similar solidarity has to exist between
teacher and student, for education to be successful. If ordinary family
and social contacts could occur within such an atmosphere of mutual
respect, psychopathology (including learning difficulties) would be
much less common.</p>
<p>Although
three individuals don&#39;t prove an argument, I think the lives and situations
of Sidis, Mill, and Russell are usefully symbolic. Sidis, who grew up
under intense pressure and social isolation and in extreme poverty,
died at the age of 46. Mill, who was educated mainly by his father,
in secure financial circumstances, experienced social isolation and
moderate pressure, and lived about 20 years longer than Sidis did. Russell,
who grew up in the highest circles of the ruling class, experienced
no pressure, and only the mild kind of social isolation that wasn&#39;t
exceptional for his class. He lived to be 97. </p>
<p>The
psychopathology of social isolation has been studied in a variety of
animals, and many features are similar across species, including humans.
Aggression, helplessness, and reduced ability to learn are typically
produced in animals by social isolation, and it&#39;s clear that certain
kinds of family environment produce the same conditions in children.
Schools seldom help, and often hinder, recovery from such early experiences.</p>
<p>“Vital
exhaustion,” decreased slow wave sleep, and anger, which are associated
with the “type A personality” and with circulatory and heart disease,
appear to have their origin in childhood experiences. Low income and
financial insecurity are strongly associated with anger, sleep disturbances,
and circulatory disease. In animals stressed by social isolation,
similar features emerge, under the influence of decreased neurosteroids,
and increased serotonin and activity of the glucocorticoid system.
</p>
<p>The
“smart drug” culture has generally been thinking pharmaceutically
rather than biologically. Behind that pharmaceutical orientation there
is sometimes the idea that the individual just isn&#39;t trying hard enough,
or doesn&#39;t have quite the right genes to excel mentally.</p>
<p>
Many stimulants--amphetamine and estrogen, for example--can increase
alertness temporarily, but at the expense of long range damage. The
first principle of stimulation should be to avoid a harmful activation
of the catabolic stress hormones. Light, play, environmental variety
and exploratory conversations stimulate the whole organism in an integral
way, stimulating repair processes and developmental processes.</p>
<p>Any
chemical support for intelligence should take into account the mind-damaging
stresses that our culture can impose, and provide defense against those.
In darkness and isolation, for example, the stress hormones increase,
and the brain-protective steroids decrease. The memory improvement that
results from taking pregnenolone or thyroid (which is needed for synthesizing
pregnenolone from cholesterol) is the result of turning off the dulling
and brain-dissolving stress hormones, allowing normal responsiveness
to be restored.</p>
<p>If
we know that rats nurtured in freedom, in an interesting environment,
grow more intelligent, then it would seem obvious that we should experiment
with similar approaches for children--if we are really interested in
fostering intelligence. And since violence and mental dullness are created
by the same social stresses, even the desire to reduce school violence
might force the society to make some improvements that will, as a side
effect, foster intelligence. </p>
<h2>References</h2>
<small>
<p>B.
Russell: “If you wish to know what men will do, you must know not
only or principally their material circumstances, but rather the whole
system of their desires with their relative strengths.”</p>
<p>John
Holt, from an interview in <em>Mother Earth News,</em> July/August, 1980<strong>:</strong>
“I suggested that we simply provide young people with schools where
there are a lot of interesting things to look at and work with . . .
but that we let the chidlren learn in their own wqys. If they have questions,
answer the questions. If they want to know where to look for something,
show them where to look.”</p>
<p>John
Holt, from the introduction to his book, <em>Teach Your Own,</em> (New
York: Dell, 1981)<strong>:</strong> “The children in the classroom, despite
their rich backgrounds and high I.Q.&#39;s, were with few exceptions frightened,
timid, evasive, and self-protecting. The infants at home were bold adventurers.”</p>
<p>“It
soon became clear to me that children are by nature and from birth very
curious about the world around them, and very energetic, resourceful,
and competent in exploring it, finding out about it, and mastering.
In short, much more eager to learn, and much better at learning, than
most adults. Babies are not blobs, but true scientists. Why not then
make schools into places in which children would be allowed, encouraged,
and (if and when they asked) helped to explore and make sense of the
world around them (in time and space) in ways that most interested them?”</p>
<p>Psychosom Med
1984 Nov-Dec;46(6):546-8. <strong>Rapid communication: whole blood serotonin
and the type A behavior pattern.</strong> Madsen D, McGuire MT.<strong> In 72
young males, whole blood serotonin is shown to have a pronounced relationship
with the Type A behavior pattern.</strong> The relationship is explored with
multivariate statistical techniques.</p>
<p>J Neurochem.
2000 Aug;75(2):732-40. Serra M, Pisu MG, Littera M, Papi G, Sanna E,
Tuveri F, Usala L, Purdy RH, Biggio G.<strong> Social isolation-induced decreases
in both the abundance of neuroactive steroids and GABA(A) receptor function
in rat brain.</strong> </p>
<p>Ann Med 2000
Apr;32(3):210-21. <strong>Role of serotonin in memory impairment.</strong> Buhot
MC, Martin S, Segu L. </p>
<p>Ivan
Illich and Etienne Verne, <strong><em>Imprisoned in the global classroom.</em></strong>
London, Writers and Readers Publishing Cooperative, 1976.</p>
<p>Ivan
Illich, <strong><em>Deschooling society.</em></strong> Harmondsworth: Penguin, 1976
(1971).</p>
<p>----Tools
for Conviviality<em> </em>(1973).</p>
<p><strong><em>----Toward
a history of needs.</em></strong> New York, Pantheon Books, c1978.</p>
<p>----Limits
to medicine. medical nemesis : the expropriation of health. Harmondsworth
New York, Penguin, 1977. </p>
<p><strong><em>----Celebration
of awareness: a call for institutional revolution.</em></strong> Harmondsworth,
Penguin Education, 1976. Pelican books Originally published: Garden
City [N.Y.]: Doubleday, 1970; London: Calder and Boyars, 1971.</p>
<p><strong><em>----Disabling
professions.</em></strong> London, Boyars, 1977, Ideas in progress series.</p>
<p>Eur J Pharmacol
1992 Feb 25;212(1):73-8. <strong>5-HT3 receptor antagonists reverse helpless
behaviour in rats.</strong> Martin P, Gozlan H, Puech AJ Departement de Pharmacologie,
Faculte de Medecine Pitie-Salpetriere, Paris, France. The effects of
the 5-HT3 receptor antagonists, zacopride, ondansetron and ICS 205-930,
were investigated in an animal model of depression, the learned helplessness
test. Rats previously subjected to a session of 60 inescapable foot-shocks
exhibited a deficit of escape performance in three subsequent shuttle-box
sessions. The 5-HT3 receptor antagonists administered i.p. twice daily
on a chronic schedule (zacopride 0.03-2 mg/kg per day; ondansetron and
ICS 205-930: 0.125-2 mg/kg per day) reduced the number of escape failures
at low to moderate daily doses. This effect was not observed with the
highest dose(s) of zacopride, ondansetron and ICS 205-930 tested.. These
results indicate that 5-HT3 antagonists may have effects like those
of conventional antidepressants in rats.</p>
<p>Neuropharmacology
1992 Apr;31(4):323-30. <strong>Presynaptic serotonin mechanisms in rats subjected
to inescapable shock.</strong> Edwards E, Kornrich W, Houtten PV, Henn FA.
“After exposure to uncontrollable shock training, two distinct groups
of rats can be defined in terms of their performance in learning to
escape from a controllable stress. Learned helpless rats do not learn
to terminate the controllable stress, whereas non-learned helpless rats
learn this response as readily as naive control rats do.” “These
results implicate presynaptic serotonin mechanisms in the behavioral
deficit caused by uncontrollable shock. In addition, a limbic-hypothalamic
pathway may serve as a control center for the behavioral response to
stress.”</p>
<p>Neurochem Int
1992 Jul;21(1):29-35.<strong> In vitro neurotransmitter release in an animal
model of depression</strong>. Edwards E, Kornrich W, van Houtten P, Henn
FA. “Sprague-Dawley rats exposed to uncontrollable shock can
be separated by a subsequent shock escape test into two groups: a &quot;helpless&quot;
(LH) group which demonstrates a deficit in escape behavior, and a &quot;nonlearned
helpless&quot; (NLH) group which shows no escape deficit and acquires
the escape response as readily as naive control rats (NC) do.” “The
major finding concerned a significant increase in endogenous and K(+)-stimulated
serotonin (5-HT) release in the hippocampal slices of LH rats. There
were no apparent differences in acetylcholine, dopamine and noradrenaline
release in the hippocampus of LH rats as compared to NLH and NC rats.
These results add further support to previous studies in our laboratory
which implicate presynaptic 5-HT mechanisms in the behavioral deficit
caused by uncontrollable shock.”</p>
<p>Psychiatry
Res 1994 Jun;52(3):285-93. <strong>In vivo serotonin release and learned
helplessness.</strong> Petty F, Kramer G, Wilson L, Jordan S Mental Health
Clinic, Dallas Veterans Affairs Medical Center, TX. Learned helplessness,
a behavioral depression caused by exposure to inescapable stress, is
considered to be an animal model of human depressive disorder. Like
human depression, learned helplessness has been associated with a defect
in serotonergic function, but the nature of this relationship is not
entirely clear. We have used in vivo microdialysis brain perfusion to
measure serotonin (5-hydroxytryptamine, 5HT) in extracellular space
of medial frontal cortex in conscious, freely moving rats. Basal 5HT
levels in rats perfused before exposure to tail-shock stress did not
themselves correlate with subsequent learned helplessness behavior.
However, 5HT release after stress showed a significant increase with
helpless behavior. <strong>These data support the hypothesis that a cortical
serotonergic excess is causally related to the development of learned
helplessness.</strong></p>
<p>Pharmacol Biochem
Behav 1994 Jul;48(3):671-6. <strong>Does learned helplessness induction by
haloperidol involve serotonin mediation?</strong> Petty F, Kramer G, Moeller
M Veterans Affairs Medical Center, Dallas 75216. Learned helplessness
(LH) is a behavioral depression following inescapable stress. Helpless
behavior was induced in naive rats by the dopamine D2 receptor blocker
haloperidol (HDL) in a dose-dependent manner, with the greatest effects
seen at 20 mg/kg (IP). Rats were tested 24 h after injection. Haloperidol
(IP) increased release of serotonin (5-HT) in medial prefrontal cortex
(MPC) as measured by in vivo microdialysis. Perfusion of HDL through
the probe in MPC caused increased cortical 5-HT release, as did perfusion
of both dopamine and the dopamine agonist apomorphine. Our previous
work found that increased 5-HT release in MPC correlates with the development
of LH. The present work suggests that increased DA release in MPC, known
to occur with both inescapable stress and with HDL, may play a necessary
but not sufficient role in the development of LH. Also, this suggests
that increased DA activity in MPC leads to increased 5-HT release in
MPC and to subsequent behavioral depression.</p>
<p>Arzneimittelforschung
1975 Nov; 25(11):1737-44<strong>. [Central action of WA-335-BS, a substance
with peripheral antiserotonin and antihistaminic activity].</strong> Kahling
J, Ziegler H, Ballhause H. “In rats and mice the serotonin and histamine
antagonistic drug <strong>. . .</strong> (WA 335-BS) caused stronger central sedative
effects than did cyproheptadine. WA 335-BS also displayed stronger activity
against reserpine- and central tremorine-induced effects than did cyproheptadine
and it slightly enhanced d-amphetamine-induced<strong> </strong>
effects:<strong> therefore it may have antidepressant properties. WA 335-BS
proved to be</strong> <strong>very effective against isolation-induced aggression
in male mice.</strong> The comparatively small anxiolytic effects may have
been caused in part by the central antiserotonin properties.” “The
results of our animal studies suggest WA 335-BS to be an antidepressant
with sedative properties.”</p>
<p>Neuroscience
2000;100(4):749-68<strong>. Behavioral, neurochemical and endocrinological
characterization of the early social isolation syndrome.</strong> Heidbreder
CA, Weiss IC, Domeney AM, Pryce C, Homberg J, Hedou G, Feldon J, Moran
MC, Nelson P. “Rearing rats in isolation has been shown to be a relevant
paradigm for studying early life stress and<strong> understanding the genesis
of depression and related affective disorders.</strong> Recent studies from
our laboratory point to the relevance of studying the social isolation
syndrome as a function of home caging conditions.”</p>
<p>Stroke 1991
Nov;22(11):1448-51. <strong>Platelet secretory products may contribute to
neuronal injury.</strong> Joseph R, Tsering C, Grunfeld S, Welch KM. BACKGROUND:
We do not fully understand the mechanisms for neuronal damage following
cerebral arterial occlusion by a thrombus that consists mainly of platelets.
The view that certain endogenous substances, such as glutamate, may
also contribute to neuronal injury is now reasonably well established.
Blood platelets are known to contain and secrete a number of substances
that have been associated with neuronal dysfunction. Therefore, we hypothesize
that a high concentration (approximately several thousand-fold higher
than in plasma, in our estimation) of locally released platelet secretory
products derived from the causative thrombus may contribute to neuronal
injury and promote reactive gliosis. SUMMARY OF COMMENT: We have recently
been able to report some direct support for this concept. When organotypic
spinal cord cultures were exposed to platelet and platelet products,
a significant reduction in the number and the size of the surviving
neurons occurred in comparison with those in controls. We further observed
that serotonin, a major platelet product, has neurotoxic properties.
There may be other platelet components with similar effect.<strong> CONCLUSIONS:
The hypothesis of platelet-mediated neurotoxicity gains some support
from these recent in vitro findings. The concept could provide a new
area of research in stroke, both at the clinical and basic levels.</strong></p>
<p>Am J Psychiatry
1981 Aug;138(8):1082-5.<strong> Tryptophan metabolism in children with attentional
deficit disorder.</strong> Irwin M, Belendiuk K, McCloskey K, Freedman DX
The authors present the first report, to their knowledge, of hyperserotonemia
in children with attentional deficit disorder who had normal intelligence.
Hyperserotonemic children had significantly lower levels of plasma total
and protein-bound tryptophan and a higher percentage of free tryptophan
than those with normal serotonin levels. Plasma kynurenine did not differ,
suggesting that the hyperserotonemia is not due to a blockade of the
kynurenine pathway but may reflect on increase in tissue tryptophan
uptake and use.</p>
<p>J Neuropsychiatry
Clin Neurosci 1990 Summer;2(3):268-74.<strong> Autistic children and their
first-degree relatives: relationships between serotonin and norepinephrine
levels and intelligence.</strong> Cook EH, Leventhal BL, Heller W, Metz J,
Wainwright M, Freedman DX “Whole-blood serotonin (5-HT) and plasma
norepinephrine (NE) were studied in 16 autistic children, 21 siblings
of autistic children, and 53 parents of autistic children. <strong>Both plasma
NE and whole-blood 5-HT were negatively correlated with vocabulary performance.” </strong>
“Eighteen subjects were hyperserotonemic (whole-blood 5-HT greater
than 270 ng/ml). For these subjects, plasma NE was significantly higher
than for subjects without hyperserotonemia.”</p>
<p>Biol Psychiatry
1998 Dec 15;44(12):1321-8. <strong>Cerebrospinal fluid monoamines in Prader-Willi
syndrome.</strong> Akefeldt A, Ekman R, Gillberg C, Mansson JE “The behavioral
phenotype of Prader-Willi syndrome (PWS) suggests hypothalamic dysfunction
and altered neurotransmitter regulation. The purpose of this study was
to examine whether there was any difference in the concentrations of
monoamine metabolites in the cerebrospinal fluid (CSF) in PWS and non-PWS
comparison cases.” “The concentrations of<strong> dopamine and particularly
serotonin metabolites were increased in the PWS group. The differences
were most prominent for 5-hydroxyindoleacetic acid. The increased concentrations
were found in all PWS cases independently of age, body mass index, and
level of mental retardation.” “The findings implicate dysfunction
of the serotonergic system and possibly also of the dopamine system </strong>
in PWS individuals . . . .”</p>
<p>Pharmacol Biochem
Behav 1976 Jul;5(1):55-61. <strong>The role of serotonergic pathways in isolation-induced
aggression in mice.</strong> Malick JB, Barnett A Male mice that became aggressive
following four weeks of social isolation were treated with seven known
serotonin receptor antagonists. All of the<strong> antiserotonergic drugs
selectively antagonized the fighting behavior of the isolated mice;
the antiaggressive activity was selective since, at antifighting doses,
none of the drugs either significantly altered spontaneous motor activity</strong>
or impaired inclined-screen performance. <strong>Antagonism of 5-HTP-induced
head-twitch was used as an in vivo measure of antiserotonergic activity
and a statistically significant correlation existed between potency
as an antiserotonergic and potency as an antiaggressive.</strong> PCPA, a
serotonin depletor, also significantly <strong>antagonized isolation-induced
aggression</strong> for at least 24 hr postdrug administration. The interrelationship
between cholinergic and serotonergic mechanisms in the mediation of
isolation aggression was investigated. The involvement of serotonergic
systems in isolation-induced aggression is discussed.</p>
<p>Probl Endokrinol
(Mosk) 1979 May-Jun;25(3):49-52<strong> [Role of serotonin receptors of the
medial-basal hypothalamus in the mechanisms of negative feedback of
the hypophyseal-testicular complex].</strong> Naumenko EV, Shishkina GT.
“Administration of serotonin into the lateral ventricle of the brain
of male rats, against the background of complete isolation of the medial-basal
hypothalamus was accompanied by the block of the compensatory elevation
of the blood testosterone level following unilateral castration.” </p>
<p>Encephale 1994
Sep-Oct;20(5):521-5. <strong>[Can a serotonin uptake agonist be an authentic
antidepressant? Results of a multicenter, multinational therapeutic
trial].</strong> Kamoun A, Delalleau B, Ozun M The classical biochemical
hypothesis of depression posits a functional deficit in central neurotransmitter
systems particularly serotonin (5-HT) and noradrenaline. The major role
suggested for 5-HT in this theory led to the development of a large
number of compounds which selectively inhibit 5-HT uptake. Numerous
clinical trials have demonstrated the antidepressant efficacy of such
types of serotoninergic agents, supporting 5-HT deficit as the main
origin of depression. <strong>Therefore, everything seemed clear: depression
was caused by 5-HT deficit. Tianeptine is clearly active in classical
animal models predictive of antidepressant activity, and is also active
in behavioral screening tests: it antagonizes isolation induced aggression
in mice and behavioral despair in rats.</strong> Biochemical studies have
revealed that in contrast to classical tricyclic antidepressant,<strong>
tianeptine stimulates 5-HT uptake </strong>
in vivo in the rat brain. This somewhat surprising property was observed
in the cortex and the hippocampus following both acute and chronic administrations.
This increase in 5-HT uptake has also been confirmed in rat platelets
after acute and<strong> chronic administrations. Moreover, in humans, a study
in depressed patients demonstrated that tianeptine significantly increased
platelet 5-HT uptake after a single administration as well as after
10 and 28 days of treatment. The antidepressant activity of tianeptine
has been evaluated in controlled studies versus reference antidepressants.
Another study aiming to compare the antidepressant efficacy of tianeptine
versus placebo and versus imiporamine is</strong> presented. 186 depressed
patients were included in this trial. They presented with either Major
Depression, single episode (24.6%) or Major Depression recurrent (66.8%)
or Bipolar Disorder (depressed) (8.6%).</p>
<p>Psychopharmacology
(Berl) 1998 Oct;139(3):255-60.<strong> Ca2+ dependency of serotonin and dopamine
release from CNS slices of chronically isolated rats.</strong> Jaffe EH.
“We have used chronic isolated housing as an animal model of depression.”
“The following questions were addressed: first, if there is a change
in the depolarization dependent release of DA and 5-HT from these CNS
structures, and second, if the release is through the classical exocytotic
mechanism. <strong>A significant increase in KCl stimulated release of 5-HT
was observed in chronically isolated animals when compared to controls. </strong>
5-HT release was completely abolished from controls or isolated animals,
when slices were incubated with Krebs containing zero Ca2+/10 mM Mg2+,
the inorganic Ca2+ channel blockers, Cd2+ or Ni2+ and the calmodulin
inhibitor, trifluoperazine.” <strong>“The basal release of DA and 5-HT
was similar in control and isolated animals and was not affected by
the Ca2+ channel antagonists. The results suggest that extracellular
Ca2+-dependent release of 5-HT and, to a lesser degree, of DA, is increased
in this chronic animal model of depression in</strong> several CNS structures.”</p>
<p>Gen Pharmacol
1994 Oct;25(6):1257-1262.<strong> Serotonin-induced decrease in brain ATP,
stimulation of brain anaerobic glycolysis and elevation of plasma hemoglobin;
the protective action of calmodulin antagonists.</strong> Koren-Schwartzer
N, Chen-Zion M, Ben-Porat H, Beitner R Department of Life Sciences,
Bar-Ilan University, Ramat Gan, Israel. <strong>1. Injection of serotonin
(5-hydroxytryptamine) to rats, induced a dramatic fall in brain ATP
level, accompanied by an increase in P(i). Concomitant to these changes,
the activity of cytosolic phosphofructokinase, the rate-limiting enzyme
of glycolysis, was significantly enhanced. Stimulation of anaerobic
glycolysis was also reflected by a marked increase in lactate content
in brain. 2. Brain glucose</strong> 1,6-bisphosphate level was decreased,
whereas fructose 2,6-bisphosphate was unaffected by serotonin. 3. All
these serotonin-induced changes in brain, which are characteristic for
cerebral ischemia, were prevented by treatment with the calmodulin (CaM)
antagonists, trifluoperazine or thioridazine. 4<strong>.. Injection of serotonin
also induced a marked elevation of plasma hemoglobin, reflecting lysed
erythrocytes,</strong> which was also prevented by treatment with the CaM
antagonists. 5.<strong> The present results suggest that CaM antagonists
may be effective drugs in treatment of many pathological conditions
and diseases in which plasma serotonin levels are known to increase.</strong></p>
<p>Gen Pharmacol
1994 Oct;25(6):1257-1262.<strong> Serotonin-induced decrease in brain ATP,
stimulation of brain anaerobic glycolysis and elevation of plasma hemoglobin;
the protective action of calmodulin antagonists.</strong> Koren-Schwartzer
N, Chen-Zion M, Ben-Porat H, Beitner R Department of Life Sciences,
Bar-Ilan University, Ramat Gan, Israel. <strong>1. Injection of serotonin
(5-hydroxytryptamine) to rats, induced a dramatic fall in brain ATP
level, accompanied by an increase in P(i). Concomitant to these changes,
the activity of cytosolic phosphofructokinase, the rate-limiting enzyme
of glycolysis, was significantly enhanced. Stimulation of anaerobic
glycolysis was also reflected by a marked increase in lactate content
in brain. 2. Brain glucose</strong> 1,6-bisphosphate level was decreased,
whereas fructose 2,6-bisphosphate was unaffected by serotonin. 3. All
these serotonin-induced changes in brain, which are characteristic for
cerebral ischemia, were prevented by treatment with the calmodulin (CaM)
antagonists, trifluoperazine or thioridazine. 4. Injection of serotonin
also induced a marked elevation of plasma hemoglobin, reflecting lysed
erythrocytes, which was also prevented by treatment with the CaM antagonists.
5. The present results suggest that CaM antagonists may be effective
drugs in treatment of many pathological conditions and diseases in which
plasma serotonin levels are known to increase. </p>
<p>J Neural Transm
1998;105(8-9):975-86. <strong>Role of tryptophan in the elevated serotonin-turnover
in hepatic encephalopathy.</strong> Herneth AM, Steindl P, Ferenci P, Roth
E, Hortnagl H. “The increase of the brain levels of 5-hydroxyindoleacetic
acid (5-HIAA) in hepatic encephalopathy (HE) suggests an increased turnover
of serotonin (5-HT).” “These results provide further evidence for
the role of tryptophan in the elevation of brain 5-HT metabolism and
for a potential role of BCAA in the treatment of HE.”</p>
<p>Tugai VA; Kurs&#39;kii
MD; Fedoriv OM. <strong>[Effect of serotonin on Ca2+ transport in mitochondria
conjugated with the respiratory chain].</strong> Ukrainskii Biokhimicheskii
Zhurnal, 1973 Jul-Aug, 45(4):408-12.</p>
<p>Kurskii MD;
Tugai VA; Fedoriv AN.<strong> [Effect of serotonin and calcium on separate
components of respiratory chain of mitochondria in some rabbit tissues].</strong>
Ukrainskii Biokhimicheskii Zhurnal, 1970, 42(5):584-8.</p>
<p>Watanabe Y;
Shibata S; Kobayashi B. <strong>Serotonin-induced swelling of rat liver mitochondria.</strong>
Endocrinologia Japonica, 1969 Feb, 16(1):133-47.</p>
<p>Mahler DJ;
Humoller FL. <strong>The influence of serotonin on oxidative metabolism of
brain mitochondria.</strong> Proceedings of the Society for Experimental
Biology and Medicine, 1968 Apr, 127(4):1074-9.</p>
<p>Eur J Pharmacol
1994 Aug 11;261(1-2):25-32. <strong>The effect of alpha 2-adrenoceptor antagonists
in isolated globally ischemic rat hearts.</strong> Sargent CA, Dzwonczyk
S, Grover G.J. “The alpha 2-adrenoceptor antagonist, yohimbine, has
been reported to protect hypoxic myocardium. Yohimbine has several other
activities, including 5-HT receptor antagonism, at the concentrations
at which protection was found.” “Pretreatment with yohimbine (1-10
microM) caused a concentration-dependent increase in reperfusion left
ventricular developed pressure and a reduction in end diastolic pressure
and lactate dehydrogenase release. The structurally similar compound
rauwolscine (10 microM) also protected the ischemic myocardium. In contrast,
idozoxan (0.3-10 microM) or tolazoline (10 microM) had no protective
effects. The<strong> cardioprotective effects of yohimbine were partially
reversed by 30 microM 5-HT. These results indicate that the mechanism
for the cardioprotective activity of yohimbine may involve 5-HT receptor
antagonistic activity.” </strong></p>
<p>Zubovskaia
AM. <strong>[Effect of serotonin on some pathways of oxidative metabolism
in the mitochondria of rabbit heart muscle].</strong> Voprosy Meditsinskoi
Khimii, 1968 Mar-Apr, 14(2):152-7.</p>
<p>Warashina Y. <strong>
[On the effect of serotonin on phosphorylation of rat liver mitochondria</strong>].
Hoppe-Seylers Zeitschrift fur Physiologische Chemie, 1967 Feb,
348(2):139-48.</p>
<p>Eur Neuropsychopharmacol
1997 Oct;7 Suppl 3:S323-S328. <strong>Prevention of stress-induced morphological
and cognitive consequences</strong>.. McEwen BS, Conrad CD, Kuroda Y, Frankfurt
M, Magarinos AM, McKittrick C. Atrophy and dysfunction of the human
hippocampus is a feature of aging in some individuals, and this dysfunction
predicts later dementia. There is reason to believe that adrenal glucocorticoids
may contribute to these changes, since the elevations of glucocorticoids
in Cushing&#39;s syndrome and during normal aging are associated with atrophy
of the entire hippocampal formation in humans and are linked to deficits
in short-term verbal memory. We have developed a model of stress-induced
atrophy of the hippocampus of rats at the cellular level, and we have
been investigating underlying mechanisms in search of agents that will
block the atrophy. Repeated restraint stress in rats for 3 weeks causes
changes in the hippocampal formation that include suppression of 5-HT1A
receptor binding and atrophy of dendrites of CA3 pyramidal neurons,
as well as impairment of initial learning of a radial arm maze task. <strong>
Because serotonin is released by stressors and may play a role in the
actions of stress on nerve cells, we investigated the actions of agents
that facilitate or inhibit serotonin reuptake.</strong> Tianeptine is known
to enhance serotonin uptake, and we compared it with fluoxetine, an
inhibitor of 5-HT reuptake, as well as with desipramine. <strong>Tianeptine
treatment (10 mg/kg/day) prevented the stress-induced atrophy of dendrites
of CA3 pycamidal neurons,</strong> whereas neither fluoxetine (10 mg/kg/day)
nor desipramine (10 mg/kg/day) had any effect. <strong>Tianeptine treatment
also prevented the stress-induced impairment of radial maze learning.</strong>
Because <strong>corticosterone- and stress-induced atrophy of CA3 dendrites
is also blocked by phenytoin, an inhibitor of excitatory amino acid
release and actions, these results suggest that serotonin released by
stress or corticosterone may interact pre- or post-synaptically with
glutamate released by stress or corticosterone, and that the final common
path may involve interactive effects between serotonin and glutamate
receptors on the dendrites of CA3 neurons innervated by mossy fibers
from the dentate gyrus. We discuss the implications of these findings
for treating cognitive impairments and the risk for dementia in the
elderly.</strong> </p>
<small>
<hr>
<p class="C">Library of GigaChad | <a href="/" target="_blank">GigaChad</a></p>
</body>
</html>