[Paleopsych] why does disaster cripple our two brains?
HowlBloom at aol.com
HowlBloom at aol.com
Sat Apr 9 23:35:19 UTC 2005
re: the old posting I’ve appended below: Why would misfortune and lack of
control turn down the body’s two leading learning machines—the cognitive brain
and the immune system? Here’s a guess. When I left the music business, I
needed to get away from music completely. Music, something I’d loved all my
life, repelled me. So I went utterly music-less for ten years. Then, when my
thirst for music kicked up again, a strange thing happened. I’d driven the
old music out of my system and was eager for the new. A kid of five or
twelve imprints on the first music he hears and loves, the music that gives flesh
to his sense of identity. Here I was, fresh as a kid, imprinting on music as
if I were twelve years old again, but imprinting not on the music of my
youth, but on the music of the 21st century. My musical death had prepared me
to be born again. It had prepared me to become a Maroon 5 fan.
So here’s the hypothesis and the question. Does woe and misery turn down
your two key learning machines to prepare you to grab hold of something new?
Does it flush your learning system so you can stitch yourself into a pattern
you previously didn’t see, a team that’s getting the things you got wrong
right? Does it prepare you to follow new leaders, new ideas, and even new
beliefs? Does it prep you to join a segment of the neural net of society that’s
contributing more than the old weave you were ejected from when you lost your
job, broke up with your girlfriend, were rejected by the grad schools you were
going for, or went through a messy divorce?
Is the disability the slings and arrows of outrageous fortune impose on you
a two-sided device used by the neural net, the collective learning machine of
which you are a part? Does it tune down your influence and your access to
resources so that you don’t get in the way of the mass mind when you are a
failed component, a component that’s chosen the wrong approach to the problems
of the moment? The evidence I’ve marshalled in The Lucifer Principle: A
Scientific Expedition Into the Forces of History and in Global Brain: The
Evolution of Mass Mind From The Big Bang to the 21st Century says yes. But does it
also prep you to become a useful module in a more promising part of the neural
net? Hb 4-09-05
We’ve known for several years now that the immune system and the brain are
joined. The brain can turn the immune system up on high or down to
underdrive depending on the way it perceives external reality. A brain that senses
social isolation will shift the immune system into low gear. So will a brain
whose perceptual powers tell it it no longer can control its circumstances or
predict what’s coming next. (Yes, future projectors that fail are hacked
away by apoptotic processes—they self destruct. By keeping only future
projectors that work, evolution compacts past knowledge into a memory that then
has future-predicting powers. But I digress.) The following press release
hints that the brain and the immune system are part of a common learning loop.
John McCrone, in material I posted last night, pointed out the value of a
hierarchical learning system. A hierarchical system may have a processing
mechanism that operates at superspeed on problems that need an instant solution. It
may have other processors working on the micro-level with a clock tailored
to nano-speed. It may also have slower processors that work on the big
picture, the macro view. All can crank input into the others—or even reset the
others’ controls. This multi-layered approach gives a neural network system
flexibility. The immune system is a learning machine par excellence, but one
that works by rewarding lymphocytes that are doing useful work. It showers
them with resources and with the ability to multiply. Like evolution itself,
the immune system ruthlessly strips assets and the right to reproduce from
lymphocytes that just don’t fit the system’s needs. The brain also works on
the Matthew Principle: “To he who hath it shall be given. From he who hath
not even what he hath shall be taken away.” It rewards neurons that are
helping it cope and strips those that aren’t of such privileges as attention and
influence--the right to connect to others, the right to feed on information,
the right to spoon its output to others, and even, in the cerebral neurons of
babies, the right to live. Yet the vast system of swiftly changing networks
in the brain gives it many levels of capability, many simultaneous processing
powers, all of them different than those of the immune system. Combine the two
—the immune system’s methods of processing and the brain’s many separate
ways of sifting input, mulling it, stewing it around, and making sense of it—
and you may have a more intricate and able team than we imagined—one doing
things throughout the body and turning literally every limb and circulatory
alleyway into an extension of the mind. Howard Ps Note that the system described
below works on attraction and repulsion signals, just like electrons,
protons, animal voices, and bacterial or human pheromones. Reprinted from
ScienceDaily Magazine ... Source: Washington University School Of Medicine Date
Posted: Friday, April 20, 2001 Web Address:
http://www.sciencedaily.com/releases/2001/04/010419072152.htm Molecule That Guides Nerve Cells Also Directs
Immune Cells St. Louis, April 19, 2001 — Researchers have the first evidence
that cues that guide migrating nerve cells also direct white blood cells called
leukocytes, which have to find their way to inflamed, infected or damaged
areas of the body. The study is reported in the April 19 issue of Nature. "This
similarity between the immune system and nervous system might suggest new
therapeutic approaches to immune system disorders such as inflammation and
autoimmune diseases," says Yi Rao, Ph.D., an associate professor of anatomy and
neurobiology at Washington University School of Medicine in St. Louis. This
study was a collaboration between the School of Medicine and Baylor College of
Medicine. Rao and Jane Y. Wu, Ph.D., an associate professor of pediatrics and
of molecular biology and pharmacology, led the Washington University teams.
Lili Feng, Ph.D., led the Baylor team. After a cell is born, it navigates to
its destination, guided by signals from other molecules already in place.
Researchers have found that the nervous system uses molecules that attract
migrating cells, molecules that stop cell migration and molecules that push cells
away. But so far, only attractive molecules have been identified in the
immune system. Neurons take minutes or hours to migrate to their destinations,
whereas leukocytes migrate within seconds. Even so, Rao and colleagues wanted to
determine whether migrating leukocytes and neurons use similar mechanisms
for finding their ways. "These experiments were carried out to address the
question whether there is mechanistic conservation between the two systems," Rao
says. His group studied a protein called Slit, a known repellent in neuronal
migration. Two of the three known Slit proteins also have been found in
organs other than the brain. The researchers simulated leukocyte migration in a
dish, using a molecule known to attract immune cells. When they added human
Slit protein (hSlit2) to the dish as well, fewer cells migrated. They repeated
the procedure in the presence of a bacterial product also known to attract
leukocytes. Again, hSlit2 inhibited cell migration. However, it did not inhibit
other functions of the bacterial product. The team then determined whether
Robo—a receptor that enables Slit to act on nerve cells—plays a similar role
in the immune system. They had previously made a fragment of Robo which blocks
the normally full-length Robo protein. When this blocker was added to the
dish, Slit no longer inhibited leukocyte migration. So Robo and a receptor on
the cells appeared to be competing for Slit. "These results suggest that Slit
also is likely to act through a Robo-like receptor on leukocytes to inhibit
their migration," Rao says. He and his colleagues also are trying to find out
whether Slit can actively repel leukocytes and whether other neuronal guidance
cues influence immune cell migration. This study bridges the gap between two
previously independent fields—immunology and neurology—and highlights the
need for collaboration. "This kind of research could have been done several
years ago," Rao says. "But we all get used to addressing questions in our own
fields. This study shows what happens if we venture out and collaborate with
scientists in other fields." Reference: Wu JY, Feng L, Park H-T, Havlioglu N,
Wen L, Tang H, Bacon KB, Jiang Z, Zhang X, Rao Y. The neuronal repellent Slit
inhibits leukocyte chemotaxis induced by chemotactic factors. Nature, April
19, 2001. Funding from the National Institutes of Health supported this
research. Copyright © 1995-2001 ScienceDaily Magazine | Email:
editor at sciencedaily.com
----------
Howard Bloom
Author of The Lucifer Principle: A Scientific Expedition Into the Forces of
History and Global Brain: The Evolution of Mass Mind From The Big Bang to the
21st Century
Visiting Scholar-Graduate Psychology Department, New York University; Core
Faculty Member, The Graduate Institute
www.howardbloom.net
www.bigbangtango.net
Founder: International Paleopsychology Project; founding board member: Epic
of Evolution Society; founding board member, The Darwin Project; founder: The
Big Bang Tango Media Lab; member: New York Academy of Sciences, American
Association for the Advancement of Science, American Psychological Society,
Academy of Political Science, Human Behavior and Evolution Society, International
Society for Human Ethology; advisory board member: Youthactivism.org;
executive editor -- New Paradigm book series.
For information on The International Paleopsychology Project, see:
www.paleopsych.org
for two chapters from
The Lucifer Principle: A Scientific Expedition Into the Forces of History,
see www.howardbloom.net/lucifer
For information on Global Brain: The Evolution of Mass Mind from the Big
Bang to the 21st Century, see www.howardbloom.net
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