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<head><title>The problem of Alzheimer's disease as a clue to immortality - Part&nbsp;1</title></head>
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The problem of Alzheimer's disease as a clue to immortality - Part&nbsp;1
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I. INTRODUCTION


II. COMMON FACTORS IN INJURY DURING GROWTH AND AGING


III. A VIEW OF ENTROPY--RENEWAL OF THE BRAIN


IV. FALSE SIGNALS FROM THE ENVIRONMENT


A. EDUCATION, DIET AND MEDICINE INTERACT

B. SIGNALS IN THE ABSTRACT


V. HORMONE IMBALANCE, LEADING TO FAILURE OF PROTECTIVE INHIBITION AND ALZHEIMER'S DISEASE


A. THE FUNCTION OF ENERGY


B. EFFECTS OF ESTROGEN AND UNSATURATED FATTY ACIDS


C. VITAMIN A AND STEROIDS

D. THE NATURE OF ALZHEIMER'S DISEASE


E. AN EXAMPLE; DIET AFFECTS HORMONES WHICH AFFECT STRUCTURE AND LEAD TO APPARENT SELF- DESTRUCTION


VI. STRUCTURE AS A REGULATORY SYSTEM--AN EMERGING VISION OF PERVASIVE EPIGENESIS


I. INTRODUCTION


The toxicity of estrogen and of the unsaturated fats has been known for most of the twentieth century, and
much has been learned about their interactions in the aging process. The body, during this time, has been
understood as a dynamic interaction of cellular trophic influences which govern both form and function. My
argument here will be that some of our adaptive, protective regulatory processes are overridden by the
excessive supply of unsaturated fats--supported by a few other toxins--in our diet, acting as a false-signal
system, and that cholesterol, pregnenolone, and progesterone which are our main long-range defenses, are
overcome by the effects of the unsaturated fats, and that the resulting cascade of ineffective and defective
reactions (including various estrogen-stimulated processes) leads to lower and lower energy production,
reduced function, and death. At certain times, especially childhood and old age, iron (which also has
important regulatory roles) accumulates to the point that its signal functions may be inappropriate.

It interacts with estrogen and unsaturated fats in ways that can change restraint and adaptation into sudden
self-destruction, apoptotic cell death. If we look at the human organism from one perspective, it seems
coherent and intelligible, but from the perspective of established academic biological doctrine, it seems
appallingly complex, lacking any visible integrating principle, and as a result simplistic mechanical,
pharmaceutical, or religious ideas are increasingly offered to fill the gap. But experimental data can be
taken out of the muddle, and put to coherent human use. In what follows, I am acting as though the doctrines
of genetic determination and regulation by membranes were mere historical relics. The emerging control
systems are now clear enough that we can begin to use them to reverse the degenerative diseases: Alzheimer's
dementia, epileptic dementia, arthritis, osteoporosis, depression, hypertension, hardening of the heart and
blood vessels, diabetes, and some types of tumor, immunodeficiencies, reflex problems, and special atrophic
problems, including clearing of amyloid and mucoid deposits. I think many people experience regenerative
age-regressing when many circumstances are just right; for example, taking a trip to the mountains in the
spring with friends can optimize several basic regulatory systems.


II. COMMON FACTORS IN BRAIN INJURY DURING GROWTH AND AGING



Most people are surprised by the number of cells in the prenatal brain, and in the very old brain: In the
human fetus at 6 months of development, there are about twice as many brain cells as there are at the time
of birth, and in old age the number of cells in the brain keeps increasing with age, so that at the age of
90 the amount of DNA in the brain (36.94 grams) is about 50%.greater than at the age of 16-20 (23.04 grams).
In the aged brain, glial cells multiply while neurons die. In the fetus, the cells that die are apparently
nerve cells that haven't yet matured. The factors that are known to reduce the brain size at birth are also
factors that are involved in the degenerating brain in old age or Alzheimer's disease: lack of oxygen,
excess unsaturated fats or deficiency of saturated fats, estrogen excess, progesterone deficiency, and lack
of glucose. A lack of carbon dioxide is probably harmful in both. Inflammation and blood clots may be
factors in the aging brain, and bleeding with vascular spasm is sometimes a contributing factor to brain
damage in both the old and the fetal brain. Endotoxemia may be a factor in nerve degeneration only during
adult life, but it is sometimes present during pregnancy.


M. C. Diamond, Enriching Heredity: The Importance of the Environment on the Anatomy of the Brain. Free
Press, N.Y., 1988. C. Finch and L. Hayflick, Handbook of the Biology of Aging. Van Nostrand Reinhold, N.Y.,
1977.


III. A VIEW OF ENTROPY: RENEWAL OF THE BRAIN

When a fertilized egg is developing into a person, each cell division creates a new environment for the
daughter cells, to which they adapt. They may run into limits and resistances (sometimes a certain gene
doesn't meet the need of the situation, or toxins are present, or nutrients and hormones are imperfectly
supplied), but the process is flexible, and a way is normally found to get around the limitation. The
embryo's brain development is my favorite example of the ways genes interact with the environment. We might
think of the "optimal brain development" of a person, or a rat, or a chicken, as something which is clearly
limited by "the genes." But if rats are given a stimulating environment, each generation gets a slightly
bigger, slightly more intelligent brain. If rats are treated during pregnancy to increase the amount of
progesterone, the offspring have bigger brains and learn more efficiently. Still, that might just be
restoring a condition that was natural for rats in some perfect environment. Chickens develop inside an egg
shell, and so the nutrients needed for their development are all present when the egg is laid.


The brain, like the other organs, stops growing when the food supply is used up. But an experimenter
(Zamenhof) opened the egg shells at the stage of development when the brain normally stops growing, and
added glucose, and found that the brain continued growing, producing chickens with bigger brains. The
"genes" of a chicken, as part of a system, have something to do with the development of that system, but the
environment existing in and around the organism is able to guide and support the way the system develops.
The size, complexity, and intelligence of the brain represents a very large part of the "information"
contained in the organism, and Zamenhof's experiment showed that the ability to realize this potential, to
create this complexity, comes from the support of the environment, and that the "genetic nature of the
chicken" didn't constitute a limit to the development of its brain.


I am going to argue that Alzheimer's disease is analogous to the situation confronted by the developing
chicken embryo or the rat or human fetus, when the environment is unable to meet the needs of the highly
energetic, demanding and sensitive brain cells, and the brain cells begin to die, instead of developing into
a more complex state, passing beyond various barriers and limitations. There are two stereotypes that are in
conflict with this view: (1) That the structure of the brain is determined at an early point in life,
sometimes explicitly stated as the age of 12 or 16, and (2) that the structure of the brain goes into an
"entropic" deterioration during the process of aging. My position is that the brain cells are in a vital
developmental process at all times, and that the same things that injure the brain of a fetus also injure
the brain of an aging person.


If novelty is really appearing during development, then it is hard to maintain that "entropy increases"
during the development of an individual. Isn't a child a richer organization than a fertilized egg? Isn't an
adult more individualized or realized than an infant? Seen from the inside, our known world gets richer with
experience. Learning is certainly anti-entropic. Where does the idea of "increasing entropy with living"
come from? Many things contribute, including a doctrine of genetic determinism, the old Platonic idea of the
imperfection of the concrete, the unreality of the existent, and the medieval idea of the "corruption of the
body." These philosophies still motivate some people in aging research. The astrophysicist, N. A. Kozyrev,
showed that the idea of an "entropic cosmos" derived simply from the assumptions of 19th century deism, "God
set the clockwork universe in motion, and left it to run down." Early in this century, Raymond Pearl argued
that the "rate of living" governed the life-span, so that "fast living" meant a short life. He based his
argument on cantaloupe seeds: the faster they grew, the sooner they died. This was because he didn't give
them anything but water, so they had to live on their stored energy; if they grew quickly, obviously they
ran out of stored energy sooner. I have never heard that described as a stupid idea, but I think politeness
is sometimes carried too far. In the clock analogy, or the seed analogy, the available energy is used up.


The clock with its wound-up spring and the seed in a dish of water may be considered as closed systems, and
we can understand their fate. But if it is foolish to argue from a confined seed to free-living organisms,
then it is just as foolish to argue from a clock to a cosmos. Unfortunately, these inferences about closed
systems are often applied to real situations that aren't energetically closed.


The "rate of living" theory of aging picked up the idea of aging as a natural physical property of time, and
gave it expression in mathematical form, arguing (Hershey, "Entropy, basal metabolism and life expectancy,"
Gerontologia 7, 245-250, 1963) that "the total lifetime entropy production" could be calculated, to give
insight into "life expectancy and evolutional development." Unfortunately, the equation Hershey used assumed
that the flow of heat out of the body into the surroundings is reversible. This suggests an image of Dr.
Frankenstein vivifying his monster with lightning, putting the heat back into the body. If heat is to be
"put back into the body," it is necessary to make sure that it is appropriate for the structure as it
exists.


Actually, it is just the directed flow of energy which generates the structures. If any biological argument
can be made from the idea of entropy, it is that it would be extremely difficult to regenerate food, by
putting heat into a person. In a few situations, it is possible to show that living structures can directly
absorb heat from their environment (causing the temperature to fall)--"negative heat production"--but the
exact meaning of this isn't clear. (B. C. Abbott, et al., "The positive and negative heat production
associated with a nerve impulse," Proc. R. Soc. B 148, 149, 1958; R. D. Keynes and J. M. Ritchie, "The
initial heat production of amphibian myelinated nerve fibres," Proc. Physiol. Soc., June 1970, page 29P-30P:
"It is now clear that in both crustacean...and mammalian (Howarth, et al., 1968) non-myelinated fibres there
is an initial production of heat during (or soon after) the action potential, 80% of which is rapidly
reabsorbed.") A. I. Zotin ("Aging and rejuvenation from the standpoint of the thermodynamics of irreversible
processes," Priroda, No. 9, 49-55, 1970), citing the theory of Prigogine-Wiame, argued that the aging
process involves both a decrease in entropy and a decrease in the rate of heat production.


Regeneration involves a production of entropy, as when an egg is formed. (The temperature fluctuation at the
time of ovulation might make a contribution to the construction of the entropic egg.) The argument that
aging of the animal (like aging of the cosmos) is governed by "the tendency of entropy to increase" has led
people to say that rejuvenation would be like unscrambling an egg. Zotin's argument is interesting, because
he says that an egg is a "scrambled animal." This view is very much like Warburg's and Szent-Gyorgyi's
theory of cancer, that it is like a reversion to a simpler state of life. To sketch out what I have argued
in different contexts, water is the part of the living substance that we can most meaningfully discuss in
terms of entropy. In fact, much of the concept of entropy has derived from the study of water, as it changed
state in steam engines, etc. Cancer cells, like egg cells, have a higher water content than the
differentiated, functioning cells of an adult, and the water is less rigidly ordered by the cellular
molecules. This different, more mobile state of the water, can be measured by the NMR (nuclear magnetic
resonance) machines which are used for MRI (magnetic resonance imaging).


Estrogen has a special place in relation to the water in an organism. It is intimately involved with the
formation of the egg cell, and wherever it operates, it increases both the quantity of water and,
apparently, the disorder of the water. Its function, I believe, is to promote regeneration, as in Zotin's
scheme, by increasing entropy, or "scrambling the animal." The way it promotes regeneration is by promoting
water uptake, stimulating cell division, and erasing the differentiated state to one degree or another,
providing a new supply of "stem cells," or cells at the beginning of a certain sequence of differentiation.
These more numerous cells then must find a hospitable environment in which to develop and adapt. If the
proper support can't be found, then they will be recycled, like the unfed cells in the brain of a fetus. If
we imagine the course of development as a summary of evolution ("ontogeny recapitulating phylogeny"), then
the egg, as it "unscrambles" itself in embryonic development, passing through stages resembling jelly fish,
worm, fish, reptile, bird, baboon, keeps finding that the available energy allows it to, in effect, say "I
want this, I don't want that," until it emerges as a human baby, saying "I want," and begins eating and
learning, and with luck continues the unscrambling, or self-actualization.. Degenerative aging, rather than
being "physically derived from the properties of time," seems to be produced situationally, by various types
of contamination of our energy supply. Unsaturated fats, interacting with an excess of iron and a deficiency
of oxygen or usable energy, redirect our developmental path.


The saturated fats, in themselves, seem to have no "signalling" functions, and when they are naturally
modified by our desaturating enzymes, the substances produced behave very differently from the plant-derived
"eicosanoids." As far as their effects have been observed, it seems that they are adaptive, rather than
dysadaptive. All of the factors that affect the brain of a fetus should be examined in relation to the aging
brain. Besides estrogen and fats, I am thinking of oxygen and carbon dioxide, glucose, iron and calcium,
cholesterol, progesterone, pregnenolone, DHEA, the endorphins, GABA, thyroid, and vitamin A. An additional
factor, endotoxin poisoning, eventually tends to intervene during stress and aging, exacerbating the trend
begun under the influence of the other factors.

IV. FALSE SIGNALS FROM THE ENVIRONMENT

The environment can be supportive, but it can also divert development from an optimal course.


Passively taking whatever you are given, by history and nature, is entropic; choosing intelligently from
possible diets, selecting courses of action, will create pattern and reduce entropy. If education contains
an element of choice and self-actualization, then the results seen in several Alzheimer's studies could have
a significance larger than what has been suggested by the investigators. A diagnostic bias has been reported
to result from the use of standardized tests based on vocabulary, because education increases vocabulary,
and tends to cover up the loss of vocabulary that occurs in dementia. In the Framingham study, it was
concluded that there was a real association of lower educational level with dementia, but the suggestion was
made that self-destructive practices such as smoking were more common among the less educated.


The Seattle study of the patients in a health maintenance organization showed a very distinct difference in
educational level between the demented and the non-demented, both of whom had roughly similar frequency of
prescriptions for estrogen. The features that seemed important to me, that weren't discussed by the authors,
were that the demented women had a much lower rate of progestogen use, and a much higher incidence of
hysterectomy, which interferes with natural progesterone production. Although Brenner, et al., in the
Seattle study concluded that "this study provides no evidence that estrogen replacement therapy has an
effect on the risk of Alzheimer's disease in postmenopausal women," they reported that "Current estrogen use
of both the oral and the vaginal routes had odds ratios below 1, while former use of both types yielded odds
ratios above 1...." (They seem to neglect the fact that Alzheimer's-type disease in old people has a long
developmental history, so it is precisely the "former" use that is relevent. 31% of the demented women had
formerly used estrogen, and only 20% of the control group. Since estrogen is a brain excitant, present use
creates exactly the same sort of effect on verbal fluency and other signs of awareness of the environment
that a little cocaine does. Anyone who neglects this effect is probably deliberately constructing a
propaganda study.)

This observation, that the demented had 155% as much former estrogen use as the normal group, as well as the
difference in rates of progestogen use (normal patients had 50% more progestogen use than demented) and
hysterectomy (demented had 44.1% vs. 17% in the normals, i.e., 259% as many; the incidence of hysterectomies
after the age of 55, which is a strong indication of a natural excess of estrogen, in the demented was 374%
of the incidence in the non-demented), should call for a larger study to clarify these observatons, which
tend to indicate that exposure to estrogen in middle-age increases the risk of Alzheimer's disease in old
age, and that even medical progestogens offer some protection against it..


(Although this study might have been bigger and better, it is far better than the junk-studies that have
been promoted by the pharmaceutical publicity machine. I have seen or heard roughly 100 mentions of the
pro-estrogen anti-scientific "studies," and none mentioning this one.)


D. E. Brenner, et al., Postmenopausal estrogen replacement therapy and the risk of Alzheimer's disease: A
population-based case-control study," Am. J. Epidemiol. 140, 262-267, 1994. "Women tend to have higher
age-specific prevalence and incidence rates of Alzheimer's disease than do men." A.F. Jorm, The Epidemiology
of Alzheimer's disease and related disorders, Chapman and Hall, London, 1990, and W. A. Rocca, et al., Ann.
Neurol. 30, 381-190, 1991.

H. C. Liu, et al., "Performance on a dementia screening test in relation to demographic variables--study of
5297 community residents in Taiwan," Arch. Neurol. 51(9), 910-915, 1994. "Commonly used dementia screening
tests may be unfair to poorly educated individuals, especially women and rural residents."


SIGNALS IN THE ABSTRACT


When I taught endocrinology, I annoyed my tidy-minded students by urging them to consider the potential
hormone-like action of everything in the body, and to think of layers of control, ranging from sugar, salt,
and carbon dioxide, through the "official hormones," to complex nervous system actions such as expectancy,
and biorhythms. Certain things that are active in very important processes deserve special attention as
"signals," but they still have to be understood in context. In this sense, we can think of Ca2+ as a signal
substance, in its many contexts; it is strongly regulated by the cell's energy charge. Magnesium and sodium
antagonize it in certain situations. Linoleic acid, linolenic acid, arachidonic acid: Their toxicity is
potentially prevented by the Mead acids, and their eicosanoid derivatives, which behave very differently
from the familiar prostaglandins, as far as they have been compared; can be drastically reduced by dietary
changes. Prostaglandins, prostacyclin, thromboxane: Formation is blocked by aspirin and other
antiinflammatory drugs.

Adenosine: Sleep inducing protective effect. Adenosine is structurally very similar to inosine, another
natural substance (found in meat, for example) which is a component of "inosiplex," an antiviral drug (Brown
and Gordon, Fed. Proc. 29, 684, 1970, and Can. J. Microbiol. 18, 1463, 1972) or immunostimulant which has
also been found to have an anti-senility effect (Doty and Gordon, Fed. Proc. 29). Adenosine is a free
radical scavenger, and protects against calcium and glutamate excitotoxicity. (I. Yokoi, et al., "Adenosines
scavenged hydroxyl radicals and prevented posttraumatic epilepsy," Free Radical Biol. Med. 19(4), 473-479,
1995; M. P. Abbracchio, et al., "Adenosine A(1) receptors in rat brain synaptosomes: Transductional
mechanisms, efects on glutamate release, and preservation after metabolic inhibition," Drug Develop. Res.
35(3), 119-129, 1995.) It also appears to protect against the relative hyperventilation that wastes carbon
dioxide, and endotoxin can interfere with its protective action. Guanosine, in this same group of
substances, might have some similar properties. Thymidine and cytidine, which are pyrimidine-based, are
endogenous analogs of the barbiturates, and like them, they might be regulators of the cytochrome P450
enzymes. Uridine, in this group, promotes glycogen synthesis, and is released from bacteria in the presence
of penicillin.


Iron: Regulator of mRNA stability, heme synthesis; reacts with reductants and unsaturated oils, to produce
free radicals and lipid peroxides; its absorption is increased by estrogen, hypothyroidism, anemia or lack
of oxygen. Glutamate and aspartate, excitotoxins, and GABA, an inhibitory transmitter.

These have metabolic links with each other, with ammonia, and with stress and energy metabolism.


Estrogen and acetylcholine, excitotoxins; see Savolainen, et al., 1994. The information on this is
overwhelmingly clear, and the publicity to the contrary is a horrifying example of the corruption of the
mass media by the drug industry.


Endorphins: Stress induced, laterally specific, involved in estrogen action, antagonized by naloxone and
similar anti-opiate drugs. I have proposed that the endorphins can cause or sustain some of the symptoms of
aging. Naloxone appears to be a useful treatment for senility. E. Roberts, Ann. N. Y. Acad. Sci. 396, 165,
1982; B. Reisberg, et al., N. Engl. J. Med. 308, 721, 1983.


Endotoxin: Antimitochondrial action, causes elevation of estrogen. It synergizes with unsaturated fats, and
naloxone opposes some of its toxic effects.

Urea, cholesterol: Structural stability of proteins and lipid-protein complexes.


Things that act directly on the water structure: I think all of the natural regulators have an effect on the
structure of water, but some unusual substances seem to act primarily on the water. Noble gases, for
example, have no chemical effects, but they tend to form "cages" of water molecules around themselves.
Camphor, adamantane, and the antiviral drug amantadine, probably have a similar water-structuring effect,
and amantadine, which is widely used as a therapy in Parkinson's disease, has an anti-excitotoxic action.

<a href="http://raypeat.com/articles/articles/alzheimers2.shtml">Article continued in Part 2 - click
here</a>

Raymond Peat, Ph.D.


Copyright 1997

<h3>SELECTED REFERENCES</h3>


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results thus strongly suggest several potential roles for LRP in brain protein and lipoprotein metabolism,
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T. Yamada, et al., "Apolipoprotein E mRNA in the brains of patients with Alzheimer's disease," J. Neurol.
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fibrillary acidic protein]. These results suggest that apoE suppresses the progression of AD, including
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G. P. Jarvik, et al., "Genetic influences on age-related change in total cholesterol, low density
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With aging, total cholesterol and LDL-C became significantly lower in the "epsilon 4 genotype" group; this
is the group at risk for AD.


S. Miller and J. M. Wehner, "Cholesterol treatment facilitates spatial learning performance in DBA/2Ibg
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A. D. Roses, "Apolipoprotein E affects the rate of Alzheimer disease expression: beta-amyloid burden is a
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F. Oyama, et al., "Apolipoprotein E genotype, Alzheimer's pathologies and related gene expression in the
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M. L. C. Maatschieman, et al., "Microglia in diffuse plaques in hereditary cerebral hemorrhage with
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plaques."


J. Poirier, "Apolipoprotein E in animal models of CNS injury and in Alzheimer's disease," Trends Neurosci.
17(12), 525-530, 1994. "The coordinated expression of ApoE and its receptor...[low density lipoprotein
(LDL)] receptor, appears to regulate the transport of cholesterol and phospholipids during the early and
intermediate phases of the reinnervation process." "...a dysfunction of the lipid-transport system
associated with compensatory sprouting and synaptic remodeling could be central to the AD process."

P. H. Chan and R. A. Fishman, "Brain edema: Induction in cortical slices by polyunsaturated fatty acids,"
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R. C. Vannucci, et al., "Carbon dioxide protects the perinatal brain from hypoxic-ischemic damage: An
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H. M. Wisniewski and P. B. Kozlowski, "Evidence for blood-brain barrier changes in senile dementia of the
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C. Nilsson, et al., "The nocturnal increase in human cerebrospinal fluid production is inhibited by a
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D. L. Williams, et al., "Cell surface 'blanket' of apolipoprotein E on rat adrenocortical cells," J. Lipid
Res. 36(4), 745-758, 1995. "...the zona fasciculata cell is encircled or covered with apoE on all faces of
the cell. ...this cell surface 'blanket' of apoE participates in the uptake of lipoprotein cholesterol by
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M. Warner and J. A. Gustafsson, "Cytochrome P450 in the brain: Neuroendocrine functions," Front
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of MPTP...-induced neuronal cell death." "The 1-amino-adamantanes amantadine and memantine have recently
been shown to be non-competitive NMDA antagonists and are widely used in Europe as antiparkinsonian agents."


R. A. Wallis, et al., "Glycine-induced CA1 excitotoxicity in the rat hippocampal slice," Brain Res. 664(1-2)
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AD brain samples were significantly thinner (that is, had less microviscosity) than corresponding
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cholesterol:phospholipid." "Addition of cholesterol restored the membrane width to that of the age-matched
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T. Reed, et al., "Lower cognitive performance in normal older adult male twins carrying the apolipoprotein E
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S.Y. Tan and M. B. Pepys, "Amyloidosis," Histopathology 25(5), 403-414, 1994. "...abnormal protein fibrils
which are derived from different proteins in different forms of the disease. Asymptomatic amyloid deposition
in a variety of tissues is a universal accompaniment of ageing, and clinical amyloidosis is not rare.
Intracerebral and cerebrovascular beta-protein amyloid deposits are a hallmark of the pathology of ...
Alzheimer's disease...." "Amyloid deposits are in a state of dynamic turnover and can regress if new fibril
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H. G. P. Swarts, et al., "Binding of unsaturated fatty acids to Na+,K+-ATPase leading to inhibition and
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voltage power supply is essential for the functioning of the computer."

<a href="http://raypeat.com/articles/articles/alzheimers2.shtml">Article continued in Part 2 - click
here</a>



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