Copyright © 1996, 1997, 1998, 2001, 2008 by Galen Daryl
Knight and VitaleTherapeutics, Inc.
VitaleTherapeutics' Goal
"VitaleTherapeutics" is Latin and Greek for "a search for the true life
treatment". As our name implies, VitaleTherapeutics is interested in
real,
long-lasting solutions for diseases having immunodeficiency,
hypersensitivity,
and autoimmune components (such as cancer,
AIDS, allergies, rheumatoid arthritis, heart disease, and diabetes). A
better understanding of how environmental toxins, metabolic imbalances,
and nutritional deficiencies can affect our immune systems to cause
these
diseases should help us to accomplish these goals. Our New Mexico based
corporation was established to identify, develop, and disseminate
information
about the causes of disease and about scientifically-documented,
non-toxic
remedies and has obtained non-profit status with the IRS.
This web site is the premier publication produced by
VitaleTherapeutics,
Inc.
Through the generous contribution of
services,
time,
expertise,
supplies,
equipment, software,
and
research funds, and with little to no budget or salary, the directors
and collaborators of VitaleTherapeutics have managed to conduct nearly
two dozen studies in the past dozen years, including aging and
differentiative studies,
studies in a murine model for AIDS, and tests of the vitaletheine
modulators
in several cancer models, including the successful treatment of dogs
and
horses with melanoma. One of the more interesting studies was helping a
major HMO sort out data on lymphedema to determine that successful
therapy depends upon very early intervention at the first onset of
edema in the affected limb. A dozen more studies are planned and
awaiting minimal
funding, including long-term follow-up of any survival stemming from
immunostimulation
in a mouse AIDS model. Making the vitaletheine modulator therapies
available for human use is planned for this year.
Part of the purpose of this Web Page is to provide a
list of current
needs for our organization so that other interested parties can
participate
in our efforts to solve these troubling problems.
EXECUTIVE SUMMARY
Those of you who have followed the news and literature about the
incidence
of cancer and other diseases in the general population have seen
genetic
approaches getting a lot of the press. One genetic researcher quoted by
the press even has stated flatly that "All cancers are diseases of
genes".
This particular characterization of the situation contradicts
epidemiological
studies and even the work of other doctors and geneticists. For
example,
in a
study of 117,988 women, aged 30 to 55,
hereditary factors (a positive family history) were found in only 2.5%
of breast cancer patients; that's only 1 in 40 cases. "Familial"
sharing
of recipes and eating habits, and residences in the same geographical
regions
with similar "familial" environmental exposures, could contribute even
to this small "familial" predisposition. A report that 95%
of breast cancer tumors contain viral proteins (RAK) and gene fragments
(similar to the proteins and genetic codes associated with another
virus,
HIV, that causes AIDS) seems to confirm the low incidence of hereditary
breast cancer by providing a possible infectious explanation for the
disease.
The logical consequence of this information is that the causes of most
breast cancers are environmental or nutritional, or both. Not long
after
the original news flash, it was reported that
97%
of cervical cancers are infected with the human papilloma virus,
another
avoidable environmental factor. Similarly, only about
2.9
to 6.9% of ovarian cancers have been liked to hereditary factors.
There
have also been reports that a genetic alteration of
chromosome
1 was detected in only about 3% of all prostate cancer cases. The
lifetime
risk of prostate cancer historically has been less than 10%, but
there
is recent evidence that this disease may already be
present
in 34% of men in the 40 to 49 age group. This statistic alone might
be the harbinger of some rather alarming environmental and/or
nutritional
trends. Other "trees" of evidence in the "forest" of proposed causes
suggest
that most human diseases (perhaps as high as 95 to 97%) arise from
factors
that we can control without genetic intervention. There is mounting
evidence
that viral infections and metabolic imbalances, such as those created
by
low
oxygen concentrations in our air, cause
genetic lesions that contribute
to the disease, so factors other than heredity, clearly, are very
important
in the etiology of cancer. Finally, we recently published a summary of
our work in the June '04 issue of the Townsend Letter, and have updated
it to include the observation that increases in cysteamine and
cystamine, a metabolic break-down product of the vitaletheine
modulators, can lead to single-strand breaks in DNA which logically
would increase the risk for mutations. Thus, correctable imbalances in
sulfur biochemistry may occur long before irreversible genetic
mutations, and even after genetic mutations, cancer can be destroyed by
humoral immunity if the sulfur biochemistry and humoral immunity
dependent upon the vitaletheine modulators can be brought back under
control.
As our ecosystems become more overtaxed by burgeoning human
populations,
it is essential for us to keep our survival needs in perspective. To
prevent
"the sun from setting" upon many of this world's "long-overshadowed"
ecosystems,
including our own, funding will have to be maintained and perhaps even
increased in the areas of nutritional and environmental research. For
example,
vaccines being touted as solutions for a variety of diseases only work
if the immune system is functional. Theoretically, this is true whether
the vaccine is made from either protein or DNA taken from affected
tissues.
By themselves, vaccines are of questionable value in established
immunodeficiency
and cancer, since the hopefully "non-infectious" antigens in the
vaccine
can divert an already poisoned immune response away from the active
infection
or cancer. Besides, those who advocate relying more and more heavily
upon
vaccines to prevent and treat disease fail to recognize that our immune
systems have a finite capacity to deal with antigenic challenges.
Immunotherapy
can sometimes work, even in seemingly terminal disease, if the antigen
and adjuvant are able to effectively target and boost a formerly
misdirected
immune response, thereby offsetting the negative effects of additional
antigen burden. For future reference,
deficiencies
of pantothenic acid, alone, are known to cause failed immunization
attempts.
Using our own studies and information referenced on our web site
from
the scientific literature (http://www.VitaleTherapeutics.org),
VitaleTherapeutics,
Inc. has attempted to document and explain why various toxic metals and
vitamin-, hormone-, and indole-like toxins negatively impact health.
Much
of this toxicity can be traced to negative effects upon a newly
discovered
family of immune stimulants,
the vitaletheine
modulators, or upon their
biological enzymic receptors, or both. In support
of this approach, unoptimized regimens of the vitaletheine modulators
have
been shown to produce lifetime cure rates in 70% of laboratory mice
with
uniformly-fatal melanoma and 100% survival rates in mice with myeloma,
all with unoptimized regimens of these compounds that have since been
optimized.
Immune stimulation in mAIDS and indications of efficacy even in a
non-immunogenic
breast cancer model also have been observed.
The potency of some of these compounds (attogram to femtogram/kg)
indicates
that they may be both, the "hair triggers" for our humoral immune
response,
and its "Achilles heel". It is difficult to avoid the minute amounts of
pollutants that chemically block the traces of vitaletheine modulators
normally present in our systems. For example, chlorine reacts with any
organic material in water to produce alkyl chlorides. Alkyl halides
(whether
chlorides, bromides, or iodides) are known to chemically modify thiol
compounds
like the vitaletheine modulators. We drink, and even breathe these
alkyl
chlorides whenever we take baths and showers. Although efforts are
underway
to systematically identify and eliminate these and other especially
problematic
pollutants, the safest strategy for now is to avoid as many
non-nutritive
environmental chemicals as possible.
WHAT ARE SOME OF THE MOST TROUBLING PROBLEMS?
New insights into what constitutes an environmental toxin, especially
in
relation to the vitaletheine modulators and its receptors, are being
disseminated
in the hopes that new regulations and remedial efforts will be studied
and implemented soon.
Endocrine Disrupters
PCBs and "dioxins" are widely recognized
as environmental endocrine disrupters
(substances that upset the delicate balance of our hormones and cause
disease).
"Dioxins" (such as 2,3,7,8-tetrachlorodibenzo-p-dioxin or TCDD), PCBs,
and the antibiotic, triclosan (in soaps), are examples of chemical
look-alikes
that can interfer with thyroid hormones, like thyroxine. One of the
most dramatic examples of an endocrine disrupter is DES
(diethylstilbestrol).
The use of this artificial estrogen in women has been associated with
increased
risks of endometriosis and of cervical, vaginal, and breast cancer.
Equol, produced metabolically from soy products, closely resembles DES
and has similar estrogenic properties.
Ironically,
in men DES is used to help slow the development of prostate cancer,
illustrating
the sensitivity and specificity of our hormonal systems to these types
of compounds. Estriol might be a safer, bioidentical alternative, and
many physicians recently have called for the investigation of
topical, bioidentical progesterone for health benefits in prostate
cancer victims.
Having only one phenolic group, preservatives such as BHA
or BHT, used in many commercial foods and packaging, can be thought of
as being half of a DES molecule (DES contains two phenolic groups). In
fact,
BHA, and to a lesser extent BHT, are known to produce
estrogen-like
responses and to enhance the
growth of
tumors in laboratory animals. Other problematic chemicals such as
herbicides,
pesticides (fungicides, insecticides, and nematocides), and phthalate
plasticizers
round out the field of "known" endocrine disrupters (Ted Schettler,
M.D.).
Alkylating Agents and Toxic Metals in Drinking Water
The occurrence of alkyl chlorides in our water makes the use of water
filters
and purifiers attractive, but this practice of water purification,
itself,
can be dangerous. Years ago, adhesives for plastics and acrylics used
in
the construction of some water purifiers added more carcinogenic alkyl
chlorides (methylene
chloride) to the water than the filters removed. Just recently, the May
1997 issue of Consumer Reports lists the recall of a Sears water filter
made by WaterWorks (Chemical Contaminant/Taste and Odor Filter
Cartridge
Premium Grade Granular Activated Carbon) that releases enough nickel
into
the water to turn it green and to cause stomach cramps, nausea, and
diarrhea
in those individuals consuming the nickel-contaminated" water. Nickel
may be particularly problematic in our environment since it is already
pervasive (present in coins, jewelry, eyeglass frames, and many types
of
stainless steel). Nickel is also a known contact carcinogen and
allergen
(NIOSH handbook). Ironically, at the same time that nickel presumably
uncouples
our protective mechanism against cancer, it overstimulates at least one
immune response (cytolytic antibody production) linked to
cancer-negating
activities. Thus, a misdirecting and uncoupling of our normal immune
surveillance
for cancer, while compensating with an
over-escalation
of an immune responses that can produce hypersensitivity and
perhaps
even auto-immunity, essentially describes the carcinogenic
immunopathology of nickel
poisoning.
"All That Glitters Isn't Gold"
Nickel is far from being our only toxic metal problem. Recently,
exposures
to other toxic metals and different combinations (mercury, manganese,
copper,
lead and copper, lead and iron, and iron and copper) have been
associated
with a
higher incidence of Parkinson's disease.
Two carcinogenic metals, nickel and cadmium, are the main components of
NiCad batteries. Cadmium, mercury (extremely
toxic), silver (irritant),
and bismuth
are commonly used in dental amalgams (fillings). Even gold
jewelry is suspect since it is seldom pure (24K), being alloyed with up
to 14K of other often unspecified metals, and gold has been listed in
toxicology texts as needing the same antidote as nickel and mercury.
Finally, according to a DOE report
cited in the Albuquerque Tribune, enough carcinogenic plutonium to
produce
46,600 counts per square meter per minute is found in some soils in
Albuquerque.
Nearly all of these metals are known to bind oxygen (hydroxide) and
sulfur
(thiols) very tightly to produce the corresponding metal oxides or
sulfides.
No data was found in the "accessible literature" for plutonium
sulfides,
but it is reasonable to expect a very tight
binding
of plutonium to thiols since
plutonium binds oxygen much more tightly
than any other metal considered and since nearly all of these other
metals
(the exception being tin) bind sulfur even more tightly than oxygen.
This
means that toxic metals tie up the cysteine in our food and, when the
protective
endogenous thiols (metallothionine and glutathione) are saturated, they
also trap vitaletheine, lipoic acid, proteins, peptides, enzymes, and
other
thiols critical to the proper functioning of our bodies. It is still
not clear if the city of Albuquerque is checking carcinogenic plutonium
levels, before and after treatment, in the Rio Grande river water
before it injects it into our pristine aquifer as a strategic
recharging effort.
It's An Indole Jungle Out There!
A group of chemicals known as indoles are less widely recognized as
environmental
toxins, but are just as problematic. There have been dramatic instances
of indole poisoning. An outbreak years ago of eosinophilia myalgia, a
painful
and life-threatening inflammation of muscle tissues, was traced to a
bad
batch of the supplementary essential amino acid, tryptophan. In
addition
to the essential amino acid and indole, tryptophan, this preparation
contained
non-nutritive
indoles that trigger the tell-tale inappropriate immune response
in
laboratory animals. However, tryptophan itself can probably poison
vitaletheine's sulfenic acid if it breaks down to kynurenine, which can
be prevented by consuming daily apple pectin with the protein in our
diets.
Other environmental indoles can be categorized as
microbial
or mycotoxins such as psilocybin (psychedelic mushrooms),
teleocidins,
and a variety of alkaloids from ergot, including LSD. Indoles are also
found in antidepressant drugs (selective
serotonin reuptake inhibitors or SSRIs) in coal tars, creosotes,
and roofing tars. The EPA has been trying
to phase out the use of creosote for wood preservation (railroad ties,
telephone poles, etc.) since about 1986. Strychnine, and vincristine
and
vinblastine of chemotherapy fame, also fall into this category of
poisonous
indole alkaloids. Another non-nutritive indole-like compound,
ethoxyquin,
is used as a preservative in tire rubber and in some dog and cat foods.
It is not known if breathing particles from tires affects our ability
to
fight off lung cancer, respiratory, and other diseases, but "immune
disruption"
does seem to be consistent i) with our preliminary observations of
animals
treated with the vitaletheine modulators when maintained on
ethoxyquin-containing
diets and ii) with the EPA's attempts to instigate new measures
restricting
particulate emissions from automobiles and power plants.
Mechanisms of Endocrine and Metabolic Disrupters
Interference with the desirable effects of melatonin and serotonin may
explain at least some of the immune suppression and resulting disease
caused
by environmental indoles. For example, teleocidins, known to promote
skin
cancer, are very similar in structure to the beneficial hormone,
melatonin.
Non-nutritive indoles can block serotonin and melatonin since the
enzymic receptors for these natural
hormones like to bind indole structures. Activities of serotonin that
may be blocked include smooth muscle contractions, gastric secretions
that
digest food and that when excessive have been linked to ulcer
formation,
and "neurotransmission" or "sending signals through our nervous
system".
Melatonin is made from serotonin and although it is known to help
control
the pigmentation of our skin, it is better known as the "sleep hormone"
produced in the dark by the pineal gland (or "third eye") to lull us to
sleep. It may be pf no small coincidence that a widely recognized side
effect
of LSD's use is insomnia (sleeplessness) or that Timothy Leary
(long-time
LSD advocate) died of prostate cancer.
These indole- and hormone-look-alikes apparently create health
problems
by binding to the receptor and transport proteins for such natural
hormones
as serotonin, melatonin, estrogen, testosterone, and thyroxine. In so
doing,
they interfere with reproductive systems, with the induction of
important
protein and enzymes in the body, and ultimately with important pathways
and processes, such as our temperature regulation, immune surveillance,
fat metabolism, nerve function, and psychology. Vitamin look-alikes,
such
as nicotine and phenarsazine, are similarly problematic, antagonizing
the
actions of their respective essential vitamins, niacin and riboflavin.
WHAT CAN BE DONE?
Avoid Known Environmental Toxins
Obviously, one way of maintaining good health and avoiding exposure to
the toxic, non-nutritive compounds resembling our natural hormones,
vitamins,
and minerals is by simply READING
PRODUCT LABELS, LITERATURE, AND RECALLS!!The
plastic housing on the Sears water filter that should be replaced
immediately
is white with a 1.5-inch-wide "green" end cap. We also wonder if
underwires
in bras are made from nickel-containing alloys, and if these contribute
to the risk of connective tissue disease and breast cancer, especially
in women who have undergone breast augmentation and who use
antipersperants to prevent nickel from sweating out of the arm pits.
Avoiding moldy foods and
agricultural products treated with various pesticides and herbicides,
and
even eating less rancid and corn, cottonseed, and peanut oils from the
southeastern
US (that are more likely to be contaminated with
carcinogenic
aflatoxins than other vegetable oils) should help us to minimize
other
environmental exposures.
Light Pollution and Other Radiation
Since melatonin appears to be present with vitalethine on its probable
receptor, a flavin-containing monooxygenase,
simply turning out our lights and not staying up late (watching our
big-screen
TV or working on our computer) is an effective way to deal with
radiation
and "light" pollution. This may be of particular concern to members of
the nursing profession, interns, and residents, and others who
literally have to work
through the night shift. As much darkness as possible is needed during
the sleep cycle to generate adequate melatonin. In other words, a nap
(in
light) is nice, but sleep (in dark) is healthy and sustaining. In
addition to the use
of melatonin supplements for insomnia or sleeplessness, there is
cautious
interest in using melatonin for the seemingly diverse diseases of
schizophrenia,
various forms of cancer, and with avoidance of toxic metals to treat
Parkinson's
disease. In a similar fashion, vitamin B2 supplements
(riboflavin) should
help to replace flavin destroyed by other
unavoidable
forms of radiation. Dietary and supplementary antioxidants, such as
Eleutherococcus
senticosus
(sic., Siberian ginseng), sulforaphane found in Daikon (Japanese)
radish, melatonin and vitamin E, can "reduce" deleterious effects of
radiation-caused
lipid epoxides. Epoxides are known to
chemically modify thiol-containing
substances, like the vitaletheine modulators.
Exercise
Native Americans (of sweat-lodge fame) will find it interesting that
one
way our body gets rid of nickel and other toxic metals is through sweating.
Scandinavians use saunas and even Americans have been known to use to
use
sweat boxes to help with weight reduction. The old entreaty "get the
lead
out" (sic., get out there and
sweat) has literal wisdom in addition to
the fat reduction and "cardiovascular benefit" attributed to exercise
by
Western medicine.
Doing Away with Depriving Diets
Since receptor and transport proteins unavoidably blocked by look-alike
toxins often are resistant to being broken down into amino acids and
reused,
amino acids and vitamins for rebuilding these contaminated proteins
must
be supplied by our diet. For example, niacin is being used to ease
withdrawal
from nicotine and to lower cholesterol, a strategy applicable to
poisonings
with other vitamin and mineral look-alikes. Essential fats and
fat-soluble
vitamins are dietary as well, so good nutrition is one of the best ways
of bolstering our overall defenses against environmental toxins. Using
starvation diets, fat substitutes, and fat-free foods for dramatic
weight
loss is not only counterproductive to good health, it can be dangerous.
For example, rapid metabolism of fat stores in the body can leave
behind
years of accumulated, fat-soluble carcinogens that concentrate in any
remaining
fatty tissue such as the breasts, particularly in women. Besides, the
newest
"rapid-" or, should we say, "rabid-weight-reduction" drugs alter our
serotonin-controlled
equilibria. The recent ban on certain combinations of rapid-weight-loss
drugs because of the permanent damage to the heart that they cause only
reinforces our concerns about this approach to losing weight.
Similarly, new concerns have arisen about the use of phytoestrogens
in roasted soybeans and flax seed as alternatives to pharmaceutical
hormonal replacement therapies even though they have been reported to
lower, not raise, the
risks of cancer. Although L-cysteine or L-cystine can help to
controlling cholesterol,
that can contribute to heart disease, by raising HDL, lowering LDL,
lowering
triglycerides, and lowering cholesterol, proteins containing these
amino acids must be digestible and the amino acids must be
assimilatable to have these beneficial effects. Soy protein apparently
does not meet this standard, and instead creates additional health
risks:
Focus on Food QUALITY not Quantity
It also is important to realize i) that many of the foods available to
us today are produced on soils that have been depleted of nutrients by
intense farming, and ii) that much of the food available in the grocery
store has been extensively processed, which depletes even more of the
vitamins,
minerals, and perhaps other nutrients that have not yet been
discovered.
One must also consider that foods picked green and chemically ripened
"to
look as good on the shelf as fresh food" are probably less nutritious
than
vine-ripened foods. Local produce, organic produce, and "Victory
Gardens"
can usually provide better and safer nutrition than imported and
chemically-treated
produce, simply because we can discover and control how this food is
processed
and limit its (and consequently our) exposure to chemicals, herbicides,
and pesticides.
Good Nutrition and Dietary Supplements
In addition to the usual vitamin and mineral supplements, other
considerations
can help to fortify our defenses against unavoidable toxins. Since the
vitamin, pantothenic acid, and the amino acid, cysteine, are the
probable
building blocks for the vitaletheine modulators, these nutritional
factors
are very important in providing protection. Pantothenic acid is readily
available in supplements and is particularly rich in
commercially-available
royal jelly. Royal jelly is fed to the fertile queen bee her entire
life,
but not to the sterile worker bees
(Would we but a sterile worker bee,
if we were made pantothenate-free?)
The disulfide, cystine, cannot bind and carry toxic metals into the
body and is probably safer than either cysteine-HCl or N-acetyl-cysteine
for additional reasons. People with cystinosis, cystinuria, or
cystinemia
or a history of kidney stones should consult with their doctor before
taking
cystine or cysteine. Even in these conditions, a B-vitamin complex
containing
pantothenic acid, folic acid, and vitamins B6 and B12
should help to metabolize
and utilize not only available cystine, but other amino acids, like
methionine, as well.
However, there is growing evidence that these three B vitamins should
always be supplemented when adequate levels of L-cystine and
pantothenic acid (B5) are also available. These steps can
help to offset any depletion of the vitaletheine modulators
and of the dietary cystine needed for rebuilding proteins, cofactors,
and
enzymes. Dietary cystine should be particularly helpful in offsetting
problems
caused by a variety of environmental toxins, including the following:
- Mycotoxins (toxins such as aflatoxin from microbes contaminating
our
food
and environment)
- Chemical Warfare Agents (nearly all, including tear gas such as
Mace
and
HN1)
- Chemotherapies, many of which are alkylating agents and/or
carcinogenic.
Mustargen is a close structural analogue of HN1 and a chemical warfare
agent known as HN2. It is used as aggressive therapy by many allopathic
practitioners by itself and in a combination therapy, known as MOPP,
with
vincristine, prednisone, and procarbazine (an indole analogue, an
immune
suppressant, and an oxidative substance that can cause cancer, birth
defects,
and mutations, respectively). Some allopathic practitioners have even
advocated
giving lethal doses of chemotherapeutic agents to cancer patients while
trying to keep them alive long enough with other drugs for the poisons
to clear their systems.
- Plant Toxins (phorbol esters and related compounds capable of
producing
epoxides or enol tautomers)
- Too Much Vitamin C Intake (anything over 200 mg/day for otherwise
healthy
people)
- Rancid Fat (polyunsaturated fats poorly stored or contaminated
with
peroxidizing
metal catalysts)
- Toxic Metals (Nickel being one of the more common and insidious
in our
environment)
Eating fresh foods rich in cysteine is another way of
bolstering
this nutrient. We should be eating more whey than curds, since the
majority
of the cysteine in milk winds up in the whey, not in casein used to
make
cheeses. The protein in human milk contains more than
twice
the cysteine and far less glutamic acid than cows milk,
contributing
to suspicions that unfermented cows' milk, processed cheese, and
glutathione may not be
the best dietary sources of cysteine-containing proteins and peptides
for
humans. Aged cheeses,
on the other hand, may be quite beneficial if one doesn't suffer from
tyramine sensitivities. Winged beans, whole grains (including oat meal
and bran, barley and even barley greens), eggs, fish like north
atlantic wine vinegar pickled herring, bison
round, and nuts (but not ground
nuts like peanuts) are
good sources of dietary
cysteine. Roasted soy beans, although appearing to be a
particularly good source of protein
and vitamins that contribute to the effective use of amino acids, do
not provide as much
protection
against heart disease and cancer
as claimed, since soy protein is poorly digested and difficult to
assimilate. Concern about the protease inhibitors
and phytic acids in roasted soy beans may be exaggerated, since there
is
some evidence that the proteases in primates are more resistant to
inhibition
than those in rodents and since phytic acids may help us excrete toxic
metals, but soy protein and other components reportedly poison the
thyroid, thymus, and hormonal status of people consuming the
unfermented versions. Similarly, consuming defatted (processed) soy
flour may not be a good idea,
since the removal of the fat probably removes the fat-soluble vitamins
and antioxidants and the essential fatty acids, leaving
behind only the binding proteins. These denuded binding proteins, until
digested, would tend to absorb fat-soluble nutrients from the body
instead of nourishing
it.
Unfortunately,
fish is often contaminated
with the counter-productive toxic metals that tie up both the cysteine
and the vitaletheine modulators, so watch the source. Open ocean fish
may
be somewhat safer than those from tidal or estuary waters simply
because
the man-made pollutants may be diluted somewhat by the time they reach
open ocean, assuming perhaps naively that our oceans are not already
largely
contaminated. Realize also that predatory fish on top of the food chain
typically concentrate toxins from their prey at a rate that is
compounded
by each link moved up the food chain. Prey fish or very young
predatory
fish, like wine vinegar pickled herring, are safer choices than that
trophy swordfish with its long
lifetime of heavily-compounded accumulations of toxic metals and other
toxins.
The RDA for cystine is about a gram. However, exceeding about 0.5%
cystine
in the protein of ones diet (such as that provided by a corn/soy diet)
may lead to a decrease in the benefit of any cystine supplementation.
Consequently,
one wants to error on the supplement side and not try to totally
replace ones dietary requirement for cysteine, e.g., without other nutritional
amino acids in dietary protein. Supplemental ranges of 400
mg cystine or less are probably most effective, especially when taken
with
dietary protein. Adjustments may have to be made for individual
variations in diet.
Since iodine and metabolites of cysteine are involved in the
synthesis
and utilization of thyroid hormone and in the regulation of other
hormonal
and metabolic pathways, iodine and cysteine probably complement each
other
nutritionally. Iodized salt is the primary source of this nutrient for
many, so iodine must be supplemented in salt-free diets designed to
control
high blood pressure. This prevents the onset of problems linked to
hypothyroidism,
including goiter, weight gain, and neurological
problems. Kelp is a good
dietary source of iodine.
Antioxidants, such as vitamin E, prevent the undesirable
oxidation of
fat to form lipid epoxides. Nickel accelerates the formation of
epoxides,
so failure by "food manufacturers" to completely remove the nickel
catalyst
from margarine ("partially hydrogenated" vegetable oils) can result in
serious health problems. Both nickel and lipid epoxides are known to
react
with thiols, so avoiding these two substances helps to prevent the
destruction
of vitaletheine and dietary cysteine. Unsaturated fats tend to oxidize
spontaneously under ambient conditions. Consequently, it is a very good
idea to consume, primarily, fats that are well-protected with natural
antioxidants
and that have neither a high degree of saturation nor a high degree of
unsaturation. This means we should i) use centrifuged coconut oil for a
cooking
oil at low temperatures and ii) get our fat-soluble vitamins and
essential fatty acids from
natural, mono- and poly-unsaturated fats, such as olive oil or even the
more stable olives. Nuts are a good source of cysteine as well,
especially Brazil
nuts, but Brazil nuts may have too much barium. Great care
(refrigeration or storage under inert gases) must be taken
to ensure that any polyunsaturated oils do not oxidize (go rancid).
Rancid
fats (e.g., nuts) "taste bad"
and "are bad" for our immune and other systems.
If these dietary fat guidelines cannot be followed for any reason, then
limiting dietary fat intake to nine ("just say nein") grams or less per
serving is a very good idea.
In addition to reducing dangerous epoxides, antioxidants are useful
in diminishing background oxidations. This "oxidative noise" can be
confused
with a true regulatory "signal" such as the "oxidation of vitaletheine"
to its sulfenic acid. Vitamin E appears to reduce background oxidation
without interfering with monooxygenase activities. At the same time,
too
much of an antioxidant (vitamin C and possibly the 20 to 50 times more
potent proanthocyanidins found in grape seed extracts) or the wrong
type
of antioxidant (carcinogenic quercetin from roasted soy beans instead
of apigenin
from oranges)
can reduce these "true" regulatory signals, thereby leading to high
cholesterol
and an improper immune response to cancer. For example, we cannot, at
this
time, advocate that people with cancer start supplements of more than
about
100
mg natural vitamin C/day. This concern is reinforced i) by vitamin
C's observed
uncoupling of an activity of the monooxygenase that down-regulates
cholesterol
production and blocks oncogene (cancer) expression and ii) by the fact
that when neither re-reduced nor protected by other, more potent
antioxidants,
vitamin C can be become oxidized to
dehydroascorbate,
which is diabetogenic.
Those healthy individuals taking synthetic vitamin C, or natural
vitamin C over 200 mg/day
and consuming adequate levels of other more potent antioxidants, might
want to consider slowly diminishing their vitamin C intake over a
period
of weeks or months, i.e., by no more than a quarter of the previous
dose
per day until their natural vitamin C intake can be maintained at about
100 mg/day. It is well-known that individuals acclimated (addicted) to
megadoses
of synthetic vitamin C will develop scurvy-like "drug withdrawal"
symptoms (including
sore gums) if their artificially high vitamin C supplementation is
diminished
too quickly.
A WAIST is a terrible thing to MIND!!
More body fat means more antioxidants are needed to control its
autooxidation.
Without them, the theoretical risk of "spontaneous combustion"
(uncontrolled
"oxidation" of accumulated fat) becomes greater, especially when helped
along with oxygen administered by anesthesiologists and sparks from
surgical electrocauterization.
The problems that many Americans have with metabolizing fat are
probably
the result of both, poor nutrition and a poisoning of the thiols found
in our fat-metabolizing cofactors and enzymes. Coenzyme A, Acyl Carrier
Protein, Lipoate Acetyl Transferase, and R-dihydrolipoic acid are among
the more obvious targets
for toxic metals and fat-soluble, environmental toxins such as alkyl
halides
(from chlorinated drinking water) and lipid epoxides. Coenzyme A is
needed,
for example, to metabolize the three major forms of energy (fat,
carbohydrates,
and protein). If fat is the energy source that can't be metabolized
(say,
for want of Coenzyme A, acyl-carrier protein, and R-lipoic acid) it
simply accumulates.
Consequently, weight gain is not something that anyone should feel
guilty
about, since in many cases it is probably just an indication of how
extensively
we have been malnourished and poisoned. A change in diet
and environment
may be needed to deal with the problem.
These insights have some far ranging consequences. When Coenzyme A
is
blocked, we cannot generate energy from the usual sources and may
suffer
from conditions known by such medical terms as "chronic fatigue
syndrome".
This, in turn, leads to less activity and eventually more weight gain.
In addition, intermediates that accumulate (when Coenzyme A is blocked)
poison other systems and lead to manifestations of other diseases. For
example, the body makes Coenzyme A from pantothenic acid and cysteine,
the latter being produced through the metabolic intermediate,
homocysteine.
Homocysteine accumulates in cancer and heart disease. Half of the heart
disease incidence has been attributed to a deficiency of the vitamins
(folic
acid and B6) that help to convert other amino acids into cysteine. A B6
deficiency alone can prevent homocysteine's conversion into cysteine.
Without
cysteine, Coenzyme A cannot be made. This problem is exacerbated
further
by any pathological accumulation of homocysteine that, through its
"like"
but not quite "cysteine" chemistry, probably interferes with the
utilization
of cysteine in producing both, Coenzyme A and vitalethine. Thus, we
have
a ready explanation for "chronic fatigue immune dysfunction syndrome"
(CFIDS).
Dimerization of homocysteine by self-lactonylation presents even
more serious consequences, since the homocysteine- thiolactonylated
homocysteine and its tautomers resemble vitaletheine and its tautomers
just a little too closely:
Carrying this argument further, poisoned individuals cannot convert
dietary lipids from animals and plants into human fat
compositions.
In essence, we would be trying to build and maintain our human
lipid-containing myelin
sheaths that surround and protect our nerve fibers with, say, cow
"parts".
This probably contributes to pathological situations in which there is
an established autoimmune component, such as in multiple sclerosis. An
environmental poisoning of the the vitaletheine modulators (immune
dysregulation)
while "cow parts" (antigens) are being used in human structures clearly
can contribute to autoimmunity. In other words, a confused and poorly
targeted
immune system, especially when one's lipid membranes are in disrepair
or
of an improper composition, may be the underlying, or at least
contributing, cause for some autoimmune
and neurodegenerative diseases. Again, obesity could be a harbinger of
dangerous metabolic imbalances (brought on by malnutrition and
environmental
poisonings) that can lead to rheumatoid conditions, Parkinson's,
Alzheimer's,
and other autoimmune, immunodeficiency, and infectious diseases.
Having a lot of accumulated fat deposits to process to find or
create
the right "parts" for nerve maintenance, certainly does not help the
body
to cope with these diseases, so weight control should help obese
individuals
with any signs of these diseases. At the same time, too little quality
fat in ones
diet, such as quality fat NOT provided by reduced-fat and fat-free
foods, may be similarly
problematic in neurodegenerative diseases. When fat is taken out of
our food, what happens to the essential fatty acids, fat-soluble
vitamins,
fat-soluble antioxidants, and other known but as yet unidentified
fat-soluble
nutritional factor(s)? They're either gone or, hopefully, at least some
of them are put back into capsules to sell to us, separately, and at
greatly inflated prices. On an unsupplemented, fat-free diet, it is not
a matter of the "right parts" being available
for nerve maintenance; there are no "parts".
Muscular dystrophy (MD) has a tentative link to obesity since it has
been associated with deficiencies of vitamin E and of selenium, both of
which are implicated metabolically in protecting lipids and therefore
thiol
compounds, such as the vitaletheine modulators, from undesirable
oxidations
and chemical modifications. Since vitamin E is fat-soluble, dietary
intakes
may be inadequate, i.e., "spread to thin", to prevent the
detrimental
effects of lipid epoxidation, especially in those obese individuals on
fat-free or starvation diets. Dietary supplements including a good
antioxidant
mix are indicated under these circumstances. Hence, moderation in both
exercise and nutritional
supplementation are essential for any safe weight "control" program; we
must supplement with vitamins, minerals and other nutrients, eat well
(focus
on "quality" not quantity), exercise,
and avoid environmental toxins
to lose weight safely.
In summary, these "steps" to avoid toxins, to improve nutrition, and
to exercise (or at least sweat) should help to fortify our defenses
against
both, environmental and infectious assaults. In fact, a growing
awareness
of endocrine disruption of our hormonal and
immune systems
has led several
researchers to call for the development of immunological treatments for
endometriosis. There are probably safer nutritional (chasteberry) and
bioidentical hormone (progesterone and estriol) alternatives to
phytoestrogens
from roasted soybeans and flax seeds, and these may be, in turn, safer
than more aggressive conventional therapies with synthetic hormone
replacement (HRTs or metabolic poisons) for estrogen- or
testosterone-linked disorders. In any case, good nutrition, vitamin and
mineral supplementation,
exercise, and environmental awareness and activism may be our best
defenses for proactively i) restoring proper immune responses, ii) for
minimizing health costs,
and iii) for providing the best "health insurance" against
pollution
and for long life. With associated insights, the vitaletheine
modulators may even
prove to be an important component of our Achilles "heal".
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