Protein Deficiency and Autism
by Dr. Brice Vickery
Many
recent studies have confirmed that all types of autism involve a malfunction
in the part of the body’s system that deals with metal regulation
(1). It has also been observed that the digestive system of these children
does not work well (2). How are these two problems related? How can
we solve this problem?
Certain metals such as iron, zinc and copper, are essential to the
body, others such as cadmium, mercury, aluminum and lead are toxic.
Too much or too little of any metal in the body will have a disrupting
effect on the system. Not everything is understood about metal metabolism,
but more studies are being done all the time that show the body’s
use of certain metals to have significant effects on the health of the
entire system. Recent autism studies have focused on a certain metal
binding protein, metallothionein (MT). MT is a biologically essential
protein that has been shown to be heavily involved in the metal regulation
of zinc, and copper as well as the chelation of toxic metals such as
cadmuim, mercury and lead. MT proteins also assist in immune function,
neuronal development, are heart protective, brain cell protective, involved
in liver cell proliferation, the absorption and of nutrients in the
small intestine, the breakdown of certain dietary proteins, cellular
respiration, neuronal development, energy metabolism and have antioxident
properties(3). Studies show that MT does not function properly in autistic
children, although it is still unclear whether this is due to genetic
factors or simply low levels of MT in the system (4).
Metalloththionein (MT) is a single chain protein. There are four kinds
of MT. MT I and II are found all over the body, MTIII is found in the
brain (mostly in the neurons of the hippocampus) and MT IV is manufactured
in the GI tract. MT contains 61 amino acids, total, 20 of which are
the sulfur containing essential amino acid, cysteine. MT has seven binding
sites for metal in two core clusters. The principle metal binding ligands
for these sites also contain cysteinal residues showing that a huge
component of the MT metal regulating system is the essential amino acid,
cysteine. The entire MT is composed of sulfur and protein (5).
Remember also that essential amino acids cannot be made by the body,
but must be obtained in the diet. One of the problems identified with
autism is a digestive system that cannot fully break down all protein
into its basic components, the amino acids, and the system will only
use amino acids to make systemic protein. This means that many necessary
amino acids are unavailable to make systemic proteins such as MT (6).
Studies have proven MT to have an affinity for zinc and an even stronger
affinity for cadmium, which will bind very much more strongly to the
metal binding sites on MT (cadmium has a half-life of ten years in the
body)(7).
Zinc is an essential metal. Adequate amounts of zinc are necessary
for proper immune function. 90% of the body’s zinc stays in the
muscle and has a very slow rate of turnover, the remaining 10% is extremely
metabolically active and very sensitive to changes in the levels of
dietary zinc. Diabetes studies showed hypoglycemia and insulinemia to
improve when cellular levels of zinc in mice were raised, whereas removing
zinc from the diet worsened these conditions.It takes only 48 hours
for all the zinc in the liver, a key area of zinc metabolism, to exchange
with the zinc in the blood plasma. Zinc is also part of the make-up
of over 300 enzymes and hundreds of zinc binding proteins. It is used
in many of the body’s systemic protein interactions as well as
in the synthesis of the hormone melatonin and its precursor, seratonin,
and it facilitates the proliferation of liver cells and has anti-oxidant
properties when it is bound to the MT protein. Studies have shown that
patients with depression, bipolar disorder, Parkinson’s disease,
Alzheimers, and autism are have severe zinc imbalances (8). Studies
also show that children with autism are often overloaded with toxic
metals, as well as zinc deficient and with MT proteins that don’t
function properly.
The presence of glutathione is critical for the healthy regulation
of zinc in the body. In order for the MT system to work optimally, glutathione
(a sulfur rich tripeptide) must be present in both a reduced (GSH) and
oxidized (GSSG) state. GSH binds the metal to the MT while GSSG releases
it. The ratio of both (GSH:GSSG) within the cell is called the redox
ratio of the cell, a healthy redox ratio is between 30:1 and 100:1.
(The redox potential of a substance is the likelihood of it undergoing
this reduction-oxidation transformation, for instance, zinc has no redox
potential at all) However, glutathione disulfide (GSSG) is also very
necessary, while GSH enhances both the rate of zinc transfer and the
number of zinc atoms released for cellular use, in the absence of GSSG,
zinc release becomes much more inhibited (9).A well-balanced redox ratio
is important. For instance, in the case of the body being under high
levels of oxidative stress, as is suspected in many autism cases, the
GSSG levels rise causing, a condition where too much zinc is released
from the MT this leads to the over inhibition of certain processes such
as, cellular respiration and the inhibition of certain enzymes in energy
metabolism. (10). Studies also show that when the metal levels are high
glutathione levels are reduced.(11) In order for GSSG to be recycled
into GSH there must be adequate amounts of the proper redox enzymes
available and as you know, enzymes are made of systemic protein Could
it be that not enough systemic protein is available for autistics to
make the proper redox enzymes?
The structure of glutathione (GSH) is composed of the amino acids (AA) glutamic acid,
glycine and once again, that sulfur containing essential amino acid,
cysteine. Studies show autistic children to be deficient in glutathione.(12)
When toxic metals such as mercury and cadmium enter the system, MT
will attempt to sequester the toxic material, this process requires
zinc and GSH. If there is not enough MT, the body will make more if
it can. (13) MT manufacture requires sufficient amounts of : cysteine,
serine, lysine, argenine, alanine, lysine, valine, aspartic acid, asparagine,
glutamic acid, glutamine, proline, threonine, and methionine (also a
sulfur containing amino acid). Exactly half of these are essential amino
acids, and one-third of the total number of AAs is made up of the sulfur-rich
cysteine. In order for the MT system to works properly the body must
have available adequate cysteine (14) Are autistic children deficient
in amino acids?
Both glutathione and MT contain large amounts of sulfur. Sulfur is
an essential mineral that is necessary for many systemic functions.
Because of the condition of our soil today our main source of organic
sulfur, plant food, is compromised. Besides the metal regulation functions
that it performs, sulfur is needed for pancreatic release of digestive
enzymes and if it is not present in the ileum of the intestine, then
leaky gut will ensue. (15). Sulfur is necessary for many enzyme reactions
as well as modulation of the nervous system, maintenance and protection
of the connective tissues, insulin production and support of the liver
detoxification Phase II pathway . Sulfur, along with molybdenum, fuels
the process that detoxifies certain food additives that may otherwise
cause allergic reaction. Sulfur containing amino acids (SAA) are cysteine
and methionine. (Studies also show that morbidity in HIV patients is
decreased with increased SAA consumption. Methionine in particular has
been shown to decrease symptoms in Parkinsons Disease and pancreatitis
) Methylsulfonylmethane (MSM) is a safe and effective form of organic
sulfur(16).
Autistic children have been identified with high toxic metal levels,
low levels of MT, MT systems that don’t work, low levels of glutathione
and zinc, low levels of sulfur and mal-functioning digestive systems
(including leaky gut and food allergies). Various different theories
for the cause of these malfunctions are proposed: genetic predisposition,
pre- and postnatal nutritional deficiencies, possible toxic effects
of infant immunizations, heavy metals exposure, and other environmental
factors. However this condition came about, the challenge remains to
somehow enable these impaired systems to function normally (17). The
functioning of any person’s system will improve when it has adequate
systemic protein.
Current therapies for autistic children involve zinc, amino acid and
glutathione supplementation. The amino acid supplementation is usually
protein specific. For instance, MT is one of the proteins in which autistic
children are deficient, leaving them open to metal toxicity. Therefore,
one therapy administers the 14 different amino acids in MT along with
GSH are given orally to the patients in an effort to raise levels of
body’s metal regulation system(18). The problem with oral GSH supplementation
is it is just not very effective (19). Glutathione and MT are systemic
proteins and the best way to get the body to manufacture these is to
enable it to fully digest its food, then it will create the proteins
it needs, where it needs them, when it needs them.
Recent studies indicate that the digestive systems of autistic children
do not fully break down food. Autistic people also show low levels of
secretin and one of the current popular theories is that orally administering
this hormone could clear up the poor digestion issues that are characteristic
of autism. The digestive system is supposed to secrete this hormone
when the stomach empties. It helps the stomach to produce digestive
enzyme (pepsin), the pancreas to produce alkaline digestive fluids,
and the liver to produce bile. However, there has only been one very
small study (three children) demonstrating the successful use of this
hormone with autism and it is unknown whether supplementation of this
hormone over long periods of time would be harmful to the body(20).
The action of secretin is to flush digestive enzymes from the pancreas
(21). If there are inadequate amounts of digestive enzymes available
to flush, how is secretin helping?
Could it not be possible that the main problem in autism is a critical
deficiency of systemic protein and sulfur in general? Secretin is a
systemic protein. It is a polypeptide consisting of 27 amino acids.
MT is a low molecular weight protein consisting of 61 amino acids, glutathione
is a tripeptide, and sulfur is an essential mineral. In order for the
proper components to be available for systemic proteins such as MT,
glutathione and secretin, dietary protein must be completely broken
down into amino acids. If this does not happen, the partially broken
down proteins will simply irritate the system resulting in conditions
such as diarrhea and allergic responses such as rashes, inflammation,
and mood disorders. (Partially broken down peptides putrefy in the system
producing indican which is easily identifiable using the Urinary Indican
Test) Partially broken down protein is not the same as amino acids and
the body will not use it to make systemic protein. A body that cannot
properly break down food will become protein deficient. If this protein
deficiency continues then systemic malfunction will eventually occur.
If food can be fully broken down then the systemic proteins will be
available to create and support systemic proteins of all sorts.
Another piece of the autism puzzle that seems to be missing from the
research is the concept of the limiting amino acid. This is a concept
that has been applied years in agriculture successfully but we do not
use it often in human nutrition. According to Donald Snyder, Ph.D, “In
every native protein there is a particular essential amino acid that
limits that protein's value to the overall diet. Once that limitation
(minimum requirement) is met or exceeded, another amino acid becomes
limiting and so on until there is derived a theoretically perfect balance
of amino acids for optimal growth and performance. Further supplementation
will not improve the diet.” (22). In other words essential amino
acids must be given in a properly balanced ratio in order for them to
be safe and effective . This means the excess of one essential amino
acid can hamper the absorption of other AAs. Therefore it would be necessary
for any AA therapy to be sure that their amino acid supplement was balanced
so that the body could effectively use it.
If the body is not digesting its dietary protein it is because the
pancreas is not producing the necessary digestive enzymes Dr. Brice
Vickery addressed this problem in the early 1980’s when he found
that all his patients with degenerative disk disease were also deficient
in systemic protein and organic sulfur. After years of testing, Dr.
Vickery solved the problem of the limiting amino acid that renders so
many other amino acid blends ineffective or, especially in the case
of cysteine, dangerous. He produced a perfectly balanced blend of essential
amino acids (Platinum Plus Essential Amino Acids, US Patent 6,203,820)
that actually enable the digestive system to produce the required enzymes
to break dietary protein into amino acids. Vickery recorded that in
ten to twelve hours of taking Platinum Plus his patient’s spinal
disks began to heal. This was proven thru countless MRI’s and CAT
Scans. Further testing showed that combined with a certain program of
use (The Vickery Protocol) Platinum Plus enabled the body to manufacture
systemic proteins, which actually boosted the immune system to the point
that it could heal other imbalance and disease conditions as well.
Heavy Metal Poisoning:
Vickery added extra organic sulfur and molybdenum to his blend to support
phase II liver detox pathways, helping the body to flush toxins such
as heavy metals out of the system. Attached charts show how quickly
Platinum Plus Essential Amino Acids enable the system to completely
flush mercury, lead, and aluminum from the body.
Fibromyalgia:
Vickery’s testing showed all Fibromyalgia patients to have five
common conditions, regardless of their symptoms. 1)protein deficiency
2)degenerating spinal disks 3)sulfur deficiency 4) heavy metal toxicity
, and 5) viral infection. When they follow the Protocol their bodies
are able to heal.
Liver Disease
If the liver does not have adequate amounts of systemic protein it
cannot make body fluid regulators like albumin, it cannot make repair
proteins used by the blood, and it cannot keep up its two-phase detoxification
system that the body uses to filter and clean the blood. These two pathways
also require glutathione and molybdenum, respectively to work properly.
If the body cannot supply these things, the liver becomes susceptible
to disease. Vickery’s research has shown Platinum Plus to allow
the liver to heal itself of diseases such as hepatitis and start functioning
normally again.
Hypoglycemia
Protein deficiency can also lead to hypoglycemia (as well as vice versa.)
If amino acids are not available in sufficient quantities to manufacture
the enzymes needed for gluconeogenesis and glycolysis, then blood sugars
will remain low after pancreatic release of insulin. Proteins also transport
the vitamins needed both of these processes. Platinum Plus blend allows
the body to produce the systemic protein it needs to help maintain blood
sugars at an optimal level.
Various viruses and bacteria
The body’s immune system is also made up of various important
systemic proteins. Alack of these proteins will lead to a weakened immune
system that is less able to protect the body from viruses and bacteria
such as staph, strep and hepatitis. Vickery’s research shows that
when the body has adequate protein it can fight off these invaders and
keep them away.
Glutathione, MT and secretin are all systemic proteins, which the body
will make itself if given adequate amounts of amino acids and co-nutrients.
The Vickery Protocol provides a balanced blend of amino acids, sulfur
and molybdenum, along with the necessary co-nutrients to allow the body
to heal its digestion, rebuild its immunity and balance its systems.
Autism shows a remarkable resemblance to the protein deficiency cases
that The Vickery Protocol has successfully helped. Dr. Vickery is currently
following several autistic patients who appear to be using his Program
with considerable success.
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