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Centrophenoxine
– The
anti-aging brain booster
by James South MA
Centrophenoxine (Lucidril®) is one of
the original anti-aging, neuro-energizing drugs. It has been
studied and used clinically for over 30 years.
Centrophenoxine is a compound of two
biochemicals- dimethylaminoethanol (DMAE) and parachlorophenoxyacetate
(pCPA). Dimthylaminoethanol is a natural food component, found
especially in fish, and is also a natural metabolite of the human
body. Centrophenoxine's other half, pCPA, is a synthetic
compound similar to a variety of plant hormones called
"auxins."
Centrophenoxine – Lipofuscin
remover
One of the earliest discoveries from
animal studies showed that centrophenoxine is extremely effective at
reducing lipofuscin levels. Lipofuscin is a "garbage
residue" biochemical conglomerate that accumulates over a
lifetime, sometimes reaching 30% of the cell volume in aged animals.
As cells accumulate ever more
lipofuscin they become ever less functional, and they may die rapidly
when a critical threshold of lipofuscin accumulation is reached.
Animal studies have shown
centrophenoxine to be highly efficient at removing this cellular
garbage- notable reductions in mice occur within 6 weeks. One study
with aged rats found a 28-42% reduction in brain lipofuscin levels
after 8 weeks of centrophenoxine treatment.
Both human and animal studies have
shown that low lipofuscin levels correlate with healthy cellular
function, while high lipofuscin accompanies poor cellular health.
Through a variety of animal experiments
measuring learning abilities and memory, aged animals whose high
lipofuscin levels were reduced by centrophenoxine, also had their
memory and learning abilities restored to a level similar to healthy
young animals, while untreated high lipofuscin control animals did
not.
Centrophenoxine – Cognition
enhancement
The chief component of centrophenoxine
is DMAE which is part of the choline betaine cycel, natural to human
and animal cells.
By adding a methyl group (CH3) to DMAE,
choline (also called trimethylaminoethanol) is formed. The choline
thus formed may then be used to make other valuable biochemicals, such
as the major neurotransmitter acetylcholine, or the essential membrane
constituents phosphatidylcholine and sphingomyelin.
Choline can also be oxidized to make
betaine (trimethylglcine), important for ridding the body of heart and
artery toxic homocysteine, now considered one of the most important
risk factors for heart disease.
Under fasting conditions, normal blood
levels of choline range from 8 to 12 micromoles. When blood choline
levels are below 14 micromoles, choline flows from brain cells into
the bloodstream. When blood choline levels are above 14 micromoles,
choline flows from the blood into the brain.
Unfortunately, when choline enters the
blood from brain cells, it is derived from auto-cannibalisation, the
choline containing phospholipids (which are critical brain cell
membrane components) are broken down to provide the choline entering
the blood.
There is evidence that excessive
neuronal choline auto-cannibalisation over a lifetime may contribute
to Alzheimer's disease.
Centrophenoxine – The need for
supplementation
While a natural foods diet, such as
liver, meat and eggs provides high dietary levels of choline, the
modern processed junk food/ synthetic diet provides little choline, as
do vegetarian diets.
Simple choline supplements, such as
choline chloride or bitartrate are often broken down, as much as 60%,
by gut bacteria. Thus, centrophenoxine derived DMAE is an especially
ideal source of blood and brain choline for several reasons.
Gut bacteria do not digest DMAE, thus
avoiding that wasteful trap. The liver quickly and easily converts
DMAE to choline as needed. Also, DMAE prevents choline from being
irreversibly oxidized to betaine, further raising blood choline
levels. Lastly, DMAE passes through the blood brain barrier far more
easily than choline.
DMAE may be incorporated into brain
cell membranes, where it functions as a powerful hydroxyl free radical
scavenger. Or the brain cells may convert the DMAE to choline for
their needs. With the help of an enzyme called "CAT",
choline is converted to the learning/ memory neurotransmitter
acetylcholine.
With aging, and even more so with
Alzheimer's disease, cholinergic neurons tend to under produce
acetylcholine. Fortunately, the popular brain nutrient
acetyl-L-carnitine that powerfully increases CAT activity, thus
increasing acetylcholine production.
The research of Dr. Raymond Bartus has
shown that the original nootropic drug- piracetam works much more
effectively to enhance learning and memory when combined with a
cholinergic compound.
Thus, centrophenoxine, piracetam and
acetyl-L-carnitine would be an "all star" combination for
cognition enhancement. Human studies have found centrophenoxine
to be effective at restoring intellectual well being.
Centrophenoxine – The human
response
One study with 76 healthy elderly, who
suffered from significant intellectual deterioration, found that
centrophenoxine increased storage of new information into long term
memory, while also increasing vigilance and alertness, after only
several weeks of treatment.
A double blind placebo controlled study
found clinical improvement from CPX in 7 out of 30 patients with
senile psychosis.
Centrophenoxine – Much more than
DMAE
Centrophenoxine, which is more than
just DMAE, also has a general activating effect on brain function.
Centrophenoxine enhances neuronal glucose (the chief brain fuel) and
oxygen uptake, while increasing carbon dioxide production, all signs
of increased brain ATP production.
Centrophenoxine also increases neuronal
RNA and protein production. RNA (derived from DNA in the cell nucleus)
"instructs" neurons how to form proteins which help encode
memory, as well as repair cell damage.
Yet brain RNA and protein production
normally drop with age, and especially when large lipofuscin deposits
form around the cell nucleus, one of the main sites where lipofuscin
accumulates in old age.
Centrophenoxine reverses this
age-related drop. It is interesting to note here that the pCPA
component of CPX is similar to plant auxins- plant hormones, which
increase RNA and protein production in growing plants.
Centrophenoxine has been shown to
increase repair of the synapses that connect nerve cells to each
other- while untreated aging synapses tend to deterio-rate in number,
structure and function.
Thus, because of the unique plant auxin
like substance pCPA that is combined with DMAE to make
centrophenoxine, centrophenoxine may be considered the ultimate
"DMAE plus."
Centrophenoxine – the dosages
In spite of the generally beneficent
anti-aging, brain energizing, repairing effects of centrophenoxine, a
few words of caution are necessary.
Centrophenoxine is a powerful enhancer
of brain and peripheral nervous system acetylcholine levels, and too
much acetylcholine can cause problems. Excessive acetylcholine levels
can lead to headaches, neck, jaw and shoulder muscle tension,
insomnia, irritability and hyperexcitability, agitation and
restlessness.
If any of these occur, simply
discontinue centrophenoxine for a few days and then try a reduced
dosage. Also, those with major depression, mania, seizure disorders or
Parkinson's disease should avoid centrophenoxine, as too much
acetylcholine may worsen these conditions. Also, pregnant women should
avoid centrophenoxine.
While elderly people with significant
intellectual decline/ loss of vigor may need 3 to 6 centrophenoxine
tablets per day (250mg each), taken preferably with breakfast and
lunch, in order to avoid insomnia.
For healthy younger people simply
wishing the brain protection/ cognitive boost/ choline benefits that
centrophenoxine provides may need only 1 or 2 centrophenoxine tablets
(250mg each) daily with breakfast or lunch.
To avoid any slight acetylcholine
excess that may slowly creep up unnoticed, it may be helpful to skip
centrophenoxine one or two days weekly.
The above
article is copyrighted and may not be copied without the written permission of
International Antiaging Systems, Les Autelets Suite A, Sark
GY9 0SF, Channel Islands, UK.
ALL INFORMATION IS EDUCATIONAL AND PROVIDED UNDER IAS TERMS AND CONDITIONS AND SHOULD NOT REPLACE THE ADVICE OF YOUR PHYSICIAN.
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