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How to Win the War
Secret Anti-biological Weapon Being Tested for Military,
Civilian Applications
by
Bill Sardi
by Bill Sardi
At
a Mountain-states laboratory researchers are testing a type of stealth
weapon against disease and infection that could virtually eradicate
most concerns about modern biological weapons such as anthrax or
ebola, overcome the growing problem of antibiotic germ resistance,
as well as disintegrate cancer cells from within, eradicate plaque
from arteries, and block every known bacterium, virus, amoeba or
fungi, including the dreaded H5N1 influenza virus.

GC: C6H10OS2
It's
not a vaccine. It's a stealth molecule known as GC.
Chemically described as C6 H10 O S2, GC is an unstable, short-lived
hydrophobic molecule that penetrates biological membranes with ease.
It disappears from the circulation within a few minutes after injection,
making it virtually nontoxic. The molecule is very small,
molecular weight of 127.27, and can penetrate through cell walls
and even barriers in the brain.
Scientists
have known about GC for years. The problem has been how to
get it to activate properly once introduced into the human gastric
tract. Even measuring its presence in the human body has been
a challenge. GC cannot be detected in the blood or urine.
Researchers have to utilize a breath test to confirm its presence
similar to how law enforcement officers utilize a breath test to
measure alcohol in the blood circulation. After oral consumption,
levels of GC can be indirectly detected in breath as elevated levels
of acetone.
Stealth
molecule
GC
is a transient molecule. Once formed, it breaks down into
other forms fairly rapidly. GC must to be introduced as two
smaller molecules that mix to become one new stealth molecule.
Even then, once formed, GC is unstable. Pure GC at room temperature
has a half-life of 2-16 hours. These problems preclude its
use as a medicine.
When
GC is introduced into the gastric tract, stomach acid destroys an
activating enzyme before GC can be converted into its biologically
active form. To date, coating oral GC pills so they won't
open up till they reach the more alkaline upper intestines has been
the only answer to this problem. However, most of the time,
the coated capsules travel all the way through the digestive tract
before they open up, often rendering them useless or unreliable.
But there is a way to activate GC to unleash its powerful disease-fighting
activity.
Military
advantage

Researchers
fully understand the importance of GC. A military force that
has GC will have a significant advantage. GC will make it
possible for any standing army to maintain more troops in the field.
Far more troops have to be removed from field operations due to
disease (diarrhea, infection, hepatitis, food poisoning, gonorrhea)
than from war-related wounds or accidents. Ask troops who
served in the middle east who came back home with Gulf War Syndrome.
A mycobacterium is believed to have caused as many as 400,000 cases
of Gulf War Syndrome.
Because
of the problem of antibiotic resistance, military doctors cannot
prescribe antibiotic drugs as prophylaxis. The overuse of antibiotics
will lead to more antibiotic resistant microorganisms. For example,
doctors are hesitant to treat a bacterium like H. pylori, which
causes ulcers and stomach cancer, even though it infects nearly
half the US population, because antibiotic treatment may induce
drug-resistant strains. So doctors wait for ulcers to occur before
prescribing triple-antibiotic therapy. On the other hand, GC does
not cause germ resistance. Theoretically, prophylactic use of GC
would eradicate most stomach ulcers and stomach cancer.
GC,
carried in the field by every soldier, can prevent or immediately
treat anthrax, Ebola, dysentery, pathogens like Salmonella, Staphylococcus,
Klebsiella, the waterborne germs Cryptosporidium and Giardia, and
viruses such as H5N1 bird flu, SARS and Herpes. Every field
soldier serving in a foreign land should consume GC daily, as prophylaxis
against potential biological threats.
While
pharmaceutical manufacturers furiously work to develop a vaccine
against bird flu, influenza viruses mutate so fast as to render
all vaccines as ineffective. GC is active against every known virus.
More
than military application
Researchers
have found GC also has many civilian applications. It has been observed
to penetrate inside cancer cells, which results in their death,
without toxicity to healthy cells. How it knows to do this
still baffles biologists.
Researchers
have noted that GC does not lower circulating levels of cholesterol,
but it does inhibit the formation of plaque in artery walls.
Unlike statin drugs, GC is not toxic to the liver; in fact, it protects
the liver.
When
scientists gave GC to rodents along with a high-fructose sugar diet,
it controlled insulin levels. But laboratory investigators
were stunned to find the sugar-fed animals given GC did not gain
weight, while the animals fed fructose sugar only, were obese.
GC may be a revolutionary weight control molecule.
What
is GC?
Just
exactly what is GC? It goes by various chemical names:
2-propene1-1sulfinothioic acid S-2-propenyl ester, 2-propenyl 2-propenethiosulfinate,
Allyl 2-propenethiosulfinate, Diallyl thiosulfinate. Actually,
you may be surprised to learn that GC stands for "garlic clove,"
or the active molecule produced by a fresh crushed garlic clove,
commonly described as allicin.
For
unexplained reasons, allicin has been overlooked by modern medicine.
In 1858 Louis Pasteur noted garlic's ability to kill germs in a
lab dish, but 62 years later medical history texts gave credit for
the discovery of the first antibiotic, penicillin, to Alexander
Fleming in 1922. Actually, French medical student Ernest Duchesne
first observed that penicillin mold killed germs in 1896. Regardless,
garlic’s microbiological discovery as an antibiotic preceded penicillin
by decades.
SUPERIORITY
OF GARLIC (ALLICIN)

Antibiotic effectiveness
is measured by the area of germs inhibited in a lab dish

Today
thousands of people needlessly die of infections caused by antibiotic-resistant
bacteria. These are mostly hospitalized patients who are subjected
to multiple antibiotics. Some hospital-acquired staph infections
are resistant to all antibiotics. Germ resistance to allicin/garlic
has never been observed.

Roman legions
used GC
The
idea of using allicin to protect soldiers or civilians from biological
threats is not new. Roman legions carried garlic cloves with them,
and quickly planted more garlic in lands they conquered. Dioscorides,
the chief medical officer in the Roman army during the 1st century
AD, treated infected soldiers with garlic. Knowing of its
prophylactic properties, Roman legions ate garlic prior to combat.
But why aren't modern armies following the way of the Romans?
The answer is simple, troops would have to carry garlic cloves with
them and endure the pungency of garlic in their stomach and odor
on their breath. Seems like a small price to pay for a life-saving
technology. The Roman army knew better.
Conventional
garlic pills simply don't contain, nor do they reliably produce,
allicin. This is confusing to consumers who see the word allicin
on most labels for garlic pills. But the label refers to garlic
powder tested in water, not stomach acid. Stomach acid destroys
the enzyme (alliinase) in garlic pills before it can mix with alliin
to produce allicin. A garlic clove has to be crushed, or preferably
mixed in a food blender, to create allicin prior to oral consumption.
A fresh crushed garlic clove can produce ~30004000 micrograms
of allicin, and up to three times more if placed in a food blender.
Despite
overwhelming evidence of garlic's health benefits, government regulations
forbid health claims even for garlic cloves. The world’s most
potent weapon against human biological threats is underused even
though it is widely available, is economical, and non-toxic. Modern
medicine’s over-reliance upon man-made drugs is resulting in the
needless early demise of millions. Think of tuberculosis, a bacterial
lung infection that now affects two billion humans on the planet.
Health authorities know that many TB patients can’t afford antibiotics
and won’t take them for a long enough period of time to eradicate
the infection. How about a garlic clove? It’s the world’s major
antidote against illness.
Selected
references:
Ankri S, Mirelman
D. Antimicrobial properties of allicin from garlic. Microbes Infection
1999; 1: 125.
Lawson LD,
Gardner CD. Composition, stability, and bioavailability of garlic
products used in a clinical trial. J Agriculture Food CHem 2005:
53, 6254.
Gonen A, Harats
D, Rabinsky A, et al., The antiatherogenic effect of allicin: possible
mode of action. Pathobiology 2005; 72: 325.
Weber ND, Andersen
DO, North JA, In vitro virucidal effects of Allium sativum (garlic)
extract and compounds. Planta Medica 1992: 58, 417.
Ruddock PS,
Liao M, Foster BC, Garlic natural health products exhibit variable
constituent levels and antimicrobial activity against Neisseria
gonorrhoeae, Staphylococcus aureus and Enterococcus faecalis. Phytotherapy
Research 2005; 19, 327.
No authors
listed, Garlic for cryptosporidiosis? Treatment Reviews 1996; No.
22, 11.
Canizares P,
Gracia I, Gomez LA, et al., Allyl-thiosulfinates, the bacteriostatic
compounds of garlic against Helicobacter pylori. Biotechnol Progress
2004; 20, 397.
Oommen S, Anto
RJ, Srinivas G, Karunagaran D. Allicin (from garlic) induces caspase-mediated
apoptosis in cancer cells. European J Pharmacology 2004: 485, 97.
Elkayam A,
Mirelman D, Peleg E, et al., The effects of allicin on weight in
fructose-induced hyperinsulinemic, hyperlipidemic, hypertensive
rats. Am J Hypertension 2003; 1053, 2003.
Hirsch K, Danilenko
M, Giat J, et al., Effect of purified allicin, the major ingredient
of freshly crushed garlic, on cancer cell proliferation. Nutrition
Cancer 2000; 38, 245.
Lawson LD,
Wang ZJ, Low allicin release from garlic supplements: a major problem
due to the sensitivities of alliinase activity. J Agriculture Food
Chem 2001; 49, 2592.
Lawson LD,
Wang ZJ, Papadimitriou D, Allicin release under simulated gastrointestinal
conditions from garlic powder tablets employed in clinical trials
on serum cholesterol. Planta Medica 2001; 67: 13.
Lawson LD,
Wang ZJ, Allicin and allicin-derived garlic compounds increase breath
acetone through allyl methyl sulfide: use in measuring allicin bioavailability.
J Agriculture Food Chem 2005; 53, 1974.
Abbruzzese
MR, Delaha EC, Garagusi VF. Absence of antimycobacterial synergism
between garlic extract and antituberculosis drugs. Diagnostic Microbiology
Infectious Disease 1987; 8: 79.
April
10, 2006
Bill
Sardi [send
him mail] is
a consumer advocate and health journalist, writing from San Dimas,
California. He offers a free downloadable book, The Collapse of
Conventional Medicine, at his
website.
Copyright
© 2006 Bill Sardi Word of Knowledge Agency, San Dimas, California.
Not intended for commercial use or posting on other websites. Permission
to reprint should be obtained from
the author.
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