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Lysine

Lysine - amino acid against herpes

By Serge Kreutz

This web site is dedicated exclusively to the amino acid l-lysine. L-lysine is an amino acids with a pharmacological use much more specific than that of most other amino acids. So far, supplementation of l-lysine is one of the best options available for the treatment of herpes simplex virus infections, especially oral forms. L-lysine is also much cheaper than antiviral drugs such as Acyclovir. L-lysine supplementation works by tilting the balance between lysine and arginine heavily in favor of lysine. This ameliorates herpes outbreaks because the herpes virus depends on the presence of arginine for its replication.

Lysine in combination with arginine is used by bodybuilders for the combination's alleged effect of stimulating the release of growth hormone.


Insures the adequate absorption of calcium; helps form collagen ( which makes up bone cartilage & connective tissues); aids in the production of antibodies, hormones & enzymes. Recent studies have shown that Lysine may be effective against herpes by improving the balance of nutrients that reduce viral growth. A deficiency may result in tiredness, inability to concentrate, irritability, bloodshot eyes, retarded growth, hair loss ,anemia & reproductive problems.  [source]


lysineLysine

L-Lysine is a basic, genetically coded amino acid. It is essential in human nutrition.

 

Symbol
lys k
Molecular formula
C6H14N2O2
Molecular weight
146.19
Isoelectric point (pH)
9.59
CAS Registry Number
39665-12-8

3D Molecular Model

lysine 3D

If you have installed MIME types for Chemistry for use with the Alchemy mol format, you may click at the 3D model above.

Deutsche Version · Overview of amino acids · Homepage


Burkhard Kirste, 1994-08-23, 1998-02-02

PAULING THERAPY Synopsis:
The Reader's Digest Version

Linus Pauling invented a cure for Heart Disease in 1991 which was announced 1993-1994.

Pauling claimed that specific non-toxic substances called Lp(a) binding inhibitors taken orally will prevent and even dissolve existing atherosclerotic plaque build-ups. Three United States of America Patents have been granted on the Pauling/Rath method.

Pauling's announcement is based on experimental proof with guinea pigs who like humans can not make their own vitamin C.

The three primary "Lp(a) binding inhibitor" substances are vitamin C, lysine and proline.

The Pauling Therapy works by itself, but in theory, Pauling's protocol makes an ideal oral adjunct to EDTA Chelation therapy and other more conventional therapies for all forms of cardiovascular disease, except radiation.

Early scientists recognized that plaques form in the same places. Usually near the heart where the blood vessels are stretched and bent, implicating high blood pressures and the mechanical stress caused by the heart beat. These scientists were ignored.

Today the majority of heart surgeries only replace a few inches of blood vessel near the heart (coronary arteries). It is unlikely that the primary cause of the lesions leading to heart disease are "poisons" circulating in the blood because plaque does not form randomly throughout the blood stream. (Note: In a heart bypass, veins from the leg are used which are without plaque.)

We know now that atherosclerotic plaques deposit in response to injury and that plaque is part of a healing process. The 1985 Nobel prize was awarded for the discovery of the Lysine Binding sites. Mainstream medical science has known since 1989 that Lp(a) (not LDL cholesterol) binds to form atherosclerotic plaques. Pauling and Rath have identified Lp(a) as an evolutionary surrogate for low vitamin C in humans. Mechanical stress then, not cholesterol or other "poisons in the blood, causes the lesions that lead to heart disease.

Modern medicine has been misguided about vitamin C since the 1940s. VItamin C is required and used up making the super protein collagen. According to the Pauling/Rath Unified Theory, the root cause of atherosclerotic plaque deposits is a vitamin C deficiency: chronic, not acute. The correct terminology for cardiovascular (heart) disease is "chronic scurvy" or "sub clinical scurvy".

Heart disease is unknown in most animal species. Pauling and Rath think humans are less resistant than other animals to arterial damage from mechanical stress (caused by the heart beat) because they become deficient in a specific protein caused by a specific vitamin deficiency. A vitamin deficiency that is impossible in most animals!

The Pauling mega-nutrient therapy to counter Lp(a) increases blood concentrations of important substances that will:

Vitamin C is required for healing the lesion, primarily through the collagen pathway.

Lysine and proline work to unbind Lp(a) from the arterial wall.

Unlike ordinary drugs, there are no health risks. These substances are required for life.

The Pauling Therapy is so safe, and the medical condition so grave, there is no reason why any physician should resist it, especially in otherwise hopeless cases.

By "cured" we mean that as first described on the LINUS PAULING VIDEO ON HEART DIEASE: End-stage CVD patients report the complete cessation of their angina pain, color returns, blood pressure drops, blood flow increases, blockages disappear, heart rates drop, lipid profiles normalize, energy increases as does the sense of well being. Patients who had failed now pass treadmill stress tests without surgery or any other medical intervention. Patients barely able to walk before the Pauling therapy report that within months they can dig fence post holes and cut down trees. Over time, elevated Lp(a) lowers. Some doctors have even told such patients that new blood vessels have "grown" as an explanation for the increased blood flow to the coronary arteries feeding the heart.

Linus Pauling's 1992 video describes these findings.

CONGRATULATIONS: YOU NOW KNOW MORE ABOUT HEART DISEASE THAN THE AVERAGE CARDIOLOGIST IN THE UNITED STATES OF AMERICA.

A great amount of money is at stake. This discovery is ignored. We can only speculate why. Regretably, not a single study has been conducted to investigate the high-dose Pauling protocol. Instead, all this is dismissed a priori as "quackery. One reason may be that every pharmaceutical company, cardiologist and heart surgeon has a vested interest in their part of the $326 billion spent annually on heart disease. Should the Pauling discovery become widely known, there will be a revolution in medicine. Certainly cardiology and heart surgery will not survive in their present form.

We are not doctors. In 1995, when we reported what Pauling had said and written, we did not know if Pauling was correct.

We now know.

Pauling nailed it.

Intelisoft Multimedia is now willing wager against others who might think otherwise. Amount negotiable. Winner takes all. Should any person or entity wish to accept this challenge and pit any competing therapy, treatment or protocol against Pauling's, in a clinical trial setting with end-stage cardiovascular patients, contact us. Terms negotiatable. There are only two up-front stipulations:

  1. The competing protocol may not include vitamin C (above the RDA), lysine or proline (or synthetic analogs), and

  2. The subjects in the Pauling Therapy group must not have been treated with any intra-arterial radiation therapy to stem restenosis.

 

We will fund the Pauling protocol subjects. Antagonist fund the patients on their protocol.

Our Prediction: 90% of the patients on the high dose Pauling vitamin C/lysine protocol will be "cured" within 30 days as measured by: lowered Arterial Stiffness (ASI measured using FDA approved Cardiovision), reductions in Chest pain, increased mobility, improved sense of well being, etc.



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