The treatment of West Nile virus with high quality grass S. John

West Nile virus, although new to the United States is
well documented. The Centers for Disease Control
identified as a flavivirus, a member of
Togavirus family. It is closely related with the yellow
Fever and dengue fever. This is important because
togavirus family are encapsulated viruses,
ie, they are having a lipid (fat) covered
Coating.

This is exciting because it means that the virus
Internet on treatment with highQuality St.
Grass S. John (St. John's wort). Several studies have been conducted
on a variety of enveloped viruses, including
Herpes simplex virus type 1 and 2, Parainfluenza
Virus, Vaccinia virus, cytomegalovirus and other
Retroviruses, including HIV-1, 2, 3, 4, 8, 9, 10

Virus non-encapsulated or "naked" viruses were
for comparison purposes10 examined 13

St. John's wort is a potent anti-viral drugs in a varietyof
encapsulated virus families, but did not show
Activity against naked viruses.

Unlike a vaccine that is specific to each
SJW is active against encapsulated organisms
Viruses from a variety of mechanisms, including
Light activation, interference with DNA
Transcription, the impairment of the assembly of intact
viral particles and the lipophilic (fat loving)
Type of ring structures (the quinone and
phenolic groups) 4, 6, 7, 9, 11, 12, 13,14, 15
These structures are essential for biological ring
Activity of SJW.

From these results it is reasonable to use high
Quality, SJW pharmaceutical grade in the fight
West Nile virus, as there is no effective
active pharmaceutical ingredients.

Quality is critical since the level of hypericin
and pseudo-hypericin are
Button. I can only recommend the SJW product
produced by Medi-Herb, which is a drug
House in Australia, comparedPharma
Production rules. The product is
distributed by Standard Process by
Alternative medical care, including
Doctors of chiropractic, acupuncturists and
Veterinarians. SJW is quite unstable and
Active ingredients degrade on store shelves. A
independent analysis of three products (all
have been certified to contain 0.3% hypericin) were
shown that much variation, with a product of 25%
under the label. E 'is of crucial importance
phytochemical that the integrity of the whole
system are retained for a maximum efficacy.16

References:
1Andersen DO, Weber ND, Wood SG et al. Antiviral
Res 1991, 16 (2): 185-196.
2Lopez-Bazzocchi I, Hudson JB, Towers GHN.
Photochem.Photopbiol. 1991, 54 (1): 95-98.
3Moraleda G, Wu TT, Jilbert AR et al. Antiviral
Res 1993, 20: 235-247.
4Tang J, Colacino JM, Larsen SH et al. Antiviral
Res 1990, 13 (6): 313-325.
5Hudson JB,Harris L, Towers GHN. Antiviral Res
1993, 20 (2) :173-178.
6Lenard J, Rabson A, Vanderoef R. Proc Natl Acad
Sci USA 1993, 90 (1): 158-162.
7Degar D, Prince AM, Pascual D et al. AIDS Res Hum
Retroviruses 1992, 8 (11): 1929-1936.
8Carpenter S, Kraus GA. Photochem Photobiol 1991;
53 (2): 169-174.
9Lavie G, Valentine F, Levin B et al. Proc Natl
Acad Sci USA 1989, 86 (15): 5963-5967.
10Meruelo D, Lavie G, Lavie D et al. Proc Natl
Acad Sci USA 1988, 85 (14):5230-5234.
11Kraus GA, Pratt D, Tössbergland J et al. Biochem
Biophys Res Commun 1990; 172 (1): 149-153.
12Takahashi I, Nakanishi S, Kobayashi E et al.
Biochem Biophys Res Commun 1989; 165 (3):
1207-1212.
13GB Witte P, Agostini P, Van Lint J et al.
Biochem Pharmacol 1993, 46 (11): 1929-1936.
14Panossian AG, Gabrielian E, V Manvelian et al.
Phytomed 1996, 3 (1): 19-28.
15Lavie G, Mazur Y, Lavie D et al. Transfusion
1995, 35 (5): 392-400.
16ConstantineGH, J. changes in Karchesy
concentrations of hypericin in Hypericum perforatum
L. and commercial products. Pharmaceuticals
Biology 1998, 36 (5): 365-367.

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