Muldner and Zoller (1984), in a clinical trial with 6 depressive women, 55-65 years old, measured
smetabolites of noradrenaline and dopamine in the urine, and found that after taking a standardized
hypericin extract, there was a significant increase in 3-methoxy-4-hydroxyphenylglucol, a marker for the
beginning of an antidepressive reaction. The same research team, working with 15 women taking a standard
hypercin extract, demonstrated an improvement in symptoms of anxiety, dysphoric mood, loss of interest,
hypersomnia, anorexia, depression (worse in the morning), insomnia, obstipation, psychomotoric
retardation, and feelings of worthlessness. They reported no side-effects (99).
Wound and Burn Healing
In a number of studies St. John's wort extracts have demonstrated anti-bacterial and wound-healing activity.
For instance, two widely prescribed Russian preparations of Hypericum, novoimanine and imanine,
have been tested for Staphylococcus aureus infection in vivo and in vitro, and been
found to be more effective than sulfonilamide (100, 101, 102). Hyperforin, a bicyclic tetraketone from H.
perforatum, is reported to be a main antibiotic constituent of novoimanine (103).
One German patent mentions that an ointment containing an extract of St. John's wort flowers shortened
healing time of burns and showed antiseptic activity (104). According to the report, first degree burns healed
in 48 hours when treated with the ointment, while second and third degree burns healed without keloid (a
type of scar tissue) formation three times faster than burns treated by conventional methods.
Other reports include that a freeze-dried St. John's-wort extract suppressed inflammation and leukocyte
infiltration in vivo (105), and that St. John's wort oil has been used in commercial products as a sun
screen. However, reports of its efficacy in this latter regard are contradictory (106, 107).
Anti-viral Effects
International interest increased in St. John's wort after researchers from New York University medical center
and the Weizmann Institute of Science in Israel demonstrated that two compounds from the plant strongly
inhibit a variety of retroviruses in vitro and in vivo (108). Several points bear citing from their
report:
- "When the compounds interact with the infecting particles shortly after in vivo administration,
disease is completely prevented."
- "Preliminary in vitro studies with pseudohypericin indicate that it can
reduce the spread of HIV."
- The total yield of hypericin and psuedohypericin from H.
triquetrifolium Turra was 0.04%.
- The compounds were still effective when administered orally or
i.p. within 1 day of infection.
- No serious toxic side effects were noticed after testing over 800 mice
with the compounds. Administration of the compounds did not result in abnormalities in any of a wide
variety of clinical tests performed on the animals.
- Hypericin shows toxicity to some human cells at very
high concentrations (>10 ug/ml, or lower for some cell types). Pseudohypericin is less toxic. Fortunately,
the compounds show remarkable antiviral potency "after one administration of a relatively small dose of the
compounds."
- "The compounds directly inactivate the virions or interfere with assembly or shedding of
assembled viral particles."
- "The compounds can cross the blood-brain barrier" (important for HIV
infection).
One word of caution, however: although Hypericum extracts appear promising for the treatment of
retroviral infections, including HIV, it must be stressed that there has been no clinical evidence of its
efficacy in humans to date (for HIV infection), and several questions remained unanswered. For instance,
there is no information about the concentration needed for efficacy, even if the compounds are effective in
HIV infection in humans. Furthermore, if a large concentration is effective, is it close to the
photosensitizing dose? Also, it must
be pointed out that the total content of these two compounds in Hypericum is quite low (dried H.
perforatum has been reported to contain 0.24% hypericin109), consequently, a standardized extract (to
hypericin content) may be the surest way to administer the plant for viral therapy.
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