St. John’s Wort
St. John’s wort (Hypericum perforatum) is a
yellow-flowered perennial European herb that has become widely naturalized in
the United States. Its name is derived from the Old English word for plant, wort, and from the fact that it often
starts blooming around June 24, St. John’s day. Although St. John’s wort has
tradi-tionally been used for wound healing, insomnia, rheumatism, and
depression, it is most popular today for the treatment of mild to moderate
depression.
The leafy parts of the herb
contain naphthodi-anthrones (e.g., hypericin),
flavonoids (e.g., quercetin), and
phloroglucinols (e.g., hypaphorine).
Although this herb is now commonly standardized
for its hypericin content, it
appears that its other constituents may also
be just as pharmacologically active.
Just how St. John’s wort
treats depression is not clearly understood. It is possible that this herb’s
various com-ponents may work synergistically rather than through a single
active substance, mimicking the action of tradi-tional antidepressants. High concentrations
can affect in vitro serotonin reuptake,
but it is unclear whether this would occur in a patient taking standard oral
doses. The hypaphorine constituent may possess serotonin reup-take inhibitor
activity, and it also inhibits synaptic up-take of amino butyric acid (GABA)
and L-glutamate. Earlier studies
demonstrated some monoamine oxidase inhibition, but this action now seems
unlikely to be clin-ically relevant. Flavonoid components and hypericin also
may weakly inhibit catechol-O-methyl-transferase
(COMT). Melatonin, surprisingly, has
also been identi-fied in St. John’s wort and may play a role in its
sleep-enhancing and antidepressant effects.
St. John’s wort is very
popular as a physician-prescribed antidepressant in Europe and is widely used
for this purpose—usually without medical guidance—in the United States. A
meta-analysis of 23 studies concluded that St. John’s wort was more effective
than placebo in treating mild to moderate depression and was as effec-tive as
imipramine and standard antidepressants. It was also better tolerated than the
antidepressants to which it was compared. A recent meta-analysis, however, failed to find St. John’s wort effective for
severe depres-sion.
St. John’s wort is usually
well tolerated, but insomnia, dizziness, fatigue, restlessness, GI upset,
constipation, dry mouth, and allergy are reported as possible side ef-fects.
Hypomania has also been reported in several cases, and rarely, photosensitivity
can be a problem fol-lowing high doses; hypericin seems to be the component
responsible for the photosensitivity. Sun-induced neuropathy has also been
described, and it is possible that hypericin may also increase the risk of
cataracts with prolonged use. While a prior allergy to the herb is the main
contraindication, St. John’s wort should also be avoided in pregnant and
breast-feeding women (it may increase uterine tone) and in children until its
safety is further established.
A major emerging concern in St. John’s wort use is the numerous
clinically significant herb–drug interac-tions that have been reported. St. John’s wort appears to be a major inducer of the cytochrome P450 3A4 (CYP3A4) enzyme system in
the liver. This first came to light following acute heart transplant rejection
in a per-son taking cyclosporin and
St. John’s wort. The cy-closporin levels remained subtherapeutic until St.
John’s wort was discontinued. A similar phenomenon was noted with AIDS patients
taking protease inhibitors and nonnucleoside reverse transcriptase
inhibitors (NNRTIs). Concomitant
use of St. John’s wort reduced the effectiveness of these medicines as well.
Since then, St. John’s wort has been shown to reduce plasma levels of digoxin, warfarin, theophylline, and oral contracep-tives. Breakthrough
bleeding has been observed in young
women taking this herb, and patients starting oral contraceptives should be
counseled to use backup contraception if they take St. John’s wort or
antibiotics. St. John’s wort can adversely affect many other com-mon
medications, including nonsedating
antihistamines, antifungals,
chemotherapeutic agents, and calcium
chan-nel blockers.
SSRIs should not be taken with St. John’s wort be-cause of the risk of
the onset of a serotonin syndrome
characterized by nausea, tremor, and weakness. Alcohol also should be avoided.
St. John’s wort can increase opioid-induced
sleep.
St. John’s wort is commonly
used at 300 mg of extract (standardized to 0.3% hypericin) three times daily
for 6 weeks or longer. Short-term treatment is usually inef-fective.
St. John’s wort is probably
effective for mild to moder-ate but not severe depression. Although well
tolerated in most patients, a major concern is its numerous herb–drug
interactions mediated by its induction of the cytochrome P450 enzyme system.
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