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Passiflora incarnata, Passifloraceae. The common name is passion flower, maypop
or apricot vine.
Passiflora was discovered in 1569 by Spanish explorers in Peru. The
ten-petal flower was seen as symbolic of the passion of Christ, and was considered
as a sign of divine approval of the Spanish conquest. The Incas brewed a tonic
tea of the plant, and the usage soon spread to Europe, where it was used as
a tranquilizer and mild sedative. The American colonists on the Gulf Coast
adopted its usage from the local Indians, who used it to soothe their nerves
and topically as a poultice, the crushed leaves being used on cuts and bruises.
The Eclectic physicians considered Passiflora an important remedy for insomnia,
restlessness, menstrual discomforts, diarrhea, epilepsy and whooping cough.
They also used the leaf juice externally for burns, scalds, wounds and toothache.
It was recognized in the National Formulary from 1916 to 1936.
There are about 400 species of the genus Passiflora, some
noted for their flowers and others for their edible fruit. It is frequently
grown as an ornamental. Passiflora species are native to tropical and subtropical
areas of the Americas. Passiflora incarnata grow from Virginia to Florida and
as far west as Missouri and Texas. It is a fast-growing, climbing perennial
vine that can reach 30 feet. The flowers are white, tinged with purple and
three inches across. They produce egg-sized yellow or orange edible fruit.
The above ground parts of the plant are used. It is available as bulk herb,
teas, capsules, hydroalcoholic extracts, and is frequently mixed with other
relaxant herbs such as valerian and skullcap.
Passiflora is used for its sedative, anxiolytic and antispasmodic effects.
It has not been determined just what the active constituents are, but flavonoids
and alkaloids are most often cited as the most probable. Passiflora has complex
action on the central nervous system.1 It has been found that there is a difference in effect between
the alcohol extract and the aqueous extract. The alcohol extracts proved to
be anxiolytic and the aqueous extract more sedative in experiments with mice.2 Early studies indicated that it has musculotropic action.3 The German Commission E recommends
it for nervous restlessness.4
In vitro experiments have shown Passiflora to be effective in killing a wide
variety of molds, yeasts and bacteria. Group A hemolytic streptococci are quite
susceptible and Candida albicans is intermediate in susceptibility. The antimicrobal
activity is quickly lost in the dried plant.5
In common usage Passiflora is a popular herb for nervousness, anxiety, reducing
pain and inducing sleep. It is frequently used as an antispasmodic for spasms,
epilepsy, menstrual pain, spasmodic coughing and asthma.6
The primary constituents of Passiflora are flavonoids,
maltol, cyanogenic glycosides and indole alkaloids. The indole alkaloids are
harman, harmin, harmalin, harmol and harmalol, which can be MAO inhibitors,
but are present in such small amounts that it is unlikely to have this effect.
The flavonoids (2.5%) consist of vitexin, isovitexin, orientin, isoorientin,
apigenin, kampferol, vicenin, lucenin, saponarin and passiflorine (similar to
morphine).7 It also
has phenolic, fatty, linoleic, linolenic, palmitic, oleic and myristic acids,
as well as formic and butyric acids, courmarins, phytosterols and essential
oil.
The German Commission E recommends 4 to 8 gr. daily or
the equivalent preparation. Hydroalcoholic extracts are used at dosages of
10 to 60 drops.
Do not use during pregnancy due to the uterine stimulating
action of the harman alkaloids. Most reports consider it nontoxic. It is possible
that large doses can cause convulsions, CNS depression and decreased myocardial
strength.8
The constituent maltol increases sleeping time induced by hexobarbital.9
1 Speroni E, Minghetti A. “Neuropharmacological
Activity of Extracts from Passiflora incarnata”. Planta Medica: 54
(6). Dec 1988.488-91.
2 Soulimani R, et al. “Behavioral
effects of Passiflora incarnata L. and its indole alkaloid and flavonoid derivative
and maltol in the mouse”. Journal of Ethnopharmacology; 57. 1997.
11-20.
3 Rugg, George H, Smith Clayton S.
“A Pharmacological Study of the Active Principles of Passiflora Incarnata”.
Journal of the American Pharmaceutical Association; 29. 1940. 245-249.
4 Blumenthal, Mark, et al. The
Complete German Commission E Monographs. American Botanical Council.
1998. 179-180.
5 “Passion Flower”.
Facts and Comparisons, The Review of Natural Products. March 1999.
6 Bergner, Paul.
“Passionflower”. Medical Herbalism: 7(1-2). Spring and Summer 1995.
13-26.
7 “Passion Flower”.
Facts and Comparisons, The Review of Natural Products. March 1999.
8 Willard, Terry,
Ph D. The Wild Rose Scientific Herbal. Wild rose College of Natural
Heeling Ltd. 1991. 257-58.
9 Brinker, Francis,
N. D. Herb Contraindications and Drug Interactions. Eclectic Institute
Inc. Oregon. 1997. 71.
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