The dried berries of Schisandra chinensis Baill. or S. sphenanthera have been
used in the traditional Chinese medicine as tonic and sedative since more than
2000 years. Schisandra (the spelling Schizandra is common but actually not
correct) is a vine belonging to the Magnoliaceae which is being been culitvated
in recent years also in Europe. Dried Schisandra berries are administered in
dosages from 2 to 5 g (KEYS 1976, TANG & EISENBRAND 1992). As Schisandrae
Fructus they are described in the chinese pharmacopoeia. Schisandra has been
subject of extensive chemical analytical anf pharmacological investigations. As
active components lignanes were identified, e.g. the groups of Schizanterines,
Gomisins and Schizandroles. The percentage of the Lignanes varies from 7.2% to
19.2% in dependence of the variety and geographical provenance. Pharmacological
studies have been carried out with the original drug, with extracts as well as
with isolated lignanes. (TANG & EISENBRAND 1992).
OHTAKI (1996) investigated
the protective effect of Gomisin A, a priincipal lignane of S. sinensis,
against experimentally induced neoplasms of the liver. The substance has
apparently an anti-promotor effect which is presumably based on an enhance
gallic acid metabolism. A further investigation of the hepatoprotective
properties of S. sinensis has been done by IP (1996). The effect of Schisandra
lignanes is assumed to be partly caused by quenching of free radicals. LIU
(1989) showed a protective effect of ethanolic Schisandra extract in cases of
tetrachloro carbon poisoning. The liver toxicity of tetrachloro carbon
poisoning is caused by the generation of trichloromethyl radicals formed in
presence of Cytochrom P450. Die trichloro methyl radicals react with oxygen to
peroxy trichloromethyl radicals which initiate a rapid lipid peroxidation. The
radical formation by tetrachloro carbon may therefore serve as a model reaction
for damages caused by free radicals in general. LU and LIU (1992) determined
the antioxidative properties of various S. sinensis lignanes in comparison with
vitamin E. The majority of the invstigated lignanes were in in-vitro assays
clearly more effective than vitmamin E. A triterpene isolated from S.
sphaerandra was described by SUN et al. (1996) as inhibitor of the reverse
transkriptase of HIV and can therefore be considered a potential anti AIDS
agent. NISHIYAMA and coworker (1995) have tested a combined phytotherapeutic
preparation of S. sinensis, Biota orientalis and P. ginseng on mice whose
learning capability had been affected by adinistration of alcohol and
scopolamine. An improvement of the memory was observed. Comparable tests
(NISHIYAMA et al., 1996) carried out on senescence accelerated mice showed a
similarly memory enhancing effect which demosntrates a potential usefulness in
cases of age related memory deterioration.
References:
IP, S.P., et al., 1996: Effect of a lignan-enriched extract of Schisandra
chinensis on aflatoxin B1 and cadmium chloride-induced hepatotoxicity in rats. Pharmacol.
Toxicol. 1996, 413-416 (1996)
KEYS, J.D., 1976: Chinese Herbs; C.E. Tuttle, Rutland (VT) and Tokyo, 1976
LU, H., & LIU, G.T., 1992: Anti-oxidant activity of dibenzocyclooctene
lignans isolated from Schisandraceae. Planta Med. 58: 311-313 (1992)
LIU, G., 1989: Pharmacological actions and clinical use of Fructus schizandrae.
Chinese Medical Journal, 102:740-749 (1989) (zitiert viele nurauf chinesisch
vorliegende Arbeiten)
NISHIYAMA, N., et al., 1995: Beneficial effects of S-113m, a novel herbal
prescription, on learning impairment model in mice. Biol. Pharm. Bull. 18:
1498-1503 (1995)
NISHIYAMA, N., et al., 1996: An herbal prescription, S-113m, consisting of
biota, ginseng and schizandra, improves learning performance in senescence
accelerated mouse. Biol. Pharm. Bull. 19: 388-393 (1996)
OHTAKI, Y., et al., 1996: Deoxycholic acid as an endogenous risk factor for
hepatocarcinogenesis and effects of gomisin A, a lignan component of Schisandra
fruits. Anticancer Res. 16: 751-755 (1996)
SUN, H.D., et al., 1996: Nigranoic acid, a triterpenoid from Schisandra
sphaerandra that inhibits HIV-1 reverse transcriptase. J. Nat. Prod. 59:
525-527 (1996)
TANG, W., & EISENBRAND, G., 1992: Chinese Drugs of Plant Origin. Springer
Verlag, Berlin, 1992
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