How It Works
Bottom Line: Schisandra has not been shown to treat cancer.
Schisandra is a fruit extract used in traditional Chinese medicine. Scientists do not know how Schisandra works, but laboratory experiments have begun to identify some of its biological activities.
Schisandra has antioxidant activity, which means that it neutralizes free radicals that can cause cellular and genetic damage. When tested in animals, schisandra had the following effects: 1) an increase in contractility of the heart 2) an increase in contractions of the uterus 3) faster breathing rate 4) and an increase in the level and activity of an important detoxifying compound, glutathione, in the liver. Schisandra also appears to affect the central nervous system of rats, but the exact effects have not been elucidated yet. One extract of schisandra was able to inhibit the activity of HIV in the test tube, but this effect has not been tested in animals or humans.
Purported Uses
To treat asthma
No scientific evidence supports this use.
To treat coughs
No scientific evidence supports this use.
To treat diarrhea
No scientific evidence supports this use.
To relieve indigestion
No scientific evidence supports this use.
To treat the flu
No scientific evidence supports this use.
To treat liver disease
Animal studies show that schisandra can protect rats' livers from chemically-induced damage, but there is no proof from clinical trials that it can treat liver disease in humans.
To prevent and treat premenstrual syndrome (PMS)
No scientific evidence supports this use.
To increase strength and stamina
No scientific evidence supports this use.
To reduce sweating
No scientific evidence supports this use.
Research Evidence
No clinical trials have tested whether schisandra has biological effects in humans, or whether it is safe to take for long periods of time.
Warnings
Although no drug interactions have been reported, schisandra may induce the activity of metabolic enzymes in the liver that are responsible for breaking down many other medications. If this is the case, it might lower the blood levels of other medications, reducing their effectiveness. Patients should talk with their doctors about the possibility of such drug interactions.
This product is regulated by the FDA as a dietary supplement. Unlike approved drugs, supplements are not required to be manufactured under specific standardized conditions. This product may not contain the labeled amount or may be contaminated. In addition, it may not have been tested for safety or effectiveness.
Side Effects
Heartburn
Sedation
Scientific Name
Common Name
Wu wei zi, schizandra, five flavor berry, fructus schisandra, gomishi, omicha, ngu mie gee
Clinical Summary
Derived from the fruit of the plant. This herb is used in traditional Chinese medicine for cough, wheezing, diarrhea and spontaneous sweating
(1). It is also used as an adaptogen. Various lignans are believed responsible for the activity of schisandra, but limited research evaluates its mechanism of action. In animal models, schisandra protects the liver against various toxins (e.g. menadione)
(7), prolongs pentobarbital sleep time
(8), and increases cardiac contractility without affecting blood pressure
(10). In vitro studies have shown that schisandra has protective effects against adriamycin-induced cardiotoxicity
(11). No human trials have been performed with this supplement. Although no drug interactions are reported, schisandra may induce cytochrome P450 and affect other metabolic pathways
(5) (9). No common adverse events are reported
(10). Additional research is necessary to understand the efficacy and to uncover possible interactions associated with this supplement.
Purported uses
- Asthma
- Cough
- Diarrhea
- Indigestion
- Influenza
- Liver disease
- Premenstrual syndrome
- Strength and stamina
- Sweating
Constituents
Lignans: Schizandrin, gamma-schizandrin, schizandrol, deoxyschizandrin (1)
Volatile oils (2)
Vitamins: A, C, E (2)
Others: Hydrocarbon derivatives (e.g. sesquicarene, beta-2-bisabolene, beta-chamigrene, alpha-ylangene) (1), triterpenoid (nigranoic acid) (3)
Mechanism of Action
The mechanism of action is unknown. Schisandra has antioxidant activity. Animal studies suggest that water- and alcohol-based extracts promote myocardial contractility without effects on blood pressure, stimulate the respiratory center, induce uterine smooth muscle contractions, and increase hepatic glutathione levels and the activities of glucose-6-phosphate and glutathione reductase
(4). Protection from hepatotoxicity and improvements in phase I metabolism are documented in rats administered 1 ml/kg carbon tetrachloride 24 hours after exposure to schisandra extract
(5) (9). Schisandra extract appears to increase DT-diaphorase activity within rat hepatocytes resulting in protection from menadione-induced toxicity
(7). In rats, repeated administration of schisandra extract at 10 mg and 25 mg doses reduces the extent of cycloheximide-induced amnesia
(6). Nigranoic acid, a triterpenoid extract from schisandra plants stems, shows limited activity against HIV-1 reverse transcriptase in vitro at an IC50 of 200 mcg/ml
(3). Schisandrin B and schisandrol B have variable effects on pentobarbital-induced sleep in mice: 12.5 mg/kg prolongs sleep while 100 mg/kg shortens the sleep interval. Schisandrin C increases pentobarbital sleep period at all doses
(8).
Pharmacokinetics
No formal pharmacokinetic studies have been performed. Animal data suggests that schisandra increases metabolism via induction of cytochrome P450 and/or glutathione reductase pathway
(1).
Adverse Reactions
CNS depression
(2), Heartburn
(10).
Herb-Drug Interactions
No significant drug interactions have been reported, but schisandra may induce cytochrome P450 and other hepatic metabolic pathways
(1).
Lab Interactions
Lower AST, ALT, Alkaline phosphate.
Literature Summary and Critique
There are no noteworthy studies.
References
- Huang KC. The Pharmacology of Chinese Herbs, 2nd ed. New York: CRC Press; 1999.
- Fetrow CW, et al. Professional's Handbook of Complementary and Alternative Medicines. Philadelphia: Springhouse; 1999.
- Sun HD, et al. Nigranoic acid, a triterpenoid from Schisandra sphaerandra that inhibits HIV-1 reverse transcriptase. J Nat Prod 1996;59:525-7.
- Ko KM, et al. Effect of a lignan-enriched fructus schisandrae extract on hepatic glutathione status in rats: protection against carbon tetrachloride toxicity. Planta Med 1995;61:134-7.
- Zhu M, et al. Evaluation of the protective effects of schisandra chinensis on phase I drug metabolism using a CCl4 intoxication model. J Ethnopharmacol 1999;67:61-8.
- Hsieh MT, et al. The ameliorating effect of the water layer of fructus schisandrae on cycloheximide-induced amnesia in rats: interaction with drugs acting at neurotransmitter receptors. Pharmacol Res 2001;43:17-22.
- Ip SP, Yiu HY, Ko KM. Schisandrin B protects against menadione-induced hepatotoxicity by enhancing DT-diaphorase activity. Mol Cell Biochem 2000;208:151-5.
- Brinker F. Herb Contraindications and Drug Interactions, 3rd ed. Sandy (OR): Eclectic Medical Publications; 2001.
- Zhu M, et al. Improvement of phase I drug metabolism with schisandra chinensis against CCl4 hepatotoxicity in a rat model. Planta Med 2000;66:521-5.
- Bensky D, Gamble A. Chinese Herbal Medicine: Materia Medica. Revised Ed. Seattle: Eastland Press; 1993.
- You JS, Pan TL, Hou YC. Schisandra chinensis protects against adriamycin-induced cardiotoxicity in rats. Chang Gung Med J 2006; 29(1): 63-70.