- Xi yang shen
- Tienchi ginseng
- western ginseng
For Patients & Caregivers
American ginseng has not been shown to treat or prevent cancer.
American ginseng has been shown to lower blood sugar levels in humans. Scientists think that the medicinal properties of this herb come from its components called ginsenosides. Most research has been done on another species, Panax ginseng. These studies indicate that ginsenosides both stimulate and inhibit the central nervous system in humans and stimulate the immune system in mice.
American ginseng was shown to reduce the number and severity of colds, and improve working memory in healthy adults. It also showed anticancer properties in lab studies, and may be useful in reducing cancer-related fatigue.
American ginseng decreases the anticoagulant effects of warfarin, a commonly used anticoagulant. Breast cancer patients should use this herb with caution because it can stimulate the growth of breast cancer cells.
- To improve athletic performance
No scientific evidence supports this use.
- To prevent and treat cancer
There are no data to back this claim. But American ginseng helps improve cance-related fatigue and improves quality of life.
- To treat diabetes
A few studies show a blood glucose-lowering effect of American ginseng.
- To stimulate the immune system
Some studies show an immunostimulant effect in animals. Human data are lacking.
- For increased strength and stamina
Although American ginseng is often promoted for this use, human data are lacking.
For Healthcare Professionals
A popular herb often confused with Asian or Panax ginseng, American ginseng has unique medicinal properties. It is frequently used in Chinese medicine to nourish “Yin” (1). American ginseng is also used in supplemental form to improve athletic performance, strength and stamina, and to treat diabetes and cancer. The saponin glycosides, also known as ginsenosides or panaxosides, are thought responsible for the herb’s biological effects.
Ginsenosides have both stimulatory and inhibitory effects on the CNS (4), alter cardiovascular tone, enhance humoral and cellular-dependent immunity, and exert anticancer effects in vitro (3) (15) (16).
Current data suggest that American ginseng may improve glucose control in diabetics (2) (6), and that it is safe for long-term use (25). It also demonstrated a modest effect in reducing the number and severity of colds (12); and enhanced working memory in healthy adults (21) and in patients with schizophrenia (24).
The anticancer activity of American ginseng was enhanced when combined with antioxidants (14). In other studies, the herb showed synergistic effects with 5-fluorouracil against colorectal cancer cells (17); and conferred protection against oxidative stress in irradiated human lymphocytes (18).
Data from an epidemiological study indicate that American ginseng improves survival and quality of life in breast cancer patients (13). Findings from a randomized controlled trial support its benefits in improving cancer-related fatigue (23).
Ginsenosides are thought responsible for American ginseng’s activity, although the exact mechanism of action is unknown. Related species, such as Panax ginseng, have been the focus of most laboratory and clinical research. Experiments using extracts from these species indicate that ginsenosides stimulate and inhibit the CNS (4). The extracts also stimulate TNF alpha production by alveolar macrophages (10).
The Rg1 ginsenoside present in American ginseng is associated with improvements in humoral and cell-mediated immune response and increases in T helper cells, T lymphocytes, and NK cells in mice (5). American ginseng was also shown to lower serum glucose and may affect carbohydrate metabolism (2) (6).
Several ginsenosides demonstrated anticancer properties in vitro (3). Current data suggest that the antiproliferative effects of American ginseng are due to compound K, a metabolite of the ginsenoside Rb1, but not Rb1 as previously thought (22). In another study, the herb was shown to significantly attenuate azoxymethane/dextran sodium sulfate (DSS)-induced colon carcinogenesis by reducing the colon tumor number and tumor load, associated with suppression of DSS-induced proinflammatory cytokine activation (26).