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* Department of Plant and Environmental Sciences,
Endocrine Physiology Laboratory, Department of Animal and Veterinary Sciences, and
Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634
To whom requests for reprints should be addressed at 1 Clemson University, Department of Animal and Veterinary Sciences, Poole Agricultural Building, Clemson, SC 29634. E-mail: sngry{at}clemson.edu
The estrogenic activity of ginseng has been the subject of conflicting reports. Cell proliferation, induction of estrogen-responsive genes, and isolated cases of adverse reactions such as postmenopausal vaginal bleeding and gynecomastia have been reported after ginseng treatment. Other studies report antiproliferative effects with no induction of estrogen-responsive genes. We developed estrogen receptor (ER)
and ER
competitive binding assays using recombinant receptors and [3H]-17
-estradiol to detect phytoestrogens in extracts of Asian ginseng root (Panax ginseng C. A. Meyer) and American ginseng root (Panax quinquefolius L.). Root extracts contained substances that bound both receptor isoforms. These substances had a two to three times greater affinity for ER
. Significantly higher binding was found in methanol extracts than in hot water extracts. Subsequent analysis of the extracts revealed significant ER binding attributable to zearalenone, the estrogenic mycotoxin produced by several Fusarium species. The ER showed no binding affinity for Rb1 and Rg1, the major ginsenosides found in P. quinquefolius and P. ginseng, respectively. Thus, ginseng extraction methods, plant species tested, and mycotoxin contaminants may help to explain the disparate literature reports. The prevalence and health significance of fungal contamination in herbal products used for medicinal purposes should be further investigated.
Key Words: ginseng estrogen receptor zearalenone phytoestrogen herbal product
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