A novel mechanism: Erxian Decoction, a Chinese medicine formula, for relieving menopausal syndrome

Many clinical and experimental reports demonstrated that Erxian Decoction (EXD) was effective in relieving menopausal syndrome. The mechanisms of action of EXD were explored on the endocrine and antioxidant regimen. Menopause causes a decline in both endocrine function and activities of antioxidant...

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Published inJournal of ethnopharmacology Vol. 123; no. 1; pp. 27 - 33
Main Authors Sze, S.C.W., Tong, Y., Zhang, Y.B., Zhang, Z.J., Lau, A.S.L., Wong, H.K., Tsang, K.W., Ng, T.B.
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 04.05.2009
Amsterdam; New York: Elsevier
Elsevier
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Summary:Many clinical and experimental reports demonstrated that Erxian Decoction (EXD) was effective in relieving menopausal syndrome. The mechanisms of action of EXD were explored on the endocrine and antioxidant regimen. Menopause causes a decline in both endocrine function and activities of antioxidant enzymes. In this study, 12-month-old female Sprague–Dawley-rats (SD-rats) with a low serum estradiol level were employed. Their endocrine functions after treatment with EXD were assessed by the determination of their serum estradiol level and ovarian mRNA levels of aromatase, which is a key enzyme for biosynthesis of estradiol. Meanwhile, superoxide dismutase-1 (SOD), catalase (CAT) and glutathione peroxidase (GPx-1) in the liver were also determined to assess the effect of EXD on the antioxidant regimen. Results revealed a significant elevation in serum estradiol level and the mRNA level of ovarian aromatase and liver CAT in the EXD-treated menopausal rat model. The results obtained from mRNA and estradiol level of the present investigation revealed that the EXD relieves the menopausal syndrome involved an increase of endocrine and antioxidant function through, at least, the activation of aromatase and CAT detoxifying pathways.
Bibliography:http://dx.doi.org/10.1016/j.jep.2009.02.034
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0378-8741
1872-7573
DOI:10.1016/j.jep.2009.02.034