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Isoflavone content and estrogenic activity of different batches of red clover (Trifolium pratense L.) extracts: An in vitro study in MCF-7 cells
Institution:1. Center for Research in Medical Pharmacology, University of Insubria, Varese, Italy;2. Linnea SA, Riazzino, TI Switzerland;1. Guangxi Medical University, Nanning 530021, China;2. The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning 530023, China;3. Ronald O. Perelman Department of Dermatology, NYU—Langone Medical Center, USA;1. Department of Neurosurgery, Affiliated Hospital of Guilin Medical University, Guilin 541001, China;2. Guilin Medical University, Guilin 541004, China;3. Department of Physiology, Guilin Medical University, Guilin 541004, China
Abstract:The estrogenicity of different batches of red clover (Trifolium pratense L., Fabaceae; RCL) extracts and its relationship with the isoflavone content were assessed by measuring MCF-7 cell proliferation by flow cytometry and propidium iodide staining. RCL extracts were compared to estradiol (E2) and to the main RCL isoflavones biochanin A, daidzein, genistein and formononetin. Isoflavone content in the extracts was assayed by HPLC.E2 and isoflavones increased MCF-7 proliferation in a concentration-dependent fashion, with the following potency order: E2 >>> genistein > biochanin A = daidzein > formononetin. Extracts increased MCF-7 proliferation with different potencies, which in four out of five extracts correlated with the ratios 5,7-dihydroxyisoflavones/7-hydroxyisoflavones. The efficacy of all extracts increased with decreasing genistein contents. A solution containing the main isoflavones at the average concentration of RCL extracts increased MCF-7 proliferation with higher potency and steeper concentration–response curve. The effects of E2, of RCL extracts and of the isoflavone solution were inhibited by the estrogen receptor antagonist 4-hydroxytamoxifen.Flow cytometric analysis of MCF-7 proliferation is a suitable bioassay for the estrogenicity of RCL extracts, thus expanding the characterization of individual batches beyond assessment of chemical composition and contributing to improved standardization of quality and activity.
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