B. Pinto, A. Bertoli, C. Noccioli
Mar 1, 2008
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0
Influential Citations
23
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Quality indicators
Journal
Phytotherapy Research
Abstract
Natural flavonoids are currently receiving much attention because of their estrogenic and antiestrogenic properties. Six isoflavones (isoprunetin, isoprunetin 7‐O‐β‐d‐glucopyranoside, isoprunetin 4′,7‐di‐O‐β‐d‐glucopyranoside, genistein, genistein 7‐O‐β‐d‐glucopyranoside, daidzein), four flavones (luteolin, luteolin 7‐O‐β‐d‐glucopyranoside, luteolin 4′‐O‐β‐d‐glucopyranoside, licoflavone C), isolated from Genista morisii and G. ephedroides (two Leguminosae plants of the Mediterranean area) together with two structurally related pterocarpans, bitucarpin A and erybraedyn C, isolated from Bituminaria bituminosa (Leguminosae), were tested for the antagonist activity by a yeast based estrogen receptor assay (Saccharomyces cerevisiae RMY326 ER‐ERE). Most compounds inhibited the estradiol‐induced transcriptional activity in a concentration dependent manner. In particular, for the flavone luteolin 77% inhibition of the induced β‐galactosidase activity was observed. Interestingly, licoflavone C exhibited a dose‐dependent antagonistic activity at concentrations up to 10−4 m, but stimulated β‐galactosidase expression at higher concentrations resulting in a U‐shaped‐like dose‐response curve. Copyright © 2007 John Wiley & Sons, Ltd.