4.7 Article

Metabolism of biochanin A and formononetin by human liver microsomes in vitro

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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 50, 期 17, 页码 4783-4790

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AMER CHEMICAL SOC
DOI: 10.1021/jf025549r

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isoflavone metabolism; cytochrome P450; biochanin A; formononetin

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Biochanin A and formononetin are abundant-in legumes.., These proestrogenic isoflavones can be converied by 4'-O-demethylation to the more potent phytoestrogens genistein and daidzein. Incubation of biochanin A or formononetin with human, liver microsomes resulted in 4'-O-demethylation and the production of additional metabolites. Three new hydroxylated formohonetin derivatives, 6,7-dihydroxy-4'-methoxyisoflavone, 7,8-dihydroxy-4'-methoxyisoflavone, and 7,3'-dihydroxy-4'-methoxyisoflavone, were isolated and characterized. We surveyed the O-demethylase competence of cytochrome P450 isoforms found in human liver. Human cytochrome P450 isoforms 1A2, 2E1, 2C9*1, 2C19, and 2D6*1 catalyzed biochanin A consumption and genistein production. Human cytochrome P450 isoforms 1A2, 2C9*1, 2A6, 2D6*1, and 2C19 catalyzed formononetin consumption and daidzein production. These, isoforms also generated other hydroxylated, metabolites. Although O-demethylation of isoflavones has been attributed to metabolism,by gut microflora, our study, demonstrates that human hepatic microsomal enzymes can perform the same transformation and may play a key role in the conversion of 4'-O-methylated isoflavones to more potent phytoestrogens.

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