Oxidative Metabolism of the Soy Isoflavones Daidzein and Genistein in Humans in Vitro and in Vivo
- 25 May 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Agricultural and Food Chemistry
- Vol. 49 (6) , 3024-3033
- https://doi.org/10.1021/jf0012695
Abstract
The soy isoflavones daidzein and genistein are found in high concentrations in human plasma and urine after soy consumption. However, in vitro and in vivo data regarding the oxidative metabolism of isoflavones in humans are scarce. Therefore, we have studied the oxidative metabolites of these compounds formed in human liver microsomes and excreted in urine of male and female humans ingesting soy products for 2 days. Human liver microsomes transformed the soy isoflavone daidzein to three monohydroxylated and three dihydroxylated metabolites according to GC/MS analysis. On the basis of a previous study with rat liver microsomes and with the help of reference substances, these metabolites were identified as 6,7,4‘-trihydroxyisoflavone, 7,3‘,4‘-trihydroxyisoflavone, 7,8,4‘-trihydroxyisoflavone, 7,8,3‘,4‘-tetrahydroxyisoflavone, 6,7,8,4‘-tetrahydroxyisoflavone, and 6,7,3‘,4‘-tetrahydroxyisoflavone. Significant amounts of the same metabolites except 6,7,8,4‘-tetrahydroxyisoflavone were also found in urine of female and male volunteers after soy intake. Genistein was metabolized by human liver microsomes to six hydroxylation products. The main metabolites were the three aromatic monohydroxylated products 5,6,7,4‘-tetrahydroxyisoflavone, 5,7,8,4‘-tetrahydroxyisoflavone and 5,7,3‘,4‘-tetrahydroxyisoflavone. The aliphatic monohydroxylated metabolite 2,5,7,4‘-tetrahydroxyisoflavone and two aromatic dihydroxylated metabolites, 5,7,8,3‘,4‘-pentahydroxyisoflavone and 5,6,7,3‘,4‘-pentahydroxyisoflavone, were formed in trace amounts. The same hydroxylated genistein metabolites except the aliphatic hydroxylated one could also be detected in human urine samples. Methylated forms of the catechol metabolites, which were generated by incubations with catechol-O-methyltransferase in vitro could be detected only in trace amounts in the urine samples. This implies that this reaction does not play a major role in the biotransformation of the hydroxylated daidzein and genistein metabolites in vivo. Most of these oxidative metabolites are described as human in vivo metabolites for the first time. Their biological significance remains to be established. Keywords: Phytoestrogens; isoflavones; daidzein; genistein; metabolism; soyKeywords
This publication has 13 references indexed in Scilit:
- A urinary profile study of dietary phytoestrogens. The identification and mode of metabolism of new isoflavonoidsPublished by Elsevier ,2000
- Biotransformation of genistein in the rat: elucidation of metabolite structure by product ion mass fragmentologynThe Journal of Steroid Biochemistry and Molecular Biology, 1999
- Antioxidant Efficacy of Phytoestrogens in Chemical and Biological Model SystemsArchives of Biochemistry and Biophysics, 1998
- DIETARY PHYTOESTROGENSAnnual Review of Nutrition, 1997
- Role of human hepatic cytochrome P450 1A2 and 3A4 in the metabolic activation of estroneCarcinogenesis: Integrative Cancer Research, 1997
- Lignan and isoflavonoid conjugates in human urineThe Journal of Steroid Biochemistry and Molecular Biology, 1995
- High-performance liquid chromatographic assay of isoflavonoids and coumestrol from human urineJournal of Chromatography B: Biomedical Sciences and Applications, 1994
- Free radical generation by redox cycling of estrogensFree Radical Biology & Medicine, 1990
- Measurement of protein using bicinchoninic acidAnalytical Biochemistry, 1985
- Die Konstitution des EquolsBerichte der deutschen chemischen Gesellschaft (A and B Series), 1939