Soybean isoflavonoids and their metabolic products inhibit in vitro lipoprotein oxidation in serum

被引:131
作者
Hodgson, JM [1 ]
Croft, KD [1 ]
Puddey, IB [1 ]
Mori, TA [1 ]
Beilin, LJ [1 ]
机构
[1] UNIV WESTERN AUSTRALIA, DEPT MED, PERTH, WA 6009, AUSTRALIA
关键词
soybeans; isoflavonoids; lipoprotein oxidation; antioxidants;
D O I
10.1016/S0955-2863(96)00133-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isoflavonoids are compounds present in many legumes, but are derived in the human diet mainly from soybeans and various soybean-based food products. The major isoflavonoids occurring in soy are the glycosides of genistein and daidzein. The metabolic products of genistein metabolism in humans have not been clearly shown. The two main products of daidzein metabolism in human appear to be equal and O-demethylangolensin. Increasing evidence suggests that oxidative modification to low-density lipoprotein is involved in atherogenesis, and that natural antioxidants that prevent or inhibit oxidative damage to low-density lipoprotein may beneficially influence atherogenesis. In the present experiments, the effects of genistein and daidzein, and the daidzein metabolites equol and O-desmethylangolensin on Cu2+-induced oxidation of lipoproteins in serum were examined. Three concentrations of each compound (0.1 mu M, 1 mu M, 10 mu M) were tested for antioxidant activity in six individual serum samples. All compounds tested inhibited lipoprotein oxidation. The minimum concentration for significant inhibition was 1 mu M for genistein and daidzein (P <0.05), and 0.1 mu M equol and O-desmethylangolensin (P <0.05). Equol and O-desmethylangolensin were more potent inhibitors of in vitro lipoprotein oxidation in serum than the two major dietary isoflavonoids. This study has demonstrated that soybean isoflavonoids and metabolic products of daidzein metabolism inhibit lipoprotein oxidation is vitro. Human intervention studies are needed to determine if these compounds can influence oxidation in vivo. (C) Elsevier Science Inc. 1996
引用
收藏
页码:664 / 669
页数:6
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