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异黄酮大豆苷元在无细胞试验中不具有抗氧化活性,但能诱导抗氧化酶过氧化氢酶。

Isoflavone daidzein possesses no antioxidant activities in cell-free assays but induces the antioxidant enzyme catalase.

作者信息

Kampkötter Andreas, Chovolou Yvonni, Kulawik Andreas, Röhrdanz Elke, Weber Nadine, Proksch Peter, Wätjen Wim

机构信息

Heinrich-Heine-Universität, Institute of Toxicology, PO Box 101007, 40001 Düsseldorf, Germany.

出版信息

Nutr Res. 2008 Sep;28(9):620-8. doi: 10.1016/j.nutres.2008.06.002.

Abstract

Epidemiologic studies have shown that dietary intake of isoflavonones is associated with several properties beneficial to human health. It has been suggested that at least some of these effects are related to the antioxidant activity of isoflavonoids. We analyzed the antioxidant activity of the major isoflavones found in soybeans, but none of these compounds showed prominent antioxidant effects in cell-free assay systems (trolox equivalent antioxidant capacity assay and 2,2-diphenyl-1-picrylhydrazyl assay). Therefore, we examined the hypothesis that the antioxidative effects of isoflavones are caused indirectly by up-regulation of antioxidative enzymes, thereby lowering intracellular concentration of reactive oxygene species. Daidzein shows a significant induction of catalase promoter activity at 100 micromol/L in a reporter gene assay and at 200 micromol/L in Northern blot experiments. Another hypothesis for antioxidant effects caused by isoflavones is due to metabolism by intestinal bacteria. Analyzing the daidzein metabolites 3'-OH-daidzein and 6-OH-daidzein in our cell culture model, we found strong antioxidant effects (2,2-diphenyl-1-picrylhydrazyl and trolox equivalent antioxidant capacity assay). We conclude that isoflavone daidzein up-regulates the antioxidant enzyme catalase but shows only little antioxidant capacity per se. Antioxidant effects of this dietary isoflavonone may also be due to formation of the antioxidant metabolites 6-OH-daidzein and 3'-OH-daidzein.

摘要

流行病学研究表明,饮食中摄入异黄酮与多种对人体健康有益的特性相关。有人提出,这些作用中至少有一些与异黄酮类化合物的抗氧化活性有关。我们分析了大豆中主要异黄酮的抗氧化活性,但在无细胞检测系统(特洛克斯等效抗氧化能力检测和2,2-二苯基-1-苦基肼检测)中,这些化合物均未表现出显著的抗氧化作用。因此,我们检验了以下假设:异黄酮的抗氧化作用是通过上调抗氧化酶间接引起的,从而降低细胞内活性氧物质的浓度。在报告基因检测中,大豆苷元在100微摩尔/升时可显著诱导过氧化氢酶启动子活性,在Northern印迹实验中,在200微摩尔/升时也有此作用。异黄酮引起抗氧化作用的另一种假设是由于肠道细菌的代谢。在我们的细胞培养模型中分析大豆苷元的代谢产物3'-羟基大豆苷元和6-羟基大豆苷元时,我们发现了很强的抗氧化作用(2,2-二苯基-1-苦基肼和特洛克斯等效抗氧化能力检测)。我们得出结论,异黄酮大豆苷元上调了抗氧化酶过氧化氢酶,但本身的抗氧化能力很小。这种膳食异黄酮的抗氧化作用也可能归因于抗氧化代谢产物6-羟基大豆苷元和3'-羟基大豆苷元的形成。

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