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饮食水平的黄酮类化合物和黄酮醇可抑制二噁英诱导的芳烃受体转化。

Flavones and flavonols at dietary levels inhibit a transformation of aryl hydrocarbon receptor induced by dioxin.

作者信息

Ashida H, Fukuda I, Yamashita T, Kanazawa K

机构信息

Laboratory of Food and Nutritional Chemistry, Faculty of Agriculture, Kobe University, Rokkodai, Nada-ku, 657-8501, Kobe, Japan.

出版信息

FEBS Lett. 2000 Jul 7;476(3):213-7. doi: 10.1016/s0014-5793(00)01730-0.

Abstract

Dioxins invade the body mainly through the diet, and produce toxicity through the transformation of aryl hydrocarbon receptor (AhR). An inhibitor of the transformation should therefore protect against the toxicity and ideally be part of the diet. We examined flavonoids ubiquitously expressed in plant foods as one of the best candidates, and found that the subclasses flavones and flavonols suppressed antagonistically the transformation of AhR induced by 1 nM of 2,3,7,8-tetrachlorodibenzo-p-dioxin, without exhibiting agonistic effects that transform AhR. The antagonistic IC(50) values ranged from 0.14 to 10 microM, close to the physiological levels in human.

摘要

二噁英主要通过饮食侵入人体,并通过芳烃受体(AhR)的转化产生毒性。因此,一种转化抑制剂应能预防毒性,并且理想情况下应成为饮食的一部分。我们研究了在植物性食物中普遍存在的黄酮类化合物,将其作为最佳候选物之一,发现黄酮和黄酮醇亚类能拮抗1 nM 2,3,7,8-四氯二苯并对二噁英诱导的AhR转化,且未表现出转化AhR的激动作用。拮抗IC(50)值范围为0.14至10 microM,接近人体生理水平。

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