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芳烃受体与其拮抗剂黄酮类化合物之间的相互作用。

Interaction between the aryl hydrocarbon receptor and its antagonists, flavonoids.

作者信息

Fukuda Itsuko, Mukai Rie, Kawase Masaya, Yoshida Ken-ichi, Ashida Hitoshi

机构信息

Research Center for Food Safety and Security, Graduate School of Agricultural Science, Kobe University, Kobe, Hyogo 657-8501, Japan.

出版信息

Biochem Biophys Res Commun. 2007 Aug 3;359(3):822-7. doi: 10.1016/j.bbrc.2007.05.199. Epub 2007 Jun 4.

Abstract

Flavonoids have been reported to be dietary antagonists of an aryl hydrocarbon receptor (AhR). However, little is known about the molecular mechanism on their antagonistic effects. In this study, the inhibitory effect of flavonoids on ligand binding to the AhR and interaction between flavonoids and the AhR complex (AhRc) were investigated in each flavonoid subclass. Flavone, flavonol, and flavanone but not catechin inhibited the specific binding between the AhR and 3-methylcholanthrene dose-dependently, indicating that the former three subclasses possibly act as competitive antagonists of the AhR. However, catechin in addition to the former three subclasses directly interacted with the AhRc by surface plasmon resonance analysis. The dissociation constant values showed an inverse correlation with the suppressive effect on the DNA binding activity. These results suggest that flavone, flavonol, and flavanone act as competitive antagonists of the AhR, while catechin associates with the AhRc and indirectly exhibits its antagonistic effects.

摘要

据报道,黄酮类化合物是芳烃受体(AhR)的膳食拮抗剂。然而,关于它们拮抗作用的分子机制却知之甚少。在本研究中,在每个黄酮类亚类中研究了黄酮类化合物对配体与AhR结合的抑制作用以及黄酮类化合物与AhR复合物(AhRc)之间的相互作用。黄酮、黄酮醇和黄烷酮而非儿茶素剂量依赖性地抑制AhR与3-甲基胆蒽之间的特异性结合,表明前三个亚类可能作为AhR的竞争性拮抗剂。然而,除了前三个亚类外,儿茶素通过表面等离子体共振分析直接与AhRc相互作用。解离常数的值与对DNA结合活性的抑制作用呈负相关。这些结果表明,黄酮、黄酮醇和黄烷酮作为AhR的竞争性拮抗剂,而儿茶素与AhRc结合并间接表现出其拮抗作用。

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