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鞣花酸是一种植物酚类化合物,可激活环氧化酶介导的前列腺素生成。

Ellagic acid, a plant phenolic compound, activates cyclooxygenase-mediated prostaglandin production.

作者信息

Wang Hui Rong, Sui Hao Chen, Zhu Bao Ting

机构信息

Department of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, P.R. China.

School of Science and Engineering, The Chinese University of Hong Kong, Shenzhen, Guangdong 518172, P.R. China.

出版信息

Exp Ther Med. 2019 Aug;18(2):987-996. doi: 10.3892/etm.2019.7667. Epub 2019 Jun 13.

Abstract

In recent years, ellagic acid (EA), a naturally-occurring phenolic compound richly contained in some of the human food sources such as and , was reported to have a number of biological effects. Based on our earlier 3D-QSAR/CoMFA models for cyclooxygenase (COX) I and II, we hypothesize that EA may have the potential to modulate the catalytic activity of COX enzymes, and this hypothesis is examined in the present study. The results from both and experiments show that EA is an activator of COX enzyme-catalyzed production of prostaglandin E2, a representative prostaglandin tested. Mechanistically, EA can activate the peroxidase active site of COX enzymes by serving as a co-substrate, presumably for the reduction of protoporphorin IX with Fe inside. The effect of EA is abrogated by the co-presence of galangin, which is known to bind to COX's peroxidase active site and thereby blocks the effect of the reducing co-substrates. In view of the known physiological functions of COX enzymes in the body, it is suggested that some of the pharmacological and/or toxicological effects of EA may result from an increased production of certain prostaglandins and their related derivatives in the body.

摘要

近年来,鞣花酸(EA)是一种天然存在的酚类化合物,在一些人类食物来源如[具体食物1]和[具体食物2]中含量丰富,据报道具有多种生物学效应。基于我们早期针对环氧化酶(COX)I和II的3D-QSAR/CoMFA模型,我们推测EA可能具有调节COX酶催化活性的潜力,本研究对这一推测进行了检验。[具体实验1]和[具体实验2]的结果均表明,EA是COX酶催化生成前列腺素E2(一种经测试的代表性前列腺素)的激活剂。从机制上讲,EA可作为共底物激活COX酶的过氧化物酶活性位点,大概是用于还原内部含有铁的原卟啉IX。高良姜素的共同存在可消除EA的作用,已知高良姜素可与COX的过氧化物酶活性位点结合,从而阻断还原共底物的作用。鉴于COX酶在体内已知的生理功能,有人提出EA的一些药理和/或毒理作用可能是由于体内某些前列腺素及其相关衍生物的生成增加所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85fa/6601391/8cd42a11b8b4/etm-18-02-0987-g00.jpg

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