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儿茶素抑制蛋白质类老年色素荧光物质生成活性的研究

  • 蔡淑娴 ,
  • 刘仲华 ,
  • 黄建安 ,
  • 罗国安 ,
  • 余兴龙 ,
  • 董新荣 ,
  • 杨志辉 ,
  • 叶飞
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  • 1. 湖南农业大学茶学教育部重点实验室,湖南 长沙 410128;
    2. 清华大学化学系 生命有机磷与化学生物学教育部重点实验室,北京 100084;
    3. 湖南农业大学动物医学院,湖南 长沙 410128
蔡淑娴(1979— ),女,广东博罗人,博士研究生,主要从事植物功能成分化学研究。

收稿日期: 2009-11-02

  修回日期: 2009-12-14

  网络出版日期: 2019-09-10

基金资助

国家973项目(2008CB117007)、湖南省科技重大专项(NK2007005)、农业部茶叶产业技术体系、农业部行业公益专项(NYHYZX07-021-12)

Study on Inhibiting Effects of Tea Catechins on the Formation of Age Pigment Fluorescence Products

  • CAI Shu-xian ,
  • LIU Zhong-hua ,
  • HUANG Jian-an ,
  • LUO Guo-an ,
  • YU Xing-long ,
  • DONG Xin-rong ,
  • YANG Zhi-hui ,
  • YE Fei
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  • 1. Key Laboratory of Ministry of Education for Tea Science, Hunan Agricultural University, Changsha 410128, China;
    2. Department of Chemistry of Tsinghua University and Key Laboratory of Biological Organic Phosphorus and Chemical Biology of Ministry of Education, Beijing 100084, China;
    3. College of Veterinary Medicine, Hunan Agricultural University, Changsha 410128, China

Received date: 2009-11-02

  Revised date: 2009-12-14

  Online published: 2019-09-10

摘要

丙二醛(Malondialdehyde, MDA)是机体内普遍存在的活性羰基化合物代表成分之一,能够与蛋白质发生羰-氨交联反应,生成老年色素荧光物质。本文探讨儿茶素单体成分对MDA应激引起的蛋白质类老年色素荧光物质生成体系的影响,并对其构效关系进行初步分析。结果表明:儿茶素能显著抑制MDA诱导的蛋白质类老年色素物质生成,且酯型儿茶素活性较强,抑制作用除与直接清除MDA外,还与其结构的亲核性有关。本研究从一个新的角度揭示了儿茶素抑制羰-氨交联反应是其预防和治疗羰基应激相关疾病的潜在作用机制之一。

本文引用格式

蔡淑娴 , 刘仲华 , 黄建安 , 罗国安 , 余兴龙 , 董新荣 , 杨志辉 , 叶飞 . 儿茶素抑制蛋白质类老年色素荧光物质生成活性的研究[J]. 茶叶科学, 2010 , 30(1) : 1 -8 . DOI: 10.13305/j.cnki.jts.2010.01.001

Abstract

Malondialdehyde (MDA) is one of the active carbonyl compounds existing in human body, which can react with protein to form age pigment fluorescence products (APFs) by carbonyl-ammonia cross linking reaction. The purpose of this study is to determine whether tea catechins can inhibit the formation of the age pigment fluorescence products induced by MDA-modified human serum albumin (HSA). Results showed that tea catechins, especially the gallated-catechin, could inhibit the formation of APFs. The structure-activity relationship studies suggested that the inhibiting effects of tea catechins on the formation of APFs were correlated with their nucleophilicity, besides their trapping MDA directly. This research indicated that inhibiting carbonyl-ammonia cross linking reaction may be one of the mechanisms of tea catechins preventing and curing diseases resulting from carbonyl stress reaction.

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