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诱变剂的细胞外截留

Extracellular interception of mutagens.

作者信息

Shankel D M, Kuo S, Haines C, Mitscher L A

机构信息

Department of Microbiology, University of Kansas, Lawrence 66045.

出版信息

Basic Life Sci. 1993;61:65-74. doi: 10.1007/978-1-4615-2984-2_5.

Abstract

Extracellular interception of mutagens by excreted enzymes or by chemical agents that react with or bind to formed mutagens provides an important means of defense against chemical mutagens/carcinogens. Kada and Shimoi have classified molecules that function in this manner as "desmutagens," and many of them are natural cellular metabolites. Among the specific mechanisms that such agents may employ are: prevention of the activation of "promutagens" to mutagens; stimulation of enzymes (e.g., glutathione-S-transferase) that catalyze the binding/inactivation of damaging electrophiles; direct binding and concomitant inactivation of promutagens or mutagens; interference with uptake of mutagens into cells; etc. De Flora and Ramel have provided an excellent discussion of the mechanisms of these agents and a proposed classification scheme. Drawing on work from our own laboratories and other recent examples in the literature, several examples of mechanistic approaches to these studies using natural plant-derived materials, e.g., humic acid, Glycyrrhiza glabra extract, glutathione, and bioflavonoids, are also described. Antioxidants and agents that conjugate electrophiles will be among the modes of action described for obtaining the goal of intercepting mutagens/carcinogens.

摘要

通过分泌的酶或与已形成的诱变剂发生反应或结合的化学试剂对诱变剂进行细胞外拦截,是抵御化学诱变剂/致癌物的重要防御手段。Kada和Shimoi将以这种方式发挥作用的分子归类为“抗诱变剂”,其中许多是天然细胞代谢产物。这类试剂可能采用的具体机制包括:防止“前诱变剂”活化为诱变剂;刺激催化有害亲电试剂结合/失活的酶(如谷胱甘肽-S-转移酶);直接结合并同时使前诱变剂或诱变剂失活;干扰诱变剂进入细胞等。De Flora和Ramel对这些试剂的作用机制及提出的分类方案进行了精彩的论述。借鉴我们自己实验室的研究工作以及文献中其他近期的实例,还描述了使用天然植物衍生材料(如腐殖酸、光果甘草提取物、谷胱甘肽和生物类黄酮)进行这些研究的几种机制方法实例。抗氧化剂和亲电试剂结合剂将属于为实现拦截诱变剂/致癌物目标而描述的作用方式。

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