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配位化学与六价铬的致癌性和致突变性。

Coordination chemistry and the carcinogenicity and mutagenicity of chromium(VI).

机构信息

Department of Chemistry, Queen Mary College, University of London, Mile End Road, E1 4NS, London, England.

出版信息

Environ Geochem Health. 1989 Dec;11(3-4):77-85. doi: 10.1007/BF01758655.

Abstract

Chromate is a known carcinogen, it is only in recent years that the molecular mechanisms by which this toxicity may be expressed have been investigated. The toxicity of chromate may be mediated by the reaction of chromium(VI) with glutathione (GSH) to generate relatively stable chromium(V) complexes and other more reactive intermediates. The conditions favouring the formation of such complexes have been studied. Reactive intermediates generated during the reduction of chromate by GSH include thionyl radicals and at least two relatively stable chromium(V) species (g -1.996 and g -.986). Mixtures of chromium(VI) and glutathione and a chromium(V) complex of glutathione, which we have isolated from the reaction (g = 1.996), are capable of causing strand breaks in bacteriophage PM2 DNA. In contrast a chromium(III) complex of GSSG, one of the final products of the reaction between GSH and chromium(VI), does not damage DNA in closed circle assays. These observations support the suggestion that reactive intermediates generated during the reduction of chromium(VI) provide one route by which the genotoxicity of chromate may be expressed.

摘要

铬酸盐是一种已知的致癌物,近年来人们才开始研究其毒性的分子机制。铬酸盐的毒性可能是由六价铬与谷胱甘肽(GSH)反应生成相对稳定的五价铬配合物和其他更具反应性的中间产物介导的。已经研究了有利于形成此类配合物的条件。GSH 还原铬酸盐过程中产生的反应性中间产物包括亚硫酸根自由基和至少两种相对稳定的五价铬物种(g = 1.996 和 g = 1.986)。我们从反应中分离出的六价铬和谷胱甘肽的混合物以及谷胱甘肽的五价铬配合物(g = 1.996)能够导致噬菌体 PM2 DNA 的链断裂。相比之下,GSH 与六价铬反应的最终产物之一 GSSG 的三价铬配合物在闭环测定中不会破坏 DNA。这些观察结果支持这样的假设,即在六价铬还原过程中产生的反应性中间产物为铬酸盐的遗传毒性表达提供了一种途径。

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