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氰化物拮抗作用的毒理学基础的最新观点。

Recent perspectives on the toxicodynamic basis of cyanide antagonism.

作者信息

Way J L, Sylvester D, Morgan R L, Isom G E, Burrows G E, Tamulinas C B, Way J L

出版信息

Fundam Appl Toxicol. 1984 Apr;4(2 Pt 2):S231-9. doi: 10.1016/0272-0590(84)90157-x.

Abstract

The mechanism of action of nitrite-thiosulfate (Chen et al., 1933a ,b; Hug , 1933) in the antagonism of the lethal effects of cyanide is much more complex than proposed 50 years ago. Some of the recent findings concerning the mechanism of nitrite action have conceptual theoretical and practical significance, as the development of newer cyanide antagonists are dependent on the elucidation of the basic mechanism of antidotal action. There are preliminary evidence which suggest a vasogenic action rather than methemoglobin formation is the primary action of nitrite, as a cyanide antagonist. Various vasogenic compounds have been uncovered and they may play an important role in the future development of a new class of cyanide antagonists. Also recent development in thiol detoxication of cyanide suggest that rhodanese may play a more complex role. The detoxification of cyanide may be viewed from a considerably more complex perspective with the elucidation of recent mechanisms. It also may provide a newer conceptual basis for a more rational development of future compounds to antagonize the lethal effects of cyanide.

摘要

亚硝酸盐-硫代硫酸盐(Chen等人,1933a,b;Hug,1933)对抗氰化物致死作用的作用机制比50年前提出的要复杂得多。最近一些关于亚硝酸盐作用机制的发现具有概念上的理论和实际意义,因为新型氰化物拮抗剂的开发依赖于解毒作用基本机制的阐明。有初步证据表明,作为氰化物拮抗剂,亚硝酸盐的主要作用是血管生成作用而非高铁血红蛋白的形成。已经发现了各种血管生成化合物,它们可能在新型氰化物拮抗剂的未来开发中发挥重要作用。此外,最近氰化物硫醇解毒方面的进展表明,硫氰酸酶可能发挥更复杂的作用。随着最近机制的阐明,氰化物解毒可能需要从一个相当复杂的角度来看待。它也可能为更合理地开发未来对抗氰化物致死作用的化合物提供一个新的概念基础。

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