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甲硝唑及其他硝基咪唑类药物的选择性毒性机制。

Mechanisms of selective toxicity of metronidazole and other nitroimidazole drugs.

作者信息

Edwards D I

出版信息

Br J Vener Dis. 1980 Oct;56(5):285-90. doi: 10.1136/sti.56.5.285.

Abstract

The selectively toxic effect of nitroimidazole drugs towards anaerobic bacteria and protozoa depends on a number of factors. The killing action of such drugs as metronidazole requires the reduction of the nitro group, a process which influences the rate of entry of the drug into the susceptible cell and which is determined by mechanisms involving ferredoxin-linked (or the equivalent) reactions in the cell. The reduced agent subsequently causes strand breakage of DNA, the extent of which depends on the A + T content of the DNA. Other effects of such drugs may include the possible inhibition of DNA repair mechanisms which exacerbate DNA damage, Inhibition of activity of nitroimidazoles may be caused by aminothiol radical scavengers and radioprotectors normally present in the cell or by the presence of other organisms in the environment (that is, the vagina) capable of inactivating the drugs.

摘要

硝基咪唑类药物对厌氧菌和原生动物的选择性毒性作用取决于多种因素。甲硝唑等此类药物的杀菌作用需要硝基的还原,这一过程会影响药物进入易感细胞的速率,并且由涉及细胞中与铁氧化还原蛋白相关(或等效)反应的机制所决定。还原后的物质随后会导致DNA链断裂,其程度取决于DNA的A+T含量。此类药物的其他作用可能包括对DNA修复机制的潜在抑制,从而加剧DNA损伤。细胞中通常存在的氨基硫醇自由基清除剂和辐射防护剂,或环境(即阴道)中存在的其他能够使药物失活的生物体,可能会导致硝基咪唑类药物活性受到抑制。

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