原生动物
细菌
厌氧菌
微生物学
甲硝唑
行动方式
无氧运动
生物化学
微生物代谢
黄多辛
铁氧还蛋白
医学
生物
抗生素
酶
生理学
遗传学
出处
期刊:PubMed
日期:1983-01-01
卷期号:93 (1 Pt 2): 165-71
被引量:49
摘要
Metronidazole and related 5-nitroimidazoles are relatively nontoxic. Reduction of their nitro group, however, leads to the production of short-lived cytotoxic intermediates, which finally decompose into nontoxic end products. The toxicity of the intermediates is due to their interaction with deoxyribonucleic acid and possibly with other macromolecules. Metabolic pathways of low redox potential that are linked to ferredoxin or flavodoxin-like electron transport components reduce nitroimidazoles with great efficacy. Such pathways are characteristic of susceptible anaerobic protozoa and bacteria and are absent in nonsusceptible aerobic cells of the host.
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