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通过简化的沙门氏菌/微粒体平板掺入试验(同步试验)筛选常用抗寄生虫药物的致突变活性。

Screening the mutagenic activities of commonly used antiparasite drugs by the Simultest, a simplified Salmonella/microsome plate incorporation assay.

作者信息

Melo M E, Ferreira L C

机构信息

Centro de Pesquisas Aggeu Magalhães, Fundação Oswaldo Cruz, Pernambuco, Brazil.

出版信息

Rev Inst Med Trop Sao Paulo. 1990 Jul-Aug;32(4):269-74. doi: 10.1590/s0036-46651990000400006.

Abstract

The mutagenic activities of 16 anti-parasite drugs were screened by the Simultest in both qualitative (spot test) and quantitative (plate incorporation) assays with a Salmonella typhimurium pool composed by the indicator strains TA97, TA98, TA100 and TA102. Four anti Chagas' disease drugs (nifurtimox, benznidazole, CL 64,855, and MK 436) and two anti-amebae drugs (metronidazole and tinidazole) gave positive results in qualitative tests and incorporation of rat liver microsomes did not alter the results. Comparative dose response curves of the mutagenic activities of CL 64,855, metronidazole and benznidazole obtained by the simultest and by individual Salmonella indicator strains demonstrated that both approaches have similar sensitivities. The results corroborate the validity of the Simultest, as a simplified, fast and economic version of the Ames test in preliminary screening of potential mutagenic drugs.

摘要

采用同步试验,通过定性(斑点试验)和定量(平板掺入法)分析,使用由指示菌株TA97、TA98、TA100和TA102组成的鼠伤寒沙门氏菌库,对16种抗寄生虫药物的致突变活性进行了筛选。四种抗恰加斯病药物(硝呋莫司、苯硝唑、CL 64,855和MK 436)以及两种抗阿米巴病药物(甲硝唑和替硝唑)在定性试验中呈阳性结果,加入大鼠肝微粒体并未改变结果。通过同步试验和单个沙门氏菌指示菌株获得的CL 64,855、甲硝唑和苯硝唑致突变活性的比较剂量反应曲线表明,两种方法具有相似的灵敏度。结果证实了同步试验作为Ames试验的一种简化、快速且经济的版本,在潜在致突变药物初步筛选中的有效性。

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