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对用硝呋替莫和苯硝唑治疗的豚鼠血液和尿液中的遗传毒性活性进行评估。

Evaluation of genotoxic activity in the blood and urine of guinea pigs treated with nifurtimox and benznidazole.

作者信息

Ferreira R C, de Melo M E, Moraes Júnior M A, Ferreira L C

机构信息

Laboratorio de Imunopatologia Keizo Asami, Universidade Federal de Pernambuco, Recife, Brasil.

出版信息

Braz J Med Biol Res. 1988;21(5):1069-77.

PMID:3248236
Abstract
  1. The mutagenicity of serum and urine from guinea pigs treated with a single oral dose (500 mg/kg) of benznidazole and nifurtimox was assayed using the Salmonella/plate incorporation test with strain TA 100 and a nitroreductase-deficient derivative, TA 100NR. 2. The urine and blood of animals treated with nifurtimox were not mutagenic for either tester strain. 3. The urine and blood of animals receiving benznidazole were mutagenic to the TA 100 but not to the TA 100NR strain. Similar results were obtained with nitrofurantoin-treated animals. Maximum mutagenicity values were obtained in serum and urine of treated animals 90 min and 24 h after administration, respectively. 4. Mutagenicity induced by benznidazole in the serum and urine of treated animals was not altered when assayed in anaerobic environments. 5. These results indicate that benznidazole and nifurtimox are not metabolized by the mammalian host into stable mutagenic derivatives detectable by the Ames test. Based on these data, we suggest that the potential cancer risk to patients treated with these drugs is small but should be further evaluated.
摘要
  1. 采用鼠伤寒沙门氏菌平板掺入试验,使用TA 100菌株和一种硝基还原酶缺陷衍生物TA 100NR,对经单次口服剂量(500毫克/千克)的苄硝唑和硝呋莫司处理的豚鼠血清和尿液的致突变性进行了测定。2. 用硝呋莫司处理的动物的尿液和血液对任何一种测试菌株均无致突变性。3. 接受苄硝唑处理的动物的尿液和血液对TA 100菌株有致突变性,但对TA 100NR菌株无致突变性。用呋喃妥因处理的动物也得到了类似结果。在给药后90分钟和24小时,分别在处理动物的血清和尿液中获得了最大致突变性值。4. 在厌氧环境中进行测定时,苄硝唑在处理动物的血清和尿液中诱导的致突变性没有改变。5. 这些结果表明,苄硝唑和硝呋莫司不会被哺乳动物宿主代谢为可通过艾姆斯试验检测到的稳定致突变衍生物。基于这些数据,我们认为用这些药物治疗的患者潜在的癌症风险很小,但应进一步评估。

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