首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Activity of a nitroalkene derivative, 1-(5-bromofur-2-il)-2-bromo-2-nitroethene, in the Salmonella/microsome assay and the mouse bone marrow micronucleus test.
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Activity of a nitroalkene derivative, 1-(5-bromofur-2-il)-2-bromo-2-nitroethene, in the Salmonella/microsome assay and the mouse bone marrow micronucleus test.

机译:沙门氏菌/微粒体测定和小鼠骨髓微核试验中硝基烯烃衍生物1-(5-溴糠-2-il)-2-溴-2-硝基乙烯的活性。

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摘要

Mutagenicity of a substituted nitroalkene, 1-(5-bromofur-2-il)-2-bromo-2-nitroethene (BNF) was tested in the Salmonella/microsome assay using the strains TA 98, TA 100 and TA 100NR (nitroreductase deficient). BNF was a direct mutagen in TA 98 and TA 100; the response was lowered when exogenous metabolic activation (S9) was used. A further decrease in mutagenicity was observed in strain TA 100NR, as compared to the parental TA 100, which showed the involvement of nitroreduction in the overall response elicited by BNF. The micronucleus assay was carried out in Swiss male mice which were given a single i.p. dose of 10-20 mg/kg of BNF dissolved in peanut oil, bone marrow being sampled 24 and 48 h later. The micronucleated polychromatic erythrocyte counts (MNPCE) showed a weak response in the dose range of 10-17.5 mg/kg at the second sampling (48 h) and a significant rise for 20 mg/kg at 24 and 48 h.
机译:使用菌株TA 98,TA 100和TA 100NR(硝基还原酶缺陷)在沙门氏菌/微粒体测定中测试了取代的硝基烯烃1-(5-溴糠-2-il)-2-溴-2-硝基乙烯(BNF)的致突变性)。 BNF是TA 98和TA 100中的直接诱变剂。当使用外源性代谢激活(S9)时,反应降低。与亲本TA 100相比,菌株TA 100NR的致突变性进一步降低,这表明硝基还原参与了BNF引发的总体反应。微核化验是在给瑞士雄性小鼠单次腹膜内注射后进行的。剂量为10-20 mg / kg的BNF溶解在花生油中,然后在24和48小时后抽取骨髓样本。微核多色红细胞计数(MNPCE)在第二次采样(48 h)的剂量范围为10-17.5 mg / kg时显示出较弱的响应,而在24和48 h则显着上升了20 mg / kg。

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