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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Biomarkers of genotoxicity and genomic instability in a non-human primate, Cebus libidinosus (Cebidae, Platyrrhini), exposed to nitroimidazole derivatives.
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Biomarkers of genotoxicity and genomic instability in a non-human primate, Cebus libidinosus (Cebidae, Platyrrhini), exposed to nitroimidazole derivatives.

机译:暴露于硝基咪唑衍生物的非人类灵长类动物Cebus libidinosus(Cebidae,Platyrrhini)中的遗传毒性和基因组不稳定的生物标志物。

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摘要

The genotoxicity of two nitroimidazole derivatives, ornidazole (ONZ) and metronidazole (MTZ) in the peripheral blood lymphocytes of Cebus libidinosus (CLI) (Primates, Cebidae) was assessed. Endpoints measured included sister chromatid exchange (SCE) frequency, cell proliferation kinetics (CPK), replication index (RI), mitotic index (MI), and damage incidence in or near CLI heterochromatin regions. MI and SCE values following ONZ or MTZ treatments were significantly different (p<0.001) from control. SCE frequency per chromosome was not proportional to chromosome length. The chromosomes most affected for SCE were 1, 2, 4, 6, 11-13, 17, and 18, many of which possess interstitial or terminal heterochromatin. In the CLI genome, chromosomes 11 and 17 showed higher susceptibility to damage RI was the only biomarker that did not show statistically significant differences between control and treated cultures. C. libidinosus bands 11q1.4 and 11q1.5 may be hot-spots in the context of nitroimidazole exposure.
机译:评估了Cebus libidinosus(CLI)(Primates,Cebidae)的外周血淋巴细胞中的两种硝基咪唑衍生物,奥硝唑(ONZ)和甲硝唑(MTZ)的遗传毒性。测量的终点包括姐妹染色单体交换(SCE)频率,细胞增殖动力学(CPK),复制指数(RI),有丝分裂指数(MI)以及CLI异染色质区域内或附近的损伤发生率。 ONZ或MTZ处理后的MI和SCE值与对照组相比有显着差异(p <0.001)。每个染色体的SCE频率与染色体长度不成比例。受SCE影响最大的染色体是1、2、4、6、11-13、17和18,其中许多具有间质或末端异染色质。在CLI基因组中,第11号和第17号染色​​体显示出更高的对RI损伤的敏感性,是唯一在对照和处理后的培养物中未显示出统计学显着差异的生物标记。在硝基咪唑暴露的情况下,C。libidinosus条带11q1.4和11q1.5可能是热点。

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