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首页> 外文期刊>DNA and Cell Biology >In vitro genotoxicity of fipronil sister chromatid exchange, cytokinesis block micronucleus test, and comet assay.
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In vitro genotoxicity of fipronil sister chromatid exchange, cytokinesis block micronucleus test, and comet assay.

机译:氟虫腈姐妹染色单体交换,胞质分裂阻滞微核试验和彗星试验的体外遗传毒性。

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Fipronil (FP) is a phenylpyrazole pesticide developed by the transnational company Rhone-Poulenc Agro in 1987. Data on the genotoxicity and toxicity of FP are rather inadequate. In this study, we aimed to evaluate the potential genotoxic activity of FP using the single-cell microgel electrophoresis or comet assay, sister chromatid exchanges (SCEs), and micronuclei (MN) in human peripheral blood lymphocytes. In addition, the cytokinesis block proliferation index (CBPI) and proliferation index (PRI) were measured for cytotoxicity. In this study, three different doses of FP were used (0.7, 0.3, 0.1 micro g/mL). Mitomycin C (2 micro g/mL) and hydrogen peroxide were used as positive controls for SCE MN test systems, and comet assay, respectively. FP induced a statistically significant increase in the MN and SCE frequency and DNA damage in a dose-dependent manner in human peripheral blood lymphocytes (p<0.01, p<0.05, for 0.7 and 0.3 micro g/mL, respectively) compared with a negative control. There is no significant difference between 0.1 micro g/mL and the negative control for MN frequency, but there is significant difference between all the doses of FP and negative control for SCE frequency, mitotic index, CBPI, and PRI values (p<0.01). Using the alkaline comet assay, we showed that all the doses of the FP induced DNA damage in human peripheral blood lymphocytes in vitro (p<0.05).
机译:Fipronil(FP)是由跨国公司Rhone-Poulenc Agro在1987年开发的苯基吡唑类农药。FP的遗传毒性和毒性数据还很不足。在这项研究中,我们旨在使用人外周血淋巴细胞中的单细胞微凝胶电泳或彗星分析,姐妹染色单体交换(SCE)和微核(MN)评估FP的潜在遗传毒性活性。另外,测量细胞分裂阻滞增殖指数(CBPI)和增殖指数(PRI)的细胞毒性。在这项研究中,使用了三种不同剂量的FP(0.7、0.3、0.1 micro g / mL)。丝裂霉素C(2微克/毫升)和过氧化氢分别用作SCE MN测试系统和彗星测定的阳性对照。与阴性相比,FP剂量依赖性地诱导了人类外周血淋巴细胞的MN和SCE频率以及DNA损伤的统计学显着增加(分别为p <0.01,p <0.05、0.7和0.3 micro g / mL)。控制。 0.1微克/毫升与MN频率阴性对照之间无显着差异,但所有FP剂量与SCE频率,有丝分裂指数,CBPI和PRI值的阴性对照之间均存在显着差异(p <0.01) 。使用碱性彗星试验,我们显示了所有剂量的FP在体外都会诱导人外周血淋巴细胞DNA损伤(p <0.05)。

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