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Environ Toxicol. 2014 May;29(5):577-87. doi: 10.1002/tox.21783. Epub 2012 May 19.
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Genotoxicity of dicrotophos, an organophosphorous pesticide, assessed with different assays in vitro.用不同的体外检测方法评估有机磷农药敌敌畏的遗传毒性。
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双硫磷杀虫剂的致突变性和遗传毒性。

Mutagenicity and genotoxicity of dicapthon insecticide.

机构信息

Faculty of Arts and Sciences, Molecular Biology and Genetics Department, Usak University, 1 Eylül Campus, 64300, Uşak, Turkey,

出版信息

Cytotechnology. 2014 Oct;66(5):741-51. doi: 10.1007/s10616-013-9623-x. Epub 2014 Jan 31.

DOI:10.1007/s10616-013-9623-x
PMID:24477548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4158013/
Abstract

Mutagenic and genotoxic effects of dicapthon were investigated by using the bacterial reverse mutation assay in Salmonella typhimurium TA97, TA98, TA100 and TA102 strains with or without metabolic activation system (S9 mix), and chromosome aberrations (CAs), sister chromatid exchanges (SCEs), and micronucleus (MN) tests in human peripheral blood lymphocytes in vitro. Dicapthon was dissolved in dimethyl sulfoxide for all test systems. 0.1, 1, 10 and 100 μg/plate doses of dicapthon were found to be weakly mutagenic on S. typhimurium TA 98 without S9 mix. The human peripheral lymphocytes were treated with four experimental concentrations of dicapthon (25, 50, 100, and 200 μg/mL) for 24 and 48 h. Dicapthon increased the frequency of SCE only at the 100 μg/mL concentration for the 24 and 48 h applications. Dicapthon also induced abnormal cell frequency, CA/cell ratio and frequency of MN dose dependently for 24 and 48 h. Dicapthon showed a statistically significant cytotoxic effect by decreasing the mitotic index in all concentrations and a cytostatic effect by decreasing nuclear division index in 100 and 200 μg/mL concentrations for both treatment periods when compared with both untreated and solvent controls. These values decreased also in a dose dependent manner.

摘要

二氯苯醌的诱变和遗传毒性作用通过沙门氏菌属鼠伤寒 TA97、TA98、TA100 和 TA102 菌株的细菌回复突变试验(加入或不加入代谢激活系统(S9 混合液))以及体外人外周血淋巴细胞的染色体畸变(CA)、姐妹染色单体交换(SCE)和微核(MN)试验进行了研究。二氯苯醌在所有试验系统中均溶解于二甲基亚砜中。结果发现,不加 S9 混合液时,0.1、1、10 和 100μg/平板剂量的二氯苯醌对 TA98 型鼠伤寒沙门氏菌具有弱致突变性。用人外周血淋巴细胞分别用二氯苯醌(25、50、100 和 200μg/mL)的四个实验浓度处理 24 和 48 小时。二氯苯醌仅在 100μg/mL 浓度下,在 24 和 48 小时应用时,增加了 SCE 的频率。二氯苯醌还剂量依赖性地诱导了异常细胞频率、CA/细胞比和 MN 频率的增加,在 24 和 48 小时的处理中均如此。与未处理和溶剂对照组相比,二氯苯醌在所有浓度下通过降低有丝分裂指数表现出统计学上显著的细胞毒性作用,在 100 和 200μg/mL 浓度下通过降低核分裂指数表现出细胞生长抑制作用,在两个处理期均如此。这些值也呈剂量依赖性下降。