首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >In vitro studies on the genotoxicity of the organophosphorus insecticide malathion and its two analogues.
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In vitro studies on the genotoxicity of the organophosphorus insecticide malathion and its two analogues.

机译:体外研究有机磷杀虫剂马拉硫磷及其两种类似物的遗传毒性。

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摘要

Malathion [S-(1,2-dicarboethoxyethyl)O,O-dimethyl phosphorodithioate] is a commonly used organophosphorus insecticide reported to be genotoxic both in vivo and in vitro, but the reports are conflicting. In order to elucidate the genotoxic potency of the main compounds present in commercial preparations of malathion, the DNA-damaging effect of this insecticide, its major metabolite malaoxon [S-(1,2-dicarboethoxyethyl)O,O-dimethyl phosphorothiolate] and its isomer isomalathion [S-(1,2-dicarboethoxyethyl)O,S-dimethyl phosphorodithioate], all at purity of at least 99.8%, was investigated by use of the alkaline single cell gel electrophoresis (comet assay). Freshly isolated human peripheral blood lymphocytes were incubated with 25, 75 and 200 microM of the chemicals for 1 h at 37 degrees C. The concentrations used are comparable to those found in blood following various non-lethal human exposures to pesticides. Malathion did not cause any significant changes in the comet length of the lymphocytes, throughout the range of concentrations tested. Malaoxon and isomalathion introduced damage to DNA in a dose-dependent manner. The effect induced by malaoxon was more pronounced than that caused by isomalathion. Treated cells were able to recover within a 60-min incubation in insecticide-free medium at 37 degrees C except the lymphocytes exposed to malaoxon at 200 microM, which did not show measurable DNA repair. The latter result suggests a considerable cytotoxic effect (cell death) of malaoxon at the highest concentration used. The reported genotoxicity of malathion might, therefore, be a consequence of its metabolic biotransformation to malaoxon or the presence of malaoxon and/or isomalathion as well as other unspecified impurities in commercial formulations of malathion. In this regard, the results of our study clearly indicate that malathion used as commercial product, i.e., containing malaoxon and isomalathion, can be considered as a genotoxic substance in vitro. This means that it may also produce DNA disturbances in vivo, such as DNA breakage at sites of oncogenes or tumor suppressor genes, thus playing a role in the induction of malignancies in individuals exposed to this agent. Therefore, malathion can be regarded as a potential mutagen/carcinogen and requires further investigation.
机译:马拉硫磷[S-(1,2-二烷乙氧基乙基)O,O-二甲基二硫代磷酸酯]是一种常用的有机磷杀虫剂,据报道在体内和体外均具有遗传毒性,但报道相互矛盾。为了阐明马拉硫磷市售制剂中存在的主要化合物的遗传毒性,使用该杀虫剂及其主要代谢产物丙氧磷[S-(1,2-二arboethoxyethyl)O,O-二甲基硫代磷酸酯]及其对DNA的破坏作用通过使用碱性单细胞凝胶电泳(彗星试验)研究了纯度至少为99.8%的异构体异马拉硫磷[S-(1,2-二芳基乙氧基乙基)O,S-二甲基二硫代磷酸酯]。将新鲜分离的人外周血淋巴细胞与25、75和200 microM的化学物质在37摄氏度下孵育1小时。所使用的浓度与在各种非致命性人类接触杀虫剂后血液中的浓度相当。在测试的整个浓度范围内,马拉硫磷对淋巴细胞的彗星长度没有造成任何重大变化。马拉松和异马拉硫磷以剂量依赖的方式对DNA造成损害。与异马拉硫磷所引起的作用相比,丙氧磷所引起的作用更为明显。处理过的细胞能够在37℃无杀虫剂的培养基中孵育60分钟后恢复,但淋巴细胞暴露于200 microM的丙氧磷中,但未显示出可测量的DNA修复作用。后一结果表明,在所使用的最高浓度下,马拉松酮具有相当大的细胞毒性作用(细胞死亡)。因此,已报道的马拉硫磷的遗传毒性可能是由于其代谢生物转化为马拉硫磷或马拉硫磷的商业配方中存在马拉硫磷和/或异马拉硫磷以及其他未指定的杂质所致。在这方面,我们的研究结果清楚地表明,用作商业产品的马拉硫磷,即含有马拉松和异马拉硫磷,可以被认为是体外的遗传毒性物质。这意味着它还可能在体内产生DNA干扰,例如在癌基因或抑癌基因的位点处DNA断裂,从而在暴露于这种药物的个体中诱发恶性肿瘤。因此,马拉硫磷可被视为潜在的诱变剂/致癌物,需要进一步研究。

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