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Impact of isomalathion on malathion cytotoxicity and genotoxicity in human HepaRG cells

机译:异马拉硫磷对人HepaRG细胞中马拉硫磷的细胞毒性和基因毒性的影响

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Isomalathion is a major impurity of technical grade malathion, one of the most abundantly applied insecticides; however little is known about its hepatotoxiciry. In the present study, cytotoxicity and genotoxicity of malathion and isomalathion either individually or in combination, were assessed using the metabolically competent human liver HepaRG cell line. Isomalathion reduced cell viability starting at a 100muM concentration after a 24 h exposure. It also significantly induced caspase-3 activity in a dose-dependent manner starting at 5 muM. On the contrary, even at concentrations as high as 500 muM malathion affected neither cell viability nor caspase-3 activity. Moreover, co-exposure of both compounds resulted in decreased toxicity of isomalathion. By contrast, malathion and isomalathion either separately or in combination, slightly induced micronuclei formation at low concentrations and had additive genotoxic effects when combined at 25 muM. Individually or combined isomalathion directly inhibited activity of carboxyesterases which are involved in detoxication of malathion. In addition, transcripts of CYP2B6 and CYP3A4, two CYPs responsible for malathion phase I metabolism, were strongly induced by the mixture while isomalathion alone only moderately decreased CYP1A2 and increased CYP2B6 transcripts. However, these CYPs were not altered at the protein or activity levels. Taken altogether, our results showed that isomalathion was much more cytotoxic than malathion while both compounds had comparable genotoxic effects in HepaRG hepatocytes at low concentrations and brought further support to the importance of considering impurities and interactions during evaluation of health risks of pesticides.
机译:异麦硫磷是工业级马拉硫磷的主要杂质,马拉硫磷是应用最广泛的杀虫剂之一。然而,人们对其肝毒性知之甚少。在本研究中,马拉硫磷和异马拉硫磷的细胞毒性和遗传毒性可通过具有代谢能力的人肝HepaRG细胞系进行单独或组合评估。暴露24小时后,异麦硫磷从100μM浓度开始降低细胞活力。从5μM开始,它还以剂量依赖性方式显着诱导caspase-3活性。相反,即使在高达500μM马拉硫磷的浓度下,也不影响细胞活力或caspase-3活性。此外,两种化合物的共同暴露导致异马拉硫磷的毒性降低。相比之下,马拉硫磷和异马拉硫磷无论是单独还是组合使用,在低浓度下都会轻微诱导微核形成,并在25μM的条件下具有累加的遗传毒性作用。单独或联合的异马拉硫磷直接抑制了与马拉硫磷脱毒有关的羧酯酶的活性。此外,混合物强烈诱导CYP2B6和CYP3A4的转录本,这两种CYP负责马拉硫磷I期代谢,而单独的异马拉硫磷仅适度降低CYP1A2和增加CYP2B6转录本。但是,这些CYP在蛋白质或活性水平上没有改变。总的来说,我们的结果表明,异马拉硫磷比马拉硫磷具有更高的细胞毒性,而两种化合物在低浓度的HepaRG肝细胞中具有相当的遗传毒性作用,并进一步支持了在评估农药健康风险时考虑杂质和相互作用的重要性。

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