首页> 外文期刊>Bulletin of Environmental Contamination and Toxicology >Effect of endosulfan on the enzymes of polyol pathway in rat Sertoli-germ cell coculture.
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Effect of endosulfan on the enzymes of polyol pathway in rat Sertoli-germ cell coculture.

机译:硫丹对大鼠睾丸胚生殖细胞共培养物中多元醇途径酶的影响。

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摘要

The effect of endosulfan (at 0, 2.0, 20.0, 40.0 and 80.0μM) on the activities of sorbitol dehydrogenase [L-iditol dehydrogenase] and aldose reductase [aldehyde reductase], measured as nmol NADPH oxidized min-1 -mg protein, was investigated using rat Sertoli-germ cell coculture. The results revealed an increase in the activity of aldose reductase in Sertoli-germ cell coculture exposed to 20-80μM endosulfan when compared with the control and the 2μM endosulfan group both after 24 and 48 h following treatment. The increase in aldose reductase activity was in a dose-dependent manner. Duration dependency was observed only in the higher dosed groups (40-80μM endosulfan). A dose-dependent increase in the activity of sorbitol dehydrogenase was recorded from 20 to 80μM exposed group after 24 h following treatment. However, the sorbitol dehydrogenase activity recorded from culture exposed to 2μM endosulfan was similar to that of the control. The trend of the activity was similar when the exposure time was further increased to 48 h -- a dose-dependent increase in sorbitol dehydrogenase activity from 20 to 80μM endosulfan. No duration-dependent changes was observed in the 48 h treatment. This study suggests that endosulfan disrupts the polyol pathwayby affecting specific enzymes, which may be one of the reasons leading to cytotoxicity in vitro.
机译:硫丹(0、2.0、20.0、40.0和80.0μM)对山梨糖醇脱氢酶[L-iditol脱氢酶]和醛糖还原酶[醛还原酶]的活性的影响,以nmol NADPH氧化的min-1 -mg蛋白测量。使用大鼠支持生殖细胞共培养进行了研究。结果显示,在处理后24小时和48小时,与对照组和2μM硫丹组相比,暴露于20-80μM硫丹的Sertoli-germ细胞共培养物中醛糖还原酶的活性增加。醛糖还原酶活性的增加是剂量依赖性的。仅在较高剂量组(40-80μM硫丹)中观察到持续时间依赖性。在治疗后24小时,从20μM至80μM暴露组记录了山梨糖醇脱氢酶活性的剂量依赖性增加。但是,暴露于2μM硫丹的培养物中记录的山梨糖醇脱氢酶活性与对照相似。当暴露时间进一步增加至48 h时,活性趋势相似-山梨糖醇脱氢酶活性从20至80μM硫丹呈剂量依赖性增加。在48小时的治疗中未观察到持续时间依赖性变化。这项研究表明,硫丹通过影响特定的酶来破坏多元醇途径,这可能是导致体外细胞毒性的原因之一。

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