首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Inhibition of extension outgrowth in differentiating rat C6 glioma cells by chlorpyrifos and chlorpyrifos oxon: effects on microtubule proteins.
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Inhibition of extension outgrowth in differentiating rat C6 glioma cells by chlorpyrifos and chlorpyrifos oxon: effects on microtubule proteins.

机译:毒死rif和毒死rifoxon抑制大鼠C6胶质瘤细胞分化中的延伸生长:对微管蛋白的影响。

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The aim of this work was to assess the toxic effects of the phosphorothionate insecticide chlorpyrifos (CPF) and its major in vivo metabolite chlorpyrifos oxon (CPO) on differentiating rat C6 glioma cells. At sublethal concentrations (1-10 microM), both compounds were able to inhibit the development of extensions from C6 cells induced to differentiate by sodium butyrate. Western blot analysis of C6 cell lysates revealed that 4 h exposure to CPF was associated with decreased levels of the cytoskeletal protein MAP1B compared to controls, whereas the levels of the cytoskeletal proteins tubulin and MAP2c were not significantly affected. Western blot analysis of extracts of cells treated with CPO showed a significant, concentration-dependent decrease in the levels of tubulin after 24 h. MAP-1B levels were also significantly decreased. The above changes were not temporally related to acetylcholinesterase (AChE) inhibition. These results suggest that both CPF and CPO can exert toxic effects directly on glial cell differentiation and that the latter compound has a potent effect on the microtubule network.
机译:这项工作的目的是评估硫磷杀虫剂毒死rif(CPF)及其主要体内代谢产物毒死ox(CPO)对分化大鼠C6胶质瘤细胞的毒性作用。在亚致死浓度(1-10 microM)下,两种化合物均能抑制丁酸钠诱导的C6细胞分化产生的延伸。对C6细胞裂解物的蛋白质印迹分析表明,与对照组相比,暴露于CPF 4 h与细胞骨架蛋白MAP1B的水平降低有关,而细胞骨架蛋白微管蛋白和MAP2c的水平没有受到显着影响。用CPO处理过的细胞提取物的Western印迹分析显示24小时后,微管蛋白水平显着,浓度依赖性降低。 MAP-1B水平也显着下降。上述变化在时间上与乙酰胆碱酯酶(AChE)抑制无关。这些结果表明,CPF和CPO均可直接对神经胶质细胞分化产生毒性作用,而后一种化合物对微管网络具有有效作用。

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