首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >The in vitro effects of Trolox on methylmercury-induced neurotoxicity.
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The in vitro effects of Trolox on methylmercury-induced neurotoxicity.

机译:Trolox对甲基汞诱导的神经毒性的体外作用。

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Methylmercury (MeHg), an environmental toxicant primarily found in fish and seafood poses a dilemma to both consumers and regulatory authorities given the nutritional benefits of fish consumption vs. possible adverse neurological damage caused by MeHg. The present study addresses whether supplementation with 6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (Trolox), alters the neuro-oxidative effects of MeHg in C6-glioma and B35-neuronal cell lines. As indicators of cytotoxicity, reduced glutathione (GSH), reactive oxygen species (ROS) and mitochondrial activity (MTT) were measured. The cellular mercury (Hg) content was measured with high resolution-inductively coupled plasma mass spectrometry (HR-ICPMS). The amount of MeHg-induced ROS was significantly reduced (p<0.05) after treatment with 50muM Trolox in C6 glial cell line. However, treatment with Trolox did not induce any significant increase in GSH levels or MTT activity in either of the cell lines. In addition, treatment with Trolox did not induce any significant changes in intracellular MeHg levels. The MeHg and Trolox treated C6 glial cell line differed significantly (p<0.05) from the B35 cell line for MTT, ROS and GSH activity. These findings provide experimental evidence that preincubation with Trolox prevents MeHg-induced ROS generation in C6 glial cell line by quenching of free radicals and not by changes in intracellular GSH or MeHg content.
机译:甲基汞(MeHg)是一种主要存在于鱼类和海鲜中的环境毒物,鉴于食用鱼类的营养益处与MeHg可能引起的不良神经系统损害,这对消费者和监管机构都是一个难题。本研究解决了补充6-羟基-2,5,7,8-四甲基苯并-2-羧酸(Trolox)是否会改变MeHg在C6-神经胶质瘤和B35神经细胞系中的神经氧化作用。作为细胞毒性的指标,测量了还原型谷胱甘肽(GSH),活性氧(ROS)和线粒体活性(MTT)。用高分辨率电感耦合等离子体质谱仪(HR-ICPMS)测量了细胞汞(Hg)含量。在C6神经胶质细胞系中用50μMTrolox处理后,MeHg诱导的ROS量显着减少(p <0.05)。但是,用Trolox处理不会在任何一种细胞系中引起GSH水平或MTT活性的明显增加。此外,用Trolox进行的治疗并未引起细胞内MeHg水平的任何显着变化。 MeHg和Trolox处理的C6神经胶质细胞系的MTT,ROS和GSH活性与B35细胞系显着不同(p <0.05)。这些发现提供了实验证据,表明与Trolox的预温育可通过自由基淬灭而不是通过细胞内GSH或MeHg含量的变化来阻止MeHg诱导的C6神经胶质细胞系中ROS的生成。

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