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使用神经毒剂 1,3-二硝基苯、3-硝基丙酸和 3-氯丙二醇进行蛋白质羰基化和线粒体功能障碍的比较研究。

A comparative study of protein carbonylation and mitochondrial dysfunction using the neurotoxicants 1,3-dinitrobenzene, 3-nitropropionic acid, and 3-chloropropanediol.

机构信息

Toxicology Program, Department of Environmental Health Sciences, School of Public Health, University of Michigan, Ann Arbor, MI 48109-2029, USA.

出版信息

Neurotoxicology. 2013 Jul;37:74-84. doi: 10.1016/j.neuro.2013.04.004. Epub 2013 Apr 23.

Abstract

This comparative evaluation of neurotoxicants previously identified as models of chemical-induced mitochondrial dysfunction and energy deprivation demonstrated that subtoxic concentrations of 1,3-dinitrobenzene (1,3-DNB), 3-nitropropionic acid (3-NPA), and 3-chloropropanediol (3-CPD) each led to concentration-dependent loss of the mitochondrial membrane potential (ΔΨm) associated with similar patterns of protein carbonylation. Subtoxic concentrations of each neurotoxicant were determined by measuring DI TNC1 cell viability using the MTS cell proliferation assay. Although exposure 1 μM, 10 μM, and 100 μM concentrations of each toxicant did not result in loss of cell viability after 48 h, exposure to each toxicant at these concentrations led to concentration-dependent loss of tetramethyl rhodamine methyl ester (TMRM) fluorescence over the same exposure period. Preincubation with the antioxidant, deferoxamine, was effective in preventing loss of TMRM flurorescence. Through the combined use of two-dimensional polyacrylamide gel electrophoresis (2D PAGE) and Oxyblot analysis, this study demonstrated that exposure to each toxicant resulted in the formation of distinctly similar patterns of protein carbonylation comprised of specific proteins identified with tandem MS/MS. Our results provide insight as to how exposure to different neurotoxicants that enhance oxidative stress may, in fact, lead to mitochondrial injury and subsequent toxicity through selective, yet shared, pathways of protein modification by oxidative carbonylation.

摘要

本研究对先前确定的化学诱导线粒体功能障碍和能量耗竭模型神经毒物进行了比较评价,结果表明,亚毒性浓度的 1,3-二硝基苯(1,3-DNB)、3-硝基丙酸(3-NPA)和 3-氯-1,2-丙二醇(3-CPD)均导致与蛋白羰基化相似模式相关的线粒体膜电位(ΔΨm)浓度依赖性丧失。通过使用 MTS 细胞增殖测定法测量 DI TNC1 细胞活力,确定了每种神经毒物的亚毒性浓度。尽管暴露于 1 μM、10 μM 和 100 μM 浓度的每种毒物 48 小时后不会导致细胞活力丧失,但在相同暴露时间内,每种毒物在这些浓度下的暴露导致四甲基罗丹明甲酯(TMRM)荧光的浓度依赖性丧失。抗氧化剂去铁胺的预孵育可有效防止 TMRM 荧光丧失。通过二维聚丙烯酰胺凝胶电泳(2D PAGE)和 Oxyblot 分析的联合使用,本研究表明,暴露于每种毒物都会导致蛋白羰基化形成明显相似的模式,其中包括通过串联 MS/MS 鉴定的特定蛋白质。我们的研究结果表明,不同的神经毒物通过增强氧化应激暴露,可能会通过选择性但共享的蛋白氧化羰基化修饰途径导致线粒体损伤和随后的毒性。

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