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接触环境毒物代森锰会诱导小鼠产生类似帕金森病的神经毒性:一项联合蛋白质组学和代谢组学分析。

Exposure to the environmentally toxic pesticide maneb induces Parkinson's disease-like neurotoxicity in mice: A combined proteomic and metabolomic analysis.

机构信息

Research Center for Environment and Health, Zhongnan University of Economics and Law, Wuhan, 430073, China; Department of Environmental Engineering, Zhongnan University of Economics and Law, Wuhan, 430073, China; Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.

Research Center for Environment and Health, Zhongnan University of Economics and Law, Wuhan, 430073, China; Department of Environmental Engineering, Zhongnan University of Economics and Law, Wuhan, 430073, China.

出版信息

Chemosphere. 2022 Dec;308(Pt 2):136344. doi: 10.1016/j.chemosphere.2022.136344. Epub 2022 Sep 7.

Abstract

Maneb is a typical dithiocarbamate fungicide that has been extensively used worldwide. Epidemiological evidence shows that exposure to maneb is an environmental risk factor for Parkinson's disease (PD). However, the mechanisms underlying maneb-induced neurotoxicity have yet to be elucidated. In this study, we exposed SH-SY5Y cells to maneb at environmentally relevant concentrations (0, 0.1, 5, 10 mg/L) and found that maneb dose-dependently decreased the cell viability. Furthermore, maneb (60 mg/kg) induced PD-like motor impairment in α-synuclein A53T transgenic mice. The results of tandem mass tag (TMT) proteomics and metabolomics studies of mouse brain and serum revealed significant changes in proteins and metabolites in the pathways involved in the neurotransmitter system. The omics results were verified by targeted metabolomics and Western blot analysis, which demonstrated that maneb induced disturbance of the PD-related pathways, including the phenylalanine and tryptophan metabolism pathways, dopaminergic synapse, synaptic vesicle cycle, mitochondrial dysfunction, and oxidative stress. In addition, the PD-like phenotype induced by maneb was attenuated by the asparagine endopeptidase (AEP) inhibitor compound #11 (CP11) (10 mg/kg), indicating that AEP may play a role in maneb-induced neurotoxicity. To the best of our knowledge, this is the first study to investigate the molecular mechanisms underlying maneb-induced PD-like phenotypes using multiomics analysis, which identified novel therapeutic targets for PD associated with pesticides and other environmental pollutants.

摘要

代森锰锌是一种典型的二硫代氨基甲酸酯类杀菌剂,在全球范围内被广泛使用。流行病学证据表明,接触代森锰锌是帕金森病(PD)的环境危险因素。然而,代森锰锌诱导神经毒性的机制尚不清楚。在这项研究中,我们将 SH-SY5Y 细胞暴露于环境相关浓度(0、0.1、5、10 mg/L)的代森锰锌中,发现代森锰锌呈剂量依赖性地降低细胞活力。此外,代森锰锌(60mg/kg)诱导α-突触核蛋白 A53T 转基因小鼠出现 PD 样运动障碍。对小鼠脑和血清的串联质量标签(TMT)蛋白质组学和代谢组学研究的结果表明,神经递质系统相关途径中的蛋白质和代谢物发生了显著变化。通过靶向代谢组学和 Western blot 分析验证了组学结果,表明代森锰锌诱导了与 PD 相关的途径的紊乱,包括苯丙氨酸和色氨酸代谢途径、多巴胺能突触、突触小泡循环、线粒体功能障碍和氧化应激。此外,天门冬酰胺内肽酶(AEP)抑制剂化合物 #11(CP11)(10mg/kg)可减轻代森锰锌诱导的 PD 样表型,表明 AEP 可能在代森锰锌诱导的神经毒性中发挥作用。据我们所知,这是首次使用多组学分析研究代森锰锌诱导 PD 样表型的分子机制的研究,该研究确定了与农药和其他环境污染物相关的 PD 新的治疗靶点。

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