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Oxidative modifications mitochondrial dysfunction and impaired protein degradation in Parkinsons disease: how neurons are lost in the Bermuda triangle

机译:帕金森氏病中的氧化修饰线粒体功能障碍和蛋白质降解受损:百慕大三角区神经元如何丢失

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摘要

While numerous hypotheses have been proposed to explain the molecular mechanisms underlying the pathogenesis of neurodegenerative diseases, the theory of oxidative stress has received considerable support. Although many correlations have been established and encouraging evidence has been obtained, conclusive proof of causation for the oxidative stress hypothesis is lacking and potential cures have not emerged. Therefore it is likely that other factors, possibly in coordination with oxidative stress, contribute to neuron death. Using Parkinson's disease (PD) as the paradigm, this review explores the hypothesis that oxidative modifications, mitochondrial functional disruption, and impairment of protein degradation constitute three interrelated molecular pathways that execute neuron death. These intertwined events are the consequence of environmental exposure, genetic factors, and endogenous risks and constitute a "Bermuda triangle" that may be considered the underlying cause of neurodegenerative pathogenesis.
机译:尽管已经提出了许多假说来解释神经退行性疾病发病机理的分子机制,但是氧化应激的理论得到了相当多的支持。尽管已经建立了许多相关性并获得了令人鼓舞的证据,但是缺乏氧化应激假说的因果关系的确凿证据,并且尚未出现潜在的治疗方法。因此,很可能其他因素可能与氧化应激有关,导致神经元死亡。本文以帕金森氏病(PD)为范例,探讨了以下假设:氧化修饰,线粒体功能破坏和蛋白质降解受损构成执行神经元死亡的三个相互关联的分子途径。这些相互交织的事件是环境暴露,遗传因素和内源性风险的结果,并构成了一个“百慕大三角”,被认为是神经退行性发病机理的根本原因。

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