The neurobiology of the substantia nigra pars compacta: from motor to sleep regulation.

Marcelo M S Lima, Angela B B Reksidler, Maria A B F Vital
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引用次数: 27

Abstract

Clinical characteristics of Parkinson's disease (PD) are the result of the degeneration of the neurons of the substantia nigra pars compacta (SNpc). Several mechanisms are implicated in the degeneration of nigrostriatal neurons such as oxidative stress, mitochondrial dysfunction, protein misfolding, disturbances of dopamine (DA) metabolism and transport, neuroinflammation, and necrosis/apoptosis. The literature widely explores the neurotoxic models elicited by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and 6-hydroxydopamine (6-OHDA). Because of the models, it is known that basal ganglia, particularly substantia nigra, have been related to a diversity of functions, from motor to sleep regulation. Nevertheless, a current debate concerning the role of DA on the sleep-wake cycle is in progress. In summary, it is suggested that the dopaminergic system is implicated in the physiology of sleep, with particular regard to the influence of the SNpc neurons. The understanding of the functioning and connectivity of the SNpc neurons has become fundamental to discovering the neurobiology of these neurons.

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黑质致密部的神经生物学:从运动到睡眠调节。
帕金森病(PD)的临床特征是黑质致密部(SNpc)神经元退行性变的结果。黑质纹状体神经元变性涉及多种机制,如氧化应激、线粒体功能障碍、蛋白质错误折叠、多巴胺(DA)代谢和运输紊乱、神经炎症和坏死/凋亡。文献广泛探讨了1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)和6-羟基多巴胺(6-OHDA)引起的神经毒性模型。由于这些模型,我们知道基底神经节,特别是黑质,与从运动到睡眠调节的多种功能有关。然而,目前关于DA在睡眠-觉醒周期中的作用的争论正在进行中。总之,这表明多巴胺能系统与睡眠生理学有关,特别是SNpc神经元的影响。对SNpc神经元的功能和连通性的理解已经成为发现这些神经元的神经生物学的基础。
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