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帕金森病中多巴胺能神经元丢失的多重打击假说

Multiple hit hypotheses for dopamine neuron loss in Parkinson's disease.

作者信息

Sulzer David

机构信息

Department of Neurology, Black 309, 650 West, 168th Street, Columbia University, New York State Psychiatric Institute, New York City, NY 10032, USA.

出版信息

Trends Neurosci. 2007 May;30(5):244-50. doi: 10.1016/j.tins.2007.03.009. Epub 2007 Apr 5.

Abstract

Parkinson's disease arises from genetic and possibly neurotoxic causes that produce massive cell death of the neuromelanin-containing dopaminergic neurons of the substantia nigra. Loss of these neurons is essential for the diagnostic parkinsonian features. Although many genetic mutations have been suggested as causes or risk factors for Parkinson's disease, the low penetrance of some mutations and the low disease concordance in relatives suggests that there must be interactions between multiple factors. We suggest that 'multiple hits' that combine toxic stress, for example, from dopamine oxidation or mitochondrial dysfunction, with an inhibition of a neuroprotective response, such as loss of function of parkin or stress-induced autophagic degradation, underlie selective neuronal death. We discuss the properties of substantia nigra dopamine neurons that might make them particular targets of such multiple hits.

摘要

帕金森病源于遗传因素以及可能的神经毒性因素,这些因素会导致黑质中含神经黑色素的多巴胺能神经元大量死亡。这些神经元的丧失是帕金森病典型特征的关键所在。尽管许多基因突变被认为是帕金森病的病因或危险因素,但一些突变的低外显率以及亲属中疾病的低一致性表明,多种因素之间必然存在相互作用。我们认为,“多重打击”,例如多巴胺氧化或线粒体功能障碍引起的毒性应激,与神经保护反应的抑制(如帕金蛋白功能丧失或应激诱导的自噬降解)相结合,是选择性神经元死亡的基础。我们讨论了黑质多巴胺能神经元的特性,这些特性可能使它们成为此类多重打击的特定靶点。

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