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帕金森病的神经病理学。

Neuropathology of Parkinson disease.

机构信息

Department of Neuroscience, Mayo Clinic, Jacksonville, FL, United States.

出版信息

Parkinsonism Relat Disord. 2018 Jan;46 Suppl 1(Suppl 1):S30-S33. doi: 10.1016/j.parkreldis.2017.07.033. Epub 2017 Aug 1.

Abstract

INTRODUCTION

Parkinson's disease (PD) is characterized by bradykinesia, rigidity, postural instability and tremor. Several pathologic processes can produce this syndrome, but neurodegeneration accompanied by neuronal inclusions composed of α-synuclein (Lewy bodies) is considered the typical pathologic correlate of PD.

METHODS

The neuropathologic features of PD are reviewed based upon personal experience and review of the literature. Molecular pathology of PD is summarized from cell biological and animal studies.

RESULTS

The pathologic feature that correlates with signs and symptoms of PD is neuronal loss in the substantia nigra with dopaminergic denervation of the striatum. Neuronal degeneration in the substantia nigra preferentially affects the ventrolateral cell group that projects to posterolateral putamen and is accompanied by formation of Lewy bodies composed of aggregated α-synuclein. Some patients with PD are found at autopsy to have other pathologic processes, such as multiple system atrophy, progressive supranuclear palsy and cerebrovascular disease (vascular Parkinsonism). The peripheral autonomic nervous system is also affected. The triggering event in PD is unknown, but recent studies suggest a role for loss of nuclear membrane integrity. Once α-synuclein aggregates forms, evidence supports cell-to-cell propagation.

CONCLUSION

PD is a multisystem synucleinopathy caused by poorly characterized genetic and environmental factors that produces degeneration in selectively vulnerable neuronal populations.

摘要

简介

帕金森病(PD)的特征为运动迟缓、肌肉僵直、姿势不稳和震颤。许多病理过程都可能导致这种综合征,但伴有α-突触核蛋白(路易体)组成的神经元内包涵体的神经退行性变被认为是 PD 的典型病理相关物。

方法

根据个人经验和文献复习,综述 PD 的神经病理学特征。从细胞生物学和动物研究中总结 PD 的分子病理学。

结果

与 PD 的症状和体征相关的病理特征是黑质神经元丧失伴纹状体多巴胺能神经支配丧失。黑质神经元变性优先影响腹外侧细胞群,该细胞群投射到后外侧壳核,并伴有聚集的α-突触核蛋白组成的路易体形成。一些 PD 患者尸检时还发现其他病理过程,如多系统萎缩、进行性核上性麻痹和脑血管病(血管性帕金森病)。周围自主神经系统也受到影响。PD 的触发事件尚不清楚,但最近的研究表明核膜完整性丧失起作用。一旦α-突触核蛋白聚集形成,就有证据支持细胞间传播。

结论

PD 是一种多系统突触核蛋白病,由特征尚不明确的遗传和环境因素引起,选择性地导致易损神经元群体的变性。

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