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职业性金属暴露与帕金森症

Occupational Metal Exposure and Parkinsonism.

作者信息

Caudle W Michael

机构信息

Department of Environmental Health, Rollins School of Public Health, Center for Neurodegenerative Disease, Emory University, 1518 Clifton Rd., NE, Claudia Nance Rollins Building, Room 2033, Atlanta, GA, 30322, USA.

出版信息

Adv Neurobiol. 2017;18:143-158. doi: 10.1007/978-3-319-60189-2_7.

Abstract

Parkinsonism is comprised of a host of neurological disorders with an underlying clinical feature of movement disorder, which includes many shared features of bradykinesia, tremor, and rigidity. These clinical outcomes occur subsequent to pathological deficits focused on degeneration or dysfunction of the nigrostriatal dopamine system and accompanying pathological inclusions of alpha-synuclein and tau. The heterogeneity of parkinsonism is equally matched with the complex etiology of this syndrome. While a small percentage can be attributed to genetic alterations, the majority arise from an environmental exposure, generally composed of pesticides, industrial compounds, as well as metals. Of these, metals have received significant attention given their propensity to accumulate in the basal ganglia and participate in neurotoxic cascades, through the generation of reactive oxygen species as well as their pathogenic interaction with intracellular targets in the dopamine neuron. The association between metals and parkinsonism is of critical concern to subsets of the population that are occupationally exposed to metals, both through current practices, such as mining, and emerging settings, like E-waste and the manufacture of metal nanoparticles. This review will explore our current understanding of the molecular and pathological targets that mediate metal neurotoxicity and lead to parkinsonism and will highlight areas of critical research interests that need to be addressed.

摘要

帕金森综合征由一系列神经系统疾病组成,其潜在临床特征为运动障碍,包括运动迟缓、震颤和僵硬等许多共同特征。这些临床症状出现在以黑质纹状体多巴胺系统变性或功能障碍以及伴随的α-突触核蛋白和tau病理包涵体为特征的病理缺陷之后。帕金森综合征的异质性与其复杂的病因相当。虽然一小部分可归因于基因改变,但大多数是由环境暴露引起的,通常包括农药、工业化合物以及金属。其中,金属因其倾向于在基底神经节中积累并通过产生活性氧以及与多巴胺神经元内细胞靶点的致病相互作用参与神经毒性级联反应而受到了广泛关注。金属与帕金森综合征之间的关联对于通过当前的做法(如采矿)以及新兴环境(如电子垃圾和金属纳米颗粒制造)职业性接触金属的人群亚组至关重要。本综述将探讨我们目前对介导金属神经毒性并导致帕金森综合征的分子和病理靶点的理解,并将突出需要解决的关键研究兴趣领域。

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