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Astrocytes in Heavy Metal Neurotoxicity and Neurodegeneration
Brain Research ( IF 2.9 ) Pub Date : 2021-01-05 , DOI: 10.1016/j.brainres.2020.147234
Baoman Li 1 , Maosheng Xia 2 , Robert Zorec 3 , Vladimir Parpura 4 , Alexei Verkhratsky 5
Affiliation  

With the industrial development and progressive increase in environmental pollution, the mankind overexposure to heavy metals emerges as a pressing public health issue. Excessive intake of heavy metals, such as arsenic (As), manganese (Mn), mercury (Hg), aluminium (Al), lead (Pb), nickel (Ni), bismuth (Bi), cadmium (Cd), copper (Cu), zinc (Zn), and iron (Fe), is neurotoxic and it promotes neurodegeneration. Astrocytes are primary homeostatic cells in the central nervous system. They protect neurons against all types of insults, in particular by accumulating heavy metals. However, this makes astrocytes the main target for heavy metals neurotoxicity. Intake of heavy metals affects astroglial homeostatic and neuroprotective cascades including glutamate/GABA-glutamine shuttle, antioxidative machinery and energy metabolism. Deficits in these astroglial pathways facilitate or even instigate neurodegeneration. In this review, we provide a concise outlook on heavy metal-induced astrogliopathies and their association with major neurodegenerative disorders. In particular, we focus on astroglial mechanisms of iron-induced neurotoxicity. Iron deposits in the brain are detected in main neurodegenerative diseases, such as Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Accumulation of iron in the brain is associated with motor and cognitive impairments and iron-induced histopathological manifestations may be considered as the potential diagnostic biomarker of neurodegenerative diseases. Effective management of heavy metal neurotoxicity can be regarded as a potential strategy to prevent or retard neurodegenerative pathologies.



中文翻译:

重金属神经毒性和神经变性中的星形胶质细胞

随着工业的发展和环境污染的日益加剧,人类过度接触重金属已成为一个紧迫的公共卫生问题。过量摄入重金属,如砷(As)、锰(Mn)、汞(Hg)、铝(Al)、铅(Pb)、镍(Ni)、铋(Bi)、镉(Cd)、铜( Cu)、锌 (Zn) 和铁 (Fe) 具有神经毒性并促进神经退行性变。星形胶质细胞是中枢神经系统中的主要稳态细胞。它们保护神经元免受所有类型的伤害,特别是通过积累重金属。然而,这使得星形胶质细胞成为重金属神经毒性的主要目标。摄入重金属会影响星形胶质细胞稳态和神经保护级联反应,包括谷氨酸/GABA-谷氨酰胺穿梭、抗氧化机制和能量代谢。这些星形胶质细胞通路的缺陷会促进甚至引发神经退行性变。在这篇综述中,我们简要介绍了重金属诱导的星形胶质细胞病及其与主要神经退行性疾病的关系。特别是,我们专注于铁诱导的神经毒性的星形胶质细胞机制。在主要的神经退行性疾病中检测到大脑中的铁沉积物,例如阿尔茨海默病、帕金森病和肌萎缩侧索硬化症。大脑中铁的积累与运动和认知障碍有关,铁诱导的组织病理学表现可能被认为是神经退行性疾病的潜在诊断生物标志物。重金属神经毒性的有效管理可被视为预防或延缓神经退行性疾病的潜在策略。

更新日期:2021-01-05
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