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神经退行性变与神经递质的运输。

Neural degeneration and the transport of neurotransmitters.

作者信息

Edwards R H

机构信息

Department of Neurology, UCLA School of Medicine 90024-1769.

出版信息

Ann Neurol. 1993 Nov;34(5):638-45. doi: 10.1002/ana.410340504.

DOI:10.1002/ana.410340504
PMID:7902065
Abstract

A number of neurodegenerative diseases selectively affect distinct neuronal populations, but the mechanisms responsible for selective cell vulnerability have generally remained unclear. The toxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) reproduces the selective degeneration of dopaminergic neurons in the substantia nigra characteristic of Parkinson's disease. The plasma membrane dopamine transporter mediates this selective toxicity through accumulation of the active metabolite N-methyl-4-phenylpyridinium (MPP+). In contrast, the vesicular amine transporter protects against this form of injury by sequestering the toxin from its primary site of action in mitochondria. Together with the identification of defects in glutamate transport from patients with amyotrophic lateral sclerosis, these observations suggest that neurotransmitter transport may have a major role in neurodegenerative disease. The recent cloning of cDNAs encoding these transport proteins will help to explore this hypothesis.

摘要

许多神经退行性疾病会选择性地影响不同的神经元群体,但导致选择性细胞易损性的机制通常仍不清楚。毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)会导致帕金森病特有的黑质中多巴胺能神经元选择性退化。质膜多巴胺转运体通过积累活性代谢物N-甲基-4-苯基吡啶鎓(MPP+)介导这种选择性毒性。相比之下,囊泡胺转运体通过将毒素与线粒体中的主要作用位点隔离来防止这种形式的损伤。结合对肌萎缩侧索硬化症患者谷氨酸转运缺陷的鉴定,这些观察结果表明神经递质转运可能在神经退行性疾病中起主要作用。最近对编码这些转运蛋白的cDNA进行克隆将有助于探索这一假说。

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