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触发帕金森病内源性神经保护机制:细胞模型研究

Triggering endogenous neuroprotective mechanisms in Parkinson's disease: studies with a cellular model.

作者信息

Zigmond M J

机构信息

Department of Neurology, University of Pittsburgh, Pittsburgh, PA 15213, USA.

出版信息

J Neural Transm Suppl. 2006(70):439-42. doi: 10.1007/978-3-211-45295-0_66.

Abstract

Glial cell line-derived neurotrophic factor (GDNF) has been implicated in the protection of dopamine (DA) neurons from oxidative stress in animal models of Parkinson's disease (PD). We have now shown that GDNF can also protect against the effects of 6-hydroxydopamine (6-OHDA) in a dopaminergic cell line and in cultures of primary DA neurons prepared from rat substantia nigra (SN). This appears to involve a rapid and transient increase in the phosphorylation of several isoforms of extracellular signal-regulated kinase (ERK). Our evidence indicates that ERK activation also can be modulated by reactive oxygen species (ROS), including those generated by endogenous DA. Identification of the ways by which these pathways can be triggered should provide insights into the pathophysiology of PD, and may offer useful avenues for retarding the progression of the disorder.

摘要

胶质细胞源性神经营养因子(GDNF)在帕金森病(PD)动物模型中对多巴胺(DA)神经元免受氧化应激损伤方面发挥了作用。我们现已表明,GDNF还能保护多巴胺能细胞系以及从大鼠黑质(SN)制备的原代DA神经元培养物免受6-羟基多巴胺(6-OHDA)的影响。这似乎涉及细胞外信号调节激酶(ERK)几种同工型磷酸化的快速短暂增加。我们的证据表明,ERK激活也可被活性氧(ROS)调节,包括内源性DA产生的ROS。确定触发这些途径的方式应能为PD的病理生理学提供见解,并可能为延缓该疾病的进展提供有用的途径。

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