帕金森病触发内源性神经保护机制:细胞模型研究

M J Zigmond
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引用次数: 16

摘要

神经胶质细胞系来源的神经营养因子(GDNF)参与了帕金森病(PD)动物模型中多巴胺(DA)神经元免受氧化应激的保护。我们现在已经证明,在多巴胺能细胞系和大鼠黑质(SN)制备的原代DA神经元培养物中,GDNF也可以防止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)的几种亚型磷酸化的快速和短暂增加。我们的证据表明,ERK的激活也可以被活性氧(ROS)调节,包括内源性DA产生的活性氧。识别这些途径的触发方式应该为PD的病理生理学提供见解,并可能为延缓疾病的进展提供有用的途径。
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Triggering endogenous neuroprotective mechanisms in Parkinson's disease: studies with a cellular model.

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.

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