Sherer Todd B, Betarbet Ranjita, Greenamyre J Timothy
Department of Neurology, Emory University, Atlanta, Georgia 30322, USA.
Neuroscientist. 2002 Jun;8(3):192-7. doi: 10.1177/1073858402008003004.
Parkinson's disease (PD) is a common and disabling neurodegenerative disease marked by progressive motor dysfunction, which results from selective degeneration of the nigrostriatal pathway. Epidemiological studies indicate that exposure to pesticides, rural living, farming, and drinking well water are associated with an increased risk of developing PD. Rare cases of PD are caused by mutations in nuclear genes, and there is increasing evidence for susceptibility genes that alter disease risk. Parkinson's disease is also associated with a systemic defect in mitochondrial complex I activity. Animal models indicate that exposure to inhibitors of mitochondrial complex I, including pesticides, is sufficient to reproduce the features of PD, but genetic factors clearly modulate susceptibility. Complex I defects may result in oxidative stress and increase the susceptibility of neurons to excitotoxic death. In this way, environmental exposures and mitochondrial dysfunction may interact and result in neurodegeneration.
帕金森病(PD)是一种常见的、使人致残的神经退行性疾病,其特征为进行性运动功能障碍,由黑质纹状体通路的选择性退化所致。流行病学研究表明,接触杀虫剂、农村生活、务农以及饮用井水与患帕金森病风险增加有关。罕见的帕金森病病例由核基因突变引起,并且越来越多的证据表明存在改变疾病风险的易感基因。帕金森病还与线粒体复合体I活性的系统性缺陷有关。动物模型表明,接触包括杀虫剂在内的线粒体复合体I抑制剂足以重现帕金森病的特征,但遗传因素显然会调节易感性。复合体I缺陷可能导致氧化应激,并增加神经元对兴奋性毒性死亡的易感性。通过这种方式,环境暴露和线粒体功能障碍可能相互作用并导致神经退行性变。