Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.
Int Rev Cell Mol Biol. 2010;281:229-66. doi: 10.1016/S1937-6448(10)81006-8.
Parkinson's disease is a complex disease characterized by a progressive degeneration of nigrostriatal dopaminergic neurons. The development of this condition is defined by the interaction between the genetic constitution of an organism and environmental factors. Analysis of the genes associated with development of monogenic forms of disease has allowed pointing out several mechanisms involved in Parkinson's disease pathogenesis such as the ubiquitin-proteasome degradation, differentiation of dopaminergic neurons, mitochondrial dysfunction, oxidative damage, and others. In this review, a variety of data which throw light on molecular mechanisms underlying pathogenesis of Parkinson's disease will be considered.
帕金森病是一种复杂的疾病,其特征是黑质纹状体多巴胺能神经元进行性退化。这种疾病的发展是由生物体的遗传构成与环境因素之间的相互作用所定义的。对与单基因疾病形式的发展相关的基因的分析,已经能够指出几种涉及帕金森病发病机制的机制,如泛素-蛋白酶体降解、多巴胺能神经元分化、线粒体功能障碍、氧化损伤等。在这篇综述中,将考虑各种阐明帕金森病发病机制的分子机制的数据。