Department of Neurology, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Prog Brain Res. 2010;184:53-87. doi: 10.1016/S0079-6123(10)84004-X.
The identification of several mutations causing familial forms of Parkinson's disease (PD) has led to the creation of multiple lines of mice expressing similar genetic alterations. These models present a unique opportunity for understanding pathophysiological mechanisms leading to PD in a mammalian brain and provide models that are suitable for the preclinical testing of new therapies. Different lines of mice recapitulate the symptoms and pathological features of PD to various extents. This chapter examines their respective advantages and highlights some of the key findings that have already emerged from the analysis of these new models of PD.
几种导致家族性帕金森病 (PD) 的突变的鉴定导致了多种表达类似遗传改变的小鼠品系的创建。这些模型为在哺乳动物大脑中理解导致 PD 的病理生理机制提供了独特的机会,并提供了适合新疗法临床前测试的模型。不同的小鼠品系在不同程度上再现了 PD 的症状和病理特征。本章考察了它们各自的优势,并强调了从这些新的 PD 模型分析中已经出现的一些关键发现。