Jinnah H A, Hess Ellen J, Ledoux Mark S, Sharma Nutan, Baxter Mark G, Delong Mahlon R
Department of Neurology, Johns Hopkins University, Baltimore, Maryland 21287, USA.
Mov Disord. 2005 Mar;20(3):283-92. doi: 10.1002/mds.20364.
A large number of different genetic and acquired disorders of the nervous system may be associated with dystonia. To elucidate its pathogenesis and to facilitate the discovery of potential novel treatments, there has been a growing interest in the development of animal models and particularly rodent models. Multiple animal models for dystonia have now been developed and partially characterized. The results obtained from studies of these models often lead in very different directions, in part because the different models target different aspects of a very heterogeneous disorder. A recent workshop addressed four main issues affecting those who conduct dystonia research with animal models, including the different ways in which dystonic disorders can be modeled in rodents, key features that constitute a useful model, methods used in the evaluation of these models, and recommendations for future research. This review summarizes the main outcomes of this conference. 2005 Movement Disorder Society.
大量不同的神经系统遗传性和后天性疾病可能与肌张力障碍有关。为了阐明其发病机制并促进潜在新疗法的发现,人们对动物模型尤其是啮齿动物模型的开发越来越感兴趣。目前已经开发出多种肌张力障碍动物模型并对其进行了部分特征描述。从这些模型研究中获得的结果往往指向非常不同的方向,部分原因是不同的模型针对的是一种非常异质性疾病的不同方面。最近的一次研讨会讨论了影响使用动物模型进行肌张力障碍研究的四个主要问题,包括在啮齿动物中模拟肌张力障碍疾病的不同方法、构成有用模型的关键特征、评估这些模型所使用的方法以及对未来研究的建议。本综述总结了本次会议的主要成果。2005年运动障碍协会。