Green S L, Tolwani R J
Department of Comparative Medicine, Stanford University School of Medicine, California, USA.
Lab Anim Sci. 1999 Oct;49(5):480-7.
Motor neuron disease is a general term applied to a broad class of neurodegenerative diseases that are characterized by fatally progressive muscular weakness, atrophy, and paralysis attributable to loss of motor neurons. At present, there is no cure for most motor neuron diseases, including amyotrophic lateral sclerosis (ALS), the most common human motor neuron disease--the cause of which remains largely unknown. Animal models of motor neuron disease (MND) have significantly contributed to the remarkable recent progress in understanding the cause, genetic factors, and pathologic mechanisms proposed for this class of human neurodegenerative disorders. Largely driven by ALS research, animal models of MND have proven their usefulness in elucidating potential causes and specific pathogenic mechanisms, and have helped to advance promising new treatments from "benchside to bedside." This review summarizes important features of selected established animal models of MND: genetically engineered mice and inherited or spontaneously occurring MND in the murine, canine, and equine species.
运动神经元病是一个通用术语,适用于一大类神经退行性疾病,其特征是由于运动神经元丧失导致致命性进行性肌肉无力、萎缩和瘫痪。目前,大多数运动神经元疾病,包括最常见的人类运动神经元疾病——肌萎缩侧索硬化症(ALS),都无法治愈,其病因在很大程度上仍然未知。运动神经元病(MND)的动物模型为最近在理解这类人类神经退行性疾病的病因、遗传因素和病理机制方面取得的显著进展做出了重大贡献。在很大程度上受ALS研究的推动,MND的动物模型已证明其在阐明潜在病因和特定致病机制方面的有用性,并有助于将有前景的新疗法从“实验室推向临床”。本综述总结了选定的已建立的MND动物模型的重要特征:基因工程小鼠以及小鼠、犬和马等物种中遗传性或自发发生的MND。