Cork L C
Division of Comparative Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Can J Neurol Sci. 1991 Aug;18(3 Suppl):432-4. doi: 10.1017/s0317167100032613.
Motor neuron diseases selectively produce degeneration and death of motor neurons; the pathogenesis of these disorders and the specificity for this population of neurons are unknown. Hereditary Canine Spinal Muscular Atrophy produces a lower motor neuron disease which is clinically and pathologically similar to human motor neuron disease: motor neurons dysfunction and degenerate. The canine model provides an opportunity to investigate early stages of disease when there are viable motor neurons still present and might be responsive to a variety of therapeutic interventions. The canine disease, like the human disease, is inherited as an autosomal dominant. The extensive canine pedigree of more than 200 characterized individuals permits genetic analysis using syntenic linkage techniques which may identify a marker for the canine trait and provide insights into homologous regions for study in human kindreds.
运动神经元疾病选择性地导致运动神经元的退化和死亡;这些疾病的发病机制以及对这一神经元群体的特异性尚不清楚。遗传性犬脊髓性肌萎缩症会引发一种下运动神经元疾病,在临床和病理上与人类运动神经元疾病相似:运动神经元功能障碍并退化。犬类模型提供了一个机会,可以在仍有存活的运动神经元且可能对多种治疗干预有反应的疾病早期阶段进行研究。犬类疾病与人类疾病一样,以常染色体显性方式遗传。超过200个已鉴定个体的广泛犬类谱系允许使用同线连锁技术进行遗传分析,这可能会识别出犬类性状的一个标记,并为在人类家族中进行研究的同源区域提供见解。