Cork L C, Griffin J W, Munnell J F, Lorenz M D, Adams R J
J Neuropathol Exp Neurol. 1979 May;38(3):209-21. doi: 10.1097/00005072-197905000-00002.
Hereditary canine spinal muscular atrophy is a newly recognized motor neuron disease occurring in Brittany Spaniels. The clinical manifestations, pattern of inheritance, electrodiagnostic findings, and muscle biopsies have features in common with human spinal muscular atrophy. Neuropathological examination discloses some loss of motor neurons in the spinal cord and brainstem. Many of the surviving motor neurons have neurofibrillary swellings in proximal axons, an abnormality similar to that which occurs early in the course of human amyotrophic lateral sclerosis. These axonal swellings are filled with maloriented skeins of neurofilaments. Since the proteins comprising neurofilaments are carried by slow axonal transport, their accumulation within axons suggest that the swellings may result from impaired slow transport, a hypothesis that can be tested in affected Brittany Spaniels. Hereditary canine spinal muscular atrophy is a new genetic, clinical, and pathological entity, and, at present, it appears to be the best currently available animal model of motor neuron disease.
遗传性犬脊髓性肌萎缩症是一种新发现的发生于不列塔尼猎犬的运动神经元疾病。其临床表现、遗传模式、电诊断结果及肌肉活检与人类脊髓性肌萎缩症有共同特征。神经病理学检查显示脊髓和脑干中有一些运动神经元缺失。许多存活的运动神经元在近端轴突中有神经原纤维肿胀,这一异常与人类肌萎缩侧索硬化症病程早期出现的异常相似。这些轴突肿胀内充满了排列紊乱的神经丝束。由于构成神经丝的蛋白质是通过轴突慢速运输携带的,它们在轴突内的积累表明肿胀可能是由慢速运输受损导致的,这一假说可在患病的不列塔尼猎犬中进行检验。遗传性犬脊髓性肌萎缩症是一种新的遗传、临床和病理实体,目前,它似乎是目前可得的最佳运动神经元疾病动物模型。