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快速进展性遗传性犬脊髓性肌萎缩症中运动神经元的病理学

Pathology of motor neurons in accelerated hereditary canine spinal muscular atrophy.

作者信息

Cork L C, Griffin J W, Choy C, Padula C A, Price D L

出版信息

Lab Invest. 1982 Jan;46(1):89-99.

PMID:7054593
Abstract

Hereditary canine spinal muscular atrophy is a dominantly inherited lower motor neuron disease with three phenotypic variants: accelerated, intermediate, and chronic. Pups with the accelerated disease develop weakness by 1.5 months and are quadriparetic by 3 months. The motor neurons of selected brainstem nuclei and ventral horn of the spinal cord are characterized by chromatolysis and by neurofibrillary abnormalities in perikarya, dendrites, and, most strikingly, proximal axons. Dendrites and axons are segmentally enlarged by accumulations of maloriented fascicles of neurofilaments; the axonal swelling usually involve internodes and are delimited by the initial segment or nodes of Ranvier. The disorganized neurofilaments appear to entrap mitochondria and other particular organelles. We have hypothesized that the neurofibrillary changes in this genetic disorder in dogs is associated with an abnormality of the cytoskeletal constituents of motor neurons. Hereditary canine spinal muscular atrophy shows features in common with human motor neuron disease.

摘要

遗传性犬脊髓性肌萎缩症是一种显性遗传的下运动神经元疾病,有三种表型变异:快速型、中间型和慢性型。患快速型疾病的幼犬在1.5个月时出现肌无力,3个月时出现四肢瘫。选定的脑干核和脊髓腹角的运动神经元表现为染色质溶解,以及核周体、树突,最显著的是近端轴突出现神经原纤维异常。树突和轴突因神经丝束排列紊乱而节段性增粗;轴突肿胀通常累及节间,并由起始段或郎飞结界定。紊乱的神经丝似乎会困住线粒体和其他特定细胞器。我们推测,犬类这种遗传疾病中的神经原纤维变化与运动神经元细胞骨架成分的异常有关。遗传性犬脊髓性肌萎缩症表现出与人类运动神经元疾病的共同特征。

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