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Spinal motor neurones in murine muscular dystrophy and spinal muscular atrophy: A quantitative histological study

机译:鼠肌营养不良和脊髓性肌萎缩症中的脊髓运动神经元:定量组织学研究

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摘要

Recent electrophysiological studies of human and mouse muscular dystrophy have prompted the hypothesis that both are of neurogenic rather than myogenic origin. A decreased number of spinal motor neurones might be expected if this hypothesis were correct. The total number of neurones in the anterior grey horns of seven normal mice, six Bar Harbor 129 strain dystrophic mice, and six mice suffering from genetically-determined spinal muscular atrophy have been counted. The number of neurones in the cell types believed to include the motor neurones was significantly reduced to 13 to 71% of normal in mice with spinal muscular atrophy. In mice with muscular dystrophy, the number of anterior horn neurones was higher rather than lower than normal. The significance of these findings is discussed.
机译:对人和小鼠肌肉营养不良症的最新电生理学研究提出了这样的假设:两者都是神经源性而非肌源性。如果这个假设是正确的,那么脊髓运动神经元的数量将会减少。已经计数了七只正常小鼠,六只Bar Harbor 129品系营养不良小鼠和六只患有遗传学确定的脊髓性肌萎缩症的小鼠的前灰角中神经元的总数。在患有脊髓性肌萎缩症的小鼠中,据信包括运动神经元的细胞类型中的神经元数量显着减少至正常的13%至71%。在患有肌营养不良症的小鼠中,前角神经元的数量多于正常人,而不是少于正常人。讨论了这些发现的意义。

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