Fukuhara N, Suzuki M, Tsubaki T, Kushiro S, Takasawa N
Acta Neuropathol. 1985;66(4):283-91. doi: 10.1007/BF00690960.
Ultrastructural studies on muscle biopsies from three patients with Becker's muscular dystrophy showed that the i.m. nerves presented loss or disarrangement of the neurofilaments and an increased number of glycogen granules and/or myelin figures not infrequently in the myelinated and unmyelinated nerve fibers. The neuromuscular junctions showed markedly widened sole-plate areas, and several terminal axons frequently abutted and formed neuromuscular junctions on the same fiber. The secondary synaptic clefts were markedly decreased in number and short in length in type I fibers but not in type II fibers. Most terminal axons showed no degenerative changes. Therefore, the participation of a neural factor might be suggested as the cause of Becker's muscular dystrophy, although it does not mean denervation in the conventional sense of an axonal degeneration.
对三名贝克型肌营养不良症患者的肌肉活检进行的超微结构研究表明,肌内神经呈现神经丝丢失或排列紊乱,并且在有髓和无髓神经纤维中,糖原颗粒和/或髓鞘样结构的数量经常增加。神经肌肉接头显示终板区域明显增宽,并且几条终末轴突经常在同一纤维上毗邻并形成神经肌肉接头。I型纤维中的次级突触间隙数量明显减少且长度较短,而II型纤维中则不然。大多数终末轴突未显示退行性变化。因此,尽管这并不意味着传统意义上轴突变性的失神经支配,但可能提示神经因素参与了贝克型肌营养不良症的病因。