Vrbová G, Ward K
J Neurol Neurosurg Psychiatry. 1981 Nov;44(11):1002-6. doi: 10.1136/jnnp.44.11.1002.
The deterioration of tibialis anterior (TA) and extensor digitorum longus (EDL) muscles in dystrophic mice (C 57 BL dy/dy) was compared. The effects of chronic electrical stimulation on various characteristic properties of these muscles were also studied. The results indicate that EDL muscles are less affected by the disease than TA. This "selectivity" is difficult to explain since both muscles have similar fibre type composition. TA and EDL muscles that were stimulated for 10-28 days developed greater tetanic tensions than the contralateral muscles, but this effect was apparent only when the muscles were severely affected by the disease, that is the contralateral TA or EDL muscles developed less than 50% of the tension produced by muscles from normal animals. In all EDL muscles, stimulation increased the fatigue resistance. The time course of contraction and relaxation of dystrophic muscles is usually slower than that of normal muscles. The stimulation reduced this slowing effect, so that the stimulated muscles became similar to homologous muscles from normal littermates.
比较了营养不良小鼠(C 57 BL dy/dy)胫前肌(TA)和趾长伸肌(EDL)的退化情况。还研究了慢性电刺激对这些肌肉各种特性的影响。结果表明,EDL肌肉受疾病影响比TA小。这种“选择性”难以解释,因为这两块肌肉具有相似的纤维类型组成。接受10 - 28天刺激的TA和EDL肌肉比其对侧肌肉产生了更大的强直张力,但这种效应仅在肌肉受到严重疾病影响时才明显,即对侧TA或EDL肌肉产生的张力不到正常动物肌肉产生张力的50%。在所有EDL肌肉中,刺激增加了抗疲劳能力。营养不良肌肉的收缩和舒张时间进程通常比正常肌肉慢。刺激减少了这种减慢效应,使得受刺激的肌肉变得与来自正常同窝小鼠的同源肌肉相似。