Niebrój-Dobosz I
J Neurol. 1976 Nov 26;214(1):61-9. doi: 10.1007/BF00313489.
In Duchenne muscular dystrophy the activity of (Na+ + K+)ATPase in erythrocyte ghosts is reduced and its reaction to ouabain is paradoxical both in low sodium and high sodium systems. No such changes were seen in a case of Becker dystrophy, in limb-girdle dystrophy, and in neurogenic atrophy of muscles. In myotonic dystrophy and congenital myotonia the activity of ATPase and its inhibition by ouabain were depressed.
在杜兴氏肌营养不良症中,红细胞膜空壳中(钠+钾)ATP酶的活性降低,并且在低钠和高钠系统中其对哇巴因的反应是反常的。在贝克肌营养不良症、肢带型肌营养不良症和肌肉神经源性萎缩病例中未观察到此类变化。在强直性肌营养不良症和先天性肌强直中,ATP酶的活性及其被哇巴因的抑制作用均降低。