WHITE L P
Calif Med. 1959 Jan;90(1):1-8.
In a study of 58 patients with various diseases of muscle or of the neuromuscular system, the serum activity of various enzymes was measured. Abnormal elevation of serum activities of aldolase, lactic dehydrogenase and, to a lesser extent, glutamic-oxalacetic transaminase and phosphohexose isomerase, was an almost constant feature in patients with progressive muscular dystrophy. These elevations were very frequent in dermatomyositis, common in acute cerebral vascular accidents, and rarely seen in other neurological disorders. Abnormal serum activity of iso-citric dehydrogenase was not observed in the course of the present study. Supplementary protein feeding of patients with muscular dystrophy had no effect on serum enzyme activity, no consistent effect on urinary creatine excretion and no effect on the strength of the patient or the course of the disease. Dystrophic muscles from a dystrophic strain of mice showed a decrease in activity of lactic dehydrogenase and aldolase below that of control muscle and an increase of iso-citric dehydrogenase activity. These findings, taken with the differences in serum activities of lactic dehydrogenase, aldolase and isocitric dehydrogenase in the dystrophic animals, support the conclusion that dystrophic animals handle these soluble enzymes in quite different ways.
在一项针对58名患有各种肌肉或神经肌肉系统疾病患者的研究中,对各种酶的血清活性进行了测定。在进行性肌营养不良患者中,醛缩酶、乳酸脱氢酶以及程度较轻的谷草转氨酶和磷酸己糖异构酶的血清活性异常升高几乎是一个恒定特征。这些升高在皮肌炎中非常常见,在急性脑血管意外中较为常见,而在其他神经系统疾病中很少见。在本研究过程中未观察到异柠檬酸脱氢酶的血清活性异常。给肌营养不良患者补充蛋白质对血清酶活性没有影响,对尿肌酸排泄没有一致的影响,对患者的肌力或疾病进程也没有影响。来自肌营养不良小鼠品系的营养不良肌肉显示,乳酸脱氢酶和醛缩酶的活性低于对照肌肉,而异柠檬酸脱氢酶活性增加。这些发现,结合营养不良动物中乳酸脱氢酶、醛缩酶和异柠檬酸脱氢酶血清活性的差异,支持了这样的结论:营养不良动物以截然不同的方式处理这些可溶性酶。