Meijer A E
Department of Neurology, University of Amsterdam, The Netherlands.
Acta Histochem. 1991;90(2):147-54. doi: 10.1016/s0065-1281(11)80053-x.
The localization of reduced glutathione in skeletal muscle fibres of patients with inherited or acquired neuromuscular diseases and of subjects with no apparent disease of the neuromuscular system was studied histochemically. In healthy human skeletal muscle fibres, the level of reduced glutathione is higher in aerobic type I fibres than in anaerobic type II fibres. This finding suggests that glutathione in these healthy fibres is held in the reduced state chiefly by the activity of the decarboxylating and NADPH regenerating enzyme NADP(+)-dependent isocitrate dehydrogenase. In diseased muscle fibres, there is generally a positive relationship between the activity of the NADPH producing enzymes glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase and the level of reduced glutathione. This positive relationship suggests that glutathione in these diseased fibres is held in the reduced state chiefly by the activity of both enzymes of the pentose phosphate pathway.
采用组织化学方法研究了遗传性或获得性神经肌肉疾病患者以及无明显神经肌肉系统疾病受试者骨骼肌纤维中还原型谷胱甘肽的定位。在健康人骨骼肌纤维中,有氧I型纤维中的还原型谷胱甘肽水平高于无氧II型纤维。这一发现表明,这些健康纤维中的谷胱甘肽主要通过脱羧和NADPH再生酶NADP(+)-依赖异柠檬酸脱氢酶的活性保持在还原状态。在患病肌肉纤维中,产生NADPH的酶葡萄糖-6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶的活性与还原型谷胱甘肽水平之间通常存在正相关。这种正相关表明,这些患病纤维中的谷胱甘肽主要通过磷酸戊糖途径的两种酶的活性保持在还原状态。