Meijer A E, Vloedman A H
Histochemistry. 1980;69(3):217-32. doi: 10.1007/BF00489769.
Isolated mitochondria from skeletal muscles of human and animals with neuromuscular diseases may reveal a loosely coupled state of oxidative phosphorylation, which is characterized by a normal phosphorylation in the presence of a phosphate acceptor and a maximal respiration in the absence of a phosphate acceptor. Moreover in these cases activity of mitochondrial Mg2+-stimulated ATPase is strongly increased and cannot be stimulated by the uncoupler 2,4-dinitrophenol. In this communication a histochemical technique for the demonstration of activity of mitochondrial Mg2+-stimulated ATPase to characterize the coupling state of muscle mitochondria in tissue sections, is described. This tissue-saving technique is especially suitable for the study of human skeletal muscle diseases.
从患有神经肌肉疾病的人和动物的骨骼肌中分离出的线粒体可能显示出氧化磷酸化的松散偶联状态,其特征是在有磷酸受体存在时磷酸化正常,在无磷酸受体时呼吸作用达到最大。此外,在这些情况下,线粒体镁离子刺激的ATP酶活性会大幅增加,且不能被解偶联剂2,4-二硝基苯酚刺激。在本通讯中,描述了一种用于在组织切片中显示线粒体镁离子刺激的ATP酶活性以表征肌肉线粒体偶联状态的组织化学技术。这种节省组织的技术特别适用于人类骨骼肌疾病的研究。