Kunz W S, Winkler K, Kuznetsov A V, Lins H, Kirches E, Wallesch C W
Klinik für Neurologie, Universitätsklinikum Magdeburg, Germany.
Mol Cell Biochem. 1997 Sep;174(1-2):97-100.
The mitochondrial function in skeletal muscle biopsies of three patients with chronic progressive external ophthalmoplegia, having deletions of the mitochondrial DNA, was studied by laser-excited fluorescence measurements of NAD(P)H and flavoproteins in saponin-skinned fibers. We detected substantially elevated steady state redox states of the mitochondrial NAD-system in the muscle fibers of these patients. Moreover, the respiratory chain-linked autofluorescence changes in the muscle fibers of these patients were larger in comparison to controls indicating substantial alterations of the mitochondrial content. These results are in line with the presence of elevated numbers of partially respiratory chain inhibited mitochondria in the skeletal muscle of chronic progressive external ophthalmoplegia patients.
对三名患有慢性进行性外眼肌麻痹且线粒体DNA缺失的患者的骨骼肌活检组织中的线粒体功能进行了研究,通过对皂素透皮纤维中NAD(P)H和黄素蛋白进行激光激发荧光测量。我们检测到这些患者肌肉纤维中线粒体NAD系统的稳态氧化还原状态显著升高。此外,与对照组相比,这些患者肌肉纤维中呼吸链相关的自发荧光变化更大,表明线粒体含量有实质性改变。这些结果与慢性进行性外眼肌麻痹患者骨骼肌中部分呼吸链受抑制的线粒体数量增加一致。