Mitsumoto H, Aprille J R, Wray S H, Nemni R, Bradley W G
Neurology. 1983 Apr;33(4):452-61. doi: 10.1212/wnl.33.4.452.
We studied skeletal muscles from eight chronic progressive external ophthalmoplegia patients with ragged-red fibers (group A), five CPEO patients without ragged-red fibers (group B), and five controls. The EM morphometric fraction of structurally abnormal mitochondria was increased in group A, and there was a similarly increased fraction of normal-appearing mitochondria in group B. State 3 respiration and uncoupled respiration were severely decreased in both groups. The morphometric mitochondrial fraction and respiratory functions were inversely related in all three groups. The cytochrome content in group A was normal; cytochromes b and cc1 were decreased in group B. These studies point to a central role of mitochondrial dysfunction in all types of CPEO, but the basic abnormalities remain to be elucidated.
我们研究了8例伴有破碎红纤维的慢性进行性眼外肌麻痹患者(A组)、5例无破碎红纤维的慢性进行性眼外肌麻痹患者(B组)的骨骼肌以及5名对照者的骨骼肌。A组结构异常线粒体的电镜形态计量分数增加,B组外观正常的线粒体分数也有类似增加。两组的状态3呼吸和非耦联呼吸均严重降低。在所有三组中,形态计量线粒体分数与呼吸功能呈负相关。A组的细胞色素含量正常;B组的细胞色素b和细胞色素c1减少。这些研究表明线粒体功能障碍在所有类型的慢性进行性眼外肌麻痹中起核心作用,但基本异常仍有待阐明。