Black J T, Judge D, Demers L, Gordon S
J Neurol Sci. 1975 Dec;26(4):479-88. doi: 10.1016/0022-510x(75)90048-9.
Histochemical, ultrastructural and biochemical studies were performed on muscle biopsy specimens from a 30-year-old man with proximal limb weakness. Modified Gomori trichome stains of anterior tibial muscle revealed accumulations of red-staining material in the subsarcolemmal and intermyofibrillar regions of virtually every fiber (ragged-red fibers); these accumulations were rich in oxidative enzymes. Electron microscopy of this muscle showed that the red-staining areas consisted of large collections of abnormal-appearing mitochondria. Mitochondria isolated from the quadriceps muscle showed lack of respiratory control with alpha-glycerophosphate as substrate. However, the lack of respiratory control with alpha-glycerophosphate must be interpreted with caution since the quadriceps muscle was severely degenerated, and biochemical alterations of mitochondria may occur secondary to muscle degeneration itself. Nevertheless, this is the second reported case of lack of respiratory control with alpha-glycerophosphate in a patient with ragged-red fibers. Further interpretation of this defect and its significance must await more studies to determine whether this muscle mitochondrial abnormality is a common finding in the disorders in which ragged-red fibers are encountered.
对一名患有近端肢体无力的30岁男性的肌肉活检标本进行了组织化学、超微结构和生化研究。胫骨前肌的改良Gomori三色染色显示,几乎每根肌纤维的肌膜下和肌原纤维间区域都有红色染色物质的积聚(破碎红纤维);这些积聚富含氧化酶。该肌肉的电子显微镜检查显示,红色染色区域由大量外观异常的线粒体聚集而成。从股四头肌分离出的线粒体以α-甘油磷酸为底物时显示出呼吸控制缺失。然而,由于股四头肌严重退化,线粒体的生化改变可能继发于肌肉退化本身,因此对α-甘油磷酸呼吸控制缺失的解释必须谨慎。尽管如此,这是第二例报道的患有破碎红纤维的患者中α-甘油磷酸呼吸控制缺失的病例。对这一缺陷及其意义的进一步解释必须等待更多研究,以确定这种肌肉线粒体异常是否是在出现破碎红纤维的疾病中的常见发现