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肌营养不良性骨骼肌线粒体的氧化代谢缺陷。

Defective oxidative metabolism of myodystrophic skeletal muscle mitochondria.

作者信息

Lee C P, Martens M E, Jankulovska L, Neymark M A

出版信息

Muscle Nerve. 1979 Sep-Oct;2(5):340-8. doi: 10.1002/mus.880020504.

Abstract

A small-scale procedure for preparing tightly coupled intact skeletal muscle mitochondria from myodystrophic (myd/myd) mice is described. Mitochondrial preparations derived from heart, liver, and skeletal muscle of myd/myd and their littermate (+/?) controls are characterized with respect to their cytochrome content and their oxidative and phosphorylative capacities. Our data indicate that there is an impairment in the NADH CoQ region of the respiratory chain of myodystrophic skeletal muscle mitochondria. Both heart and liver mitochondria of myd/myd exhibited normal activities of respiratory chain-linked oxidative phosphorylation.

摘要

本文描述了一种从小鼠肌营养不良症(myd/myd)小鼠制备紧密偶联的完整骨骼肌线粒体的小规模方法。对来自myd/myd小鼠及其同窝对照(+/?)的心脏、肝脏和骨骼肌的线粒体提取物进行了细胞色素含量、氧化能力和磷酸化能力的表征。我们的数据表明,肌营养不良症骨骼肌线粒体呼吸链的NADH辅酶Q区域存在损伤。myd/myd小鼠的心脏和肝脏线粒体均表现出呼吸链相关氧化磷酸化的正常活性。

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