Rowland L P
Muscle Nerve. 1980 Jan-Feb;3(1):3-20. doi: 10.1002/mus.880030103.
In Duchenne muscular dystrophy, as in other genetic diseases, there must be a biochemical abnormality. This fundamental genetic fault has not been identified, but several indirect lines of evidence suggest that the surface membranes of skeletal muscle are affected. The biochemical evidence implies abnormal egress of soluble enzymes and other proteins from muscle, abnormal permeability, and altered properties of membrane-bound enzymes. As a result of the presumed genetic abnormality, functional properties are altered, and impaired regulation of intracellular calcium content could be responsible for the hallmarks of the disease--progressive weakness and degeneration of muscle. The evidence is by no means conclusive, however, and some of it is contradictory. Technical advances must be made before isolated membranes can be characterized biochemically. Other theories are also being evaluated.
在杜兴氏肌营养不良症中,与其他遗传性疾病一样,必定存在生化异常。这种根本的基因缺陷尚未得到确认,但几条间接证据表明骨骼肌的表面膜受到了影响。生化证据表明,可溶性酶和其他蛋白质从肌肉中异常流出、通透性异常以及膜结合酶的性质改变。由于推测的基因异常,功能特性发生改变,细胞内钙含量调节受损可能是该疾病特征——进行性肌无力和肌肉退化的原因。然而,这些证据绝非确凿无疑,其中一些相互矛盾。在能够对分离出的膜进行生化特性分析之前,必须取得技术进步。其他理论也正在评估之中。