Martin H, Ontell M
Department of Neurobiology, Anatomy, and Cell Science, University of Pittsburgh, School of Medicine, PA.
Muscle Nerve. 1988 Jun;11(6):588-96. doi: 10.1002/mus.880110611.
Regenerated myofibers formed subsequent to orthotopic transplantation of young, dystrophic mouse muscle fail to display the extensive histopathological changes characteristics of murine dystrophy. In order to determine whether this modification of the phenotypic expression of murine dystrophy is unique to the transplantation system or whether it can be found when other extreme trauma induces dystrophic muscle to regenerate, the extensor digitorum longus muscles of 4-6-week-old normal (129 ReJ +/+) and dystrophic (129 ReJ dy/dy) mice were given two series of injections of the myotoxin bupivacaine, spaced 12 hours apart. These injections resulted in necrosis of approximately 90% of the original myofibers. At 100 days after injection, the regenerated normal muscle appeared "healthy," whereas the regenerated dystrophic muscle displayed histopathological changes. It is suggested that the differences in the time course of innervation of the myotubes in the transplantation system as compared with that in the bupivacaine system may be a factor in determining whether regenerated dystrophic myofibers express a dystrophic morphology.
将年轻的营养不良小鼠肌肉原位移植后形成的再生肌纤维,并未表现出鼠类营养不良所特有的广泛组织病理学变化特征。为了确定这种鼠类营养不良表型表达的改变是移植系统所特有的,还是在其他极端创伤诱导营养不良肌肉再生时也能发现,对4 - 6周龄正常(129 ReJ +/+)和营养不良(129 ReJ dy/dy)小鼠的趾长伸肌进行了两组布比卡因(一种肌毒素)注射,间隔12小时。这些注射导致约90%的原始肌纤维坏死。注射后100天,再生的正常肌肉看起来“健康”,而再生的营养不良肌肉则表现出组织病理学变化。有人认为,与布比卡因系统相比,移植系统中肌管神经支配时间进程的差异可能是决定再生的营养不良肌纤维是否表现出营养不良形态的一个因素。