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肌肉萎缩症:中心核可能反映了缺陷肌核的代偿性激活。

Muscular dystrophy: centronucleation may reflect a compensatory activation of defective myonuclei.

作者信息

Totsuka T, Watanabe K, Uramoto I, Sakuma K, Mizutani T

机构信息

Department of Physiology, Aichi Prefectural Institute for Developmental Research, Kasugai, Japan.

出版信息

J Biomed Sci. 1998;5(1):54-61. doi: 10.1007/BF02253356.

Abstract

Muscular dystrophy has long been believed to be characterized by degeneration and abortive regeneration of muscle fibers (the muscle degeneration theory), but unfortunately its pathogenesis is still unclear and an effective treatment has yet to be developed. As a challenge to the theory, we have proposed an alternative muscle-defective-growth theory and a further bone muscle growth imbalance hypothesis supposing possible defects in bone-growth-dependent muscle growth based on our findings in hereditary dystrophic dy mice (C57BL/6J dy/dy). This review presents some new insights into the pathogenesis of the disease along with our hypothesis, focusing on the physiological meaning of centronucleation, one of the major pathological changes commonly observed in dystrophic muscles of man and experimental animals.

摘要

长期以来,人们一直认为肌肉萎缩症的特征是肌纤维变性和再生失败(肌肉变性理论),但不幸的是,其发病机制仍不清楚,尚未开发出有效的治疗方法。作为对该理论的挑战,基于我们对遗传性营养不良dy小鼠(C57BL/6J dy/dy)的研究结果,我们提出了一种替代性的肌肉生长缺陷理论以及进一步的骨骼肌肉生长失衡假说,假定骨生长依赖性肌肉生长可能存在缺陷。本综述结合我们的假说,对该疾病的发病机制提出了一些新见解,重点关注中心核化的生理意义,中心核化是在人类和实验动物的营养不良性肌肉中常见的主要病理变化之一。

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