Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse

• Published in: Acta neuropathologica Vol. 69; no. 1-2; pp. 91 - 95
• Main Authors: Tanabe, Y, Esaki, K, Nomura, T
• Format: Journal Article
• Language: English
• Published: Germany 01-01-1986
• Subjects: Animals; Body Weight; Cell Count; Genetic Linkage; Mice; Mice, Inbred C57BL; Muscles - pathology; Muscular Dystrophy, Animal - diagnosis; Muscular Dystrophy, Animal - genetics; Muscular Dystrophy, Animal - pathology; X Chromosome
• ISSN: 0001-6322; 1432-0533
• DOI: 10.1007/bf00687043

Histological, histochemical, and morphometric analyses were performed chronologically on muscles from mutant mice with X chromosome-linked muscular dystrophy (mdx), and the findings were compared with those in nondystrophic control animals (C57BL/10ScSn). Massive grouped muscle fiber destruction, followed by complete regeneration, occurred abruptly at 20 days of age. There were no preceding changes in body weight, the number and mean diameter of fibers, and fiber type differentiation before the initial episode of muscle fiber necrosis. Muscle fiber necrosis decreased in intensity after 60 days of age. Even after repeated muscle fiber necrosis and regeneration, the most striking finding was that interstitial fibrosis and adipose tissue replacement were minimal, and there was no apparent fiber loss. Since the necrosis was probably well compensated by the active regenerative process, the mdx mice developed no obvious muscle weakness and thus differed from human and other animal muscular dystrophies with the exception of the dystrophic hamster.