Branched fibers in dystrophic mdx muscle are associated with a loss of force following lengthening contractions

被引:69
作者
Chan, S.
Head, S. I. [1 ]
Morley, J. W.
机构
[1] Univ New S Wales, Sch Med Sci, Sydney, NSW 2052, Australia
[2] Univ Western Sydney, Sch Med, Sydney, NSW, Australia
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2007年 / 293卷 / 03期
关键词
skeletal muscle; mdx mouse; lengthening contraction; Duchenne muscular dystrophy;
D O I
10.1152/ajpcell.00128.2007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We demonstrated that the susceptibility of skeletal muscle to injury from lengthening contractions in the dystrophin-deficient mdx mouse is directly linked with the extent of fiber branching within the muscles and that both parameters increase as the mdx animal ages. We subjected isolated extensor digitorum longus muscles to a lengthening contraction protocol of 15% strain and measured the resulting drop in force production ( force deficit). We also examined the morphology of individual muscle fibers. In mdx mice 1-2 mo of age, 17% of muscle fibers were branched, and the force deficit of 7% was not significantly different from that of age-matched littermate controls. In mdx mice 6-7 mo of age, 89% of muscle fibers were branched, and the force deficit of 58% was significantly higher than the 25% force deficit of age-matched littermate controls. These data demonstrated an association between the extent of branching and the greater vulnerability to contraction-induced injury in the older fast-twitch dystrophic muscle. Our findings demonstrate that fiber branching may play a role in the pathogenesis of muscular dystrophy in mdx mice, and this could affect the interpretation of previous studies involving lengthening contractions in this animal.
引用
收藏
页码:C985 / C992
页数:8
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