Hindlimb immobilization applied to 21-day-old mdx mice prevents the occurrence of muscle degeneration

被引:45
作者
Mokhtarian, A
Lefaucheur, JP
Even, PC
Sebille, A
机构
[1] Fac Med St Antoine, INSERM, U153, Atelier Regenerat Neuromusculaire,Lab Physiol, F-75571 Paris 12, France
[2] Coll France, CNRS, URA 1860, Lab Neurobiol Regulat, F-75231 Paris, France
关键词
dystrophinopathy; muscle regeneration;
D O I
10.1152/jappl.1999.86.3.924
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Dystrophin-deficient skeletal muscles of mdx mice undergo their first rounds of degeneration-regeneration at the age of 14-28 days. This feature is thought to result from an increase in motor activity at weaning. In this study, we hypothesize that if the muscle is prevented from contracting, it will avoid the degenerative changes that normally occur. For this purpose, we developed a procedure of mechanical hindlimb immobilization in 3-wk-old mice to restrain soleus (Sol) and extensor digitorum longus (FDL) muscles in the stretched or shortened position. After a 14-day period of immobilization, the striking feature was the low percentage of regenerated (centronucleated) myofibers in Sol and EDL muscles, regardless of the length at which they were fixed, compared with those on the contralateral side (stretched Sol: 8.4 +/- 6.5 vs. 46.6 +/- 10.3%, P = 0.0008; shortened Sol: 1.2 +/- 1.6 vs. 50.4 +/- 16.4%, P = 0.0008; stretched EDL: 05 +/- 0.5 vs. 32.9 +/- 17.5%, P = 0.002; shortened EDL: 3.3 +/- 3.1 vs. 34.7 +/- 11.1%, P = 0.002). Total numbers of myofibers did not change with immobilization. This study shows that limb immobilization prevents the occurrence of the first round of myofiber necrosis in mdx mice and suggests that muscle contractions play a role in the skeletal muscle degeneration of dystrophin-deficient mdx mouse muscles.
引用
收藏
页码:924 / 931
页数:8
相关论文
共 32 条
[1]   HISTOPATHOLOGICAL CHANGES IN DUCHENNE MUSCULAR DYSTROPHY [J].
BELL, CD ;
CONEN, PE .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1968, 7 (03) :529-&
[2]   X-CHROMOSOME-LINKED MUSCULAR-DYSTROPHY (MDX) IN THE MOUSE [J].
BULFIELD, G ;
SILLER, WG ;
WIGHT, PAL ;
MOORE, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1189-1192
[3]   EFFECT OF VOLUNTARY WHEEL-RUNNING EXERCISE ON MUSCLES OF THE MDX MOUSE [J].
CARTER, GT ;
WINEINGER, MA ;
WALSH, SA ;
HORASEK, SJ ;
ABRESCH, RT ;
FOWLER, WM .
NEUROMUSCULAR DISORDERS, 1995, 5 (04) :323-332
[4]   Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle [J].
Cullen, MJ ;
Walsh, J ;
Roberds, SL ;
Campbell, KP .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1996, 22 (01) :30-37
[5]   PROGRESSIVE DETERIORATION OF MUSCLES IN MDX MICE INDUCED BY OVERLOAD [J].
DICK, J ;
VRBOVA, G .
CLINICAL SCIENCE, 1993, 84 (02) :145-150
[6]   Exercise and clenbuterol as strategies to decrease the progression of muscular dystrophy in mdx mice [J].
DupontVersteegden, EE .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (03) :734-741
[7]   VOLUNTARY EXERCISE DECREASES PROGRESSION OF MUSCULAR-DYSTROPHY IN DIAPHRAGM OF MDX MICE [J].
DUPONTVERSTEEGDEN, EE ;
MCCARTER, RJ ;
KATZ, MS .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (04) :1736-1741
[8]   IS LIMB IMMOBILIZATION A MODEL OF MUSCLE DISUSE [J].
FOURNIER, M ;
ROY, RR ;
PERHAM, H ;
SIMARD, CP ;
EDGERTON, VR .
EXPERIMENTAL NEUROLOGY, 1983, 80 (01) :147-156
[9]   Beneficial effects of voluntary wheel running on the properties of dystrophic mouse muscle [J].
Hayes, A ;
Williams, DA .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (02) :670-679
[10]   THE EFFECTS OF ENDURANCE EXERCISE ON DYSTROPHIC MDX MICE .1. CONTRACTILE AND HISTOCHEMICAL PROPERTIES OF INTACT MUSCLES [J].
HAYES, A ;
LYNCH, GS ;
WILLIAMS, DA .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1993, 253 (1336) :19-25