Effects of Exercise and Steroid on Apoptosis in Skeletal Muscle of Mdx Mouse.
- Author:
Moon Suk BANG
1
;
Jung Hun LIM
;
Dai Youl KIM
Author Information
1. Department of Rehabilitation Medicine, Seoul National University College of Medicine, Korea. rheumagene@hotmail.com
- Publication Type:Original Article
- Keywords:
Exercise;
Steroid;
Apoptosis;
Mdx mouse;
Muscular dystrophy
- MeSH:
Animals;
Apoptosis*;
Blotting, Western;
DNA;
DNA Fragmentation;
Immobilization;
In Situ Nick-End Labeling;
Mice;
Mice, Inbred mdx*;
Models, Animal;
Muscle, Skeletal*;
Muscular Dystrophies;
Muscular Dystrophy, Duchenne;
Social Conditions
- From:Journal of the Korean Academy of Rehabilitation Medicine
2003;27(2):232-239
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: To investigate the effect of exercise and steroid to the muscle of animal model of Duchenne muscular dystrophy. METHOD: We used 15 mdx and 15 control mice. To grade exercise loading, control and mdx mice were divided into free-living, exercise and immobilization groups. Free-living and exercise groups were further divided into steroid-treated and sham-treated groups to evaluate the effect of steroid administration. We measured the apoptotic changes using in situ DNA nick-end labling (TUNEL), DNA fragmentation assay and western blots for Bcl-2 and BAX. RESULT: With TUNEL method, the largest number of myonuclei became positive in sham-treated exercise group while apoptosis was significantly reduced in steroid-treated exercise group in mdx mice. Steroid-treated free-living group showed higher rate of apoptotic change than sham-treated free-living group. With western blots for Bcl-2 and BAX, the value of BAX/Bcl-2 ratio was highest in sham-treated exercise group and among free living mdx mice, it was higher in steroid-treated group than sham-treated one. CONCLUSION: Apoptosis can be minimized in free living condition while exercise loading or immobilization can cause apoptotic change in muscular dystrophy animal model. Steroid administration induces apoptosis in free living muscle and it alleviates apoptotic damage caused by exercise loading in mdx mice.
