Differential expression of caveolins and myosin heavy chains in response to forced exercise in rats.
- Author:
Sookyoung PARK
1
;
Yunkyung HONG
;
Youngjeon LEE
;
Jinyoung WON
;
Kyu Tae CHANG
;
Yonggeun HONG
Author Information
- Publication Type:Original Article
- Keywords: Forced exercise; caveolins; myosin heavy chain; TGFbeta-1
- MeSH: Animals; Caveolin 3; Caveolins; Female; Humans; Male; Muscle, Skeletal; Muscles; Muscular Atrophy; Myosin Heavy Chains; Myosins; Nervous System; Protein Isoforms; Rats; RNA; Spinal Cord Injuries; Stroke
- From:Laboratory Animal Research 2012;28(1):1-9
- CountryRepublic of Korea
- Language:English
- Abstract: Exercise training can improve strength and lead to adaptations in the skeletal muscle and nervous systems. Skeletal muscles can develop into two types: fast and slow, depending on the expression pattern of myosin heavy chain (MHC) isoforms. Previous studies reported that exercise altered the distribution of muscle fiber types. It is not currently known what changes in the expression of caveolins and types of muscle fiber occur in response to the intensity of exercise. This study determined the changes in expression of caveolins and MHC type after forced exercise in muscular and non-muscular tissues in rats. A control (Con) group to which forced exercise was not applied and an exercise (Ex) group to which forced exercise was applied. Forced exercise, using a treadmill, was introduced at a speed of 25 m/min for 30 min, 3 times/day (07:00, 15:00, 23:00). Homogenized tissues were applied to extract of total RNA for further gene analysis. The expression of caveolin-3 and MHC2a in the gastrocnemius muscle of female rats significantly increased in the Ex group compared with the Con group (P<0.05). Furthermore, in the gastrocnemius muscle of male rats, the expression of MHC2x was significantly different between the two groups (P<0.05). There was an increased expression in caveolin-3 and a slightly decreased expression in TGFbeta-1 in muscular tissues implicating caveolin-3 influences the expression of MHC isoforms and TGFbeta-1 expression. Eventually, it implicates that caveolin-3 has positive regulatory function in muscle atrophy induced by neural dysfunction with spinal cord injury or stroke.