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Effects of unweighting and clenbuterol on myosin light and heavy chains in fast and slow muscles of rat

Authors :
STEVENS, LAURENCE
FIRINGA, CAROLE
GOHLSCH, BARBEL
BASTIDE, BRUNO
MOUNIER, YVONNE
PETTE, DIRK
Source :
The American Journal of Physiology. Nov, 2000, Vol. 279 Issue 5, C1558
Publication Year :
2000

Abstract

Stevens, Laurence, Carole Firinga, Barbel Gohlsch, Bruno Bastide, Yvonne Mounier, and Dirk Pette. Effects of unweighting and clenbuterol on myosin light and heavy chains in fast and slow muscles of rat. Am J Physiol Cell Physiol 279: C1558-C1563, 2000.--To investigate, the plasticity of slow and fast muscles undergoing slow-to-fast transition, rat soleus (SOL), gastrocnemius (GAS), and extensor digitorum longus (EDL) muscles were exposed for 14 days to 1) unweighting by hindlimb suspension (HU), or 2) treatment with the [Beta.sub.2]-adrenergic agonist clenbuterol (CB), or 3) a combination of both (HU-CB). In general, HU elicited atrophy, CB induced hypertrophy, and HU-CB partially counteracted the HU-induced atrophy. Analyses of myosin heavy (MHC) and light chain (MLC) isoforms revealed HU- and CB-induced slow-to-fast transitions in SOL (increases of MHCIIa with small amounts of MHCIId and MHCIIb) and the upregulation of the slow MHCIa isoform. The HU- and CB-induced changes in GAS consisted of increases in MHCIId and MHCIIb ('fast-to-faster transitions'). Changes in the MLC composition of SOL and GAS consisted of slow-to-fast transitions and mainly encompassed an exchange of MLC1s with MLC1f. In addition, MLC3f was elevated whenever MHCIId and MHCIIb isoforms were increased. Because the EDL is predominantly composed of type IID and IIB fibers, HU, CB, and HU-CB had no significant effect on the MHC and MLC patterns. extensor digitorum longus; gastrocnemius; hindlimb suspension; myosin; slow-to-fast transition; soleus

Details

ISSN :
00029513
Volume :
279
Issue :
5
Database :
Gale General OneFile
Journal :
The American Journal of Physiology
Publication Type :
Academic Journal
Accession number :
edsgcl.67629070