Influence of overload on phenotypic remodeling in regenerated skeletal muscle

Am J Physiol Cell Physiol. 2001 Nov;281(5):C1686-94. doi: 10.1152/ajpcell.2001.281.5.C1686.

Abstract

We studied the effects of 10 wk of functional overload on the expression of myosin heavy chain (MHC), sarcoplasmic reticulum Ca(2+)-ATPase isoforms (SERCA), and the activity of several metabolic enzymes in sham and regenerated plantaris muscles. Overload was accomplished by bilateral surgical ablation of its synergists 4 wk after right plantaris muscles regenerated after myotoxic infiltration. The overload-induced muscle enlargement was slightly less in regenerated than in sham muscles [28% (P < 0.005) and 43% (P < 0.001), respectively]. Overload led to an increase in type I MHC expression (P < 0.01) to a similar extent in sham and regenerated plantaris, while the expected shift from type IIb to type IIa MHC was less marked in regenerated than in sham plantaris. The overload-induced decrease in the expression of the fast SERCA isoform and in the activity of the M subunit of lactate dehydrogenase occurred to a similar extent in sham and regenerated plantaris [66% (P < 0.01) and 27% (P < 0.005), respectively]. In conclusion, the lesser responses of muscle mass and fast MHC composition of regenerated plantaris to mechanical overload suggest an alteration of the transcriptional, translational, and/or posttranslational control of gene expression in regenerated muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Body Weight / drug effects
  • Body Weight / physiology
  • Calcium-Transporting ATPases / metabolism
  • Citrate (si)-Synthase / metabolism
  • Creatine Kinase / metabolism
  • Elapid Venoms / toxicity
  • Immunohistochemistry
  • Isoenzymes / metabolism
  • L-Lactate Dehydrogenase / metabolism
  • Male
  • Muscle Fibers, Skeletal / drug effects
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiology*
  • Muscular Diseases / chemically induced
  • Muscular Diseases / pathology
  • Myosin Heavy Chains / metabolism
  • Organ Size / drug effects
  • Organ Size / physiology
  • Phenotype
  • Rats
  • Rats, Wistar
  • Regeneration / drug effects
  • Regeneration / physiology*
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases

Substances

  • Elapid Venoms
  • Isoenzymes
  • L-Lactate Dehydrogenase
  • Citrate (si)-Synthase
  • Creatine Kinase
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases
  • Myosin Heavy Chains
  • Calcium-Transporting ATPases