Functional overloading facilitates the regeneration of injured soleus muscles in mice

J Physiol Sci. 2008 Dec;58(6):397-404. doi: 10.2170/physiolsci.RP004008.

Abstract

The effect of functional overloading on the regenerating process of injured skeletal muscle was investigated in 10-week-old male mice (C57BL/6J). Functional overloading on soleus of both hindlimbs was performed by cutting the distal tendons of plantaris and gastrocnemius muscles for 2 weeks before cardiotoxin (CTX) injection as the preconditioning and also during 10 weeks of recovery. To activate the necrosis-regeneration cycle, 0.1 ml of 10-microM CTX was injected into soleus muscle. The mean values of absolute muscle weight and the percentage of Pax7-positive nuclei in soleus were increased by the preconditioning. These values, as well as total muscle protein content, in the group with CTX injection plus overloading were larger than in the group with CTX injection alone. Fibers with central nucleus were noted in the group with CTX injection with or without overloading. The rate of disappearance of fibers having central nucleus during recovery was stimulated by overloading. Histological analyses revealed that the regeneration of injured soleus muscle with overloading proceeded more rapidly than the muscle without overloading. These results, in combination with previous lines of evidence, strongly suggest that functional overloading may facilitate the regeneration of injured skeletal muscles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Nucleus / metabolism
  • Cell Nucleus / pathology
  • Cell Proliferation
  • Disease Models, Animal
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle Contraction*
  • Muscle Fibers, Skeletal / metabolism
  • Muscle Fibers, Skeletal / pathology
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiopathology*
  • Muscular Diseases / chemically induced
  • Muscular Diseases / pathology
  • Muscular Diseases / physiopathology*
  • Necrosis
  • Organ Size
  • PAX7 Transcription Factor / metabolism
  • Regeneration*
  • Stress, Mechanical
  • Tendons / surgery
  • Time Factors
  • Toxins, Biological

Substances

  • Muscle Proteins
  • PAX7 Transcription Factor
  • Pax7 protein, mouse
  • Toxins, Biological