Role of IGF-I and IGFBPs in the changes of mass and phenotype induced in rat soleus muscle by clenbuterol

Am J Physiol Endocrinol Metab. 2002 Jan;282(1):E31-7. doi: 10.1152/ajpendo.2002.282.1.E31.

Abstract

Clenbuterol induces hypertrophy and a slow-to-fast phenotype change in skeletal muscle, but the signaling mechanisms remain unclear. We hypothesized that clenbuterol could act via local expression of insulin-like growth factor I (IGF-I). Administration of clenbuterol to 3-mo-old female Wistar rats resulted in a 10 and 13% increase of soleus muscle mass after 3 and 9 days, respectively, reaching 16% after 4 wk. When associated with triiodothyronine, clenbuterol induced a dramatic slow-to-fast phenotype change. In parallel, clenbuterol administration induced in soleus muscle a fivefold increase in IGF-I mRNA levels associated with an eightfold increase in IGF-binding protein (IGFBP)-4 and a fivefold increase of IGFBP-5 mRNA levels on day 3. This increased IGF-I gene expression was associated with an increase in muscle IGF-I content, already detected on day 1 and persisting until day 5 without increase in serum IGF-I concentrations. These data show that muscle hypertrophy induced by clenbuterol is associated with a local increase in muscle IGF-I content. They suggest that clenbuterol-induced muscle hypertrophy could be mediated by local production of IGF-I.

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Blood / metabolism
  • Clenbuterol / pharmacology*
  • Female
  • Gene Expression
  • Insulin-Like Growth Factor Binding Protein 4 / genetics
  • Insulin-Like Growth Factor Binding Protein 4 / metabolism
  • Insulin-Like Growth Factor Binding Protein 5 / genetics
  • Insulin-Like Growth Factor Binding Protein 5 / metabolism
  • Insulin-Like Growth Factor Binding Proteins / physiology*
  • Insulin-Like Growth Factor I / chemistry
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Insulin-Like Growth Factor I / physiology*
  • Isoenzymes / metabolism
  • Muscle, Skeletal / anatomy & histology*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / physiology*
  • Myosin Heavy Chains / metabolism
  • Organ Size / physiology
  • Peptide Fragments / metabolism
  • Phenotype
  • Rats
  • Rats, Wistar
  • Time Factors

Substances

  • Adrenergic beta-Agonists
  • Insulin-Like Growth Factor Binding Protein 4
  • Insulin-Like Growth Factor Binding Protein 5
  • Insulin-Like Growth Factor Binding Proteins
  • Isoenzymes
  • Peptide Fragments
  • Insulin-Like Growth Factor I
  • Myosin Heavy Chains
  • Clenbuterol