Mechanical load increases muscle IGF-I and androgen receptor mRNA concentrations in humans

Am J Physiol Endocrinol Metab. 2001 Mar;280(3):E383-90. doi: 10.1152/ajpendo.2001.280.3.E383.

Abstract

The mechanism(s) of load-induced muscle hypertrophy is as yet unclear, but increasing evidence suggests a role for locally expressed insulin-like growth factor I (IGF-I). We investigated the effects of concentric (CON) vs. eccentric (ECC) loading on muscle IGF-I mRNA concentration. We hypothesized a greater IGF-I response after ECC compared with CON. Ten healthy subjects (24.4 +/- 0.7 yr, 174.5 +/- 2.6 cm, 70.9 +/- 4.3 kg) completed eight sets of eight CON or ECC squats separated by 6-10 days. IGF-I, IGF binding protein-4 (IGFBP-4), and androgen receptor (AR) mRNA concentrations were determined in vastus lateralis muscle by RT-PCR before and 48 h after ECC and CON. Serum total testosterone (TT) and IGF-I were measured serially across 48 h, and serum creatine kinase activity (CK), isometric maximum voluntary contraction (MVC), and soreness were determined at 48 h. IGF-I mRNA concentration increased 62% and IGFBP-4 mRNA concentration decreased 57% after ECC (P < 0.05). Changes after CON were similar but not significant (P = 0.06-0.12). AR mRNA concentration increased (P < 0.05) after ECC (63%) and CON (102%). Serum TT and IGF-I showed little change. MVC fell 10% and CK rose 183% after ECC (P < 0.05). Perceived soreness was higher (P < 0.01) after ECC compared with CON. Results indicate that a single bout of mechanical loading in humans alters activity of the muscle IGF-I system, and the enhanced response to ECC suggests that IGF-I may somehow modulate tissue regeneration after mechanical damage.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Biomechanical Phenomena
  • Creatine Kinase / blood
  • Exercise*
  • Female
  • Humans
  • Hypertrophy
  • Insulin-Like Growth Factor Binding Protein 4 / genetics
  • Insulin-Like Growth Factor I / analysis
  • Insulin-Like Growth Factor I / genetics*
  • Kinetics
  • Male
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • RNA, Messenger / metabolism*
  • Receptors, Androgen / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Testosterone / blood
  • Weight-Bearing*

Substances

  • Insulin-Like Growth Factor Binding Protein 4
  • RNA, Messenger
  • Receptors, Androgen
  • Testosterone
  • Insulin-Like Growth Factor I
  • Creatine Kinase