Intensified exercise training does not alter AMPK signaling in human skeletal muscle

Am J Physiol Endocrinol Metab. 2004 May;286(5):E737-43. doi: 10.1152/ajpendo.00462.2003. Epub 2003 Dec 23.

Abstract

The AMP-activated protein kinase (AMPK) cascade has been linked to many of the acute effects of exercise on skeletal muscle substrate metabolism, as well as to some of the chronic training-induced adaptations. We determined the effect of 3 wk of intensified training (HIT; 7 sessions of 8 x 5 min at 85% Vo2 peak) in skeletal muscle from well-trained athletes on AMPK responsiveness to exercise. Rates of whole body substrate oxidation were determined during a 90-min steady-state ride (SS) pre- and post-HIT. Muscle metabolites and AMPK signaling were determined from biopsies taken at rest and immediately after exercise during the first and seventh HIT sessions, performed at the same (absolute) pre-HIT work rate. HIT decreased rates of whole body carbohydrate oxidation (P < 0.05) and increased rates of fat oxidation (P < 0.05) during SS. Resting muscle glycogen and its utilization during intense exercise were unaffected by HIT. However, HIT induced a twofold decrease in muscle [lactate] (P < 0.05) and resulted in tighter metabolic regulation, i.e., attenuation of the decrease in the PCr/(PCr + Cr) ratio and of the increase in [AMPfree]/ATP. Resting activities of AMPKalpha1 and -alpha2 were similar post-HIT, with the magnitude of the rise in response to exercise similar pre- and post-HIT. AMPK phosphorylation at Thr172 on both the alpha1 and alpha2 subunits increased in response to exercise, with the magnitude of this rise being similar post-HIT. Acetyl-coenzyme A carboxylase-beta phosphorylation was similar at rest and, despite HIT-induced increases in whole body rates of fat oxidation, did not increase post-HIT. Our results indicate that, in well-trained individuals, short-term HIT improves metabolic control but does not blunt AMPK signaling in response to intense exercise.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases
  • Acetyl-CoA Carboxylase / metabolism
  • Acidosis / enzymology*
  • Adult
  • Analysis of Variance
  • Exercise / physiology*
  • Glycogen / metabolism
  • Humans
  • Lactic Acid / metabolism
  • Multienzyme Complexes / metabolism*
  • Muscle, Skeletal / enzymology*
  • Oxygen Consumption / physiology
  • Phosphorylation
  • Physical Fitness / physiology*
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction / physiology

Substances

  • Multienzyme Complexes
  • Lactic Acid
  • Glycogen
  • PRKAA2 protein, human
  • Protein Serine-Threonine Kinases
  • AMP-Activated Protein Kinases
  • PRKAA1 protein, human
  • Acetyl-CoA Carboxylase