Effect of endurance training on lipid metabolism in women: a potential role for PPARalpha in the metabolic response to training

Am J Physiol Endocrinol Metab. 2000 Aug;279(2):E348-55. doi: 10.1152/ajpendo.2000.279.2.E348.

Abstract

Endurance training increases fatty acid oxidation (FAO) and skeletal muscle oxidative capacity. However, the source of the additional fat and the mechanisms for increasing FAO capacity in muscle are not clear. We measured whole body and regional lipolytic activity and whole body and plasma FAO in six lean women during 90 min of bicycling exercise (50% pretraining peak O(2) consumption) before and after 12 wk of endurance training. We also assessed skeletal muscle content of peroxisome proliferator-activated receptor-alpha (PPARalpha) and its target proteins that regulate FAO [medium-chain and very long chain acyl-CoA dehydrogenase (MCAD and VLCAD)]. Despite a 25% increase in whole body FAO during exercise after training (P < 0.05), training did not alter regional adipose tissue lipolysis (abdominal: 0.56 +/- 0.26 and 0.57 +/- 0.10 micromol x 100 g(-1) x min(-1); femoral: 0.13 +/- 0.07 and 0.09 +/- 0.02 micromol x 100 g(-1) x min(-1)), whole body palmitate rate of appearance in plasma (168 +/- 18 and 150 +/- 25 micromol/min), and plasma FAO (554 +/- 61 and 601 +/- 45 micromol/min). However, training doubled the levels of muscle PPARalpha, MCAD, and VLCAD. We conclude that training increases the use of nonplasma fatty acids and may enhance skeletal muscle oxidative capacity by PPARalpha regulation of gene expression.

Publication types

  • Clinical Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acyl-CoA Dehydrogenase
  • Acyl-CoA Dehydrogenase, Long-Chain / metabolism
  • Adipose Tissue / metabolism
  • Adult
  • Citrate (si)-Synthase / metabolism
  • Epinephrine / blood
  • Fatty Acids / blood
  • Female
  • Glycerol / blood
  • Humans
  • Insulin / blood
  • Lipid Metabolism*
  • Lipolysis / physiology
  • Muscle, Skeletal / metabolism
  • Norepinephrine / blood
  • Oxidation-Reduction
  • Physical Endurance / physiology*
  • Physical Exertion / physiology*
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Transcription Factors / metabolism*

Substances

  • Fatty Acids
  • Insulin
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Acyl-CoA Dehydrogenase
  • Acyl-CoA Dehydrogenase, Long-Chain
  • Citrate (si)-Synthase
  • Glycerol
  • Norepinephrine
  • Epinephrine