Human mRNA response to exercise and temperature

Int J Sports Med. 2012 Feb;33(2):94-100. doi: 10.1055/s-0031-1287799. Epub 2011 Nov 23.

Abstract

The purpose of this research was to determine the mRNA response to exercise in different environmental temperatures. 9 recreationally active males (27±1 years, 77.4±2.7 kg, 13.5±1.5% fat, 4.49±0.15 L · min (-1) VO2 max) completed 3 trials consisting of 1 h cycling exercise at 60% Wmax followed by a 3 h recovery in the cold (7°C), room temperature (20°C), and hot (33°C) environments. Muscle biopsies were obtained pre, post, and 3 h post exercise for the analysis of glycogen and mRNA. Expired gases were collected to calculate substrate use. PGC-1α increased to a greater degree in the cold trial than in the room temperature trial (p=0.036) and the hot trial (p=0.006). PGC1-α mRNA was also higher after the room temperature trial than the hot trial (p=0.050). UCP3 and MFN2 mRNA increased with exercise (p<0.05), but were unaffected by temperature. COX was unaffected by exercise or temperature. Muscle glycogen decreased with exercise (p<0.05), but was no different among trials. Whole body VO2 was lower during exercise in the cold than exercise in the heat. However, VO2 was higher during recovery in the cold trial than in the room temperature and hot trials (p<0.05). This study presents evidence of PGC-1α temperature sensitivity in human skeletal muscle.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Bicycling / physiology*
  • Biopsy
  • Cold Temperature
  • Cross-Over Studies
  • Exercise Test
  • GTP Phosphohydrolases / genetics
  • Glycogen / metabolism*
  • Heat-Shock Proteins / genetics*
  • Hot Temperature
  • Humans
  • Ion Channels / genetics
  • Male
  • Mitochondrial Proteins / genetics
  • Muscle, Skeletal / metabolism
  • Oxygen / metabolism
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA, Messenger / metabolism*
  • Temperature
  • Transcription Factors / genetics*
  • Uncoupling Protein 3

Substances

  • Heat-Shock Proteins
  • Ion Channels
  • Mitochondrial Proteins
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA, Messenger
  • Transcription Factors
  • UCP3 protein, human
  • Uncoupling Protein 3
  • Glycogen
  • GTP Phosphohydrolases
  • MFN2 protein, human
  • Oxygen