Local muscle cooling does not impact expression of mitochondrial-related genes

J Therm Biol. 2017 Jul:67:35-39. doi: 10.1016/j.jtherbio.2017.04.008. Epub 2017 Apr 25.

Abstract

Recovery that takes place in a cold environment after endurance exercise elevates PGC-1α mRNA whereas ERRα and NRF2 mRNA expression are inhibited. However, the effect of local skeletal muscle cooling on mitochondrial-related gene expression is unknown.

Purpose: To determine the impact of local skeletal muscle cooling during recovery from an acute bout of exercise on mitochondrial-related gene expression.

Methods: Recreationally-trained male cyclists (n=8, age 25±3 y, height 181±6cm, weight 79±8kg, 12.8±3.6% body fat, VO2peak 4.52±0.88L·min-1 protocol) completed a 90-min variable intensity cycling protocol followed by 4h of recovery. During recovery, ice was applied intermittently to one leg (ICE) while the other leg served as a control (CON). Intramuscular temperature was recorded continuously. Muscle biopsies were taken from each vastus lateralis at 4h post-exercise for the analysis of mitochondrial-related gene expression.

Results: Intramuscular temperature was colder in ICE (26.7±1.1°C) than CON (35.5±0.1°C) throughout the 4h recovery period (p<0.001). There were no differences in expression of PGC-1α, TFAM, NRF1, NRF2, or ERRα mRNA between ICE and CON after the 4h recovery period.

Conclusion: Local muscle cooling after exercise does not impact the expression of mitochondrial biogenesis-related genes compared to recovery from exercise in control conditions. When these data are considered with previous research, the stimuli for cold-induced gene expression alterations may be related to factors other than local muscle temperature. Additionally, different intramuscular temperatures should be examined to determine dose-response of mitochondrial-related gene expression.

Keywords: Exercise; Ice; PGC-1alpha; Vastus Lateralis.

MeSH terms

  • Bicycling / physiology
  • Cold Temperature*
  • Gene Expression Regulation / physiology*
  • Genes, Mitochondrial / genetics*
  • Humans
  • Male
  • Muscle, Skeletal / metabolism*