Transcriptional activation of the IL-6 gene in human contracting skeletal muscle: influence of muscle glycogen content

FASEB J. 2001 Dec;15(14):2748-50. doi: 10.1096/fj.01-0507fje. Epub 2001 Oct 29.

Abstract

In humans, the plasma interleukin 6 (IL-6) concentration increases dramatically during low-intensity exercise. Measurements across the working limb indicate that skeletal muscle is the source of IL-6 production. To determine whether energy availability influences the regulation of IL-6 expression during prolonged exercise, six male subjects completed two trials consisting of 180 min of two-legged dynamic knee extensor with either normal or low (~60% of control) pre-exercise muscle glycogen levels. Increases in plasma IL-6 during exercise were significantly higher (P<0.05) in the low-glycogen (16-fold) trial verses the control (10-fold) trial. Transcriptional activation of the IL-6 gene in skeletal muscle was also higher in the low-glycogen trial; it increased by about 40-fold after 90 min of exercise and about 60-fold after 180 min of exercise. Muscle IL-6 mRNA followed a similar but delayed pattern, increasing by more than 100-fold in the low-glycogen trial and by about 30-fold in the control trial. These data demonstrate that exercise activates transcription of the IL-6 gene in working skeletal muscle, a response that is dramatically enhanced when glycogen levels are low. These findings also support the hypothesis that IL-6 may be produced by contracting myofibers when glycogen levels become critically low as a means of signaling the liver to increase glucose production.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Exercise / physiology
  • Glycogen / metabolism
  • Humans
  • Interleukin-6 / blood
  • Interleukin-6 / genetics*
  • Male
  • Muscle Contraction / genetics*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transcription, Genetic
  • Transcriptional Activation

Substances

  • Interleukin-6
  • RNA, Messenger
  • Glycogen