Role of muscle IL-6 in gender-specific metabolism in mice

PLoS One. 2017 Mar 20;12(3):e0173675. doi: 10.1371/journal.pone.0173675. eCollection 2017.

Abstract

The aim of the present work was to further explore the physiological roles of muscle-derived IL-6. Adult-floxed and conditional skeletal muscle IL-6 knock out male and female mice were used to study energy expenditure (indirect calorimetry at rest and during treadmill exercise, and body temperature cycle during the light phase) and energy intake (response to fast/refeeding). We also evaluated the responses to leptin and the activity of the insulin signalling pathway in skeletal muscle and liver by phosphorylation of Akt at Ser 473. The stress response was also studied. Results indicate a relevant role of muscle IL-6 in maintaining energy homeostasis, especially in males. Absence of muscle IL-6 in male mice results in lower core body temperature in the light phase, increased respiratory exchange ratio (RER) both at rest and during exercise, increased expression of TCA cycle marked gene, citrate synthase in muscle, reduced fat storage and decreased body weight and food consumption in response to leptin. In females, muscle IL-6 deficiency increases VO2 and CO2 levels similarly. Also in contrast to males, energy expenditure (EE) measured over 48h reveals a significant elevation in female mice with muscle IL-6 deficiency; moreover, they show a modified response to fasting-refeeding and to restraint stress. The present results contribute to the understanding of the role of muscle IL-6 in male and female mouse metabolism, not only during exercise but also in the basal state and in situations where energy balance is altered.

MeSH terms

  • Animals
  • Body Temperature
  • Energy Metabolism*
  • Exercise Test
  • Fasting / metabolism
  • Fasting / physiology
  • Gene Knockout Techniques
  • Insulin / metabolism
  • Interleukin-6 / deficiency
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Male
  • Mice
  • Muscle, Skeletal / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / chemistry
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rest
  • Serine / metabolism
  • Sex Characteristics*
  • Signal Transduction
  • Stress, Physiological / drug effects

Substances

  • Insulin
  • Interleukin-6
  • Serine
  • Proto-Oncogene Proteins c-akt

Grants and funding

The authors are grateful to grants SAF2011-23272 and SAF2014-56546-R to JH, and Spanish Ministry of Economy and Competitiveness (MINECO grants BFU2014-52149-R) and Instituto de Salud Carlos III to M.V. CIBERDEM is an initiative of the Instituto de Salud Carlos III, Madrid, Spain". OFG acknowledges the support of fellowship FPU2012-00365.