Sepsis in mice stimulates muscle proteolysis in the absence of IL-6

Am J Physiol. 1998 Dec;275(6):R1983-91. doi: 10.1152/ajpregu.1998.275.6.R1983.

Abstract

We tested the role of interleukin-6 (IL-6) in sepsis-induced muscle proteolysis by determining ubiquitin mRNA levels and protein breakdown rates in incubated extensor digitorum longus muscles from septic and sham-operated IL-6 knockout and wild-type mice. In addition, the effect of treatment of mice with human recombinant IL-6 on muscle protein breakdown rates was determined. Finally, protein breakdown rates were measured in myotubes treated for up to 48 h with different concentrations of IL-6. Sepsis in wild-type mice resulted in an approximately ninefold increase in plasma IL-6 levels, whereas IL-6 was not detectable in plasma of sham-operated or septic IL-6 knockout mice. Total and myofibrillar muscle protein breakdown rates were increased by approximately 30% and threefold, respectively, in septic IL-6 wild-type mice with an almost identical response noted in septic IL-6 knockout mice. Ubiquitin mRNA levels determined by dot blot analysis were increased during sepsis in muscles from both IL-6 knockout and wild-type mice, although the increase was less pronounced in IL-6 knockout than in wild-type mice. Treatment of normal mice or of cultured L6 myotubes with IL-6 did not influence protein breakdown rates. The present results suggest that IL-6 does not regulate muscle proteolysis during sepsis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Humans
  • Infections / metabolism*
  • Interleukin-6 / blood
  • Interleukin-6 / deficiency*
  • Interleukin-6 / genetics
  • Interleukin-6 / pharmacology
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mice, Knockout / genetics
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism*
  • Myofibrils / metabolism
  • Peptide Hydrolases / metabolism
  • RNA, Messenger / metabolism
  • Recombinant Proteins
  • Reference Values
  • Ubiquitins / genetics

Substances

  • Interleukin-6
  • Muscle Proteins
  • RNA, Messenger
  • Recombinant Proteins
  • Ubiquitins
  • Peptide Hydrolases