Pentoxifylline improves insulin action limiting skeletal muscle catabolism after infection

J Endocrinol. 1999 Oct;163(1):15-24. doi: 10.1677/joe.0.1630015.

Abstract

We investigated the ability of pentoxifylline (PTX) to modulate protein synthesis and degradation in the presence and absence of insulin during incubation of epitrochlearis muscle, 2 or 6 days after injection of Escherichia coli. On days 2 and 6 after infection, protein synthesis was inhibited by 25%, whereas proteolysis was enhanced by 75%. Insulin (2 nM) in vitro stimulated protein synthesis in muscles from infected rats to the same extent as in controls. The ability of insulin to limit protein degradation was severely blunted 48 h after infection. On day 6 after infection, insulin inhibited proteolysis to a greater extent than on day 2. PTX suppressed the increase in plasma concentrations of tumor necrosis factor more than 600-fold after injection of bacteria, and partially prevented the inhibition of protein synthesis and stimulation of protein degradation during sepsis. Moreover, PTX administration maintained the responsiveness of protein degradation to insulin during sepsis. Thus cytokines may influence skeletal muscle protein metabolism during sepsis, both indirectly through inhibition of the effects of insulin on proteolysis, and directly on the protein synthesis and degradation machinery.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Animals
  • Culture Techniques
  • Escherichia coli Infections / drug therapy
  • Escherichia coli Infections / metabolism*
  • Forelimb
  • Insulin / therapeutic use*
  • Male
  • Muscle Proteins / biosynthesis
  • Muscle Proteins / metabolism*
  • Muscle, Skeletal / metabolism*
  • Pentoxifylline / therapeutic use*
  • Phenylalanine / metabolism
  • Phosphodiesterase Inhibitors / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Tumor Necrosis Factor-alpha / metabolism
  • Tyrosine / metabolism

Substances

  • Insulin
  • Muscle Proteins
  • Phosphodiesterase Inhibitors
  • Tumor Necrosis Factor-alpha
  • Tyrosine
  • Phenylalanine
  • Pentoxifylline