Cytokines stimulate lipolysis and decrease lipoprotein lipase activity in cultured fat cells by a prostaglandin independent mechanism

Biochem Biophys Res Commun. 1992 Jul 15;186(1):237-43. doi: 10.1016/s0006-291x(05)80798-3.

Abstract

We previously showed that indomethacin blocked the effect of tumor necrosis factor (TNF) and other cytokines on lipolysis. We now show that TNF stimulates prostaglandin (PG) production, enhances lipolysis and decreases lipoprotein lipase (LPL) activity in 3T3-F442A adipocytes and indomethacin blocks these activities, suggesting that the actions of TNF are mediated by PG's. However, exogenous PGE2 at the levels induced by TNF is not sufficient to affect lipolysis or LPL activity and low doses of indomethacin and flurbiprofen block PG production without affecting TNF's action. Interleukin-1 and interferon-alpha and gamma induce lipolysis and decrease LPL activity but do not stimulate much PG production. These results demonstrate that cytokines enhance lipolysis and decrease LPL activity in 3T3 adipocytes by a PG independent mechanism.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Animals
  • Cells, Cultured
  • Cytokines / pharmacology*
  • Dinoprostone / pharmacology*
  • Flurbiprofen / pharmacology
  • Humans
  • Indomethacin / pharmacology
  • Interferon Type I / pharmacology
  • Interferon-gamma / pharmacology
  • Interleukin-1 / pharmacology
  • Kinetics
  • Lipolysis / drug effects*
  • Lipoprotein Lipase / metabolism*
  • Mice
  • Prostaglandins / metabolism*
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Cytokines
  • Interferon Type I
  • Interleukin-1
  • Prostaglandins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Flurbiprofen
  • Interferon-gamma
  • Lipoprotein Lipase
  • Dinoprostone
  • Indomethacin