Lipoxygenase inhibitors suppress formation of tumor necrosis factor in vitro and in vivo

Biochem Biophys Res Commun. 1989 Mar 15;159(2):748-54. doi: 10.1016/0006-291x(89)90058-2.

Abstract

Injection of endotoxin in D-galactosamine sensitized mice resulted in increased serum levels of tumor necrosis factor as determined in a fibroblast cytolysis assay. Concomitant injection of different lipoxygenase inhibitors decreased the titer of TNF. When the lipoxygenase inhibitors were tested in macrophage cultures stimulated with LPS, they prevented the production of TNF. Indomethacin, a blocker of cyclooxygenase was neither in vivo nor in vitro effective in the prevention of the endotoxin-induced synthesis of TNF. The involvement of superoxide anion in this effect was excluded by use of superoxide dismutase which did not influence the formation of TNF in macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Female
  • Galactosamine / administration & dosage
  • Lipopolysaccharides
  • Lipoxygenase Inhibitors*
  • Macrophages / drug effects
  • Macrophages / enzymology
  • Macrophages / metabolism*
  • Mice
  • Mice, Inbred Strains
  • SRS-A / biosynthesis
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Lipopolysaccharides
  • Lipoxygenase Inhibitors
  • SRS-A
  • Tumor Necrosis Factor-alpha
  • Galactosamine