Prostaglandin-independent stimulation of interleukin-6 production by fibrinogen degradation product D in perfused murine liver

Scand J Immunol. 1998 Sep;48(3):269-71. doi: 10.1046/j.1365-3083.1998.00395.x.

Abstract

Bacterial endotoxin (LPS) and fibrinogen degradation product D (FDP-D) are both potent stimulators of interleukin-6 (IL-6) production in liver, however, there are differences in their metabolic effects. The aim of the present study was to compare the role of prostaglandins in the enhancement of IL-6 production by LPS or FDP-D in perfused mouse livers. Indomethacin inhibited the effect of LPS significantly but was ineffective in the case of FDP-D. Accordingly, production of prostaglandins D2 and E2 was not elevated following the addition of FDP-D, while their formation was increased several fold by LPS. At the same time interleukin-1 (IL-1) production in perfused liver rose markedly upon the addition of FDP-D. It is suggested that prostaglandins are not involved in the effects of FDP-D on the liver. The stimulatory effect of FDP-P on IL-6 production might be the consequence of elevated IL-1 levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dinoprostone / biosynthesis
  • Fibrin Fibrinogen Degradation Products / pharmacology*
  • In Vitro Techniques
  • Indomethacin / pharmacology
  • Interleukin-1 / biosynthesis
  • Interleukin-6 / biosynthesis*
  • Liver / drug effects*
  • Liver / metabolism*
  • Male
  • Mice
  • Perfusion
  • Prostaglandin D2 / biosynthesis
  • Prostaglandins / pharmacology*

Substances

  • Fibrin Fibrinogen Degradation Products
  • Interleukin-1
  • Interleukin-6
  • Prostaglandins
  • Dinoprostone
  • Prostaglandin D2
  • Indomethacin