Inhibition of nitric oxide synthase or cyclo-oxygenase pathways in organum vasculosum laminae terminalis attenuates interleukin-1 beta fever in rabbits

Neurosci Lett. 1996 Apr 26;208(3):155-8. doi: 10.1016/0304-3940(96)12578-7.

Abstract

Fever was induced in rabbits by i.v. administration of lipopolysaccharide (LPS) or administration of interleukin-1 beta (IL-1 beta) into the organum vasculosum laminae terminalis (OVLT). Intra-OVLT injection of IL-1 receptor antagonist (IL-lra), 1 h before LPS or IL-1 beta injection, inhibited the LPS- or IL-1 beta-induced fever. Dexamethasone (a potent inhibitor of the transcription of inducible nitric oxide synthase, iNOS), L-N5-(1-iminoethyl)ornithine (an irreversible NOS inhibitor), aminoguanidine (a specific iNOS inhibitor), or indomethacin (an inhibitor of cyclo-oxygenase, COX) also inhibited IL-1 beta-induced fever when injected into the OVLT 1 h before IL-1 beta injection. These results suggest that iNOS or COX pathways in the OVLT mediate the IL-1 beta-induced fever in rabbits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Fever / chemically induced*
  • Interleukin-1 / pharmacology*
  • Lipopolysaccharides / pharmacology
  • Male
  • Membrane Potentials / drug effects
  • Nitric Oxide Synthase / drug effects*
  • Prostaglandin-Endoperoxide Synthases / drug effects*
  • Rabbits
  • Time Factors

Substances

  • Interleukin-1
  • Lipopolysaccharides
  • Nitric Oxide Synthase
  • Prostaglandin-Endoperoxide Synthases