Unresponsiveness of mu-opioid receptor knockout mice to lipopolysaccharide-induced fever

Br J Pharmacol. 2005 Apr;144(8):1029-31. doi: 10.1038/sj.bjp.0706145.

Abstract

Recently, we demonstrated that lipopolysaccharide (LPS)-induced fever could be suppressed by a selective mu-opioid receptor antagonist, indicating that the mu-opioid system is involved in the LPS fever. In the present study, to confirm the role of the mu-opioid system in the pathogenesis of LPS fever, we used mice lacking the mu-opioid receptor. In the wild type (WT), following intraperitoneal (i.p.) injection of 100 microg kg(-1) of LPS, body temperature (T(b)) increased approximately 1 degrees C and remained elevated during the 360-min recording period. In the mu-opioid receptor knockout (MOR-KO) mice, the administration of 100 microg kg(-1) i.p. of LPS did not induce fever during the recording period. Saline by itself, given i.p., did not alter the T(b), either in WT or MOR-KO. These results confirm that the mu-opioid system is involved in LPS-induced fever.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Body Temperature / drug effects
  • Body Temperature / genetics
  • Drug Tolerance / genetics*
  • Fever / chemically induced
  • Fever / genetics*
  • Fever / metabolism*
  • Lipopolysaccharides / toxicity*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Opioid, mu / deficiency*
  • Receptors, Opioid, mu / genetics*
  • Receptors, Opioid, mu / physiology

Substances

  • Lipopolysaccharides
  • Receptors, Opioid, mu