Kupffer cell-generated PGE2 triggers the febrile response of guinea pigs to intravenously injected LPS

Am J Physiol Regul Integr Comp Physiol. 2006 May;290(5):R1262-70. doi: 10.1152/ajpregu.00724.2005. Epub 2006 Jan 12.


Because the onset of fever induced by intravenously (i.v.) injected bacterial endotoxic lipopolysaccharides (LPS) precedes the appearance in the bloodstream of pyrogenic cytokines, the presumptive peripheral triggers of the febrile response, we have postulated previously that, in their stead, PGE2 could be the peripheral fever trigger because it appears in blood coincidentally with the initial body core temperature (Tc) rise. To test this hypothesis, we injected Salmonella enteritidis LPS (2 microg/kg body wt i.v.) into conscious guinea pigs and measured their plasma levels of LPS, PGE2, TNF-alpha, IL-1beta, and IL-6 before and 15, 30, 60, 90, and 120 min after LPS administration; Tc was monitored continuously. The animals were untreated or Kupffer cell (KC) depleted; the essential involvement of KCs in LPS fever was shown previously. LPS very promptly (<10 min) induced a rise of Tc that was temporally correlated with the elevation of plasma PGE2. KC depletion prevented the Tc and plasma PGE2 rises and slowed the clearance of LPS from the blood. TNF-alpha was not detectable in plasma until 30 min and in IL-1beta and IL-6 until 60 min after LPS injection. KC depletion did not alter the times of appearance or magnitudes of rises of these cytokines, except TNF-alpha, the maximal level of which was increased approximately twofold in the KC-depleted animals. In a follow-up experiment, PGE2 antiserum administered i.v. 10 min before LPS significantly attenuated the febrile response to LPS. Together, these results support the view that, in guinea pigs, PGE2 rather than pyrogenic cytokines is generated by KCs in immediate response to i.v. LPS and triggers the febrile response.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibodies, Blocking / pharmacology
  • Body Temperature / drug effects
  • Cytokines / blood
  • Dinoprostone / antagonists & inhibitors
  • Dinoprostone / biosynthesis*
  • Dinoprostone / genetics
  • Fever / chemically induced
  • Fever / metabolism*
  • Guinea Pigs
  • Injections, Intravenous
  • Jugular Veins
  • Kupffer Cells / metabolism*
  • Lipopolysaccharides / administration & dosage
  • Lipopolysaccharides / pharmacology*


  • Antibodies, Blocking
  • Cytokines
  • Lipopolysaccharides
  • Dinoprostone