Endogenous interleukin-10 is required for the defervescence of fever evoked by local lipopolysaccharide-induced and Staphylococcus aureus-induced inflammation in rats

J Physiol. 2003 Jun 1;549(Pt 2):653-64. doi: 10.1113/jphysiol.2002.037291. Epub 2003 Apr 11.

Abstract

We tested the hypothesis that endogenous interleukin (IL)-10 limits the fever induced by a Gram-negative bacterial toxin (Escherichia coli lipopolysaccharide, LPS) and a Gram-positive bacterial toxin (Staphylococcus aureus), when these toxins are injected into a subcutaneous air pouch (I.PO.) in rats. Injection of LPS or S. aureus caused fevers that were reduced in amplitude and duration by simultaneous administration of rat recombinant IL-10. The inhibition of fever by IL-10 was accompanied by a significant reduction in the toxin-evoked increases in concentrations of immunoreactive IL-6 at the site of inflammation and of IL-6 and IL-1 receptor antagonist in the circulation. Conversely, neutralisation of endogenous IL-10 in the pouch increased the amplitude and dramatically increased the duration of toxin-evoked fever, and augmented toxin-induced increases in pouch tumour necrosis factor-alpha, IL-1beta, and especially IL-6. Our data support a crucial regulatory role for endogenous IL-10 in limiting the fever responses during both Gram-negative and Gram-positive infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Temperature
  • Female
  • Fever / etiology*
  • Fever / metabolism
  • Fever / physiopathology*
  • Inflammation / complications*
  • Inflammation / etiology
  • Inflammation / microbiology
  • Interleukin-1 / metabolism
  • Interleukin-10 / metabolism*
  • Interleukin-10 / pharmacology
  • Interleukin-6 / metabolism
  • Lipopolysaccharides
  • Male
  • Osmolar Concentration
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Staphylococcal Infections
  • Subcutaneous Tissue / microbiology
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-1
  • Interleukin-6
  • Lipopolysaccharides
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-10