Hepatoprotective role of interleukin 10 in galactosamine/lipopolysaccharide mouse liver injury

Louis, H;Lemoine, O.;Peny, MO;Gulbis, B.;Devière, Jacques;et.al.
(1997) Gastroenterology — Vol. 112, n° 3, p. 935-942 (1997)

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Authors
  • Louis, H
    Author
  • Lemoine, O.
    Author
  • Peny, MO
    Author
  • Gulbis, B.
    Author
  • Nisol, FrançoiseUCLouvain
    Author
  • Devière, Jacques
    Author
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Abstract
Background & Aims: Interleukin (IL)-10 is a potent antiinflammatory cytokine. Its role in modulating liver injury induced by galactosamine and lipopolysaccharide (Gal/LPS) was investigated. Methods: The. effects of recombinant IL-10 (rIL-10), anti-IL-10 monoclonal antibodies, or gadolinium chloride (GdCl3) pretreatment were studied in mice challenged with Gal/LPS. Tumor necrosis factor (TNF) alpha and IL-10 serum concentrations were measured and liver injury was assessed by alanine aminotransferase (ALT) serum concentrations and by histology. Results: (1) IL-10 is pvoduced early and together with TNF-alpha after Gal/LPS challenge. (2) Anti-IL-10 pretreatment increases TNF-alpha (+443%, P = 0.04), ALT (+160%, P = 0.04) serum levels, and the percentage of severe necrosis compared with control monoclonal antibodies. (3) Administration of vIL-10 30 minutes before Gal/LPS decreases TNF-alpha (-67%, P = 0.02), ALI (-94%, P = 0.01) serum concentrations, and the proportion of severe necrosis. The hepatoprotective effect is still observed when rIL-10 is injected 30 or 120 minutes after Gal/LPS. (4) GdCl3 pretreatment protects against hepatotoxicity, decreases TNF-alpha, but increases IL-10 serum concentrations. Conclusions: These results indicate that IL-10 protects the liver in the Gal/LPS mouse model. Increased IL-10 and decreased TNF-a secretion ave potentially involved in the hepatoprotection observed after GdCl3 pretreatment.
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Citations

Louis, H., Lemoine, O., Peny, M., Gulbis, B., Nisol, F., Goldman, M., & Devière, J. (1997). Hepatoprotective role of interleukin 10 in galactosamine/lipopolysaccharide mouse liver injury. Gastroenterology, 112(3), 935-942. https://doi.org/10.1053/gast.1997.v112.pm9041256 (Original work published 1997)