Modulation of inflammatory response in a cirrhotic rat model with induced bacterial peritonitis

PLoS One. 2013;8(3):e59692. doi: 10.1371/journal.pone.0059692. Epub 2013 Mar 20.

Abstract

Bacterial peritonitis is a severe complication in patients with cirrhosis and ascites and despite antibiotic treatment, the inflammatory response to infection may induce renal dysfunction leading to death. This investigation evaluated the effect of TNF-α blockade on the inflammatory response and mortality in cirrhotic rats with induced bacterial peritonitis treated or not with antibiotics. Sprague-Dawley rats with carbon-tetrachloride-induced cirrhosis were treated with an intraperitoneal injection of 10(9) CFU of Escherichia coli diluted in 20 mL of sterile water to induce bacterial peritonitis and randomized to receive subcutaneously-administered placebo, ceftriaxone, anti-TNF-α mAb and ceftriaxone, or anti-TNF-α mAb alone. No differences were observed between groups at baseline in respect to renal function, liver hepatic tests, serum levels of nitrite/nitrate and TNF-α. Treatment with ceftriaxone reduced mortality (73.3%) but differences did not reach statistical significance as compared to placebo. Mortality in rats treated with ceftriaxone and anti-TNF-α mAb was significantly lower than in animals receiving placebo (53% vs. 100%, p<0.01). Serum TNF-α decreased significantly in surviving rats treated with ceftriaxone plus anti-TNF-α mAb but not in treated with antibiotics alone. Additional studies including more animals are required to assess if the association of antibiotic therapy and TNF-α blockade might be a possible approach to reduce mortality in cirrhotic patients with bacterial peritonitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology*
  • Carbon Tetrachloride / toxicity
  • Ceftriaxone / pharmacology*
  • Escherichia coli / drug effects*
  • Immunoassay
  • Liver Cirrhosis / chemically induced
  • Liver Cirrhosis / complications*
  • Male
  • Peritonitis / drug therapy*
  • Peritonitis / etiology
  • Peritonitis / microbiology
  • Peritonitis / physiopathology*
  • Rats
  • Rats, Sprague-Dawley
  • Statistics, Nonparametric
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha / blood
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Antibodies, Monoclonal
  • Tumor Necrosis Factor-alpha
  • Ceftriaxone
  • Carbon Tetrachloride

Grants and funding

This study was partially funded by unrestricted grants from the Generalitat de Catalunya (AGAUR) (2005SGR01085), Fondo de Investigaciones Sanitarias (FIS) PI08-0262 and from the Fundación de Investigación del Hospital General Universitario de Alicante. Centocor (Malvern, PA, USA) also provided funding to conduct this investigation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.