Treatment with Met-RANTES decreases bacterial translocation in experimental colitis

Am J Surg. 2006 Jan;191(1):77-83. doi: 10.1016/j.amjsurg.2005.10.005.

Abstract

Background: During colitis, epithelial function is impaired, leading to increased bacterial translocation. Recent studies have shown the important role of proinflammatory cytokines and chemokines, including RANTES (regulated on activation, normal T-cell expressed and secreted), in inflammatory bowel diseases (IBDs). In this study, we evaluated the role of Met-RANTES, an antagonist of the RANTES receptor, on the impairment of bacterial translocation in a rat model of colitis.

Methods: Rats were randomly assigned to 3 groups. Group 1 = control, group 2 = experimental colitis, and group 3 = colitis plus Met-RANTES treatment. On day 7 after colitis was induced, plasma tumor necrosis factor-alpha colon tissue myeloperoxidase and portal blood endotoxin levels were measured. Lymph node, liver, and spleen culture quantified bacterial translocation.

Results: Met-RANTES treatment resulted in significant decreases in colonic damage as well as bacterial translocation in experimental colitis.

Conclusions: These results suggest that chemokine receptor antagonists may potentially be useful in the treatment of IBDs.

Publication types

  • Evaluation Study

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Bacterial Translocation / drug effects*
  • Chemokine CCL5 / analogs & derivatives*
  • Chemokine CCL5 / pharmacology
  • Colitis / chemically induced
  • Colitis / microbiology
  • Colitis / physiopathology*
  • Colon / drug effects*
  • Disease Models, Animal
  • Male
  • Noxae / adverse effects
  • Rats
  • Rats, Wistar
  • Trinitrobenzenesulfonic Acid / adverse effects

Substances

  • Anti-Inflammatory Agents
  • Chemokine CCL5
  • Noxae
  • RANTES, Met-
  • Trinitrobenzenesulfonic Acid