A protective effect of the synthetic coumarine derivative Cloricromene against DNB-colitis in the rat

Walter Fries, Emanuela Mazzon, Sergio Sturiale, Maria R. Giofré, Maria A. Lo Presti, Salvatore Cuzzocrea, Giuseppe M. Campo, Achille P. Caputi, Giuseppe Longo, Giacomo C. Sturniolo

Research output: Contribution to journalArticlepeer-review

Abstract

Biologic therapies, namely antibodies against tumor necrosis factor-α (TNF- α) or its receptors, have been recently introduced for the treatment of patients with inflammatory bowel disease (IBD). In the present study the effects of cloricromene, an agent with known antithrombotic actions and with demonstrated anti-TNF- α activity were investigated in a rat model of experimental colitis induced with dinitrobenzenesulphonic acid (DNB)/ethanol. We investigated three experimental groups: (i) sham-colitis with vehicle-treatment (controls, n = 6), (ii) colitis with vehicle-treatment (saline, 0.1 ml s.c., daily) (DNB-V, n = 7), (iii) colitis with cloricromene-treatment (10 mg/kg/day s.c.; DNB-C, n = 8). After 7 days, the weight gain, colon wet weight, macroscopic damage score, coagulation parameters, colon mucosal myeloperoxidase activity (MPO), and tissue concentrations of TNF- α and of macrophage inhibitory peptide-2 (MIP-2) were assessed. The macroscopic damage scores, colon wet weights, and tissue MIP-2 levels were significantly increased in untreated and in cloricromene-treated rats compared with controls. Cloricromene treatment was associated with a minor body weight loss (p <0.025) and significantly reduced tissue concentrations of MPO and TNF-α (p <0.02, both). Blood coagulation parameters were not affected by treatment. In the DNB-model treatment with cloricromene effectively reduces tissue levels of TNF- α and of myeloperoxidase, whereas MIP-2 concentrations were not influenced. Blood coagulation parameters remained unchanged indicating safety of treatment. Since biological therapies frequently fail to improve disease course of IBD, other therapies with similar targets should be further investigated.

Original languageEnglish
Pages (from-to)2749-2756
Number of pages8
JournalLife Sciences
Volume74
Issue number22
DOIs
Publication statusPublished - Apr 16 2004

Keywords

  • Cloricromene
  • Experimental colitis
  • Heparin
  • MIP-2
  • Rat
  • Thromboembolism
  • TNF-α

ASJC Scopus subject areas

  • Pharmacology

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