Role of inducible nitric oxide synthase in trinitrobenzene sulphonic acid induced colitis in mice

• Published in: Gut Vol. 45; no. 6; pp. 864 - 873
• Main Authors: McCafferty, D-M, Miampamba, M, Sihota, E, Sharkey, K A, Kubes, P
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group Ltd and British Society of Gastroenterology 01.12.1999; BMJ; BMJ Publishing Group LTD
• Subjects: Acute Disease; Animals; Biological and medical sciences; Biopsy; Chronic Disease; Colitis - chemically induced; Colitis - enzymology; Crohns disease; Deoxyribonucleic acid; DNA; epithelial permeability; Female; Fluorescent Antibody Technique; Gastroenterology. Liver. Pancreas. Abdomen; Gene Expression; Inflammation; Inflammatory bowel disease; Laboratories; Male; Medical research; Medical sciences; Mice; Mice, Mutant Strains; Neutrophils; Neutrophils - enzymology; Nitric oxide; nitric oxide synthase; Nitric Oxide Synthase - deficiency; Nitric Oxide Synthase - genetics; Nitric Oxide Synthase - physiology; Nitric Oxide Synthase Type II; Other diseases. Semiology; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; Rodents; Stem cells; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Studies; Trinitrobenzenesulfonic Acid; New Jersey; Enzyme; Induction; Leukocyte; Pathogenesis; Rodentia; Nitric-oxide synthase; Vertebrata; Experimental disease; Mammalia; Mouse; Animal; Digestive diseases; Intestinal disease; Oxidoreductases; Colitis
• ISSN: 0017-5749; 1468-3288; 1458-3288
• DOI: 10.1136/gut.45.6.864

BACKGROUND Studies using inhibitors of nitric oxide synthase (NOS) to date are inconclusive regarding the role of inducible NOS (iNOS) in intestinal inflammation. AIMS (1) To examine the role of iNOS in the development of chronic intestinal inflammation; (2) to identify the cellular source(s) of iNOS. METHODS Colitis was induced by an intrarectal instillation of trinitrobenzene sulphonic acid (TNBS, 60 mg/ml, 30% ethanol), in wild type (control) or iNOS deficient mice. Mice were studied over 14 days; the colons were scored for injury and granulocyte infiltration was quantified. Blood to lumen leakage of51Cr-EDTA was measured as a quantitative index of mucosal damage. RESULTS At 24 and 72 hours, iNOS deficient mice had significantly increased macroscopic inflammation compared with wild type mice. Granulocyte infiltration increased significantly at 24 hours and remained elevated in iNOS deficient mice at 72 hours, but significantly decreased in controls. However, by seven days post-TNBS macroscopic damage, microscopic histology, granulocyte infiltration, and mucosal permeability did not differ between wild type and iNOS deficient mice. A four- to fivefold increase in iNOS mRNA was observed in wild type mice at 72 hours and seven days post-TNBS and was absent in iNOS deficient mice. Immunohistochemistry techniques showed that iNOS expression was predominantly localised in neutrophils, with some staining also in macrophages. CONCLUSIONS These results suggest that leucocyte derived iNOS ameliorates the early phase, but does not impact on the chronic phase of TNBS induced colitis despite the presence of iNOS.