Monochloramine induces acute and protracted colitis in the rat: Response to pharmacological treatment
- 作者：Ballester ; Isabel ; Gonz脙脙lez ; Raquel ; Nieto ; Ana ; Zarzuelo ; Antonio ; S脙脙nchez de Medina ; Ferm脙脙n
- 关键词：Monochloramine ; Oxidative stress ; Inflammatory bowel disease ; Alkaline phosphatase ; Myeloperoxidase
- 刊名：Life Sciences
- 出版年：2005
- 期刊代码：62_00243205
- 类别：imm
- 出版时间：May 6, 2005
- 卷：76
- 期：25
- 页码：2965-2980
- 文件大小：703 K
摘要
Monochloramine is a powerful oxidative molecule that is produced in inflammatory sites. We investigated the effect of intrarectally administered monochloramine (3.2 mg) in the rat. A single enema induced after 24 h an intense inflammatory reaction characterized by mucosal necrosis, submucosal edema, hemorrhage and colonic thickening, as well as induction of nitric oxide synthase and tumor necrosis factor and an increase in the interferon γ/interleukin 4 ratio. The inflammatory response peaked 3–5 days after monochloramine administration and then followed a extended recovery phase. At 1 week there was substantial but incomplete mucosal repair, submucosal edema, neutrophil/macrophage infiltration and increased myeloperoxydase and alkaline phosphatase activities. Oxidative stress, as determined by malonyldialdehyde levels, was prominent only in the acute phase (3–5 days). Monochloramine colitis was amenable to pharmacological treatment with sulphasalazine or prednisolone, suggesting that it may be used as an experimental model of inflammatory bowel disease. In conclusion, monochloramine induces acute and protracted colonic inflammation in the rat. Locally produced monochloramine might contribute to the perpetuation of inflammatory bowel disease.