Abstract | BACKGROUND: Overproduction of nitric oxide by the inducible form of nitric oxide synthase (iNOS) has been implicated in colitis. Different authors have postulated both toxic and protective effects of nitric oxide (NO) in the pathophysiology of active inflammation. The objective of this study was to examine the role of iNOS in experimental chronic colitis using iNOS-deficient mice. METHODS: RESULTS: After DSS treatment, a moderate colitis with marked cell infiltration was observed. Intense expression of iNOS was observed on infiltrating cells as well as on the colonic mucosal epithelium in these animals. In the iNOS-deficient mice, tissue damage was significantly diminished. No iNOS or nitrotyrosine staining was found in iNOS-deficient mice. The number of infiltrating cells and the expression of mucosal adressin cell adhesion molecule-1 were significantly attenuated in the DSS-treated colon of iNOS-deficient mice. CONCLUSION: Induction of iNOS seems to act as a critical toxic effector molecule in the pathogenesis of chronic colonic inflammation.
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Authors | R Hokari, S Kato, K Matsuzaki, M Kuroki, A Iwai, A Kawaguchi, S Nagao, T Miyahara, K Itoh, E Sekizuka, H Nagata, H Ishii, S Miura |
Journal | Free radical biology & medicine
(Free Radic Biol Med)
Vol. 31
Issue 2
Pg. 153-63
(Jul 15 2001)
ISSN: 0891-5849 [Print] United States |
PMID | 11440827
(Publication Type: Journal Article)
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Chemical References |
- Cell Adhesion Molecules
- Immunoglobulins
- Madcam1 protein, mouse
- Mucoproteins
- Nitric Oxide
- 3-nitrotyrosine
- Tyrosine
- Dextran Sulfate
- Nitric Oxide Synthase
- Nitric Oxide Synthase Type II
- Nos2 protein, mouse
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Topics |
- Animals
- Cell Adhesion Molecules
- Chronic Disease
- Colitis
(enzymology, etiology, genetics, pathology)
- Dextran Sulfate
(toxicity)
- Immunoglobulins
(metabolism)
- Immunohistochemistry
- Intestinal Mucosa
(drug effects, metabolism, pathology)
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Mucoproteins
(metabolism)
- Nitric Oxide
(physiology)
- Nitric Oxide Synthase
(deficiency, genetics)
- Nitric Oxide Synthase Type II
- Tyrosine
(analogs & derivatives, metabolism)
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