Increases in free radicals and cytoskeletal protein oxidation and nitration in the colon of patients with inflammatory bowel disease. Issue 5 (1st May 2003)

• Record Type: Journal Article
• Authors: Keshavarzian, A; Banan, A; Farhadi, A; Komanduri, S; Mutlu, E; Zhang, Y; Fields, J Z
• Is Part Of: Gut. Volume 52:Issue 5(2003)
• Page Start: 720
• Page End: 728
• Publication Date: 2003-05-01
• Subjects: inflammatory bowel disease -- ulcerative colitis -- Crohn's disease -- free radicals -- intestinal barrier -- cytoskeleton -- nitric oxide -- oxidative stress -- inflammation; ROM, reactive oxygen metabolite -- RNM, reactive nitrogen metabolite -- NO, nitric oxide -- iNOS, inducible NO synthase -- IBD, inflammatory bowel disease -- UC, ulcerative colitis -- CD, Crohn's disease -- UCAI, ulcerative colitis disease activity index -- CDAI, Crohn's disease activity index -- PVDF, polyvinylidene difluoride -- TBS, Tris buffered saline -- ECL, enhanced chemiluminescence -- OD, optical density -- DNPH, 2, 4, dinitrophenylhydrazine -- BSA, bovine serum albumin -- PBS, phosphate buffered saline -- HRP, horseradish peroxidase -- LSCM, laser scanning confocal microscope; Gastroenterology -- Periodicals; 616.33
• DOI: 10.1136/gut.52.5.720
• Languages: English
• ISSNs: 0017-5749

Abstract

Abstract : Background: Overproduction of colonic oxidants contributes to mucosal injury in inflammatory bowel disease (IBD) but the mechanisms are unclear. Our recent findings using monolayers of intestinal cells suggest that the mechanism could be oxidant induced damage to cytoskeletal proteins. However, oxidants and oxidative damage have not been well characterised in IBD mucosa. Aims: To determine whether there are increases in oxidants and in tissue and cytoskeletal protein oxidation in IBD mucosa. Methods: We measured nitric oxide (NO) and markers of oxidative injury (carbonylation and nitrotyrosination) to tissue and cytoskeletal proteins in colonic mucosa from IBD patients (ulcerative colitis, Crohn's disease, specific colitis) and controls. Outcomes were correlated with IBD severity score. Results: Inflamed mucosa showed the greatest increases in oxidants and oxidative damage. Smaller but still significant increases were seen in normal appearing mucosa of patients with active and inactive IBD. Tissue NO levels correlated with oxidative damage. Actin was markedly (>50%) carbonylated and nitrated in inflamed tissues of active IBD, less so in normal appearing tissues. Tubulin carbonylation occurred in parallel; tubulin nitration was not observed. NO and all measures of oxidative damage in tissue and cytoskeletal proteins in the mucosa correlated with IBD severity. Disruption of the actin cytoarchitecture was primarily within the epithelial cells and paracellular area. Conclusions: Oxidant levels increase in IBD along with oxidation of tissue and cytoskeletal proteins. Oxidative injury correlated with disease severity but is also present in substantial amounts in normal appearing mucosa of IBD patients, suggesting that oxidative injury does not necessarily lead to tissue injury and is not entirely a consequence of tissue injury. Marked actin oxidation (>50%)—which appears to result from cumulative oxidative damage—was only seen in inflamed mucosa, suggesting that oxidant induced cytoskeletal disruption is required for tissue injury, mucosal disruption, and IBD flare up.