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pubmed-article:15472512pubmed:abstractTextPolyamines and their acetylated derivatives are a prerequisite for cellular metabolism and considered to be essential for proliferation and differentiation of the rapidly renewing intestinal mucosa. However, their role during mucosal inflammation is less clear. Polyamine concentrations were determined in isolated colonic epithelial cells (CECs) from endoscopic biopsies from 26 patients with inflammatory bowel disease (IBD) and 40 controls as well as colon samples from mice with and without acute or chronic dextran sodium sulfate (DSS)-induced colitis. In patients with ulcerative colitis, CEC spermidine and N8-acetylspermidine levels were significantly enhanced and spermine levels were reduced compared with healthy controls. A correlation of polyamine levels of patients with IBD with their corresponding inflammatory index revealed that increased concentrations of spermidine, N8-acetylspermidine, and N1-acetylspermine were found in CECs from the most severe inflamed mucosal areas. Using acute and chronic DSS colitis as a model of mucosal inflammation, we found enhanced levels of spermidine and spermine in acute colitis, whereas in chronic inflammation, CEC spermine concentrations were decreased. Our data indicate a lack of the anti-inflammatory polyamine spermine in severe ulcerative colitis and chronic DSS colitis, which may aggravate the disease. Increased spermidine and N8-acetylspermidine levels reflect increased uptake and metabolism likely due to accelerated proliferation and regeneration of CECs.lld:pubmed
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pubmed-article:15472512pubmed:copyrightInfoCopyright 2004 Lippincott Williams & Wilkinslld:pubmed
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pubmed-article:15472512pubmed:pagination529-35lld:pubmed
pubmed-article:15472512pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:15472512pubmed:articleTitleIntracellular polyamine levels of intestinal epithelial cells in inflammatory bowel disease.lld:pubmed
pubmed-article:15472512pubmed:affiliationDepartment of Surgery, University of Regensburg, Germany. thomas.weiss@klinik.uni-regensburg.delld:pubmed
pubmed-article:15472512pubmed:publicationTypeJournal Articlelld:pubmed