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  • 1
    ISSN: 1573-2568
    Keywords: ANTIOXIDANTS ; EICOSANOIDS ; FATTY ACIDS ; FREE RADICALS ; INFLAMMATORY BOWEL DISEASE ; ULCERATIVE COLITIS ; TRINITROBENZENE SULFONIC ACID
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The intrarectal administration oftrinitrobenzene sulfonic acid in rats induces ulcerativecolitis, which results in histological alterations ofcolonic mucosa, severe modification of the cellularantioxidant defense system, and enhanced production ofinflammatory eicosanoids. This study evaluated theinfluence of different dietary fatty acids, ie,monounsaturated, n-3, and n-3 + n-6 polyunsaturatedfatty acids, on the recovery of the colonic mucosahistological pattern, the cellular antioxidant defensesystem of colon, and PGE2 and LTB4colonic mucosa contents in a model of ulcerative colitisinduced by intrarectal administration of trinitrobenzene sulfonicacid. Administration of dietary n-3 polyunsaturatedfatty acids led to a minimum stenosis score, a higherhistological recovery, lower colon alkaline phosphatase and gamma-glutamyltranspeptidase activities,and lower mucosal levels of PGE2 andLTB4 compared with the other two experimentalgroups. However, glutathione transferase, glutathionereductase, glutathione peroxidase, and catalase activities were lowerin the group treated with n-3 polyunsaturated fattyacids than in the groups fed with either themonounsaturated or the n-6 + n-3 polyunsaturatedenriched diet. We conclude that n-3 polyunsaturatedfatty acids can be administered to prevent inflammationin ulcerative colitis, but they cause a decrease in thecolonic antioxidant defense system, promoting oxidative injury at the site of inflammation.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-2568
    Keywords: COLON ; FATTY ACID ; INFLAMMATORY BOWEL DISEASE ; ULCERATIVE COLITIS ; TRINITROBENZENESULFONIC ACID
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Polyunsaturated fatty acids have a key role inthe pathogenesis of inflammatory bowel disease sincesome of the arachidonic acid-derived eicosanoids havebeen found to be increased in inflamed intestinal mucosa in the acute phase of human disease. Theaim of this study was to prospectively assess plasma andcolon mucosa fatty acid patterns in rats withexperimental ulcerative colitis. Twenty rats weretreated with trinitrobenzene sulfonic acid and 20 withNaCl; two groups were killed after one week and twoafter two weeks to evaluate colon damage. Plasma wasobtained by aortic puncture and colonic mucosa was scraped off and the fatty acid pattern wasdetermined by gas-liquid chromatography. Total,saturated, and monounsaturated plasma fatty acids weresignificantly higher in both periods of ulcerativecolitis as compared to controls. Plasma n-6 fatty acidswere increased after treatment, but no significantchanges were observed concerning to n-3 fatty acids.With regard to colon mucosa, saturated andmonounsaturated fatty acids did not change because of thedisease; however, n-6 fatty acids decreased in the firstweek and increased in the second week and n-3 fattyacids were increased. Changes on the fatty aciddistribution in plasma did not parallel to those of colonicmucosa except for 22:6(n-3). We have also found thatexperimental ulcerative colitis induced bytrinitrobenzene sulfonic acid reproduces many of thefeatures related to changes in plasma and colon mucosafatty acids observed in the human disease.
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  • 3
    ISSN: 1573-2568
    Keywords: INFLAMMATORY BOWEL DISEASE ; TRINITROBENZENESULFONIC ACID ; HISTOLOGY ; ULTRASTRUCTURE
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Inflammatory bowel disease (IBD) of humans is achronic and devastating disease of unknown etiology.Models of acute colitis in animals have been achieved byintrarectal administration of agents such as 2,4,6-trinitrobenzenesulfonic acid (TNBS) intorat colon. This agent induces focal inflammation andalterations in the colon with features similar to thosefound in chronic inflammatory diseases in humans. The aim of this study was to assess the effectof TNBS administration on histological andultrastructural features of the rat colon, especially inareas not affected by transmural inflammation. Also in areas without transmural inflammation, weobserved a significant increase in crypt diameter and inthe number and area of the goblet cells, as well asalterations in the contents of mucin in goblet cells. We conclude that TNBS treatment in rats led tosevere changes in normal architecture of the colon andalso in damaged areas where no direct inflammation wasproduced.
    Type of Medium: Electronic Resource
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