Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8221
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dc.contributor.authorTeke, Z.-
dc.contributor.authorBostanci, E.B.-
dc.contributor.authorYenisey, C.-
dc.contributor.authorKelten, Esra Canan-
dc.contributor.authorSacar, M.-
dc.contributor.authorSimsek, N.G.-
dc.contributor.authorDüzcan, Süleyman Ender-
dc.date.accessioned2019-08-16T12:37:15Z
dc.date.available2019-08-16T12:37:15Z
dc.date.issued2013-
dc.identifier.issn0894-1939-
dc.identifier.urihttps://hdl.handle.net/11499/8221-
dc.identifier.urihttps://doi.org/10.3109/08941939.2012.687434-
dc.description.abstractPurpose: We aimed to investigate whether caffeic acid phenethyl ester (CAPE) prevents detrimental systemic effects of intestinal ischemia-reperfusion (IR) injury on colonic anastomotic wound healing. Methods: This experimental study was conducted on 48 male Wistar albino rats. The rats were randomly allocated into four groups and a left colonic anastomosis was performed in all rats: (i) sham-operated group (n = 12), laparatomy without intestinal IR injury; (ii) sham + CAPE group (n = 12), identical to Group 1 except for CAPE treatment (10 µmol/kg, intravenously); (iii) intestinal IR group (n = 12), 60 min of superior mesenteric ischemia followed by reperfusion; and (iv) IR + CAPE-treated group (n = 12) (10 µmol/kg, intravenously, 30 min before the construction of colonic anastomosis). On the postoperative day 7, the rats were subjected to relaparotomy for in vivo measurement of the colonic anastomotic bursting pressure. A colonic segment including the anastomotic site was resected for histopathological evaluation and biochemical analyses. The plasma proinflammatory cytokine levels were measured. Body weight changes were examined. Results: CAPE treatment significantly increased colonic anastomotic bursting pressures, and colonic anastomotic tissue hydroxyproline contents and antioxidant parameters (p < .05), and significantly decreased oxidative stress markers in colonic anastomotic tissues and plasma proinflammatory cytokine levels (p < .05). Histopathological scores were significantly better due to CAPE administration (p < .05). Conclusions: This study clearly showed that CAPE treatment prevented the delaying effects of remote IR injury on colonic anastomotic wound healing. Further clinical studies are required to determine whether CAPE has a useful role in the enhancement of gastrointestinal anastomotic wound healing during particular surgeries in which IR-induced organ injury occurs. © 2013 Informa Healthcare USA, Inc.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Investigative Surgeryen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBursting pressuresen_US
dc.subjectCaffeic acid phenethyl esteren_US
dc.subjectCatalaseen_US
dc.subjectColonic anastomosisen_US
dc.subjectGlutathioneen_US
dc.subjectGlutathione peroxidaseen_US
dc.subjectGlutathione reductaseen_US
dc.subjectHydroxyprolineen_US
dc.subjectIschemia-reperfusionen_US
dc.subjectMalondialdehydeen_US
dc.subjectMyeloperoxidaseen_US
dc.subjectNitric oxideen_US
dc.subjectWound healingen_US
dc.subjectXanthine oxidaseen_US
dc.subjectantiinflammatory agenten_US
dc.subjectantioxidanten_US
dc.subjectcaffeic acid phenethyl esteren_US
dc.subjecthydroxyprolineen_US
dc.subjectinterleukin 1betaen_US
dc.subjectinterleukin 6en_US
dc.subjecttumor necrosis factor alphaen_US
dc.subjectanimal experimenten_US
dc.subjectanimal modelen_US
dc.subjectantiinflammatory activityen_US
dc.subjectantioxidant activityen_US
dc.subjectarticleen_US
dc.subjectbody weighten_US
dc.subjectchemical analysisen_US
dc.subjectcolon anastomosisen_US
dc.subjectcontrolled studyen_US
dc.subjectexperimental studyen_US
dc.subjecthistopathologyen_US
dc.subjectin vivo studyen_US
dc.subjectintestine injuryen_US
dc.subjectlaparotomyen_US
dc.subjectmaleen_US
dc.subjectmeasurementen_US
dc.subjectmesenteric ischemiaen_US
dc.subjectnonhumanen_US
dc.subjectoxidative stressen_US
dc.subjectpriority journalen_US
dc.subjectraten_US
dc.subjectreoperationen_US
dc.subjectreperfusion injuryen_US
dc.subjectsuperior mesenteric arteryen_US
dc.subjectwound healingen_US
dc.subjectAnastomosis, Surgicalen_US
dc.subjectAnimalsen_US
dc.subjectAnti-Inflammatory Agents, Non-Steroidalen_US
dc.subjectCaffeic Acidsen_US
dc.subjectColonen_US
dc.subjectCytokinesen_US
dc.subjectDrug Evaluation, Preclinicalen_US
dc.subjectLaparotomyen_US
dc.subjectMaleen_US
dc.subjectMesenteric Artery, Superioren_US
dc.subjectOxidative Stressen_US
dc.subjectPhenylethyl Alcoholen_US
dc.subjectRandom Allocationen_US
dc.subjectRatsen_US
dc.subjectRats, Wistaren_US
dc.subjectReperfusion Injuryen_US
dc.subjectSurgical Wound Dehiscenceen_US
dc.subjectWound Healingen_US
dc.subjectXanthine Oxidaseen_US
dc.titleCaffeic acid phenethyl ester prevents detrimental effects of remote ischemia-reperfusion injury on healing of colonic anastomosesen_US
dc.typeArticleen_US
dc.identifier.volume26en_US
dc.identifier.issue1en_US
dc.identifier.startpage16
dc.identifier.startpage16en_US
dc.identifier.endpage29en_US
dc.identifier.doi10.3109/08941939.2012.687434-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid22646141en_US
dc.identifier.scopus2-s2.0-84873675895en_US
dc.identifier.wosWOS:000314650400004en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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