Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/33073
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dc.contributor.authorYıldar, Murat-
dc.contributor.authorAkşit, Hasan Z.-
dc.contributor.authorKorkut, Oǧuzhan-
dc.contributor.authorSunay, Bahar-
dc.contributor.authorSeyrek, Kamil-
dc.date.accessioned2023-06-18T08:03:24Z-
dc.date.available2023-06-18T08:03:24Z-
dc.date.issued2014-04-
dc.identifier.citationÖzyiǧit, M. Ö. vd. (2014). "Protective effect of 2-aminoethyl diphenylborinate on acute ischemia-reperfusion injury in the rat kidney". Journal of Surgical Research, 187(2), 683-689.en_US
dc.identifier.issn0022-4804-
dc.identifier.issn1095-8673-
dc.identifier.urihttps://doi.org/10.1016/j.jss.2013.11.009-
dc.identifier.urihttp://hdl.handle.net/11452/33073-
dc.description.abstractBackground: To investigate the protective effect of 2-aminoethyl diphenylborinate (2-APB) against ischemia-reperfusion (I/R) injury in the rat kidney by an experimental study. Materials and methods: Thirty male Sprague-Dawley rats were randomly divided into the following three groups: (1) sham group, (2) I/R group, and (3) I/R + 2-APB group. Renal I/ R injury was induced by clamping the left renal pedicle for 45 min after right nephrectomy, followed by 3 h of reperfusion. The therapeutic agent 2-APB was administered intravenously at a dose of 2 mg/kg 10 min before renal ischemia. Glutathione, superoxide dismutase, total antioxidant capacity, malondialdehyde, tumor necrosis factor a, interleukin 6, aspartate aminotransferase, alanine aminotransferase, and creatinine levels were measured from blood samples, and the rats were sacrificed subsequently. Tissue samples were scored histopathologically. Visualization of apoptotic cells was performed using the terminal deoxynucleotidyl transferase dUTP nick end labeling staining method. Results: 2-APB significantly reduced serum malondialdehyde, tumor necrosis factor a, interleukin 6, aspartate aminotransferase, alanine aminotransferase, and creatinine levels in the I/R injury group. However, glutathione, superoxide dismutase, and total antioxidant capacity levels increased significantly. Histopathologic scores were significantly better and the rate of apoptosis was lower in the 2-APB group. Conclusions: 2-APB reduces oxidative stress and damage caused by renal I/R injury. The results of this study demonstrate that 2-APB can be used as an effective agent against I/R injury in the kidney.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject2-APBen_US
dc.subjectKidney failureen_US
dc.subjectCalcium channelsen_US
dc.subjectAntioxidantsen_US
dc.subjectOxidative stressen_US
dc.subjectFree-radicalsen_US
dc.subjectMechanismsen_US
dc.subjectBlockeren_US
dc.subjectToxicityen_US
dc.subjectSurgeryen_US
dc.subject.meshAcute kidney injuryen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAntioxidantsen_US
dc.subject.meshApoptosisen_US
dc.subject.meshBoron compoundsen_US
dc.subject.meshCalcium channel agonistsen_US
dc.subject.meshCreatinineen_US
dc.subject.meshDisease models, animalen_US
dc.subject.meshGlutathioneen_US
dc.subject.meshInterleukin-6en_US
dc.subject.meshMaleen_US
dc.subject.meshMalondialdehydeen_US
dc.subject.meshOxidative stressen_US
dc.subject.meshRandom allocationen_US
dc.subject.meshRatsen_US
dc.subject.meshRats, sprague-dawleyen_US
dc.subject.meshReperfusion injuryen_US
dc.subject.meshSuperoxide dismutaseen_US
dc.subject.meshTumor necrosis factor-alphaen_US
dc.titleProtective effect of 2-aminoethyl diphenylborinate on acute ischemia-reperfusion injury in the rat kidneyen_US
dc.typeArticleen_US
dc.identifier.wos000332770600043tr_TR
dc.identifier.scopus2-s2.0-84900564665tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Veteriner Fakültesi/Patoloji Anabilim Dalı.tr_TR
dc.identifier.startpage683tr_TR
dc.identifier.endpage689tr_TR
dc.identifier.volume187tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalJournal of Surgical Researchen_US
dc.contributor.buuauthorÖzyiǧit, Musa Özgür-
dc.contributor.researcheridAAR-6478-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed24331939tr_TR
dc.subject.wosSurgeryen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid6507338060tr_TR
dc.subject.scopusStaining; Acids; Ironen_US
dc.subject.emtreeAlanine aminotransferase blood levelen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAnimal modelen_US
dc.subject.emtreeAnimal tissueen_US
dc.subject.emtreeAntioxidant activityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeAspartate aminotransferase blood levelen_US
dc.subject.emtreeBlood samplingen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug effecten_US
dc.subject.emtreeHistopathologyen_US
dc.subject.emtreeKidney ischemiaen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNephrectomyen_US
dc.subject.emtreeNick end labelingen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeOxidative stressen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeRenal protectionen_US
dc.subject.emtreeReperfusion injuryen_US
dc.subject.emtree2 aminoethoxydiphenylboraneen_US
dc.subject.emtreeAlanine aminotransferaseen_US
dc.subject.emtreeAntioxidanten_US
dc.subject.emtreeAspartate aminotransferaseen_US
dc.subject.emtreeCreatinineen_US
dc.subject.emtreeDna nucleotidylexotransferaseen_US
dc.subject.emtreeGlutathioneen_US
dc.subject.emtreeInterleukin 6en_US
dc.subject.emtreeMalonaldehydeen_US
dc.subject.emtreeSuperoxide dismutaseen_US
dc.subject.emtreeTumor necrosis factor alphaen_US
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