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dc.contributor.authorAbalı, Remzi
dc.contributor.authorTaşdemir, Nicel
dc.contributor.authorYüksel, Mehmet Aytaç
dc.contributor.authorGüzel, Savaş
dc.contributor.authorÖznur, Meltem
dc.contributor.authorNalbantoğlu, Burçin
dc.contributor.authorTaşdemir, Ufuk Göker
dc.date.accessioned2022-05-11T14:07:39Z
dc.date.available2022-05-11T14:07:39Z
dc.date.issued2013
dc.identifier.issn0301-2115
dc.identifier.issn1872-7654
dc.identifier.urihttps://doi.org/10.1016/j.ejogrb.2013.09.037
dc.identifier.urihttps://hdl.handle.net/20.500.11776/5166
dc.description.abstractObjective: The aim of this study was to investigate the effect of infliximab on experimentally induced ovarian ischernia/reperfusion injury (IRi). Study design: A total of 42 female rats were equally divided into 6 experimental groups; group 1: sham operation, group 2: 3-h ischemia, group 3 and 4: 3-h ischemia, 3-h reperfusion, group 5 and 6: 3-h ischemia, 24 h reperfusion. In group 4 and group 6, 30 min before reperfusion, infliximab was administered intraperitoneally at a dose of 5 mg/kg. Bilateral ovaries were removed for histopathologic and biochemical analysis. Serum MDA (sMDA), tissue MDA (tMDA), serum NO (sNO), tissue NO (tNO) and serum catalase concentrations were analyzed. Tissue damage of ovarian tissue was scored by histological examination. Results: The infliximab administration significantly lowered the sNO, tNO and sMDA concentrations in group 4 compared to group 3 (p = 0.041, p = 0.025 and p = 0.035, respectively). sNO, tNO and sMDA concentrations were also lower in group 6 when compared to group 5, but this differences were not significant (p > 0.05). On the other hand, tMDA concentrations were lower in infliximab-applied groups when compared to ischemia/reperfusion groups (group 3 vs. 4 and 5 vs. 6) (p = 0.045 and p = 0.048, respectively). Moreover, histopathologic tissue damage scores in infliximab administration groups were significantly lower than in ischemia/reperfusion groups (p < 0.001). Conclusion: Infliximab attenuates I/R-induced ovarian tissue injury in rats subjected to ischemia/reperfusion. (C) 2013 Elsevier Ireland Ltd. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.identifier.doi10.1016/j.ejogrb.2013.09.037
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTumor necrosing factor alpha antagonisten_US
dc.subjectInfliximaben_US
dc.subjectOvarian torsionen_US
dc.subjectIschemiaen_US
dc.subjectReperfusionen_US
dc.subjectRaten_US
dc.subjectIschemia-Reperfusion Injuryen_US
dc.subjectAcid Phenethyl Esteren_US
dc.subjectTorsionen_US
dc.subjectDetorsionen_US
dc.titleProtective effect of infliximab on ischemia/reperfusion injury in a rat ovary model: biochemical and histopathologic evaluationen_US
dc.typearticleen_US
dc.relation.ispartofEuropean Journal of Obstetrics & Gynecology and Reproductive Biologyen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kadın Hastalıkları ve Doğum Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyokimya Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Tıbbi Patoloji Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Çocuk Cerrahisi Ana Bilim Dalıen_US
dc.authorid0000-0002-6396-3168
dc.authorid0000-0002-5630-3399
dc.identifier.volume171en_US
dc.identifier.issue2en_US
dc.identifier.startpage353en_US
dc.identifier.endpage357en_US
dc.institutionauthorAbalı, Remzi
dc.institutionauthorTaşdemir, Nicel
dc.institutionauthorGüzel, Savaş
dc.institutionauthorÖznur, Meltem
dc.institutionauthorNalbantoğlu, Burçin
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid6506061779
dc.authorscopusid23986422400
dc.authorscopusid41862830000
dc.authorscopusid23968920100
dc.authorscopusid15844109600
dc.authorscopusid36165893600
dc.authorscopusid56499067400
dc.authorwosidNALBANTOGLU, BURCIN/A-5386-2018
dc.identifier.wosWOS:000329599000032en_US
dc.identifier.scopus2-s2.0-84890435349en_US
dc.identifier.pmid24169036en_US


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