Oxidative renal damage in rats subjected to Ovarian Ischemia reperfusion and protective effect of tianeptine

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Ischemia reperfusion (I/R) injury in an organ can also cause damage in other organs. The aim of this study was to research the effect of tianeptine on oxidative ovarian injury induced by I/R in rats, and on the complication of this damage on the kidney. Albino Wistar female rats were assigned into groups, control subjected to ovarian I/R (OIR), exposed to 25 mg/kg tianeptine + ovarian I/R (TOIR), sham operation + 25 mg/kg tianeptin (TSG) and sham operated (SHAM). MDA, MPO, TNF-α and IL-1β levels in OIR group were found to be significantly higher compared to the TOIR,TSG and SHAM groups, and the tGSH level was found to be lower. Histopathologically, dilated and congested blood vessel, edema, hemorrhage, and PNL infiltration were observed in the OIR group ovarian and kidney tissues. In the ovarian and kidney tissues of TOIR group, dilated and congested blood vessel was found. This information obtained suggests that tianeptine may be useful in the treatment of ovarian I/R injury and its complications on kidney. © 2017, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.

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AlanDeğerDil
dc.contributor.authorKaraca, Ibrahim
dc.contributor.authorDelibaş, Ilhan B.
dc.contributor.authorYapça, Ömer E.
dc.contributor.authorIngeç, Metin
dc.contributor.authorKumbasar, Serkan
dc.contributor.authorHirik, Erkan
dc.contributor.authorKuzucu, Mehmet
dc.contributor.authorBilgin, Aslı Ö.
dc.date.accessioned2026-10-18T20:29:32.165279158Z
dc.date.available2026-10-18T20:29:32.165279158Z
dc.date.issued2017
dc.description.abstractIschemia reperfusion (I/R) injury in an organ can also cause damage in other organs. The aim of this study was to research the effect of tianeptine on oxidative ovarian injury induced by I/R in rats, and on the complication of this damage on the kidney. Albino Wistar female rats were assigned into groups, control subjected to ovarian I/R (OIR), exposed to 25 mg/kg tianeptine + ovarian I/R (TOIR), sham operation + 25 mg/kg tianeptin (TSG) and sham operated (SHAM). MDA, MPO, TNF-α and IL-1β levels in OIR group were found to be significantly higher compared to the TOIR,TSG and SHAM groups, and the tGSH level was found to be lower. Histopathologically, dilated and congested blood vessel, edema, hemorrhage, and PNL infiltration were observed in the OIR group ovarian and kidney tissues. In the ovarian and kidney tissues of TOIR group, dilated and congested blood vessel was found. This information obtained suggests that tianeptine may be useful in the treatment of ovarian I/R injury and its complications on kidney. © 2017, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.
dc.identifier.endpage2347
dc.identifier.issn0326-2383
dc.identifier.issue12
dc.identifier.scopus2-s2.0-85038370237
dc.identifier.startpage2339
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14726
dc.identifier.volume36
dc.language.isoen
dc.publisherColegio de Farmaceuticos de la Provincia de Buenos Aires
dc.relation.ispartofLatin American Journal of Pharmacy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectKidney
dc.subjectOvarian injury
dc.subjectRat
dc.subjectTianeptine
dc.subjectglutathione
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectmyeloperoxidase
dc.subjecttumor necrosis factor
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectbleeding
dc.subjectblood vessel occlusion
dc.subjectcontrolled study
dc.subjectedema
dc.subjectenzyme linked immunosorbent assay
dc.subjecthistopathology
dc.subjectkidney injury
dc.subjectkidney tissue
dc.subjectlipid peroxidation
dc.subjectnonhuman
dc.subjectovarian ischemia reperfusion
dc.subjectovary disease
dc.subjectovary tissue
dc.subjectoxidative stress
dc.subjectreperfusion injury
dc.titleOxidative renal damage in rats subjected to Ovarian Ischemia reperfusion and protective effect of tianeptine
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.source.indexSCOPUS