The molecular mechanism involved in the protective effect of etodolac against ovarian injury induced with ischemia/reperfusion in rats

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This study investigated the protective effect at the molecular level of etodolac against ovarian injury induced in rats with ischemia/reperfusion (I/R). Rats were divided into four groups. The 25 mg/kg etodolac + ovarian ischemia/reperfusion (EIR 25) and 50 mg/kg etodolac+ovarian ischemia/reperfusion (EIR 50) groups were given etodolac by the oral route 1 h before administration of anesthesia. Two h of ischemia and 2 h of reperfusion were applied to ovarian tissue in all groups (except for (SG) sham operation group) 1 h after etodolac administration. The experimental results showed that etodolac at a dose of 50 mg/kg suppressed MPO (myeloperoxidase), TNF-α, IL-1β gene expression in ovarian tissue with I/R better than at a dose of 25 mg/kg. In addition, etodolac at these doses prevented a decrease in SOD gene expression in ovarian tissue subjected to I/R to a significant extent (p < 0.0001). In conclusion, etodolac can be used in the treatment of I/R-related ovarian injury. © 2015, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.

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AlanDeğerDil
dc.contributor.authorAl, Ragip A.
dc.contributor.authorYapca, Omer E.
dc.contributor.authorDogan, Hasan
dc.contributor.authorMammadov, Renad
dc.contributor.authorAltuner, Durdu
dc.contributor.authorSuleyman, Bahadir
dc.contributor.authorCetin, Nihal
dc.date.accessioned2026-10-18T20:30:11.752530656Z
dc.date.available2026-10-18T20:30:11.752530656Z
dc.date.issued2015
dc.description.abstractThis study investigated the protective effect at the molecular level of etodolac against ovarian injury induced in rats with ischemia/reperfusion (I/R). Rats were divided into four groups. The 25 mg/kg etodolac + ovarian ischemia/reperfusion (EIR 25) and 50 mg/kg etodolac+ovarian ischemia/reperfusion (EIR 50) groups were given etodolac by the oral route 1 h before administration of anesthesia. Two h of ischemia and 2 h of reperfusion were applied to ovarian tissue in all groups (except for (SG) sham operation group) 1 h after etodolac administration. The experimental results showed that etodolac at a dose of 50 mg/kg suppressed MPO (myeloperoxidase), TNF-α, IL-1β gene expression in ovarian tissue with I/R better than at a dose of 25 mg/kg. In addition, etodolac at these doses prevented a decrease in SOD gene expression in ovarian tissue subjected to I/R to a significant extent (p < 0.0001). In conclusion, etodolac can be used in the treatment of I/R-related ovarian injury. © 2015, Colegio de Farmaceuticos de la Provincia de Buenos Aires. All rights reserved.
dc.identifier.endpage541
dc.identifier.issn0326-2383
dc.identifier.issue3
dc.identifier.scopus2-s2.0-84926472518
dc.identifier.startpage537
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15376
dc.identifier.volume34
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.subjectEtodolac
dc.subjectIL-1β
dc.subjectIschemia/reperfusion
dc.subjectRat
dc.subjectTNF-α
dc.subjectinterleukin 1beta
dc.subjectmyeloperoxidase
dc.subjectsuperoxide dismutase
dc.subjecttumor necrosis factor alpha
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectDNA synthesis
dc.subjectfemale
dc.subjectgene expression
dc.subjectischemia
dc.subjectnonhuman
dc.subjectovarian injury
dc.subjectovary disease
dc.subjectreal time polymerase chain reaction
dc.subjectreperfusion injury
dc.titleThe molecular mechanism involved in the protective effect of etodolac against ovarian injury induced with ischemia/reperfusion in rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus3
rdl.source.indexSCOPUS