The molecular mechanism of the protective effect of tianeptine against ovarian ischemia-reperfusion injury

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Özet

Torsion of the ovary is a gynecologic emergency that occurs when the ovary and fallopian tube rotate around the infundibulopelvic ligament, causing ischemic changes in the adnexa. Tianeptine is an atypical antidepressant that has been shown to be effective in treatment-resistant depression and has fewer side effects than other antidepressants. In this study, the protective effect of tianeptine on ovarian ischemia-reperfusion (I/R) injury in female rats was evaluated. Four groups were created from twenty-four female albino Wistar rats before surgery (n = 6/each group): TPG (5 mg/kg/orally tianeptine-only), SG (sham operation), OIR (ovarian I/R), and TOIR (5 mg/kg/orally tianeptine + I/R). One hour before surgery procedures, the TPG and TOIR applied tianeptine. Tianeptine administration procedure was repeated once daily for six days. Under 60 mg/kg intraperitoneal (IP) ketamine and sevoflurane (inhaler) anesthesia, the right ovaries, fallopian tubes, and vessels in the OIR and TOIR groups were clamped by torsion. After 3 h of ischemia, a 6-day reperfusion period was started. Tianeptine administration procedure was repeated once daily for six days. In the SG group, the abdominal cavity was opened and closed with sutures without any intervention on the ovaries. On the seventh day, rats were sacrificed (120 mg/kg ketamine, IP), and ovaries were extracted. Levels of oxidants (malondialdehyde), antioxidants (total glutathione, superoxide dismutase, and catalase), and pro-inflammatory cytokines (tumor necrosis factor-alpha, interleukin-1β, interleukin-6) were measured in excised ovarian tissue. Ovarian tissues also examined histopathologically and immunohistochemically. I/R increased the levels of oxidants and pro-inflammatory cytokines and decreased the levels of antioxidants in rat ovaries. In parallel, histopathologic and immunohistochemical examination of the ovarian tissue revealed the presence of severe (grade 3) oxidative damage. Tianeptine significantly suppressed oxidative stress and pro-inflammatory cytokine increases related with I/R in the ovarian tissue, while also alleviating histopathological damage and oxidative DNA damage. Our experimental results suggest that tianeptine treatment may be effective against I/R-induced ovarian injury. © The Author(s) 2025.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/10577Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1038/s41598-025-13875-7Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKalkan, Betul
dc.contributor.authorYavuzer, Bulent
dc.contributor.authorAliyev, Aydin
dc.contributor.authorCakir, Osman Kagan
dc.contributor.authorGozen, Fusun
dc.contributor.authorMendil, Ali Sefa
dc.contributor.authorCoban, Taha Abdulkadir
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:25:46.205565323Z
dc.date.available2026-10-18T20:25:46.205565323Z
dc.date.issued2025
dc.description.abstractTorsion of the ovary is a gynecologic emergency that occurs when the ovary and fallopian tube rotate around the infundibulopelvic ligament, causing ischemic changes in the adnexa. Tianeptine is an atypical antidepressant that has been shown to be effective in treatment-resistant depression and has fewer side effects than other antidepressants. In this study, the protective effect of tianeptine on ovarian ischemia-reperfusion (I/R) injury in female rats was evaluated. Four groups were created from twenty-four female albino Wistar rats before surgery (n = 6/each group): TPG (5 mg/kg/orally tianeptine-only), SG (sham operation), OIR (ovarian I/R), and TOIR (5 mg/kg/orally tianeptine + I/R). One hour before surgery procedures, the TPG and TOIR applied tianeptine. Tianeptine administration procedure was repeated once daily for six days. Under 60 mg/kg intraperitoneal (IP) ketamine and sevoflurane (inhaler) anesthesia, the right ovaries, fallopian tubes, and vessels in the OIR and TOIR groups were clamped by torsion. After 3 h of ischemia, a 6-day reperfusion period was started. Tianeptine administration procedure was repeated once daily for six days. In the SG group, the abdominal cavity was opened and closed with sutures without any intervention on the ovaries. On the seventh day, rats were sacrificed (120 mg/kg ketamine, IP), and ovaries were extracted. Levels of oxidants (malondialdehyde), antioxidants (total glutathione, superoxide dismutase, and catalase), and pro-inflammatory cytokines (tumor necrosis factor-alpha, interleukin-1β, interleukin-6) were measured in excised ovarian tissue. Ovarian tissues also examined histopathologically and immunohistochemically. I/R increased the levels of oxidants and pro-inflammatory cytokines and decreased the levels of antioxidants in rat ovaries. In parallel, histopathologic and immunohistochemical examination of the ovarian tissue revealed the presence of severe (grade 3) oxidative damage. Tianeptine significantly suppressed oxidative stress and pro-inflammatory cytokine increases related with I/R in the ovarian tissue, while also alleviating histopathological damage and oxidative DNA damage. Our experimental results suggest that tianeptine treatment may be effective against I/R-induced ovarian injury. © The Author(s) 2025.
dc.identifier.doi10.1038/s41598-025-13875-7
dc.identifier.issn2045-2322
dc.identifier.issue1
dc.identifier.pmcidPMC12317024
dc.identifier.pmid40750657
dc.identifier.scopus2-s2.0-105012387153
dc.identifier.startpage28141
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10577
dc.identifier.volume15
dc.identifier.wosWOS:001542644100023
dc.language.isoen
dc.publisherNature Research
dc.relation.ispartofScientific Reports
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject8-OHdG
dc.subjectIschemia-reperfusion injury
dc.subjectOvary
dc.subjectRats
dc.subjectTianeptine
dc.subjectAnimals
dc.subjectDisease Models, Animal
dc.subjectFemale
dc.subjectOxidative Stress
dc.subjectProtective Agents
dc.subjectRats, Wistar
dc.subjectReperfusion Injury
dc.subjectThiazepines
dc.subjectprotective agent
dc.subjectthiazepine derivative
dc.subjectanimal
dc.subjectdisease model
dc.subjectdrug effect
dc.subjectdrug therapy
dc.subjectmetabolism
dc.subjectpathology
dc.subjectprevention and control
dc.subjectrat
dc.subjectvascularization
dc.subjectWistar rat
dc.titleThe molecular mechanism of the protective effect of tianeptine against ovarian ischemia-reperfusion injury
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus3
rdl.citation.wos3
rdl.departmentDepartment of Obstetrics and Gynecology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, 24100, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, 24100, Turkey. | Department of Medical Biochemistry, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, 24100, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, Erzincan, 24100, Turkey. halis.suleyman@gmail.com.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)