The investigation of the protective effects of nimesulide on experimental testicular ischemia-reperfusion injury in rats; [La investigación de los efectos protectores de nimesulida en la lesión de isquemia y reperfusión testicular experimental en ratas]

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Introduction and objectives: Testicular ischemia/reperfusion (I/R) injury develops after torsion and following detorsion of the testis. Reactive oxygen species were produced and oxidative damage begins to occur due to I/R process. Nimesulide, which is a specific cyclooxygenase-2 inhibitor drug, have antioxidant, antiinflammatory, analgesics and antipyretic effects. We aimed to investigate biochemically and histopathologically effect of nimesulide on testis I/R injury in rats induced by the testicular torsion–detorsion. Material and methods: In this study, 24 albino Wistar male rats were divided into four groups (6 rats in each group): ischemia/reperfusion applied + 50 mg/kg nimesulide administrated (NIM-50), ischemia/reperfusion applied + 100 mg/kg nimesulide administrated (NIM-100), ischemia/reperfusion applied (IR) and Sham surgery (SS) groups. Nimesulide was administered to NIM-50 and NIM-100 groups at the 50 mg/kg and 100 mg/kg doses before 2 h applied I/R procedures. The IR group were applied only I/R procedures, no drug treatment was applied. Animals were sacrificed under high dose anesthesia and left testes were extracted. Testes were examined biochemically and histopathologically. Results: Total glutathione (tGSH) and cyclooxygenase-1 (COX-1) levels were increased in the NIM-50 and NIM-100 groups compared to IR group. The levels of COX-2, malondialdehyde (MDA), interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) were lower in the NIM-50 and NIM-100 groups than in the IR group. Some histopathological changes seen in IR group. This findings were decreased in NIM-50 group and prevented in NIM-100 group. Conclusion: Nimesulide prevented inflammation and oxidative stress. Our results suggest that nimesulide may be have a protective effect on testicular I/R injury. © 2018 Asociación Española de Andrología, Medicina Sexual y Reproductiva

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AlanDeğerDil
dc.contributor.authorPolat, Eyüp Can
dc.contributor.authorBozkurt, Ali Seydi
dc.contributor.authorKeskin Cimen, Ferda
dc.contributor.authorGulaboglu, Mine
dc.contributor.authorAltuner, Durdu
dc.date.accessioned2026-10-18T20:28:45.007747827Z
dc.date.available2026-10-18T20:28:45.007747827Z
dc.date.issued2020
dc.description.abstractIntroduction and objectives: Testicular ischemia/reperfusion (I/R) injury develops after torsion and following detorsion of the testis. Reactive oxygen species were produced and oxidative damage begins to occur due to I/R process. Nimesulide, which is a specific cyclooxygenase-2 inhibitor drug, have antioxidant, antiinflammatory, analgesics and antipyretic effects. We aimed to investigate biochemically and histopathologically effect of nimesulide on testis I/R injury in rats induced by the testicular torsion–detorsion. Material and methods: In this study, 24 albino Wistar male rats were divided into four groups (6 rats in each group): ischemia/reperfusion applied + 50 mg/kg nimesulide administrated (NIM-50), ischemia/reperfusion applied + 100 mg/kg nimesulide administrated (NIM-100), ischemia/reperfusion applied (IR) and Sham surgery (SS) groups. Nimesulide was administered to NIM-50 and NIM-100 groups at the 50 mg/kg and 100 mg/kg doses before 2 h applied I/R procedures. The IR group were applied only I/R procedures, no drug treatment was applied. Animals were sacrificed under high dose anesthesia and left testes were extracted. Testes were examined biochemically and histopathologically. Results: Total glutathione (tGSH) and cyclooxygenase-1 (COX-1) levels were increased in the NIM-50 and NIM-100 groups compared to IR group. The levels of COX-2, malondialdehyde (MDA), interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) were lower in the NIM-50 and NIM-100 groups than in the IR group. Some histopathological changes seen in IR group. This findings were decreased in NIM-50 group and prevented in NIM-100 group. Conclusion: Nimesulide prevented inflammation and oxidative stress. Our results suggest that nimesulide may be have a protective effect on testicular I/R injury. © 2018 Asociación Española de Andrología, Medicina Sexual y Reproductiva
dc.identifier.doi10.1016/j.androl.2018.08.001
dc.identifier.endpage62
dc.identifier.issn1698-031X
dc.identifier.issue2
dc.identifier.pmid30477960
dc.identifier.scopus2-s2.0-85056990403
dc.identifier.startpage55
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13950
dc.identifier.volume18
dc.identifier.wosWOS:000531163100003
dc.language.isoen
dc.publisherEdiciones Doyma, S.L.
dc.relation.ispartofRevista Internacional de Andrologia
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectIschemia/reperfusion
dc.subjectNimesulide
dc.subjectTestis
dc.subjectAnimals
dc.subjectAnti-Inflammatory Agents, Non-Steroidal
dc.subjectAntioxidants
dc.subjectCyclooxygenase Inhibitors
dc.subjectDose-Response Relationship, Drug
dc.subjectInflammation
dc.subjectMale
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectReactive Oxygen Species
dc.subjectReperfusion Injury
dc.subjectSpermatic Cord Torsion
dc.subjectSulfonamides
dc.subjectantioxidant
dc.subjectnonsteroid antiinflammatory agent
dc.subjectprostaglandin synthase inhibitor
dc.subjectreactive oxygen metabolite
dc.subjectsulfonamide
dc.subjectanimal
dc.subjectdose response
dc.subjectdrug effect
dc.subjectmetabolism
dc.subjectpathophysiology
dc.subjectrat
dc.subjecttestis torsion
dc.subjectWistar rat
dc.titleThe investigation of the protective effects of nimesulide on experimental testicular ischemia-reperfusion injury in rats; [La investigación de los efectos protectores de nimesulida en la lesión de isquemia y reperfusión testicular experimental en ratas]
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus9
rdl.citation.wos11
rdl.departmentDepartment of Clinical Pharmacy, Faculty of Pharmacy, Erzincan University, 24100 Erzincan, Turkey. | Department of Urology, Faculty of Medicine, Erzincan University, 24100 Erzincan, Turkey. | Department of Pathology, Faculty of Medicine, Erzincan University, 24100 Erzincan, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan University Erzincan, Turkey. Electronic address: durdualtuner@hotmail.com.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)