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]
Özet
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
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Polat, Eyüp Can | |
| dc.contributor.author | Bozkurt, Ali Seydi | |
| dc.contributor.author | Keskin Cimen, Ferda | |
| dc.contributor.author | Gulaboglu, Mine | |
| dc.contributor.author | Altuner, Durdu | |
| dc.date.accessioned | 2026-10-18T20:28:45.007747827Z | |
| dc.date.available | 2026-10-18T20:28:45.007747827Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | 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 | |
| dc.identifier.doi | 10.1016/j.androl.2018.08.001 | |
| dc.identifier.endpage | 62 | |
| dc.identifier.issn | 1698-031X | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 30477960 | |
| dc.identifier.scopus | 2-s2.0-85056990403 | |
| dc.identifier.startpage | 55 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/13950 | |
| dc.identifier.volume | 18 | |
| dc.identifier.wos | WOS:000531163100003 | |
| dc.language.iso | en | |
| dc.publisher | Ediciones Doyma, S.L. | |
| dc.relation.ispartof | Revista Internacional de Andrologia | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Ischemia/reperfusion | |
| dc.subject | Nimesulide | |
| dc.subject | Testis | |
| dc.subject | Animals | |
| dc.subject | Anti-Inflammatory Agents, Non-Steroidal | |
| dc.subject | Antioxidants | |
| dc.subject | Cyclooxygenase Inhibitors | |
| dc.subject | Dose-Response Relationship, Drug | |
| dc.subject | Inflammation | |
| dc.subject | Male | |
| dc.subject | Oxidative Stress | |
| dc.subject | Rats | |
| dc.subject | Rats, Wistar | |
| dc.subject | Reactive Oxygen Species | |
| dc.subject | Reperfusion Injury | |
| dc.subject | Spermatic Cord Torsion | |
| dc.subject | Sulfonamides | |
| dc.subject | antioxidant | |
| dc.subject | nonsteroid antiinflammatory agent | |
| dc.subject | prostaglandin synthase inhibitor | |
| dc.subject | reactive oxygen metabolite | |
| dc.subject | sulfonamide | |
| dc.subject | animal | |
| dc.subject | dose response | |
| dc.subject | drug effect | |
| dc.subject | metabolism | |
| dc.subject | pathophysiology | |
| dc.subject | rat | |
| dc.subject | testis torsion | |
| dc.subject | Wistar rat | |
| dc.title | 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] | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 9 | |
| rdl.citation.wos | 11 | |
| rdl.department | Department 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.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
