Effect of anakinra, an interleukin one beta antagonist, on oxidative testicular damage induced in rats with ischemia reperfusion; [Efecto de la anakinra, que es un antagonista de la interleucina 1 beta en oxidativo daño testicular, inducida en ratas con isquemia reperfusión]
Özet
Background: It has been reported in the literature that proinflammatory interleukin-1 beta (IL-1β) is increased in cases of testicular ischemia reperfusion (I/R) damage. This information suggests that anakinra, an IL-1β antagonist, may be effective in testicular I/R damage. Objective: In our study, we investigated the effect of anakinra on testicular I/R damage induced in rats with torsion/detorsion. Methods: The 50 mg/kg anakinra + testicular torsion/detorsion (KTD-50) and 100 mg/kg anakinra + testicular torsion/detorsion (KTD-100) groups received an intraperitoneal (i.p.) injection of 50 mg/kg and 100 mg/kg of anakinra, respectively. In turn, the testicular torsion/detorsion (TTD) and sham operation (SOG) groups received a single dose of distilled water as a solvent 1 h before ketamine anaesthesia. After the testes of the TTD, KTD-50 and KTD-100 groups were subjected to torsion and detorsion for 4 h each, the rats were killed with a high-dose anaesthesia, and their testicles were removed and evaluated through biochemical, gene expression and histopathological examinations. The results were evaluated in comparison with those of the SOG group. Results: The levels of malondialdehyde (MDA), myeloperoxidase (MPO) and IL-1β showed significant increases in the TTD group, which underwent torsion/detorsion, compared to the KTD-50, KTD-100 and SOG groups. Conversely, the levels of glutathione (tGSH), glutathione peroxidase (GPO) and glutathione s-transferase (GST) were found to be significantly higher in the KTD-50, KTD-100 and SOG groups than in the TTD group. Conclusion: Anakinra at a 100 mg/kg dose histologically suppressed better oxidative stress and tunica albuginea, germ cell, seminiferous tubule and interstitial damage in the testicular tissue compared to a 50 mg/kg dose. Experimental results indicate that anakinra might be beneficial in the attenuation of testicular I/R damage. © 2017 Asociación Española de Andrología, Medicina Sexual y Reproductiva; Antecedentes: Se ha reportado en la literatura que citoquinas interleuquina-1 beta (IL-1β) es mayor en el daño de la isquemia reperfusión testicular (I/R). Esta información sugiere que la anakinra, que es un antagonista IL-1β puede ser eficaz en daño testicular I/R. Objetivo: En nuestro estudio se investigó el efecto de este medicamento en daño testicular I/R inducida en ratas con detorsion/torsión. Métodos: KTD-50 grupo recibido intraperitonealmente (i.p.) inyección de 50 mg/kg y KTD-100 Grupo 100 mg/kg de anakinra, mientras TTD (control) y SOG (sham grupo operación) recibieron una dosis única de agua destilada como solvente, una hora antes de ketamina anestesia. Después de que los testículos de TTD, KTD-50 y KTD-100 grupos fueron sometidas a torsión y detorsion para cuatro por cuatro horas, las ratas fueron asesinados con altas dosis de anestesia, sus testículos fueron extraídos y evaluados a través de la expresión génica, bioquímicas e histopatológicas de exámenes. Los resultados fueron evaluado en comparación con la de SCG grupo. Resultados: Los niveles de MDA, MPO y IL- 1β mostraron incrementos significativos en el grupo TTD/torsión detorsion administrados frente a-50, KTD KTD-100 y SOG grupos. Por el contrario, los niveles de tGSH, GPO y GST resultaron significativamente más altas en KTD-50 KTD-100 y grupos SOG de TTD en grupo. Conclusión: La anakinra en 100 mg/kg dosis mejor histológicamente suprime el estrés oxidativo y la túnica albuginea, células germinales, túbulos seminíferos apretadamente enrollados intersticial y daño en el tejido testicular en comparación con la dosis de 50 mg/kg. Los resultados experimentales indican que la anakinra puede ser beneficiosa en la atenuación de los daños I/R testicular.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Hirik, Erkan | |
| dc.contributor.author | Suleyman, Bahadir | |
| dc.contributor.author | Mammadov, Renad | |
| dc.contributor.author | Yapanoglu, Turgut | |
| dc.contributor.author | Cimen, Ferda Keskin | |
| dc.contributor.author | Cetin, Nihal | |
| dc.contributor.author | Kurt, Nezahat | |
| dc.date.accessioned | 2026-10-18T20:29:00.230912394Z | |
| dc.date.available | 2026-10-18T20:29:00.230912394Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | Background: It has been reported in the literature that proinflammatory interleukin-1 beta (IL-1β) is increased in cases of testicular ischemia reperfusion (I/R) damage. This information suggests that anakinra, an IL-1β antagonist, may be effective in testicular I/R damage. Objective: In our study, we investigated the effect of anakinra on testicular I/R damage induced in rats with torsion/detorsion. Methods: The 50 mg/kg anakinra + testicular torsion/detorsion (KTD-50) and 100 mg/kg anakinra + testicular torsion/detorsion (KTD-100) groups received an intraperitoneal (i.p.) injection of 50 mg/kg and 100 mg/kg of anakinra, respectively. In turn, the testicular torsion/detorsion (TTD) and sham operation (SOG) groups received a single dose of distilled water as a solvent 1 h before ketamine anaesthesia. After the testes of the TTD, KTD-50 and KTD-100 groups were subjected to torsion and detorsion for 4 h each, the rats were killed with a high-dose anaesthesia, and their testicles were removed and evaluated through biochemical, gene expression and histopathological examinations. The results were evaluated in comparison with those of the SOG group. Results: The levels of malondialdehyde (MDA), myeloperoxidase (MPO) and IL-1β showed significant increases in the TTD group, which underwent torsion/detorsion, compared to the KTD-50, KTD-100 and SOG groups. Conversely, the levels of glutathione (tGSH), glutathione peroxidase (GPO) and glutathione s-transferase (GST) were found to be significantly higher in the KTD-50, KTD-100 and SOG groups than in the TTD group. Conclusion: Anakinra at a 100 mg/kg dose histologically suppressed better oxidative stress and tunica albuginea, germ cell, seminiferous tubule and interstitial damage in the testicular tissue compared to a 50 mg/kg dose. Experimental results indicate that anakinra might be beneficial in the attenuation of testicular I/R damage. © 2017 Asociación Española de Andrología, Medicina Sexual y Reproductiva; Antecedentes: Se ha reportado en la literatura que citoquinas interleuquina-1 beta (IL-1β) es mayor en el daño de la isquemia reperfusión testicular (I/R). Esta información sugiere que la anakinra, que es un antagonista IL-1β puede ser eficaz en daño testicular I/R. Objetivo: En nuestro estudio se investigó el efecto de este medicamento en daño testicular I/R inducida en ratas con detorsion/torsión. Métodos: KTD-50 grupo recibido intraperitonealmente (i.p.) inyección de 50 mg/kg y KTD-100 Grupo 100 mg/kg de anakinra, mientras TTD (control) y SOG (sham grupo operación) recibieron una dosis única de agua destilada como solvente, una hora antes de ketamina anestesia. Después de que los testículos de TTD, KTD-50 y KTD-100 grupos fueron sometidas a torsión y detorsion para cuatro por cuatro horas, las ratas fueron asesinados con altas dosis de anestesia, sus testículos fueron extraídos y evaluados a través de la expresión génica, bioquímicas e histopatológicas de exámenes. Los resultados fueron evaluado en comparación con la de SCG grupo. Resultados: Los niveles de MDA, MPO y IL- 1β mostraron incrementos significativos en el grupo TTD/torsión detorsion administrados frente a-50, KTD KTD-100 y SOG grupos. Por el contrario, los niveles de tGSH, GPO y GST resultaron significativamente más altas en KTD-50 KTD-100 y grupos SOG de TTD en grupo. Conclusión: La anakinra en 100 mg/kg dosis mejor histológicamente suprime el estrés oxidativo y la túnica albuginea, células germinales, túbulos seminíferos apretadamente enrollados intersticial y daño en el tejido testicular en comparación con la dosis de 50 mg/kg. Los resultados experimentales indican que la anakinra puede ser beneficiosa en la atenuación de los daños I/R testicular. | |
| dc.identifier.doi | 10.1016/j.androl.2017.03.001 | |
| dc.identifier.endpage | 94 | |
| dc.identifier.issn | 1698-031X | |
| dc.identifier.issue | 3 | |
| dc.identifier.pmid | 30300135 | |
| dc.identifier.scopus | 2-s2.0-85020207803 | |
| dc.identifier.startpage | 87 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/14213 | |
| dc.identifier.volume | 16 | |
| dc.identifier.wos | WOS:000440257400001 | |
| 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 | Anakinra | |
| dc.subject | Interleucina-1β | |
| dc.subject | Interleukin-1β | |
| dc.subject | Ischemia/reperfusion | |
| dc.subject | Isquemia/reperfusión | |
| dc.subject | Rat | |
| dc.subject | Rata | |
| dc.subject | Testes damage | |
| dc.subject | Testis daños | |
| dc.subject | Animals | |
| dc.subject | Disease Models, Animal | |
| dc.subject | Dose-Response Relationship, Drug | |
| dc.subject | Glutathione | |
| dc.subject | Glutathione Peroxidase | |
| dc.subject | Interleukin 1 Receptor Antagonist Protein | |
| dc.subject | Interleukin-1beta | |
| dc.subject | Male | |
| dc.subject | Malondialdehyde | |
| dc.subject | Oxidative Stress | |
| dc.subject | Peroxidase | |
| dc.subject | Rats | |
| dc.subject | Rats, Wistar | |
| dc.subject | Reperfusion Injury | |
| dc.subject | Seminiferous Tubules | |
| dc.subject | Spermatic Cord Torsion | |
| dc.subject | interleukin 1 receptor blocking agent | |
| dc.subject | interleukin 1beta | |
| dc.subject | malonaldehyde | |
| dc.subject | animal | |
| dc.subject | comparative study | |
| dc.title | Effect of anakinra, an interleukin one beta antagonist, on oxidative testicular damage induced in rats with ischemia reperfusion; [Efecto de la anakinra, que es un antagonista de la interleucina 1 beta en oxidativo daño testicular, inducida en ratas con isquemia reperfusión] | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 16 | |
| rdl.citation.wos | 13 | |
| rdl.department | Department of Urology, Faculty of Medicine, Erzincan University, Erzincan, Turkey. Electronic address: ehirik@gmail.com. | Department of Pharmacology, Faculty of Medicine, Erzincan University, Erzincan, Turkey. | Department of Urology, Faculty of Medicine, Atatürk University, Erzincan, Turkey. | Department of Pathology, Faculty of Medicine, Erzincan University, Erzincan, Turkey. | Department of Biochemistry, Faculty of Medicine, Atatürk University, Erzincan, Turkey. | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
