The effect of anakinra to nephrotoxicity with cisplatin induced in rats: Biochemical, gene expression and histopathological evaluation

ArticleAçık Erişim

Özet

Background. Oxidative stress and interleukin-1 beta (IL-1β) have been reported to play a role in the pathogenesis of nephrotoxicity induced by cisplatin. Objectives. The objective of this study was to investigate the effect of anakinra, which is an IL-1β receptor antagonist, on cisplatin-induced nephrotoxicity in rats, through biochemical, gene expression and histopathological analyses. Material and methods. The study was designed with 4 groups. For 1 week, the control group (C) and the cisplatin (Cis) group received distilled water, while the cisplatin + anakinra 50 (Cis + ANA50) group and the cisplatin + anakinra 100 (Cis + ANA100) group were intraperitoneally administered 50 mg/kg and 100 mg/kg of anakinra, respectively. The Cis, Cis + ANA50 and Cis + ANA100 groups were intraperitoneally injected with a 2.5 mg/kg dose of cisplatin for 7 days. After sacrifice, the kidney tissue of each rat was extracted for the assessment of the malondialdehyde (MDA) and total glutathione (tGSH) levels, and for gene expression analyses of IL-1β. The kidney tissues were histopathologically evaluated. Statistical analyses of the data were performed using one-way analysis of variance (ANOVA). Results. The administration of cisplatin (the Cis group) yielded a higher level of MDA (4.75 ±0.25 nmol/mL; p < 0.001) and lower levels of tGSH (1.80 ±0.35 mg/L; p < 0.001) compared to other groups. Cisplatin also increased IL-1β gene expression (6.33 ±0.27 gene expression levels; p < 0.001) compared to other groups. The impact of anakinra on the MDA and tGSH levels, and on IL-1β gene expression induced by cisplatin was observed as a reversal of these findings (p < 0.05). Anakinra better prevented an increase of the levels of MDA and IL-1β at a dose of 100 mg/kg compared to a 50 mg/kg dose. Conclusions. Anakinra prevents oxidative kidney damage induced by cisplatin in a dose-dependent manner. This result suggests that anakinra may be useful in the treatment of cisplatin-induced kidney damage. © 2018 by Wroclaw Medical University.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/14015Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17219/acem/75775Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorOzcicek, Adalet
dc.contributor.authorOzcicek, Fatih
dc.contributor.authorCimen, Ferda Keskin
dc.contributor.authorMammadov, Renad
dc.contributor.authorCankaya, Murat
dc.contributor.authorEzmeci, Talat
dc.contributor.authorAltuner, Durdu
dc.date.accessioned2026-10-18T20:28:48.882486742Z
dc.date.available2026-10-18T20:28:48.882486742Z
dc.date.issued2018
dc.description.abstractBackground. Oxidative stress and interleukin-1 beta (IL-1β) have been reported to play a role in the pathogenesis of nephrotoxicity induced by cisplatin. Objectives. The objective of this study was to investigate the effect of anakinra, which is an IL-1β receptor antagonist, on cisplatin-induced nephrotoxicity in rats, through biochemical, gene expression and histopathological analyses. Material and methods. The study was designed with 4 groups. For 1 week, the control group (C) and the cisplatin (Cis) group received distilled water, while the cisplatin + anakinra 50 (Cis + ANA50) group and the cisplatin + anakinra 100 (Cis + ANA100) group were intraperitoneally administered 50 mg/kg and 100 mg/kg of anakinra, respectively. The Cis, Cis + ANA50 and Cis + ANA100 groups were intraperitoneally injected with a 2.5 mg/kg dose of cisplatin for 7 days. After sacrifice, the kidney tissue of each rat was extracted for the assessment of the malondialdehyde (MDA) and total glutathione (tGSH) levels, and for gene expression analyses of IL-1β. The kidney tissues were histopathologically evaluated. Statistical analyses of the data were performed using one-way analysis of variance (ANOVA). Results. The administration of cisplatin (the Cis group) yielded a higher level of MDA (4.75 ±0.25 nmol/mL; p < 0.001) and lower levels of tGSH (1.80 ±0.35 mg/L; p < 0.001) compared to other groups. Cisplatin also increased IL-1β gene expression (6.33 ±0.27 gene expression levels; p < 0.001) compared to other groups. The impact of anakinra on the MDA and tGSH levels, and on IL-1β gene expression induced by cisplatin was observed as a reversal of these findings (p < 0.05). Anakinra better prevented an increase of the levels of MDA and IL-1β at a dose of 100 mg/kg compared to a 50 mg/kg dose. Conclusions. Anakinra prevents oxidative kidney damage induced by cisplatin in a dose-dependent manner. This result suggests that anakinra may be useful in the treatment of cisplatin-induced kidney damage. © 2018 by Wroclaw Medical University.
dc.identifier.doi10.17219/acem/75775
dc.identifier.eissn2451-2680
dc.identifier.endpage1650
dc.identifier.issn1899-5276
dc.identifier.issue12
dc.identifier.pmid30484291
dc.identifier.scopus2-s2.0-85058709609
dc.identifier.startpage1643
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14015
dc.identifier.volume27
dc.identifier.wosWOS:000453577800005
dc.language.isoen
dc.publisherWroclaw University of Medicine
dc.relation.ispartofAdvances in Clinical and Experimental Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAnakinra
dc.subjectCisplatin-nephrotoxicity
dc.subjectRats
dc.subjectAnimals
dc.subjectAntineoplastic Agents
dc.subjectAntioxidants
dc.subjectAntirheumatic Agents
dc.subjectCisplatin
dc.subjectDrug Administration Schedule
dc.subjectGlutathione
dc.subjectInjections, Intraperitoneal
dc.subjectInterleukin 1 Receptor Antagonist Protein
dc.subjectKidney
dc.subjectKidney Diseases
dc.subjectMalondialdehyde
dc.subjectOxidative Stress
dc.subjectProtective Agents
dc.subjectRats, Wistar
dc.subjectdistilled water
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectantineoplastic agent
dc.subjectantioxidant
dc.subjectantirheumatic agent
dc.subjectinterleukin 1 receptor blocking agent
dc.subjectprotective agent
dc.subjectanalysis of variance
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectArticle
dc.titleThe effect of anakinra to nephrotoxicity with cisplatin induced in rats: Biochemical, gene expression and histopathological evaluation
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos2
rdl.departmentDepartment of Internal Medicine, Faculty of Medicine, Erzincan University, Turkey. | Department of Pathology, Faculty of Medicine, Erzincan University, Turkey. | Department of Pharmacology, Faculty of Medicine, Erzincan University, Turkey. | Department of Biology, Arts and Sciences, Erzincan University, Turkey. | Department of Public Health, Faculty of Medicine, Erzincan University, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)