The effect of anakinra to nephrotoxicity with cisplatin induced in rats: Biochemical, gene expression and histopathological evaluation
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
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Ozcicek, Adalet | |
| dc.contributor.author | Ozcicek, Fatih | |
| dc.contributor.author | Cimen, Ferda Keskin | |
| dc.contributor.author | Mammadov, Renad | |
| dc.contributor.author | Cankaya, Murat | |
| dc.contributor.author | Ezmeci, Talat | |
| dc.contributor.author | Altuner, Durdu | |
| dc.date.accessioned | 2026-10-18T20:28:48.882486742Z | |
| dc.date.available | 2026-10-18T20:28:48.882486742Z | |
| dc.date.issued | 2018 | |
| dc.description.abstract | 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. | |
| dc.identifier.doi | 10.17219/acem/75775 | |
| dc.identifier.eissn | 2451-2680 | |
| dc.identifier.endpage | 1650 | |
| dc.identifier.issn | 1899-5276 | |
| dc.identifier.issue | 12 | |
| dc.identifier.pmid | 30484291 | |
| dc.identifier.scopus | 2-s2.0-85058709609 | |
| dc.identifier.startpage | 1643 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/14015 | |
| dc.identifier.volume | 27 | |
| dc.identifier.wos | WOS:000453577800005 | |
| dc.language.iso | en | |
| dc.publisher | Wroclaw University of Medicine | |
| dc.relation.ispartof | Advances in Clinical and Experimental Medicine | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Anakinra | |
| dc.subject | Cisplatin-nephrotoxicity | |
| dc.subject | Rats | |
| dc.subject | Animals | |
| dc.subject | Antineoplastic Agents | |
| dc.subject | Antioxidants | |
| dc.subject | Antirheumatic Agents | |
| dc.subject | Cisplatin | |
| dc.subject | Drug Administration Schedule | |
| dc.subject | Glutathione | |
| dc.subject | Injections, Intraperitoneal | |
| dc.subject | Interleukin 1 Receptor Antagonist Protein | |
| dc.subject | Kidney | |
| dc.subject | Kidney Diseases | |
| dc.subject | Malondialdehyde | |
| dc.subject | Oxidative Stress | |
| dc.subject | Protective Agents | |
| dc.subject | Rats, Wistar | |
| dc.subject | distilled water | |
| dc.subject | interleukin 1beta | |
| dc.subject | malonaldehyde | |
| dc.subject | antineoplastic agent | |
| dc.subject | antioxidant | |
| dc.subject | antirheumatic agent | |
| dc.subject | interleukin 1 receptor blocking agent | |
| dc.subject | protective agent | |
| dc.subject | analysis of variance | |
| dc.subject | animal experiment | |
| dc.subject | animal tissue | |
| dc.subject | Article | |
| dc.title | The effect of anakinra to nephrotoxicity with cisplatin induced in rats: Biochemical, gene expression and histopathological evaluation | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 2 | |
| rdl.citation.wos | 2 | |
| rdl.department | Department 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.status | gold | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
