The effects of sorafenib in healthy and cisplatin-treated rats
Özet
Background. Sorafenib is a multikinase inhibitor currently used in the treatment of hepatocellular carcinoma, renal cell carcinoma and thyroid cancer. Objectives. The literature on this agent is scarce. This study aimed to evaluate the effects of sorafenib when administered to both healthy and cisplatin-induced rats. Materials and methods. The animals were divided into 4 groups: 1) control group that received 0.9% saline intraperitoneally (C); 2) group administered a single dose (7 mg/kg) of cisplatin (Cis); 3) a group administered 20 mg/kg of sorafenib for 7 days (Sor); 4) group administered 20 mg/kg of sorafenib followed by 7 mg/kg of cisplatin for 7 days (Cis+Sor). All animals were sacrificed 7 days after the completion of their treatment arm, and serum and tissue samples were taken. Results. Alanine aminotransferase (ALT), aspartate aminotransferase (AST) and interleukin 38 (IL-38) levels were increased in the Sor and Cis+Sor groups compared to the control group. When compared with the control group, serum urea, creatinine, kidney IL-1β, and tumor necrosis factor alpha (TNF-α) levels did not change in the Sor group. When compared to the Cis group, the levels of these parameters decreased in the Cis+Sor group. Conclusions. According to the data obtained, sorafenib caused liver toxicity when given to both healthy and cisplatin-induced rats. While sorafenib did not cause any significant changes in the kidneys when given to healthy rats, it had a healing effect in kidneys after stress induced by cisplatin. © 2023 Wroclaw University of Medicine. All rights reserved.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Demirtas, Levent | |
| dc.contributor.author | Gürbüzel, Mehmet | |
| dc.contributor.author | Tahirler, Hilal | |
| dc.contributor.author | Akbas, Emin Murat | |
| dc.contributor.author | Karatas, Ozhan | |
| dc.contributor.author | Arslan, Yusuf Kemal | |
| dc.date.accessioned | 2026-10-18T20:27:06.074322475Z | |
| dc.date.available | 2026-10-18T20:27:06.074322475Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Background. Sorafenib is a multikinase inhibitor currently used in the treatment of hepatocellular carcinoma, renal cell carcinoma and thyroid cancer. Objectives. The literature on this agent is scarce. This study aimed to evaluate the effects of sorafenib when administered to both healthy and cisplatin-induced rats. Materials and methods. The animals were divided into 4 groups: 1) control group that received 0.9% saline intraperitoneally (C); 2) group administered a single dose (7 mg/kg) of cisplatin (Cis); 3) a group administered 20 mg/kg of sorafenib for 7 days (Sor); 4) group administered 20 mg/kg of sorafenib followed by 7 mg/kg of cisplatin for 7 days (Cis+Sor). All animals were sacrificed 7 days after the completion of their treatment arm, and serum and tissue samples were taken. Results. Alanine aminotransferase (ALT), aspartate aminotransferase (AST) and interleukin 38 (IL-38) levels were increased in the Sor and Cis+Sor groups compared to the control group. When compared with the control group, serum urea, creatinine, kidney IL-1β, and tumor necrosis factor alpha (TNF-α) levels did not change in the Sor group. When compared to the Cis group, the levels of these parameters decreased in the Cis+Sor group. Conclusions. According to the data obtained, sorafenib caused liver toxicity when given to both healthy and cisplatin-induced rats. While sorafenib did not cause any significant changes in the kidneys when given to healthy rats, it had a healing effect in kidneys after stress induced by cisplatin. © 2023 Wroclaw University of Medicine. All rights reserved. | |
| dc.description.sponsorship | This research was partially supported with a grant from the Research Fund of Erzincan Binali Yıldırım University (Project No. SAG-A-070114-0051). | |
| dc.identifier.doi | 10.17219/acem/155216 | |
| dc.identifier.eissn | 2451-2680 | |
| dc.identifier.endpage | 456 | |
| dc.identifier.issn | 1899-5276 | |
| dc.identifier.issue | 4 | |
| dc.identifier.pmid | 36413179 | |
| dc.identifier.scopus | 2-s2.0-85146788442 | |
| dc.identifier.startpage | 449 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12164 | |
| dc.identifier.volume | 32 | |
| dc.identifier.wos | WOS:000890460800001 | |
| 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 | cisplatin | |
| dc.subject | IL-38 | |
| dc.subject | nephrotoxicity | |
| dc.subject | rat | |
| dc.subject | sorafenib | |
| dc.subject | Animals | |
| dc.subject | Antioxidants | |
| dc.subject | Kidney | |
| dc.subject | Liver Neoplasms | |
| dc.subject | Oxidative Stress | |
| dc.subject | Rats | |
| dc.subject | alanine aminotransferase | |
| dc.subject | aspartate aminotransferase | |
| dc.subject | creatinine | |
| dc.subject | cytokine | |
| dc.subject | interleukin 1 | |
| dc.subject | interleukin 1beta | |
| dc.subject | interleukin 38 | |
| dc.subject | sodium chloride | |
| dc.subject | tumor necrosis factor | |
| dc.subject | unclassified drug | |
| dc.subject | urea | |
| dc.subject | antioxidant | |
| dc.subject | alanine aminotransferase blood level | |
| dc.subject | animal experiment | |
| dc.subject | animal model | |
| dc.subject | animal tissue | |
| dc.subject | Article | |
| dc.subject | aspartate aminotransferase blood level | |
| dc.subject | bleeding | |
| dc.title | The effects of sorafenib in healthy and cisplatin-treated rats | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 4 | |
| rdl.citation.wos | 3 | |
| rdl.department | Department of Internal Medicine, Faculty of Medicine, Erzincan Binali Yıldırım University, Türkiye. | Department of Medical Biology, Faculty of Medicine, Erzincan Binali Yıldırım University, Türkiye. | Department of Endocrinology, Faculty of Medicine, Erzincan Binali Yıldırım University, Türkiye. | |
| 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) |
