The effects of sorafenib in healthy and cisplatin-treated rats

ArticleAçık Erişim

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.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12164Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17219/acem/155216Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDemirtas, Levent
dc.contributor.authorGürbüzel, Mehmet
dc.contributor.authorTahirler, Hilal
dc.contributor.authorAkbas, Emin Murat
dc.contributor.authorKaratas, Ozhan
dc.contributor.authorArslan, Yusuf Kemal
dc.date.accessioned2026-10-18T20:27:06.074322475Z
dc.date.available2026-10-18T20:27:06.074322475Z
dc.date.issued2023
dc.description.abstractBackground. 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.sponsorshipThis research was partially supported with a grant from the Research Fund of Erzincan Binali Yıldırım University (Project No. SAG-A-070114-0051).
dc.identifier.doi10.17219/acem/155216
dc.identifier.eissn2451-2680
dc.identifier.endpage456
dc.identifier.issn1899-5276
dc.identifier.issue4
dc.identifier.pmid36413179
dc.identifier.scopus2-s2.0-85146788442
dc.identifier.startpage449
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12164
dc.identifier.volume32
dc.identifier.wosWOS:000890460800001
dc.language.isoen
dc.publisherWroclaw University of Medicine
dc.relation.ispartofAdvances in Clinical and Experimental Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcisplatin
dc.subjectIL-38
dc.subjectnephrotoxicity
dc.subjectrat
dc.subjectsorafenib
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectKidney
dc.subjectLiver Neoplasms
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectalanine aminotransferase
dc.subjectaspartate aminotransferase
dc.subjectcreatinine
dc.subjectcytokine
dc.subjectinterleukin 1
dc.subjectinterleukin 1beta
dc.subjectinterleukin 38
dc.subjectsodium chloride
dc.subjecttumor necrosis factor
dc.subjectunclassified drug
dc.subjecturea
dc.subjectantioxidant
dc.subjectalanine aminotransferase blood level
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectaspartate aminotransferase blood level
dc.subjectbleeding
dc.titleThe effects of sorafenib in healthy and cisplatin-treated rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus4
rdl.citation.wos3
rdl.departmentDepartment 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.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)