The effects of sorafenib in healthy and cisplatin-treated rats


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DEMİRTAŞ L., GÜRBÜZEL M., Tahirler H., AKBAŞ E. M., KARATAŞ Ö., ARSLAN Y. K.

ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, cilt.32, ss.449-456, 2023 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 32
  • Basım Tarihi: 2023
  • Doi Numarası: 10.17219/acem/155216
  • Dergi Adı: ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE
  • Sayfa Sayıları: ss.449-456
  • Anahtar Kelimeler: IL-38, cisplatin, rat, nephrotoxicity, sorafenib, RAF/MEK/ERK PATHWAY, NEPHROTOXICITY, MECHANISMS, TARGETS, CELLS, LIVER, RESISTANCE, INJURY
  • Çukurova Üniversitesi Adresli: Evet

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-1 beta, and tumor necrosis factor alpha (TNF-alpha) 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 it had a effect in after stress induced