Cardiotoxicity of sorafenib is mediated through elevation of ROS level and CaMKII activity and dysregulation of calcium homoeostasis. Issue 2 (7th October 2019)

• Record Type: Journal Article
• Authors: Ma, Wenzhuo; Liu, Mei; Liang, Fanfan; Zhao, Lili; Gao, Chenying; Jiang, Xixi; Zhang, Xin; Zhan, Heqin; Hu, Hao; Zhao, Zhenghang
• Is Part Of: Basic & clinical pharmacology & toxicology. Volume 126:Issue 2(2020)
• Page Start: 166
• Page End: 180
• Publication Date: 2019-10-07
• Subjects: Ca2+ abnormality -- cardiotoxicity -- mPTP -- N‐(2‐mercaptopropionyl)‐glycine -- ROS -- sorafenib; Pharmacology -- Periodicals; Toxicology -- Periodicals; Pharmacology -- Periodicals; Toxicology -- Periodicals; Pharmacology, Clinical -- Periodicals; Computer network resources; Electronic journals; 615.1
• DOI: 10.1111/bcpt.13318
• Languages: English
• ISSNs: 1742-7835

Abstract

Abstract: Sorafenib, a multi‐kinase inhibitor, is recommended as a new standard therapy for advanced hepatocellular carcinoma (HCC); however, it also exhibits severe cardiotoxicity and the toxicity mechanisms are not completely elucidated. Recent studies suggested that sorafenib‐enhanced ROS may partially contribute to its anti‐HCC effect, which implies that redox mechanism might also be involved in sorafenib's cardiotoxicity. In this study, we aimed to investigate if sorafenib is able to induce oxidative stress and how this may impair cellular functions in cardiomyocyte, ultimately accounting for its cardiotoxicity. Our results showed that in isolated rat hearts, sorafenib caused ventricular arrhythmias and left ventricular dysfunction, which were alleviated by the antioxidant N‐(2‐mercaptopropionyl)‐glycine (MPG). In isolated ventricular myocytes, sorafenib increased diastolic intracellular Ca 2+ levels, decreased Ca transients and the occurrence of Ca 2+ waves. These changes were eliminated by MPG, CaMKII inhibitor KN‐93 and the mitochondrial permeability transition pore (mPTP)inhibitor cyclosporin A (CsA). Moreover, the levels of oxidized and phosphorylated CaMKII were significantly increased. Sorafenib elevated ROS levels, which was reversed by CsA and MPG; additionally, sorafenib reduced the activity of mitochondrial complex III and augmented mitochondrial ROS production. In vivo rats treated with sorafenib exhibited a reduction of antioxidant defence and abnormal histological alterations including hypertrophy, increased fibrosis, disordered myofibrils and damaged mitochondria, which were protected by MPG. We conclude that sorafenib induces the disruption of Ca 2+ homoeostasis and cardiac injury via enhanced ROS potentially through inhibiting mitochondrial complex III, the opening of mPTP and overactivating CaMKII. These results provide a potential strategy for preventing or reducing cardiotoxicity of sorafenib.