LCZ696 ameliorates doxorubicin-induced cardiomyocyte toxicity in rats

• Published in: Scientific reports Vol. 12; no. 1; p. 4930
• Main Authors: Miyoshi, Toru, Nakamura, Kazufumi, Amioka, Naofumi, Hatipoglu, Omer F., Yonezawa, Tomoko, Saito, Yukihiro, Yoshida, Masashi, Akagi, Satoshi, Ito, Hiroshi
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23.03.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 692/4019/592/75/230; 692/4028/67/1059; Adenosine kinase; Aminobutyrates; AMP; Angiotensin; Animals; Antioxidants; Apoptosis; BAX protein; Bcl-2 protein; Biphenyl Compounds; Calcium-binding protein; Cardiomyocytes; Cardiotoxicity; Cardiotoxicity - drug therapy; Cardiotoxicity - etiology; Cardiotoxicity - metabolism; Cell viability; Chemotherapy; Doxorubicin; Doxorubicin - metabolism; Doxorubicin - toxicity; Drug Combinations; Humanities and Social Sciences; Kinases; Male; Mitochondria; multidisciplinary; Myocytes, Cardiac - metabolism; Neprilysin; Oxidative Stress; Phosphorylation; Protein kinase; Rats; Rats, Sprague-Dawley; Reactive oxygen species; Reactive Oxygen Species - metabolism; Science; Science (multidisciplinary); Troponin; Troponin T; Valsartan - pharmacology; Valsartan - therapeutic use
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-09094-z

Doxorubicin (DOX)-based chemotherapy induces cardiotoxicity, which is considered the main bottleneck for its clinical application. In this study, we investigated the potential benefit of LCZ696, an angiotensin receptor–neprilysin inhibitor against DOX-induced cardiotoxicity in rats and H9c2 cells and determined whether the mechanism underlying any such effects involves its antioxidant activity. Male Sprague–Dawley rats were randomly separated into four groups, each consisting of 15 rats (DOX (1.5 mg/kg/day intraperitoneally for 10 days followed by non-treatment for 8 days); DOX + valsartan (31 mg/kg/day by gavage from day 1 to day 18); DOX + LCZ696 (68 mg/kg/day by gavage from day 1 to day 18); and control (saline intraperitoneally for 10 days). DOX-induced elevation of cardiac troponin T levels on day 18 was significantly reduced by LCZ696, but not valsartan. The DOX-induced increase in myocardial reactive oxygen species (ROS) levels determined using dihydroethidium was significantly ameliorated by LCZ696, but not valsartan, and was accompanied by the suppression of DOX-induced increase in p47phox. LCZ696 recovered the DOX-induced decrease in phosphorylation of adenosine monophosphate-activated protein kinase and increased the ratio of Bax and Bcl-2. In H9c2 cardiomyocytes, LCZ696 reduced DOX-induced mitochondrial ROS generation and improved cell viability more than valsartan. Our findings indicated that LCZ696 ameliorated DOX-induced cardiotoxicity in rat hearts in vivo and in vitro, possibly by mediating a decrease in oxidative stress.