Article Publish Status: FREE
Abstract Title:

Asiatic Acid Protects against Doxorubicin-Induced Cardiotoxicity in Mice.

Abstract Source:

Oxid Med Cell Longev. 2020 ;2020:5347204. Epub 2020 May 15. PMID: 32509145

Abstract Author(s):

Xiaoping Hu, Baijun Li, Luocheng Li, Bowen Li, Jinlong Luo, Bin Shen

Article Affiliation:

Xiaoping Hu


The use of doxorubicin (DOX) can result in depression of cardiac function and refractory cardiomyopathy. Currently, there are no effective approaches to prevent DOX-related cardiac complications. Asiatic acid (AA) has been reported to provide cardioprotection against several cardiovascular diseases. However, whether AA could attenuate DOX-related cardiac injury remains unclear. DOX (15 mg/kg) was injected intraperitoneally into the mice to mimic acute cardiac injury, and the mice were given AA (10 mg/kg or 30 mg/kg) for 2 weeks for protection. The data in our study found that AA-treated mice exhibited attenuated cardiac injury and improved cardiac function in response to DOX injection. AA also suppressed myocardial oxidative damage and apoptosis without affecting cardiac inflammation in DOX-treated mice. AA also provided protection in DOX-challenged cardiomyocytes, improved cell viability, and suppressed intracellular reactive oxygen species (ROS) in vitro. Detectionof signaling pathways showed that AA activated protein kinase B (AKT) signaling pathway in vivo and in vitro. Furthermore, we found that AA lost its protective effects in the heart with AKT inactivation. In conclusion, our results found that AA could attenuate DOX-induced myocardial oxidative stressand apoptosis via activation of the AKT signaling pathway.

Study Type : Animal Study, In Vitro Study

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