Details

Autor(en) / Beteiligte

• Sun, Xiao
• Sun, Ping
• Zhen, Dong
• Xu, Xiangli
• Yang, Li
• Fu, Danni
• Wei, Chengxi
• Niu, Xiaofeng
• Tian, Jiawei
• Li, Hairu

Titel

Melatonin alleviates doxorubicin-induced mitochondrial oxidative damage and ferroptosis in cardiomyocytes by regulating YAP expression

Ist Teil von

• Toxicology and applied pharmacology, 2022-02, Vol.437, p.115902-115902, Article 115902

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2022

Quelle

Access via ScienceDirect (Elsevier)

Beschreibungen/Notizen

• Doxorubicin (Dox) is a high-efficiency agent for cancer therapy. However, it causes cardiotoxicity which limits its clinical application. Despite more efforts has been made to seek protective decisions, unfortunately, the poor prognosis suggests the need for new treatments. As a powerful mitochondrial antioxidant, melatonin (Mel) has been found to confer cardioprotection against various cardiovascular diseases. Currently, the mechanism through which Mel confers protection is not well understood. In this study, we established a Dox-induced cardiotoxicity model in H9c2 cardiomyocytes, zebrafish, and SD rats to explore the mechanism by which Mel alleviates Dox-induced cardiotoxicity. In vivo and in vitro experiments showed that Dox significantly decreased the viability of H9c2 cells, induced apoptosis, myocardial injury, and effectively up-regulated the expression of p-YAP but down-regulated the expression of YAP. Furthermore, we found that Dox significantly up-regulated the expression of ferroptosis-associated protein ACSL4 and down-regulated expression of GPX4. Interestingly, these effects of Dox were reversed following treatment with Mel, indicating that ferroptosis mediated the protective effects of Mel against Dox-induced cardiomyocyte injury. Furthermore, we used YAP-siRNA in vitro and verteporfin (Ver) in vivo to down-regulate the expression level of YAP. The results showed that YAP down-regulation abolished the protective effects of Mel including apoptosis, mitochondrial lipid peroxidation, and ferroptosis. Collectively, these results show that Mel regulates ferroptosis by modulating YAP expression to counteract Dox-induced cardiotoxicity. •Doxorubicin induces myocardial injury and ferroptosis.•Melatonin mitigates doxorubicin-induced cardiotoxicity and myocardial ferroptosis.•Melatonin inhibites myocardial ferroptosis by preserving the expression of YAP.•Melatonin alleviates cardiotoxicity by regulating ferroptosis via YAP/ACSL4 axis.•The mechanism of melatonin's anti-ferroptosis involves mitochondrial protection.