Dapagliflozin alleviates myocardial ischemia/reperfusion injury by reducing ferroptosis via MAPK signaling inhibition

被引:50
|
作者
Chen, Weixiang [1 ]
Zhang, Yue [1 ]
Wang, Zuoxiang [1 ]
Tan, Mingyue [1 ]
Lin, Jia [1 ]
Qian, Xiaodong [1 ]
Li, Hongxia [1 ]
Jiang, Tingbo [1 ]
机构
[1] Soochow Univ, Dept Cardiol, Affiliated Hosp 1, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
myocardial ischemia/reperfusion; dapagliflozin; ferroptosis; MAPK pathway; treatment; SGLT2; INHIBITORS; OXIDATIVE STRESS; PATHWAY; MECHANISMS;
D O I
10.3389/fphar.2023.1078205
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Reperfusion is essential for ischemic myocardium but paradoxically leads to myocardial damage that worsens cardiac functions. Ferroptosis often occurs in cardiomyocytes during ischemia/reperfusion (I/R). The SGLT2 inhibitor dapagliflozin (DAPA) exerts cardioprotective effects independent of hypoglycemia. Here, we investigated the effect and potential mechanism of DAPA against myocardial ischemia/reperfusion injury (MIRI)-related ferroptosis using the MIRI rat model and hypoxia/reoxygenation (H/R)-induced H9C2 cardiomyocytes. Our results show that DAPA significantly ameliorated myocardial injury, reperfusion arrhythmia, and cardiac function, as evidenced by alleviated ST-segment elevation, ameliorated cardiac injury biomarkers including cTnT and BNP and pathological features, prevented H/R-triggered cell viability loss in vitro. In vitro and in vivo experiments showed that DAPA inhibited ferroptosis by upregulating the SLC7A11/GPX4 axis and FTH and inhibiting ACSL4. DAPA notably mitigated oxidative stress, lipid peroxidation, ferrous iron overload, and reduced ferroptosis. Subsequently, network pharmacology and bioinformatics analysis suggested that the MAPK signaling pathway was a potential target of DAPA and a common mechanism of MIRI and ferroptosis. DAPA treatment significantly reduced MAPK phosphorylation in vitro and in vivo, suggesting that DAPA might protect against MIRI by reducing ferroptosis through the MAPK signaling pathway.
引用
收藏
页数:15
相关论文
empty
未找到相关数据