From: Ferroptosis in cardiovascular diseases: role and mechanism
Reagents | Mechanisms | CADs | References |
---|---|---|---|
BMSCS-EXO | Increases GSH level | Myocardial I/R injury | [88] |
FRATAXIN | Reduces mitochondrial iron and ROS level | Myocardial I/R injury | [91] |
RESVERATROL | Regulates USP19-Beclin1 autophagy | Myocardial I/R injury | [92] |
NARINGIN | Regulates the NRF2 /System xc—/GPX4 pathway | Myocardial I/R injury | [93] |
SMI | Activates Nrf2/GPX4 pathway | Myocardial I/R injury | [94] |
SSYXC | Increases transferrin level | Atrial fibrillation | [164] |
DESFERRIAMINE | Inhibits iron overload | COVID-19-associated cardiomyopathy | [104] |
LACTOFERRIN | Inhibits iron overload | COVID-19-associated cardiomyopathy | [107] |
MELATONIN | Reduces ACSL4 level and increases GPX4 level | Chemotherapy-related cardiomyopathy | [121] |
EMPAGLIFLOZIN | Regulates NLRP3 and myd88 related pathways | Chemotherapy-related cardiomyopathy | [122] |
FERROSTATIN-1 | Inhibits lipids peroxidation | Hypertrophic cardiomyopathy | [127] |
DHA | Increases SLC7A11 level | Hypertrophic cardiomyopathy | [165] |
ABCB7 | Interacts with mitochondrial complex IV and V | Hypertrophic cardiomyopathy | [134] |
PUERARIN | Inhibits iron overload and lipids peroxidation | Hypertrophic cardiomyopathy | [135] |
Losartan | Inhibits iron overload | Hypertrophic cardiomyopathy | [136] |