Table 3 Pharmacological treatment of cardiovascular diseases
Drug | Mechanism | Results | Action |
|---|---|---|---|
Perhexiline/ Etomoxir | Inhibit CPT1 | Inhibit FAO, enhance glucose oxidation | Improve myocardial ischemia and heart failure |
Trimetazidine | Block Long-chain 3-ketoacyl CoA Thioesterase | Inhibit FAO, increase glucose oxidation, Improve insulin sensitivity | Improve myocardial ischemia |
Trimetazidine | Upregulate the expression of AMPK and PPAR-α | Facilitate the absorption of energy substrates and protein expression, especially ketones | Improve heart failure |
Trimetazidine | Activate the AMPK/ERK pathway | Inhibiting FAO to enhance glucose oxidation | Reduce reperfusion injury |
Trimetazidine | Activate the SIRT1-AMPK pathway | Enhance ATP production and SOD activity, while decreasing LPO, FFA, and NO levels | Improve myocardial infarction |
Glucose-Insulin-Potassium (GIK) Solution | Reduce circulating free fatty acid levels | Inhibit FAO, Enhance Glycolysis | Reduce myocardial infarct size |
Lipstatin-1 | Reduce ROS | Reduce lipid peroxides | Reduce myocardial infarct size and ischemia-reperfusion injury |
Simvastatin/Fluvastatin | Block the MVA pathway | Reduce lipid peroxides | Lower cholesterol levels, maintain normal heart function |
Simvastatin | Activating the JAK/STAT3 pathway | Alleviate mitochondrial damage | Improve heart failure |
Coenzyme Q10 | Clear free radicals | Enhance mitochondrial energy production | Improve myocardial ischemia |
Ferrostatin-1 | Reduce ROS, prevent lipid peroxidation | Reduce iron death, maintain mitochondrial function | Protect myocardial cells |
Mitotane | Reduce ROS | Reduce lipid peroxides | Rescue from DOX-induced cardiomyopathy |
Dexrazoxane | Reduce ROS | Reduce lipid peroxides | Maintain mitochondrial function |
Fenofibrate | Activate PPAR-α | Promote FAO, regulate cardiac energy metabolism, alleviate oxidative stress | Improve heart failure |
Dichloroacetic Acid (DCA) | Inhibit PDK | Enhance glucose oxidation and reduce glycolysis | Reduce reperfusion injury |
Carvedilol | Improve insulin resistance, reduce oxidative stress. | Enhance glucose oxidation | Improve heart failure |
Pioglitazone | Activate PPAR-γ, Anti-inflammatory | Alleviate mitochondrial damage | Reduce reperfusion injury |
Metformin | Activate AMPK | Increase glucose uptake, improve insulin resistance | Improve diabetic cardiomyopathy |
Metformin | Up-regulate Sirt3, reduce the acetylation level of PGC-1a | Inhibit mitochondrial damage, improve mitochondrial respiratory function | Improve heart failure |
Empagliflozin | Reduce pACC, CPT1, CD36; Enhance GLUT4 | Block FAO, increase glucose uptake | Improve diabetic cardiomyopathy |
SGLT2 Inhibitors | Increase levels of beta-hydroxybutyrate in the blood | Decrease energy demand, stabilize mitochondria | Improve energy metabolism in heart failure |