Table 2. Metabolic Therapies Used in the Treatment of Heart Failure.
Italics indicate therapies with reported adverse effects. mCPT1, muscle form of carnitine palmitoyl transferase 1; PDK, pyruvate dehydrogenase kinase; MCD, malonyl CoA decarboxylase; PPAR, peroxisome proliferator-activated receptor; PDE, phosphodiesterase; AMPK, AMP-activated protein kinase; MitoQ, mitochondrial-targeted antioxidant; MitoTEMPO, Mitochondria-targeted antioxidant with superoxide and alkyl radical scavenging properties; EUK-8, superoxide dismutase and catalase mimetic; SS peptide, Szeto-Schiller peptide; PUFAs, polyunsaturated fatty acids.
| Substrate Preference: |
| mCPT1 Inhibitors |
| Partial β-oxidation inhibitors |
| PDK Inhibitors |
| MCD inhibitors |
| Nicotinic Acid Derivatives |
| PPAR Agonists |
| Insulin Sensitivity: |
| Glucagon Like Peptides (GLP-1) |
| Metformin |
| Thiazolidinediones |
| Mitochondrial Function: |
| PDE inhibitors |
| AMPK Activators |
| MitoQ |
| MitoTEMPO |
| EUK-8 |
| SS peptides |
| Dietary Modulation: |
| PUFAs |
| Vitamin E |