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. Author manuscript; available in PMC: 2014 Aug 16.
Published in final edited form as: Circ Res. 2013 Aug 16;113(5):10.1161/CIRCRESAHA.113.302095. doi: 10.1161/CIRCRESAHA.113.302095

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