Table 1.
Properties of the main antioxidant therapeutics.
| Components of standard heart failure therapy that possess antioxidant properties | |
| ACEi, ARBs, ARNi, antialdosterone drugs: interference with RAAS signaling | |
| Carvedilol: β1- and β2-adrenergic receptor blocker that also increase NO production or decrease inactivation | |
| β3AR agonists: enhancement of myocardial β3-adrenergic coupling with NO-cGMP signaling | |
| ARNi: enhancement of NPs/cGMP/PKG pathway | |
|
| |
| Drugs with redox effect that are not mainstream therapeutic approach in heart failure | |
| PDE5 inhibition and BH4 supplementation: potentiating NO/cGMP/PKG signaling | |
| Statins: NADPH oxidase inhibitors | |
| Allopurinol: xanthine oxidases inhibitor | |
| Ranolazine: inhibitor of elevated late INa | |
| MAO inhibitors: blunting ROS production from MAOs | |
|
| |
| Novel therapeutic compounds that target ROS/RNS signaling pathways | |
| SS-31 (MTP-131, Bendavia): direct action on mitochondrial function | |
| Resveratrol: preservation of the LKB1-AMPK-eNOS signaling axis | |
| HNO donors: improving Ca2+ cycling and myofilament Ca2+ sensitivity | |
ARNi: angiotensin receptor-neprilysin inhibitor.
AMPK: AMP-activated protein kinase.
NPs: natriuretic peptides.