Antioxidant Cardioprotection against Reperfusion Injury: Potential Therapeutic Roles of Resveratrol and Quercetin.
Ramón RodrigoCatalina RetamalDenisse SchupperDiego Vergara-HernándezSarmistha SahaElisabetta ProfumoElisabetta ProfumoSarmistha SahaPublished in: Molecules (Basel, Switzerland) (2022)
Ischemia-reperfusion myocardial damage is a paradoxical tissue injury occurring during percutaneous coronary intervention (PCI) in acute myocardial infarction (AMI) patients. Although this damage could account for up to 50% of the final infarct size, there has been no available pharmacological treatment until now. Oxidative stress contributes to the underlying production mechanism, exerting the most marked injury during the early onset of reperfusion. So far, antioxidants have been shown to protect the AMI patients undergoing PCI to mitigate these detrimental effects; however, no clinical trials to date have shown any significant infarct size reduction. Therefore, it is worthwhile to consider multitarget antioxidant therapies targeting multifactorial AMI. Indeed, this clinical setting involves injurious effects derived from oxygen deprivation, intracellular pH changes and increased concentration of cytosolic Ca 2+ and reactive oxygen species, among others. Thus, we will review a brief overview of the pathological cascades involved in ischemia-reperfusion injury and the potential therapeutic effects based on preclinical studies involving a combination of antioxidants, with particular reference to resveratrol and quercetin, which could contribute to cardioprotection against ischemia-reperfusion injury in myocardial tissue. We will also highlight the upcoming perspectives of these antioxidants for designing future studies.
Keyphrases
- acute myocardial infarction
- percutaneous coronary intervention
- oxidative stress
- left ventricular
- early onset
- st segment elevation myocardial infarction
- ischemia reperfusion injury
- acute coronary syndrome
- reactive oxygen species
- st elevation myocardial infarction
- antiplatelet therapy
- coronary artery disease
- clinical trial
- patients undergoing
- end stage renal disease
- coronary artery bypass grafting
- late onset
- heart failure
- newly diagnosed
- ejection fraction
- induced apoptosis
- randomized controlled trial
- prognostic factors
- dna damage
- chronic kidney disease
- drug delivery
- atrial fibrillation
- signaling pathway
- stem cells
- peritoneal dialysis
- bone marrow
- mesenchymal stem cells
- heat shock protein
- heat shock
- cell therapy
- protein kinase