Effects of Metformin on Ischemia/Reperfusion Injury: New Evidence and Mechanisms.
Estefanie Osorio-LlanesWendy Villamizar-VillamizarMaría Clara Ospino GuerraLuis Antonio Díaz-ArizaSara Camila Castiblanco-ArroyaveLuz MedranoDaniela MengualRicardo BelónJairo Castellar-LópezYanireth SepúlvedaCésar Vásquez-TrincadoAileen Y ChangSamir BolívarEvelyn Mendoza-TorresPublished in: Pharmaceuticals (Basel, Switzerland) (2023)
The search for new drugs with the potential to ensure therapeutic success in the treatment of cardiovascular diseases has become an essential pathway to follow for health organizations and committees around the world. In June 2021, the World Health Organization listed cardiovascular diseases as one of the main causes of death worldwide, representing 32% of them. The most common is coronary artery disease, which causes the death of cardiomyocytes, the cells responsible for cardiac contractility, through ischemia and subsequent reperfusion, which leads to heart failure in the medium and short term. Metformin is one of the most-used drugs for the control of diabetes, which has shown effects beyond the control of hyperglycemia. Some of these effects are mediated by the regulation of cellular energy metabolism, inhibiting apoptosis, reduction of cell death through regulation of autophagy and reduction of mitochondrial dysfunction with further reduction of oxidative stress. This suggests that metformin may attenuate left ventricular dysfunction induced by myocardial ischemia; preclinical and clinical trials have shown promising results, particularly in the setting of acute myocardial infarction. This is a review of the molecular and pharmacological mechanisms of the cardioprotective effects of metformin during myocardial ischemia-reperfusion injury.
Keyphrases
- left ventricular
- oxidative stress
- ischemia reperfusion injury
- acute myocardial infarction
- cell death
- cell cycle arrest
- induced apoptosis
- cardiovascular disease
- heart failure
- diabetic rats
- coronary artery disease
- cardiac resynchronization therapy
- hypertrophic cardiomyopathy
- clinical trial
- endoplasmic reticulum stress
- left atrial
- signaling pathway
- type diabetes
- percutaneous coronary intervention
- healthcare
- mitral valve
- dna damage
- aortic stenosis
- public health
- pi k akt
- cell proliferation
- stem cells
- coronary artery bypass grafting
- atrial fibrillation
- mesenchymal stem cells
- cardiovascular events
- phase ii
- human health
- heat shock protein
- acute coronary syndrome
- cerebral ischemia
- smooth muscle
- brain injury
- single molecule
- open label
- heat stress
- insulin resistance
- adipose tissue
- double blind
- randomized controlled trial