Abstract

Myocardial ischaemia-reperfusion (I/R) injury is a well-known term for exacerbation of cellular destruction and dysfunction after the restoration of blood flow to a previously ischaemic heart. A vast number of studies that have demonstrated that the role of mineralocorticoids in cardiovascular diseases is based on the use of pharmacological mineralocorticoid receptor (MR) antagonists. This review paper aimed to summarize current knowledge on the effects of MR antagonists on myocardial I/R injury as well as postinfarction remodeling. Animal models, predominantly the Langendorff technique and left anterior descending coronary artery occlusion, have confirmed the potency of MR antagonists as preconditioning and postconditioning agents in limiting infarct size and postinfarction remodeling. Several preclinical studies in rodents have established and proved possible mechanisms of cardioprotection by MR antagonists, such as reduction of oxidative stress, reduction of inflammation, and apoptosis, therefore limiting the infarct zone. However, the results of some clinical trials are inconsistent, since they reported no benefit of MR antagonists in acute myocardial infarction. Due to this, further studies and the results of ongoing clinical trials regarding MR antagonist administration in patients with acute myocardial infarction are being awaited with great interest.

Highlights

  • A vast number of studies that has demonstrated the role of mineralocorticoids in cardiovascular diseases is based on the use of pharmacological mineralocorticoid receptor (MR) antagonists (Weldon and Brown 2019)

  • The results of some clinical trials are inconsistent since they reported no benefit of MR antagonists in acute myocardial infarction

  • Further studies and the results of on-going clinical trials regarding MR antagonists administration in patients with acute myocardial infarction are being awaited with great interest

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Summary

Introduction

A vast number of studies that has demonstrated the role of mineralocorticoids in cardiovascular diseases is based on the use of pharmacological mineralocorticoid receptor (MR) antagonists (Weldon and Brown 2019) These antagonists have shown a beneficial effect in various animal models of disease as well as in several clinical trials and represent potential prevention therapy for patients at risk of ischemic disease. The most used MR antagonists in humans are spironolactone and eplerenone Both have similar therapeutic benefit but different pharmacological characteristics (Weldon and Brown 2019; Namsolleck and Unger 2014). Ischaemia-reperfusion (I/R) injury can be defined as the exacerbation of cellular destruction and dysfunction, after the restoration of blood flow to previously ischaemic tissues. Up until now several animal models of myocardial I/R injury have been established with three predominantly used methods such as the Langendorff model of global ischemia, the isolated working heart model according to Neely, and the left anterior descending coronary artery (LAD) occlusion model

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