Caspase inhibition via A3 adenosine receptors: a new cardioprotective mechanism against myocardial infarction

Cardiovasc Drugs Ther. 2014 Feb;28(1):19-32. doi: 10.1007/s10557-013-6500-y.

Abstract

Purpose: 2-CL-IB-MECA, (A3 adenosine receptor agonist)(A3AR) mediated cardioprotection is well documented although the associated intracellular signalling pathways remain unclear. Here we demonstrate a role of the pro-survival signalling pathways MEK1/2-ERK1/2 and PI3K/AKT and their effect on modifying Caspase-3 activity in A3AR mediated cardioprotection.

Methods: Isolated perfused rat hearts or primary adult rat cardiac myocytes were subjected to ischaemia/hypoxia and reperfusion/reoxygenation, respectively. 2-CL-IB-MECA (1 nM) was administered at the onset of reperfusion/reoxygenation in the presence and absence of either the PI3K inhibitor Wortmannin (5 nM) or MEK1/2 inhibitor UO126 (10 μM). Heart tissues were harvested for assessment of p-ERK1/2(Thr202/Tyr204) or p-AKT (Ser-473) status or underwent infarct size assessment. Cardiac myocytes underwent flow-cytometric analysis for apoptosis, necrosis, cleaved-caspase 3/p-BAD (Ser-112 and Ser-136) activity post-reoxygenation.

Results: 2-CL-IB-MECA significantly reduced infarct size compared to non-treated controls, where co-administration with either of the kinase inhibitors abolished the infarct sparing effects. Administration of 2-CL-IB-MECA at reperfusion significantly upregulated the status of p-ERK1/2 and p-AKT compared to time matched controls in a UO126 and Wortmannin sensitive manner respectively. 2-CL-IB-MECA when administered throughout reoxygenation significantly reduced apoptosis, necrosis, cleaved-caspase 3 activity and increased p-BAD (Ser-112) and p-BAD (Ser-136) activity in myocytes subjected to hypoxia/reoxygenation injury. The cytoprotective effect was abolished by co-administration with the kinase inhibitors Wortmannin and/or UO126.

Conclusions: We have described the molecular mechanisms associated with A3AR mediated cardioprotection indicating a role for the pro-survival signalling pathways that decrease caspase-3 activity. These observations provide novel insight into the pharmacological effects of A3ARs in ameliorating myocardial ischaemia/reperfusion injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / analogs & derivatives
  • Adenosine / pharmacology
  • Adenosine A3 Receptor Agonists / pharmacology*
  • Androstadienes / pharmacology
  • Animals
  • Apoptosis / drug effects
  • Butadienes / pharmacology
  • Cardiotonic Agents / pharmacology
  • Caspase 3 / metabolism
  • Disease Models, Animal
  • Male
  • Myocardial Infarction / etiology
  • Myocardial Infarction / pathology
  • Myocardial Infarction / prevention & control*
  • Myocardial Reperfusion Injury / physiopathology*
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / pathology
  • Nitriles / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Adenosine A3 / metabolism*
  • Signal Transduction / drug effects
  • Wortmannin

Substances

  • Adenosine A3 Receptor Agonists
  • Androstadienes
  • Butadienes
  • Cardiotonic Agents
  • Nitriles
  • Receptor, Adenosine A3
  • U 0126
  • Caspase 3
  • Adenosine
  • Wortmannin
  • 2-chloro-N(6)-(3-iodobenzyl)adenosine-5'-N-methyluronamide