4.5 Article

The divergent roles of protein kinase C epsilon and delta in simulated ischaemia-reperfusion injury in human myocardium

Journal

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
Volume 46, Issue 5, Pages 758-764

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.yjmcc.2009.02.013

Keywords

Ischaemia; Reperfusion; Preconditioning; Apoptosis; Human; Myocardium

Funding

  1. British Heart Foundation
  2. Department of Health's NIHR Biomedical Research Centres

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Experimental studies suggest that cardioprotection can be achieved through either the activation of PKC-epsilon prior to the index ischaemic episode or the inhibition of PKC-delta at the onset of reperfusion. However, whether these PKC isoforms exert such divergent roles in human myocardium, subjected to simulated ischaemia-reperfusion injury, is unclear. Human atrial trabeculae were isolated from right atrial appendages harvested from patients undergoing elective cardiac surgery. These were subjected to 90 min of hypoxia followed by 120 min of reoxygenation, at the end of which the recovery of baseline contractile function was determined. Atrial trabeculae were randomised to receive various treatment protocols comprising a peptide activator of PKC-epsilon, a peptide inhibitor of PKC-delta and their respective inactive control peptides. Administering the PKC-delta peptide inhibitor at reoxygenation improved the recovery of function at all the concentrations tested (39.3 +/- 1.4% at 5 nM, 52.4 +/- 2.9% at 50 nM and 46.8 +/- 2.9% at 500 nM versus the control group, 27.5 +/- 1.4%: N >= 6/ group: P<0.02). Preconditioning with the PKC-epsilon peptide activator improved the recovery of function (40.0 +/- 0.8% at 50 nM and 49.7 +/- 3.1% at 500 nM versus the control group 27.5 +/- 1.4%: N >= 6/group: P<0.02). This cardioprotective effect was comparable to that achieved by a standard hypoxic preconditioning protocol (52.3 +/- 3.2%). Interestingly, administering the PKC-epsilon activator (500 nM) at the onset of reperfusion also improved the recovery of contractile function (40.7 +/- 2.1% versus 27.5 +/- 1.5%: N >= 6/group: P<0.05). In human myocardium, cardioprotection can be achieved by either inhibiting PKC-delta or activating PKC-epsilon at the onset of reperfusion. in addition, PKC-e activation offers cardioprotection when administered as a preconditioning strategy. (C) 2009 Elsevier Inc. All rights reserved.

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