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Survival kinases in ischemic preconditioning and postconditioning

Hausenloy, DJ; Yellon, DM; (2006) Survival kinases in ischemic preconditioning and postconditioning. CARDIOVASC RES , 70 (2) 240 - 253. 10.1016/j.cardiores.2006.01.017.

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Abstract

Despite nearly twenty years of research into the field of ischemic preconditioning, the actual mechanism of protection remains unclear. However, much progress has been made in elucidating the signal transduction pathways that convey the extracellular signal initiated by the preconditioning stimulus to the intracellular targets of cardioprotection, with many of these pathways involving the activation of a diverse array of survival protein kinase cascades. The powerful protective benefits of ischemic preconditioning have not yet been realised in the clinical arena, not least because of the prerequisite for any preconditioning intervention to be applied prior to the onset of index ischemia, which in the case of an acute myocardial infarction is difficult to institute. In this regard, the newly described phenomenon of ischemic postconditioning, which comprises a cardioprotective intervention that can be applied at the time of myocardial reperfusion, offers a far more attractive and amenable approach to myocardial protection. Interestingly, certain survival protein kinase cascades recruited at the time of myocardial reperfusion appear to be shared by both ischemic preconditioning and postconditioning, thereby offering a potentially common target of cardioprotection. The often disputed roles these different protein kinases play in mediating the cardioprotective effects of ischemic preconditioning and postconditioning are reviewed in this article, and include protein kinases C, G, and A, members of the MAPK family (Erk1/2, p38, INK and BMK1), the PI3K-Akt cascade, and the JAK-STAT pathway. (c) 2006 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.

Type: Article
Title: Survival kinases in ischemic preconditioning and postconditioning
DOI: 10.1016/j.cardiores.2006.01.017
Keywords: signalling, preconditioning, kinases, ACTIVATED PROTEIN-KINASE, MITOCHONDRIAL PERMEABILITY TRANSITION, RABBIT VENTRICULAR MYOCYTES, K-ATP CHANNELS, MYOCARDIAL ISCHEMIA/REPERFUSION INJURY, REDUCES INFARCT SIZE, PERFUSED RAT-HEART, JAK-STAT PATHWAY, REPERFUSION INJURY, IN-VIVO
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Institute of Cardiovascular Science > Pre-clinical and Fundamental Science
URI: http://discovery.ucl.ac.uk/id/eprint/183530
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