Literature DB >> 18033009

Protecting the acutely ischemic myocardium beyond reperfusion therapies: are we any closer to realizing the dream of infarct size elimination?

R Tissier1, M V Cohen, J M Downey.   

Abstract

Patients currently treated for acute myocardial infarction receive reperfusion therapy as their only anti-infarct intervention. Although pharmacologic agents have been evaluated in the past for their ability to salvage ischemic myocardium when administered at reperfusion, until very recently none has demonstrated clear efficacy in clinical trials. However, a new generation of interventions has emerged which protects the heart by activating the reperfusion-induced salvage kinase (RISK) pathway. Unlike the disappointing results documented with previously touted putative cardioprotective agents, the preclinical experience with these newer interventions is very consistent indicating that there is a high likelihood that they will be effective clinically. Ischemic postconditioning, which also acts by activating the RISK pathway, has shown marked reduction in infarct size in small-scale trials. Finally, if a strategy for rapidly cooling the heart can be devised so that the in-hospital normothermic ischemic time can be significantly reduced, then infarct size can be even further decreased. In our opinion it is well within our reach using existing technologies to see the day when infarction can be virtually eliminated in the patient with acute coronary occlusion.

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Mesh:

Year:  2007        PMID: 18033009

Source DB:  PubMed          Journal:  Arch Mal Coeur Vaiss        ISSN: 0003-9683


  9 in total

1.  Modulation of receptor sensitivity: possible therapeutic target?

Authors:  Michel V Cohen; James M Downey
Journal:  Br J Pharmacol       Date:  2009-03       Impact factor: 8.739

2.  Triple therapy greatly increases myocardial salvage during ischemia/reperfusion in the in situ rat heart.

Authors:  Xi-Ming Yang; Lin Cui; Ahmad Alhammouri; James M Downey; Michael V Cohen
Journal:  Cardiovasc Drugs Ther       Date:  2013-10       Impact factor: 3.727

3.  Cardioprotective PKG-independent NO signaling at reperfusion.

Authors:  Michael V Cohen; Xi-Ming Yang; Yanping Liu; Nataliya V Solenkova; James M Downey
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-09-17       Impact factor: 4.733

4.  Cardioprotection: spotlight on PKG.

Authors:  M V Cohen; J M Downey
Journal:  Br J Pharmacol       Date:  2007-09-17       Impact factor: 8.739

5.  Two classes of anti-platelet drugs reduce anatomical infarct size in monkey hearts.

Authors:  Xi-Ming Yang; Yanping Liu; Lin Cui; Xiulan Yang; Yongge Liu; Narendra Tandon; Junichi Kambayashi; James M Downey; Michael V Cohen
Journal:  Cardiovasc Drugs Ther       Date:  2013-04       Impact factor: 3.727

6.  Acidosis, oxygen, and interference with mitochondrial permeability transition pore formation in the early minutes of reperfusion are critical to postconditioning's success.

Authors:  Michael V Cohen; Xi-Ming Yang; James M Downey
Journal:  Basic Res Cardiol       Date:  2008-07-14       Impact factor: 17.165

Review 7.  Signalling pathways and mechanisms of protection in pre- and postconditioning: historical perspective and lessons for the future.

Authors:  Michael V Cohen; James M Downey
Journal:  Br J Pharmacol       Date:  2014-11-24       Impact factor: 8.739

Review 8.  Adenosine-associated delivery systems.

Authors:  Mehdi Kazemzadeh-Narbat; Nasim Annabi; Ali Tamayol; Rahmi Oklu; Amyl Ghanem; Ali Khademhosseini
Journal:  J Drug Target       Date:  2015       Impact factor: 5.121

9.  Protective effect of the combinations of glycyrrhizic, ferulic and cinnamic acid pretreatment on myocardial ischemia-reperfusion injury in rats.

Authors:  Yuqin Gao; Jiping Hao; Hongkao Zhang; Guoqiang Qian; Renwang Jiang; Jing Hu; Jianing Wang; Zhang Lei; Guoping Zhao
Journal:  Exp Ther Med       Date:  2014-12-16       Impact factor: 2.447

  9 in total

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