Literature DB >> 16830072

Protection from post-conditioning depends on the number of short ischemic insults in anesthetized pigs.

Efstathios K Iliodromitis1, Michael Georgiadis, Michael V Cohen, James M Downey, Elias Bofilis, Dimitrios T Kremastinos.   

Abstract

Post-conditioning in the early reperfusion period confers protection to the heart after a potentially lethal episode of prolonged ischemia. Protection from this novel intervention has been documented in rat, rabbit and canine hearts, but one group has reported that it is ineffective in pigs, a large-animal species that should be most relevant to humans. We hypothesized that this negative result was related to an inappropriate post-conditioning protocol rather than the species. The present study, therefore, tested whether an effective post-conditioning protocol could be identified that limits infarct size in anesthetized pigs. Domestic Landrace pigs weighing 25-29 kg were anesthetized, and after a mid-sternal thoracotomy and pericardiotomy the left anterior descending coronary artery was ligated for 60 min followed by 3 h of reperfusion. Three groups were studied: control group (n = 5) with no other intervention, 4-30 PostC group (n = 5) with 4 cycles of 30-s reperfusion/30-s ischemia, and 8-30 PostC group (n = 6) with 8 cycles of 30-s reperfusion/30-s ischemia. The two post-conditioning protocols started immediately after termination of the 60-min coronary occlusion. Region at risk and infarct size were delineated with the aid of pre-mortem monastral blue injection and postmortem staining with triphenyltetrazolium chloride, respectively. In control hearts 33.5 +/- 7.6% of the risk zone infarcted and 36.7 +/- 3.7% in the 4-30 PostC group (P = NS). But there was only 10.5 +/- 0.5% infarction in the 8-30 PostC group (P < 0.01 vs. the other two groups). Post-conditioning confers protection in pigs but requires more than 4 ischemia/reperfusion cycles. Post-conditioning may protect by inhibiting mitochondrial permeability transition pore formation by keeping the heart acidotic as it is reoxygenated. If true, then it would be difficult to employ too many occlusion cycles.

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Year:  2006        PMID: 16830072     DOI: 10.1007/s00395-006-0606-3

Source DB:  PubMed          Journal:  Basic Res Cardiol        ISSN: 0300-8428            Impact factor:   17.165


  27 in total

1.  The Protective Effects of Ischemic Postconditioning against Stroke: From Rapid to Delayed and Remote Postconditioning.

Authors:  Heng Zhao
Journal:  Open Drug Discov J       Date:  2011-12-24

Review 2.  From rapid to delayed and remote postconditioning: the evolving concept of ischemic postconditioning in brain ischemia.

Authors:  Heng Zhao; Chuancheng Ren; Xingmiao Chen; Jiangang Shen
Journal:  Curr Drug Targets       Date:  2012-02       Impact factor: 3.465

Review 3.  Ischemic Conditioning and Atrial Fibrillation: Hope for a NewTherapy?

Authors:  Heiko Schmitt; Bruce T Liang; Christopher Pickett
Journal:  J Atr Fibrillation       Date:  2013-04-06

Review 4.  Myocardial ischemic conditioning: Physiological aspects and clinical applications in cardiac surgery.

Authors:  Radhouane Bousselmi; Mohamed Anis Lebbi; Mustapha Ferjani
Journal:  J Saudi Heart Assoc       Date:  2013-11-13

5.  Ischemic post-conditioning reduces infarct size of the in vivo rat heart: role of PI3-K, mTOR, GSK-3beta, and apoptosis.

Authors:  Claudia Wagner; Diana Tillack; Gregor Simonis; Ruth H Strasser; Christof Weinbrenner
Journal:  Mol Cell Biochem       Date:  2010-01-07       Impact factor: 3.396

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

7.  Myocardial ischemic postconditioning against ischemia-reperfusion is impaired in ob/ob mice.

Authors:  Omar Bouhidel; Sandrine Pons; Richard Souktani; Roland Zini; Alain Berdeaux; Bijan Ghaleh
Journal:  Am J Physiol Heart Circ Physiol       Date:  2008-08-08       Impact factor: 4.733

8.  Ischemic postconditioning confers cardioprotection and prevents reduction of Trx-1 in young mice, but not in middle-aged and old mice.

Authors:  Virginia Perez; Verónica D Annunzio; Tamara Mazo; Timoteo Marchini; Lourdes Caceres; Pablo Evelson; Ricardo J Gelpi
Journal:  Mol Cell Biochem       Date:  2016-03-01       Impact factor: 3.396

9.  The cardioprotection of the late phase of ischemic preconditioning is enhanced by postconditioning via a COX-2-mediated mechanism in conscious rats.

Authors:  Hiroshi Sato; Roberto Bolli; Gregg D Rokosh; Qiuli Bi; Shujing Dai; Gregg Shirk; Xian-Liang Tang
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-08-17       Impact factor: 4.733

10.  Apyrase treatment of myocardial infarction according to a clinically applicable protocol fails to reduce myocardial injury in a porcine model.

Authors:  Jesper van der Pals; Sasha Koul; Michael I Götberg; Göran K Olivecrona; Martin Ugander; Mikael Kanski; Andreas Otto; Matthias Götberg; Håkan Arheden; David Erlinge
Journal:  BMC Cardiovasc Disord       Date:  2010-01-04       Impact factor: 2.298

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