Back to Search Start Over

Argon Exposure Induces Postconditioning in Myocardial Ischemia-Reperfusion

Authors :
Laurent Coulbault
Christophe Simard
Jacques H. Abraini
Laurent Sallé
Alain Manrique
Stéphane Allouche
Jean-Luc Hanouz
Mathieu Souplis
Damien Legallois
René Rouet
Sandrine Lemoine
Katrien Blanchart
Adrien Lemaitre
Romain Guinamard
Source :
Journal of cardiovascular pharmacology and therapeutics. 22(6)
Publication Year :
2017

Abstract

Background and Purpose: Cardioprotection against ischemia–reperfusion (I/R) damages remains a major concern during prehospital management of acute myocardial infarction. Noble gases have shown beneficial effects in preconditioning studies. Because emergency proceedings in the context of myocardial infarction require postconditioning strategies, we evaluated the effects of argon in such protocols on mammalian cardiac tissue. Experimental Approaches: In rat, cardiac I/R was induced in vivo by transient coronary artery ligature and cardiac functions were evaluated by magnetic resonance imaging. Hypoxia–reoxygenation (H/R)-induced arrhythmias were evaluated in vitro using intracellular microelectrodes on both rat-isolated ventricle and a model of border zone in guinea pig ventricle. Hypoxia–reoxygenation loss of contractile force was assessed in human atrial appendages. In those models, postconditioning was induced by 5 minutes application of argon at the time of reperfusion. Key Results: In the in vivo model, I/R produced left ventricular ejection fraction decrease (24%) and wall motion score increase (36%) which was prevented when argon was applied in postconditioning. In vitro, argon postconditioning abolished H/R-induced arrhythmias such as early after depolarizations, conduction blocks, and reentries. Recovery of contractile force in human atrial appendages after H/R was enhanced in the argon group, increasing from 51% ± 2% in the nonconditioned group to 83% ± 7% in the argon-treated group ( P < .001). This effect of argon was abolished in the presence of wortmannin and PD98059 which inhibit prosurvival phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt) and MEK/extracellular receptor kinase 1/2 (ERK 1/2), respectively, or in the presence of the mitochondrial permeability transition pore opener atractyloside, suggesting the involvement of the reperfusion injury salvage kinase pathway. Conclusion and Implications: Argon has strong cardioprotective properties when applied in conditions of postconditioning and thus appears as a potential therapeutic tool in I/R situations.

Details

ISSN :
19404034
Volume :
22
Issue :
6
Database :
OpenAIRE
Journal :
Journal of cardiovascular pharmacology and therapeutics
Accession number :
edsair.doi.dedup.....de0340931ccc7db9d20a5e00b08b861c