Myocardial postconditioning is lost in vascular nitrate tolerance

Organic nitrates play an important role in the therapy of ischemic heart disease; however, their clinical application is limited by the development of vascular nitrate tolerance. We have previously shown attenuation of the cardioprotective effect of preconditioning in vascular nitrate tolerance. Her...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Fekete Veronika
Murlasits Zsolt
Aypar Eda
Bencsik Péter
Sárközy Márta
Szénási Gábor
Ferdinandy Péter
Csont Tamás Bálint
Dokumentumtípus: Cikk
Megjelent: 2013-09
Sorozat:Journal of cardiovascular pharmacology 62 No. 3
doi:10.1097/FJC.0b013e3182993ae0

mtmt:2322814
Online Access:http://publicatio.bibl.u-szeged.hu/6593
Leíró adatok
Tartalmi kivonat:Organic nitrates play an important role in the therapy of ischemic heart disease; however, their clinical application is limited by the development of vascular nitrate tolerance. We have previously shown attenuation of the cardioprotective effect of preconditioning in vascular nitrate tolerance. Here, we studied whether the development of vascular nitrate tolerance affects the infarct size, limiting effect of ischemic postconditioning (IPost) in the myocardium, and whether the activation of survival kinases plays a role in the molecular mechanism of postconditioning in the presence or absence of vascular nitrate tolerance. Male Wistar rats were treated with nitroglycerin/vehicle for 3 days to induce vascular nitrate tolerance. On the fourth day, isolated hearts were subjected to 30-minute coronary occlusion followed by 120-minute reperfusion with or without IPost. In nontolerant hearts, postconditioning significantly decreased infarct size as compared with ischemia/reperfusion; however, postconditioning failed to decrease infarct size in hearts of nitrate tolerant rats. Phosphorylation of ERK 1/2, Akt, or endothelial nitric oxide synthetase showed no significant differences between the groups at the 10th minute of reperfusion. Vascular nitrate tolerance interferes with the infarct size limiting effect of IPost. Activation of survival kinases is not crucial in the molecular mechanism of postconditioning, which remains unaffected in nitrate tolerance.
Terjedelem/Fizikai jellemzők:298-303
ISSN:1533-4023