Preconditioning decreases ischemia/reperfusion-induced peroxynitrite formation

被引:40
作者
Csonka, C
Csont, T
Onody, A
Ferdinandy, P
机构
[1] Univ Szeged, Fac Med, Dept Biochem, Cardiovasc Res Grp, H-6720 Szeged, Hungary
[2] Univ Alberta, Dept Pharmacol, Cardiovasc Res Grp, Edmonton, AB, Canada
基金
匈牙利科学研究基金会;
关键词
peroxynitrite; nitrotyrosine; preconditioning; ischemia/reperfusion; rat heart;
D O I
10.1006/bbrc.2001.5308
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The role for peroxynitrite (ONOO-) in the mechanism of preconditioning is not known. Therefore, we studied effects of preconditioning and subsequent ischemia/reperfusion on myocardial ONOO- formation in isolated rat hearts. Hearts were subjected to a preconditioning protocol (three intermittent periods of global ischemia/reperfusion of 5 min duration each) followed by a test ischemia/reperfusion (30 min global ischemia and 15 min reperfusion). When compared to nonpreconditioned controls, preceding preconditioning improved postischemic cardiac performance and significantly decreased test ischemia/reperfusion-induced formation of free nitrotyrosine measured in the perfusate as a marker for cardiac endogenous ONOO- formation. During preconditioning, however, the first period of ischemia/reperfusion increased nitrotyrosine formation, which was attenuated after the third period of ischemia/reperfusion. We conclude that classic preconditioning inhibits ischemia/reperfusion-induced cardiac formation of ONOO- and that subsequent periods of ischemia/reperfusion result in a gradual attenuation of ischemia/reperfusion-induced ONOO- generation. This mechanism might be involved in ischemic adaptation of the heart. (C) 2001 Academic Press.
引用
收藏
页码:1217 / 1219
页数:3
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