Suppr超能文献

预处理可减少缺血/再灌注诱导的过氧亚硝酸盐形成。

Preconditioning decreases ischemia/reperfusion-induced peroxynitrite formation.

作者信息

Csonka C, Csont T, Onody A, Ferdinandy P

机构信息

Cardiovascular Research Group, Department of Biochemistry, University of Szeged, Szeged, Hungary.

出版信息

Biochem Biophys Res Commun. 2001 Aug 3;285(5):1217-9. doi: 10.1006/bbrc.2001.5308.

Abstract

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.

摘要

过氧亚硝酸根(ONOO⁻)在预处理机制中的作用尚不清楚。因此,我们研究了预处理及随后的缺血/再灌注对离体大鼠心脏中ONOO⁻形成的影响。心脏接受预处理方案(三个间歇性的全脑缺血/再灌注期,每期持续5分钟),随后进行测试性缺血/再灌注(30分钟全脑缺血和15分钟再灌注)。与未预处理的对照组相比,预处理可改善缺血后心脏功能,并显著降低测试性缺血/再灌注诱导的灌注液中游离硝基酪氨酸的形成,该物质作为心脏内源性ONOO⁻形成的标志物。然而,在预处理期间,第一个缺血/再灌注期会增加硝基酪氨酸的形成,而在第三个缺血/再灌注期后这种增加会减弱。我们得出结论,经典预处理可抑制缺血/再灌注诱导的心脏ONOO⁻形成,并且随后的缺血/再灌注期会导致缺血/再灌注诱导的ONOO⁻生成逐渐减弱。这种机制可能参与了心脏的缺血适应过程。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验