Pagliaro Pasquale, Mancardi Daniele, Rastaldo Raffaella, Penna Claudia, Gattullo Donatella, Miranda Katrina M, Feelisch Martin, Wink David A, Kass David A, Paolocci Nazareno
Dipartimento di Scienze Cliniche e Biologiche, Università degli Studi di Torino, Orbassano, Italy.
Free Radic Biol Med. 2003 Jan 1;34(1):33-43. doi: 10.1016/s0891-5849(02)01179-6.
Nitric oxide (NO) donors mimic the early phase of ischemic preconditioning (IPC). The effects of nitroxyl (HNO/NO(-)), the one-electron reduction product of NO, on ischemia/reperfusion (I/R) injury are unknown. Here we investigated whether HNO/NO(-), produced by decomposition of Angeli's salt (AS; Na(2)N(2)O(3)), has a cardioprotective effect in isolated perfused rat hearts. Effects were examined after intracoronary perfusion (19 min) of either AS (1 microM), the NO donor diethylamine/NO (DEA/NO, 0.5 microM), vehicle (100 nM NaOH) or buffer, followed by global ischemia (30 min) and reperfusion (30 min or 120 min in a subset of hearts). IPC was induced by three cycles of 3 min ischemia followed by 10 min reperfusion prior to I/R. The extent of I/R injury under each intervention was assessed by changes in myocardial contractility as well as lactate dehydrogenase (LDH) release and infarct size. Postischemic contractility, as indexed by developed pressure and dP/dt(max), was similarly improved with IPC and pre-exposure to AS, as opposed to control or DEA/NO-treated hearts. Infarct size and LDH release were also significantly reduced in IPC and AS groups, whereas DEA/NO was less effective in limiting necrosis. Co-infusion in the triggering phase of AS and the nitroxyl scavenger, N-acetyl-L-cysteine (4 mM) completely reversed the beneficial effects of AS, both at 30 and 120 min reperfusion. Our data show that HNO/NO(-) affords myocardial protection to a degree similar to IPC and greater than NO, suggesting that reactive nitrogen oxide species are not only necessary but also sufficient to trigger myocardial protection against reperfusion through species-dependent, pro-oxidative, and/or nitrosative stress-related mechanisms.
一氧化氮(NO)供体可模拟缺血预处理(IPC)的早期阶段。一氧化氮的单电子还原产物硝酰基(HNO/NO⁻)对缺血/再灌注(I/R)损伤的影响尚不清楚。在此,我们研究了由安吉利盐(AS;Na₂N₂O₃)分解产生的HNO/NO⁻在离体灌注大鼠心脏中是否具有心脏保护作用。在冠状动脉内灌注(19分钟)AS(1微摩尔)、NO供体二乙胺/NO(DEA/NO,0.5微摩尔)、溶媒(100纳摩尔氢氧化钠)或缓冲液后,接着进行全心缺血(30分钟)和再灌注(部分心脏为30分钟或120分钟),然后检测相关效应。在I/R之前,通过3分钟缺血然后10分钟再灌注的三个循环诱导IPC。通过心肌收缩力的变化以及乳酸脱氢酶(LDH)释放和梗死面积来评估每种干预下的I/R损伤程度。与对照或DEA/NO处理的心脏相反,以舒张期压力和dP/dt(max)为指标的缺血后收缩力在IPC和预先暴露于AS时同样得到改善。IPC组和AS组的梗死面积和LDH释放也显著降低,而DEA/NO在限制坏死方面效果较差。在触发阶段同时输注AS和硝酰基清除剂N-乙酰-L-半胱氨酸(4毫摩尔)在再灌注30分钟和120分钟时均完全逆转了AS的有益作用。我们的数据表明,HNO/NO⁻提供的心肌保护程度与IPC相似且大于NO,这表明活性氮氧化物不仅是触发心肌抗再灌注保护所必需的,而且通过依赖于物种、促氧化和/或亚硝化应激相关机制也是足够的。