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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Morphine induces preconditioning via activation of mitochondrial K(Ca) channels.
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Morphine induces preconditioning via activation of mitochondrial K(Ca) channels.

机译:吗啡通过激活线粒体K(Ca)通道诱导预处理。

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摘要

PURPOSE: Mitochondrial calcium sensitive potassium (mK(Ca)) channels are involved in cardioprotection induced by ischemic preconditioning. In the present study we investigated whether morphine-induced preconditioning also involves activation of mK(Ca) channels. METHODS: Isolated rat hearts (six groups; each n = 8) underwent global ischemia for 30 min followed by a 60-min reperfusion. Control animals were not further treated. Morphine preconditioning (MPC) was initiated by two five-minute cycles of morphine 1 microM infusion with one five-minute washout and one final ten-minute washout period before ischemia. The mK(Ca) blocker, paxilline 1 microM, was administered, with and without morphine administration (MPC + Pax and Pax). As a positive control, we added an ischemic preconditioning group (IPC) alone and combined with paxilline (IPC + Pax). At the end of reperfusion, infarct sizes were determined by triphenyltetrazoliumchloride staining. RESULTS: Infarct size was (mean +/- SD) 45 +/- 9% of the area at risk in the Control group. The infarct size was less in the morphine or ischemic preconditioning groups (MPC: 23 +/- 8%, IPC: 20 +/- 5%; each P < 0.05 vs Control). Infarct size reduction was abolished by paxilline (MPC + Pax: 37 +/- 7%, P < 0.05 vs MPC and IPC + Pax: 36 +/- 6%, P < 0.05 vs IPC), whereas paxilline alone had no effect (Pax: 46 +/- 7%, not significantly different from Control). CONCLUSION: Cardioprotection by morphine-induced preconditioning is mediated by activation of mK(Ca) channels.
机译:目的:线粒体钙敏感钾(mK(Ca))通道参与缺血预处理引起的心脏保护作用。在本研究中,我们调查了吗啡诱导的预处理是否也涉及mK(Ca)通道的激活。方法:将离体大鼠心脏(六组;每组n = 8)进行整体缺血30分钟,然后再灌注60分钟。对照动物没有进一步治疗。吗啡预处理(MPC)是通过两个5分钟的吗啡1 microM输注周期进行的,每次缺血前进行5分钟冲洗,最后一次进行10分钟冲洗。给予mK(Ca)阻滞剂Paxilline 1 microM,同时接受和不给予吗啡(MPC + Pax和Pax)。作为阳性对照,我们添加了单独的缺血预处理组(IPC)并与Paxilline(IPC + Pax)联合使用。在再灌注结束时,通过三苯基四唑鎓氯化物染色确定梗塞大小。结果:梗塞面积为对照组中风险区域的(平均值+/- SD)45 +/- 9%。吗啡或缺血预处理组的梗塞面积较小(MPC:23 +/- 8%,IPC:20 +/- 5%;与对照组相比,每个P <0.05)。茶碱消除了梗死面积的缩小(MPC + Pax:37 +/- 7%,P <0.05 vs MPC和IPC + Pax:36 +/- 6%,P <0.05 vs IPC),而单独使用Paxilline则没有效果( Pax:46 +/- 7%,与对照组无显着差异。结论:吗啡诱导的预处理对心脏的保护作用是通过激活mK(Ca)通道介导的。

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