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吗啡通过激活线粒体 K(Ca)通道诱导预处理。

Morphine induces preconditioning via activation of mitochondrial K(Ca) channels.

机构信息

Department of Anesthesiology, Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Can J Anaesth. 2010 Aug;57(8):767-73. doi: 10.1007/s12630-010-9325-1. Epub 2010 May 12.

Abstract

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.

摘要

目的

线粒体钙敏感钾(mK(Ca))通道参与缺血预处理诱导的心脏保护。本研究旨在探讨吗啡预处理是否也涉及 mK(Ca)通道的激活。

方法

分离大鼠心脏(六组;每组 n = 8)进行 30 分钟的整体缺血,随后进行 60 分钟的再灌注。对照动物不再进一步处理。吗啡预处理(MPC)通过两次 1μM 吗啡输注 5 分钟的循环,每次 5 分钟冲洗,然后在缺血前进行最后 10 分钟冲洗来启动。给予 mK(Ca)阻滞剂 1μM 巴氯芬,同时给予和不给予吗啡(MPC + Pax 和 Pax)。作为阳性对照,我们单独添加了一个缺血预处理组(IPC),并与巴氯芬联合添加(IPC + Pax)。再灌注结束时,通过三苯基四唑氯化物染色确定梗死面积。

结果

对照组的梗死面积为危险区域的 45% ± 9%。吗啡或缺血预处理组的梗死面积较小(MPC:23% ± 8%,IPC:20% ± 5%;均 P <0.05 与对照相比)。巴氯芬消除了梗死面积的减少(MPC + Pax:37% ± 7%,P <0.05 与 MPC 和 IPC + Pax 相比:36% ± 6%,P <0.05 与 IPC 相比),而巴氯芬单独使用则没有效果(Pax:46% ± 7%,与对照相比无显著差异)。

结论

吗啡诱导的预处理的心脏保护作用是通过激活 mK(Ca)通道介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7c7/2899019/690f7ad4eede/12630_2010_9325_Fig1_HTML.jpg

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