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线粒体ATP敏感性钾通道在七氟醚对大鼠体内预处理和后处理心脏保护作用中的影响

The influence of mitochondrial KATP-channels in the cardioprotection of preconditioning and postconditioning by sevoflurane in the rat in vivo.

作者信息

Obal Detlef, Dettwiler Saskia, Favoccia Christian, Scharbatke Horst, Preckel Benedikt, Schlack Wolfgang

机构信息

Klinik für Anaesthesiologie, Universitätsklinikum Düsseldorf, Düsseldorf, Germany.

出版信息

Anesth Analg. 2005 Nov;101(5):1252-1260. doi: 10.1213/01.ANE.0000181336.96511.32.

Abstract

Volatile anesthetics induce myocardial preconditioning and can also protect the heart when given at the onset of reperfusion-a practice recently termed "postconditioning." We investigated the role of mitochondrial KATP (mKATP)-channels in sevoflurane-induced cardioprotection for both preconditioning and postconditioning alone and whether there is a synergistic effect of both. Rats were subjected to 25 min of coronary artery occlusion followed by 120 min of reperfusion. Infarct size was determined by triphenyltetrazolium staining. The following protocols were used: 1) preconditioning (S-Pre, n = 10, achieved by 2 periods of 5 min sevoflurane administration (1 MAC) followed by 10 min of washout); 2) sevoflurane postconditioning (1 MAC of sevoflurane given for 2 min at the beginning of reperfusion; S-Post, n = 10); 3) administration before and after ischemia (S-Pre + S-Post, n = 10). Protocols 1-3 were repeated in the presence of 5-hydroxydecanoate (5HD), a specific mKATP-channel-blocker (S-Pre + S-Post + 5HD, S-Pre + 5HD: n = 10; S-Post + 5HD: n = 9). Nine rats served as untreated controls (CON) or received 5HD alone (5HD, n = 10). Both S-Pre (23% +/- 13% of the area at risk, mean +/- sd) and S-Post (18% +/- 5%) reduced infarct size compared with CON (49% +/- 11%, both P < 0.05). S-Pre + S-Post resulted in a larger reduction of infarct size (12% +/- 5%, P = 0.054 versus S-Pre) compared with administration before or after ischemia alone. 5HD diminished the protection in all three sevoflurane treated groups (S-Pre + 5HD, 35% +/- 12%; S-Post + 5HD, 44% +/- 12%; S-Pre + S-Post + 5HD, 46% +/- 14%;) but given alone had no effect on infarct size (41% +/- 13%). Sevoflurane preconditioning and postconditioning protects against myocardial ischemia-reperfusion injury. The combination of preconditioning and postconditioning provides additive cardioprotection and is mediated, at least in part, by mKATP-channels.

摘要

挥发性麻醉剂可诱导心肌预处理,并且在再灌注开始时给予时也能保护心脏——这种做法最近被称为“后处理”。我们研究了线粒体ATP敏感性钾通道(mKATP通道)在七氟醚诱导的预处理和后处理单独的心脏保护作用中的作用,以及两者是否存在协同效应。将大鼠冠状动脉闭塞25分钟,随后再灌注120分钟。通过三苯基四氮唑染色确定梗死面积。采用以下方案:1)预处理(S-Pre,n = 10,通过给予2个5分钟的七氟醚(1MAC),随后冲洗10分钟来实现);2)七氟醚后处理(在再灌注开始时给予2分钟的七氟醚(1MAC);S-Post,n = 10);3)缺血前后给药(S-Pre + S-Post,n = 10)。在存在特异性mKATP通道阻滞剂5-羟基癸酸(5HD)的情况下重复方案1-3(S-Pre + S-Post + 5HD,S-Pre + 5HD:n = 10;S-Post + 5HD:n = 9)。9只大鼠作为未处理对照(CON)或单独接受5HD(5HD,n = 10)。与CON组(49%±11%)相比,S-Pre组(危险区域面积的23%±13%,平均值±标准差)和S-Post组(18%±5%)的梗死面积均减小(均P <0.05)。与单独缺血前或缺血后给药相比,S-Pre + S-Post导致梗死面积减小幅度更大(12%±5%,与S-Pre相比P = 0.054)。5HD减弱了所有三个七氟醚处理组的保护作用(S-Pre + 5HD,35%±12%;S-Post + 5HD,44%±12%;S-Pre + S-Post + 5HD,46%±14%),但单独给予对梗死面积无影响(41%±13%)。七氟醚预处理和后处理可防止心肌缺血-再灌注损伤。预处理和后处理的联合提供了相加的心脏保护作用,并且至少部分由mKATP通道介导。

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