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模拟微重力通过AMP激活的蛋白激酶缺乏增加心肌对缺血再灌注损伤的易感性。

Simulated microgravity increases myocardial susceptibility to ischemia-reperfusion injury via a deficiency of AMP-activated protein kinase.

作者信息

Lu Yuan-Ming, Jiao Bo, Lee Jun, Zhang Lin, Yu Zhi-Bin

机构信息

a Department of Aerospace Physiology, Fourth Military Medical University, Key Laboratory of Aerospace Medicine, Ministry of China, Xi'an, 710032, China.

b Department of Cardiology, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710038, China.

出版信息

Can J Physiol Pharmacol. 2017 Jan;95(1):59-71. doi: 10.1139/cjpp-2015-0456. Epub 2016 Sep 1.

Abstract

Gravitation is an important factor in maintaining cardiac contractility. Our study investigated whether simulated microgravity increases myocardial susceptibility to ischemia-reperfusion (IR) injury. Using the Langendorff-perfused heart model with 300 beats/min pacing, 4-week tail suspension (SUS) and control (CON) male Sprague-Dawley rats (n = 10 rats/group) were subjected to 60 min of left anterior descending coronary artery (LAD) occlusion followed by 120 min of reperfusion. Left ventricular end-systolic pressure (LVESP), left ventricular end-diastolic pressure (LVEDP), creatine kinase (CK) and lactate dehydrogenase (LDH) activity, and infarct size were assessed. Data demonstrated that there were significantly increased LVEDP, CK, LDH, and infarct size in SUS compared with CON (P < 0.05), accompanied by decreased LVESP (P < 0.05). Furthermore, TUNEL-positive cardiomyocytes were higher in SUS than that in CON (P < 0.01), and AMP-activated protein kinase (AMPK) phosphorylation and Bcl-2/Bax in SUS were less compared with CON (P < 0.05). Similarly, isolated hearts pre-treated with A-769662 exhibited better recovery of cardiac function, increased AMPK phosphorylation, and reduced necrosis and apoptosis. Furthermore, AMPKα protein showed a significant suppression in 4-week hindlimb unweighting rats. These results suggest that AMPK deficiency increases myocardial susceptibility to IR injury in rats subjected to simulated microgravity.

摘要

重力是维持心脏收缩力的一个重要因素。我们的研究调查了模拟微重力是否会增加心肌对缺血再灌注(IR)损伤的易感性。使用以300次/分钟起搏的Langendorff灌注心脏模型,将4周悬吊(SUS)和对照(CON)雄性Sprague-Dawley大鼠(每组n = 10只大鼠)左冠状动脉前降支(LAD)闭塞60分钟,然后再灌注120分钟。评估左心室收缩末期压力(LVESP)、左心室舒张末期压力(LVEDP)、肌酸激酶(CK)和乳酸脱氢酶(LDH)活性以及梗死面积。数据表明,与CON组相比,SUS组的LVEDP、CK、LDH和梗死面积显著增加(P < 0.05),同时LVESP降低(P < 0.05)。此外,SUS组TUNEL阳性心肌细胞高于CON组(P < 0.01),SUS组的AMP激活蛋白激酶(AMPK)磷酸化以及Bcl-2/Bax低于CON组(P < 0.05)。同样,用A-769662预处理的离体心脏表现出更好的心脏功能恢复、AMPK磷酸化增加以及坏死和凋亡减少。此外,在4周后肢去负荷大鼠中AMPKα蛋白表现出显著抑制。这些结果表明,在模拟微重力环境下,AMPK缺乏会增加大鼠心肌对IR损伤的易感性。

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