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κ-阿片受体激动剂通过激活 AMPK/Akt/eNOS 信号通路保护心肌缺血再灌注损伤。

κ-opioid receptor activation protects against myocardial ischemia-reperfusion injury via AMPK/Akt/eNOS signaling activation.

机构信息

Department of Physiology, National Key Discipline of Cell Biology, Fourth Military Medical University, Xi'an 710032, Shaanxi Province, China.

Department of Neurosurgery, Tangdu Hospital, Fourth Military Medical University, Xi'an 710033, Shaanxi Province, China.

出版信息

Eur J Pharmacol. 2018 Aug 15;833:100-108. doi: 10.1016/j.ejphar.2018.05.043. Epub 2018 May 30.

Abstract

This study aims to investigate the effect of κ-opioid receptor activation on myocardial ischemia and reperfusion(I/R) injury and elucidate the underlying mechanisms. Myocardial I/R rat model and simulated I/R cardiomyocytes model were established. In vivo study showed that U50,488 H improved cardiac function, reduced myocardial infarct size and serum cTnT significantly. The effect of U50,488 H was abolished by nor-BNI(a κ-opioid receptor antagonist), Compound C(an AMPK inhibitor), Akt inhibitor and L-NAME(an eNOS inhibitor). AICAR, an AMPK activator, mimicked the effect of U50,488 H. U50,488 H up-regulated p-AMPK, p-Akt, and p-eNOS, which were abolished by nor-BNI. AICAR increased p-Akt and p-eNOS, which was abolished by Compound C. In vitro study showed that U50,488 H increased p-AMPK, p-Akt, and p-eNOS via κ-OR activation. The effect of U50,488 H on p-AMPK was abolished by compound C, but not Akt inhibitor and L-NAME. The effect of U50,488 H on p-Akt was abolished by compound C and Akt inhibitor, but not L-NAME. AICAR increased p-Akt and p-eNOS, which was abolished by Akt inhibitor, but not L-NAME. U50,488 H and AICAR also increased the viability of cardiomyocytes subjected to simulated I/R, the effects of U50,488 H and AICAR were blocked by nor-BNI, Compound C, Akt inhibitor, and L-NAME, respectively. In conclusion, κ-OR activation confers cardioprotection via AMPK/Akt/eNOS signaling.

摘要

本研究旨在探讨κ-阿片受体激活对心肌缺血再灌注(I/R)损伤的影响,并阐明其潜在机制。建立了心肌 I/R 大鼠模型和模拟 I/R 心肌细胞模型。体内研究表明,U50,488H 可改善心功能,显著减少心肌梗死面积和血清 cTnT。U50,488H 的作用被 nor-BNI(κ-阿片受体拮抗剂)、Compound C(AMPK 抑制剂)、Akt 抑制剂和 L-NAME(eNOS 抑制剂)所阻断。AICAR(AMPK 激活剂)模拟了 U50,488H 的作用。U50,488H 上调了 p-AMPK、p-Akt 和 p-eNOS,这些作用被 nor-BNI 所阻断。AICAR 增加了 p-Akt 和 p-eNOS,这一作用被 Compound C 所阻断。体外研究表明,U50,488H 通过 κ-OR 激活增加了 p-AMPK、p-Akt 和 p-eNOS。U50,488H 对 p-AMPK 的作用被 Compound C 阻断,但不受 Akt 抑制剂和 L-NAME 的影响。U50,488H 对 p-Akt 的作用被 Compound C 和 Akt 抑制剂阻断,但不受 L-NAME 的影响。AICAR 增加了 p-Akt 和 p-eNOS,这一作用被 Akt 抑制剂阻断,但不受 L-NAME 的影响。U50,488H 和 AICAR 还增加了模拟 I/R 后心肌细胞的活力,U50,488H 和 AICAR 的作用分别被 nor-BNI、Compound C、Akt 抑制剂和 L-NAME 阻断。总之,κ-OR 激活通过 AMPK/Akt/eNOS 信号通路发挥心脏保护作用。

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