电针预处理通过nrf2介导的氧化应激和焦亡减轻大鼠心肌缺血再灌注损伤。

IF 5.5
The American journal of Chinese medicine Pub Date : 2025-01-01 Epub Date: 2025-03-20 DOI:10.1142/S0192415X25500132
Xuefeng Xia, Yaping Ding, Chunmei Zhou, Hanyu Zhang, Xinran Yang, Chuchu Shen, Senlei Xu, Hongru Zhang, Yihuang Gu, Hua Bai
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引用次数: 0

摘要

氧化应激和焦亡是心肌缺血再灌注损伤(MIRI)的关键因素。虽然以前的研究报道了电针(EA)预处理具有心脏保护作用,但其潜在的机制仍然难以捉摸。因此,本研究旨在探讨EA预处理对MIRI大鼠氧化应激和焦亡的影响,并探讨核因子e2相关因子2 (Nrf2)在这一过程中的作用。结扎大鼠左冠状动脉前降支30 min,再灌注4 h,构建MIRI模型。造模前,大鼠内关穴电刺激3天。此外,研究人员给药Nrf2抑制剂ML385,以研究Nrf2在EA预处理后调节氧化应激和焦亡中的作用。结果显示,EA预处理改善了MIRI后左心室功能,减少了心肌梗死面积和cTnT水平。同时,EA预处理可减轻miri诱导的氧化应激和焦亡,表现为ROS、MDA、NF-[公式:见文]bp65、caspase-1、IL-1[公式:见文]、GSDMD-N下调,SOD和HO-1上调。机制上,EA上调Nrf2的表达。然而,其心脏保护作用和减轻氧化应激和焦亡的能力被Nrf2的抑制所抑制。综上所述,我们的研究表明,EA预处理通过减轻氧化应激和焦亡来减轻大鼠的MIRI, Nrf2在这一保护机制中起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electroacupuncture Preconditioning Attenuates Myocardial Ischemia-Reperfusion Injury in Rats Partially Through Nrf2-Mediated Reduction of Oxidative Stress and Pyroptosis.

Oxidative stress and pyroptosis have been established as key contributors to myocardial ischemia-reperfusion injury (MIRI). While previous studies reported that electroacupuncture (EA) preconditioning exerted cardioprotective effects, the underlying mechanisms remain elusive. Thus, this study aimed to investigate the effects of EA preconditioning on oxidative stress and pyroptosis in MIRI rats, and explore the role of nuclear factor E2-associated factor 2 (Nrf2) throughout that process. A MIRI model was constructed by ligating the left anterior descending coronary artery for 30 min, followed by 4 h of reperfusion in rats. Prior to modeling, rats were subjected to EA at the Neiguan Point for three days. Furthermore, ML385, a Nrf2 inhibitor, was administered in order to examine the role of Nrf2 in regulating oxidative stress and pyroptosis following EA preconditioning. The results revealed that EA preconditioning improved left ventricular function after MIRI and reduced both the myocardial infarction area and cTnT levels. Meanwhile, EA preconditioning alleviated MIRI-induced oxidative stress and pyroptosis, as evidenced by the downregulation of ROS, MDA, NF-κB p65, caspase-1, IL-1β, and GSDMD-N, and the upregulation of SOD and HO-1. Mechanistically, EA up-regulated enhanced the expression of Nrf2. However, its cardioprotective effects and ability to attenuate oxidative stress and pyroptosis were suppressed by the inhibition of Nrf2. Taken together, our study indicated that EA preconditioning attenuated MIRI in rats by mitigating oxidative stress and pyroptosis, with Nrf2 playing a vital role in this protective mechanism.

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