Anesthetic-mediated cardioprotection: from molecular mechanisms to clinical translation challenges.

IF 3.2 3区 医学 Q2 PHYSIOLOGY
Frontiers in Physiology Pub Date : 2025-09-17 eCollection Date: 2025-01-01 DOI:10.3389/fphys.2025.1688142
Tingting Fu, Xiao Jia, Can Tang, Dan Yu, Hui Zhou, Xinghe Wang, Su Liu, Kunwei Wu
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引用次数: 0

Abstract

Anesthetics have long been recognized as essential pharmacological agents for surgical procedures, primarily valued for their ability to induce unconsciousness and provide analgesia. However, emerging research over the past 3 decades has revealed an additional and potentially transformative property of certain anesthetics: their ability to protect the heart against ischemic injury. This comprehensive review examines the cardioprotective effects of both intravenous and volatile anesthetics, with particular focus on propofol, ketamine, isoflurane, and sevoflurane. We analyze the molecular mechanisms underlying their protective actions, including modulation of mitochondrial function, reduction of oxidative stress, and regulation of key survival pathways such as PI3K/Akt/GSK3βand p53 signaling. The review evaluates preclinical evidence from cellular and animal models, as well as clinical studies investigating anesthetic-mediated cardioprotection in cardiac surgery patients. Special attention is given to the phenomenon of anesthetic preconditioning and postconditioning, their comparative efficacy, and the challenges in translating these protective strategies into clinical practice. We also discuss emerging concepts such as the role of microRNAs in mediating anesthetic-induced protection and the potential cardioprotective benefits of anesthetic combinations. Finally, we identify critical gaps in current knowledge and propose future research directions that may enhance the clinical application of anesthetic-mediated cardioprotection.

Abstract Image

Abstract Image

麻醉介导的心脏保护:从分子机制到临床翻译的挑战。
长期以来,麻醉药一直被认为是外科手术中必不可少的药物,主要因其诱导无意识和提供镇痛的能力而受到重视。然而,在过去的30年里,新兴的研究揭示了某些麻醉剂的另一个潜在的变革性特性:它们保护心脏免受缺血性损伤的能力。本文综述了静脉麻醉药和挥发性麻醉药的心脏保护作用,特别关注异丙酚、氯胺酮、异氟醚和七氟醚。我们分析了其保护作用的分子机制,包括线粒体功能的调节,氧化应激的减少,以及关键生存途径如PI3K/Akt/ gsk3 β和p53信号的调节。该综述评估了来自细胞和动物模型的临床前证据,以及研究麻醉介导的心脏保护在心脏手术患者中的临床研究。特别关注麻醉前调理和后调理的现象,它们的比较功效,以及将这些保护策略转化为临床实践的挑战。我们还讨论了新兴的概念,如microrna在介导麻醉诱导保护中的作用以及麻醉组合的潜在心脏保护作用。最后,我们确定了当前知识的关键空白,并提出了未来的研究方向,以加强麻醉介导的心脏保护的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.50
自引率
5.00%
发文量
2608
审稿时长
14 weeks
期刊介绍: Frontiers in Physiology is a leading journal in its field, publishing rigorously peer-reviewed research on the physiology of living systems, from the subcellular and molecular domains to the intact organism, and its interaction with the environment. Field Chief Editor George E. Billman at the Ohio State University Columbus is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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