缺血再灌注损伤后的心脏保护策略。

IF 2.8 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Honghong Zhang, Huilin Hu, Changlin Zhai, Lele Jing, Hongen Tian
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引用次数: 0

摘要

急性心肌梗死(AMI)在世界范围内具有较高的发病率和死亡率。尽管早期再灌注是挽救缺血心肌最有效的策略,但再灌注损伤可以随着血流的恢复而发展。因此,确定心肌梗死后对心脏的保护机制和策略具有重要意义。最近的研究表明,多种细胞内分子和信号通路参与心脏保护。同时,基于设备的心脏保护模式,如心脏左心室负荷、低温、冠状窦介入、过饱和氧(SSO2)和远程缺血条件(RIC),已成为重要的研究领域。在此,我们综述了心肌缺血再灌注损伤(IRI)后心脏保护的分子机制和心脏保护模式,以确定降低AMI患者死亡率和改善预后的潜在方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cardioprotective Strategies After Ischemia–Reperfusion Injury

Cardioprotective Strategies After Ischemia–Reperfusion Injury

Acute myocardial infarction (AMI) is associated with high morbidity and mortality worldwide. Although early reperfusion is the most effective strategy to salvage ischemic myocardium, reperfusion injury can develop with the restoration of blood flow. Therefore, it is important to identify protection mechanisms and strategies for the heart after myocardial infarction. Recent studies have shown that multiple intracellular molecules and signaling pathways are involved in cardioprotection. Meanwhile, device-based cardioprotective modalities such as cardiac left ventricular unloading, hypothermia, coronary sinus intervention, supersaturated oxygen (SSO2), and remote ischemic conditioning (RIC) have become important areas of research. Herein, we review the molecular mechanisms of cardioprotection and cardioprotective modalities after ischemia–reperfusion injury (IRI) to identify potential approaches to reduce mortality and improve prognosis in patients with AMI.

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来源期刊
CiteScore
6.70
自引率
3.30%
发文量
38
审稿时长
>12 weeks
期刊介绍: Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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