Suppr超能文献

心房颤动中的电代谢耦联:对代谢驱动因素的更深入理解。

Electro-metabolic coupling in atrial fibrillation: A deeper understanding of the metabolic driver.

机构信息

Xi'an Key Laboratory of Special Medicine and Health Engineering, School of Life Sciences, Northwestern Polytechnical University, Xi'an, Shaanxi 710072, China.

Department of Cardiology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710004, China.

出版信息

Biomed Pharmacother. 2024 Nov;180:117536. doi: 10.1016/j.biopha.2024.117536. Epub 2024 Oct 8.

Abstract

Atrial fibrillation (AF), the most common sustained heart rhythm abnormality, disrupts the normal link between electrical activity and atrial muscle contraction; this disruption is termed "excitation-contraction uncoupling". It weakens atrial contractions and contributes to the development and persistence of AF. In addition to electrical dysfunction, AF is increasingly recognized as a metabolic disorder. Metabolic remodeling may reportedly precede electrophysiological, contractile, and structural changes in AF. Both clinical observations and experimental studies have underscored the critical importance of metabolic homeostasis, and its disturbance is considered a key initial factor in the development of AF. Research in this field has progressed, and a consensus has emerged that metabolic status (energy flux) and electrophysiological signaling (ion flux) are interactively regulated, highlighting the concept of "electro-metabolic coupling." Their uncoupling or decompensation constitutes a common pathological basis of AF. Despite growing recognition of the importance of metabolic balance, the role of electro-metabolic coupling in AF remains unclear. Thus, this review aimed to discuss 1) a comprehensive understanding of electro-metabolic alterations post-AF, 2) the pivotal role of metabolic homeostasis in AF pathogenesis, and 3) the mutual regulation of electro-metabolic signaling, along with potential therapeutic strategies targeting these imbalances.

摘要

心房颤动(房颤)是最常见的持续性心律失常,它破坏了电活动和心房肌收缩之间的正常联系;这种破坏被称为“兴奋-收缩脱偶联”。它削弱了心房收缩,并导致房颤的发生和持续。除了电功能障碍外,房颤越来越被认为是一种代谢紊乱。据报道,代谢重构可能先于房颤的电生理、收缩和结构变化。临床观察和实验研究都强调了代谢稳态的关键重要性,其紊乱被认为是房颤发展的一个关键初始因素。该领域的研究取得了进展,人们已经达成共识,即代谢状态(能量通量)和电生理信号(离子通量)是相互调节的,突出了“电-代谢偶联”的概念。它们的解偶联或失代偿构成了房颤的共同病理基础。尽管人们越来越认识到代谢平衡的重要性,但电-代谢偶联在房颤中的作用仍不清楚。因此,本综述旨在讨论 1)房颤后电-代谢改变的全面理解,2)代谢稳态在房颤发病机制中的关键作用,以及 3)电-代谢信号的相互调节,以及针对这些失衡的潜在治疗策略。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验