机械-化学转导对心脏交替的动力学影响。

IF 3.2 3区 生物学 Q2 BIOPHYSICS Biophysical journal Pub Date : 2025-01-16 DOI:10.1016/j.bpj.2025.01.006
Daisuke Sato,Asuka Hatano,Donald M Bers,Ye Chen-Izu,Leighton T Izu
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引用次数: 0

摘要

在每一次心跳中,心肌细胞执行兴奋- ca2 +信号-收缩(EC)耦合来泵血对抗血管阻力。心肌细胞可以感知机械负荷并激活机械-化学-转导(mechano-chemo-transduction, MCT)机制,对EC耦合提供反馈调节。MCT反馈对于心脏在负荷增加时调节收缩以维持心输出量很重要。MCT反馈增强l型Ca2+电流,使ryanodine受体(RyRs)敏化,并增强SERCA泵活性,从而在负荷增加的情况下保持收缩幅度。然而,在某些条件下,MCT反馈也可以促进心脏交替,被视为动作电位持续时间、Ca2+瞬态和收缩强度的搏动变化,这是心律不齐的前兆。虽然交替可以由膜电压或细胞内Ca2+循环的不稳定引起,但mct诱导的交替的潜在机制,特别是机电不协调交替,其中更强的节拍矛盾地与更短的动作电位相关,目前尚不清楚。在这项研究中,我们使用心室肌细胞的数学模型来研究MCT反馈对产生交替的动力系统的影响。我们系统地分析了MCT反馈如何通过l型Ca2+通道(ltcc), RyRs或SERCA作用,影响膜电压和Ca2+循环的稳定性,以及它们之间的耦合。我们的研究结果表明,MCT反馈通常可以促进动作电位和Ca2+瞬态的协调和不协调交替,这取决于潜在的不稳定机制。我们发现,通过RyRs的MCT反馈主要增加Ca2+不稳定性,而LTCC和SERCA反馈由于稳定性和耦合改变之间的相互作用而具有复杂的影响。我们还展示了如何从实验和临床观察中确定潜在的机制。我们的建模研究为心脏交替的复杂动力学提供了新的见解,并强调了MCT反馈在机械负荷下心脏中危及生命的心律失常发展中的重要性。
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Dynamical effects of Mechano-Chemo-Transduction on Cardiac Alternans.
In every heartbeat, cardiac muscle cells perform excitation-Ca2+ signaling-contraction (EC) coupling to pump blood against the vascular resistance. Cardiomyocytes can sense the mechanical load and activate mechano-chemo-transduction (MCT) mechanism, which provides feedback regulation of EC coupling. MCT feedback is important for the heart to upregulate contraction in response to increased load to maintain cardiac output. MCT feedback enhances the L-type Ca2+ current, sensitizes ryanodine receptors (RyRs), and augments SERCA pump activity, thereby maintaining contraction amplitude despite increased load. However, under certain conditions, MCT feedback can also promote cardiac alternans, seen as beat-to-beat variations in action potential duration, Ca2+ transients, and contraction strength, which is a precursor to arrhythmias. While alternans can arise from instabilities in either membrane voltage or intracellular Ca2+ cycling, underlying mechanisms of MCT-induced alternans, particularly electromechanically discordant alternans where stronger beats are paradoxically associated with shorter action potentials, remain unclear. In this study, we used a mathematical model of the ventricular myocyte to investigate the effects of MCT feedback on the dynamical system that generates alternans. We systematically analyzed how MCT feedback, acting through L-type Ca2+ channels (LTCCs), RyRs, or SERCA, affects the stability of membrane voltage and Ca2+ cycling, as well as the coupling between them. Our results show that MCT feedback can generally promote both concordant and discordant alternans in action potential and Ca2+ transients, depending on the underlying instability mechanism. We found that MCT feedback through RyRs predominantly increases Ca2+ instability, while LTCC and SERCA feedback have complex effects due to the interplay between stability and coupling alterations. We also showed how to determine underlying mechanisms from experimental and clinical observations. Our modeling studies provide new insights into the complex dynamics underlying cardiac alternans and highlight the importance of MCT feedback in the development of life-threatening arrhythmias in the heart under mechanical load.
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来源期刊
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
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