Acute Biomechanical Effects of Cardiac Contractility Modulation in Living Myocardial Slices from End-Stage Heart Failure Patients.

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL Bioengineering Pub Date : 2025-02-12 DOI:10.3390/bioengineering12020174
Mark F A Bierhuizen, Jorik H Amesz, Sanne J J Langmuur, Bobby Lam, Paul Knops, Kevin M Veen, Olivier C Manintveld, Jolanda Kluin, Natasja M S de Groot, Yannick J H J Taverne
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Abstract

Proof-of-concept to determine the direct biomechanical effects of cardiac contractility modulation (CCM) on living myocardial slices (LMS) from patients with end-stage heart failure (HF). Left ventricular LMS from patients with end-stage HF were produced and cultured in a biomimetic system with mechanical loading and electrical stimulation. CCM stimulation (80 mA, 40 ms delay, 21 ms duration) enhanced maximum contractile force (CCM: 1229 µN (587-2658) vs. baseline: 1066 µN (529-2128), p = 0.05) and area under the contractile curve (CCM: 297 (151-562) vs. baseline: 243 (129-464), p = 0.05) but did not significantly impact contractile duration, time to peak, or time to relaxation. Increasing CCM stimulation delay, duration, and amplitude resulted in a higher fraction of LMS with a positive inotropic response. Furthermore, CCM attenuated the negative force-frequency relationship in HF-LMS. CCM stimulation enhanced contractile force in HF-LMS. The fraction of LMS exerting a positive inotropic response to CCM increased with increasing delay, duration, and amplitude settings, suggesting that personalizing stimulation parameters could optimize the beneficial effects of CCM. CCM is a novel device-based therapy that may improve contractile function, ejection fraction, functional outcomes, and quality of life in patients with heart failure. However, continuous efforts are needed to identify true responders to CCM therapy, understand the exact mechanisms, and optimize the contractile response to CCM stimulation. The present study revealed that CCM enhanced the contractile force of HF-LMS in a stimulation setting-dependent manner, reaching a larger fraction of the myocardium while increasing delay, duration, and amplitude. This understanding may contribute to the individualization of CCM stimulation settings.

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心肌收缩力调节对终末期心力衰竭患者活体心肌切片的急性生物力学影响
确定心脏收缩性调节(CCM)对终末期心力衰竭(HF)患者活体心肌切片(LMS)的直接生物力学影响的概念验证。在机械负荷和电刺激的仿生系统中培养终末期HF患者的左心室LMS。CCM刺激(80 mA, 40 ms延迟,21 ms持续时间)增强了最大收缩力(CCM: 1229µN (587-2658) vs基线:1066µN (529-2128), p = 0.05)和收缩曲线下面积(CCM: 297 (151-562) vs基线:243 (129-464),p = 0.05),但对收缩持续时间、峰值时间或松弛时间没有显著影响。增加CCM刺激延迟、持续时间和振幅导致LMS呈正性肌力反应的比例更高。此外,CCM减弱了HF-LMS的负力-频率关系。CCM刺激可增强HF-LMS的收缩力。LMS对CCM产生正性肌力反应的比例随着延迟、持续时间和振幅设置的增加而增加,这表明个性化刺激参数可以优化CCM的有益效果。CCM是一种基于装置的新型治疗方法,可以改善心力衰竭患者的收缩功能、射血分数、功能结局和生活质量。然而,需要持续的努力来确定对CCM治疗的真正应答者,了解确切的机制,并优化对CCM刺激的收缩反应。本研究显示,CCM以刺激设置依赖的方式增强了HF-LMS的收缩力,在增加延迟、持续时间和幅度的同时,到达更大比例的心肌。这种理解可能有助于CCM刺激设置的个性化。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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