起搏部位对犬模型收缩力学恢复曲线的影响。

Sarah E Ahlberg, Nathan A Grenz, Daniel L Ewert, Paul A Iaizzo, Lawrence J Mulligan
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引用次数: 0

摘要

导读:已知起搏部位会影响心室的收缩状态。非生理性起搏部位,如右心室心尖(RVA)或左心室自由壁(LVFW),由于异常的电传播,已被证明可以降低正常心肌的收缩状态。起搏对这些部位的影响可能会改变机械恢复(MR),这是一种涉及收缩的机电调节的基本心脏特性。这反过来又可能影响心脏功能。本研究旨在确定起搏部位是否会改变MR: tau的时间常数。方法和结果:麻醉犬(n = 6)在右心房(RA)、右心室(RVA)、右室间隔(RVS)和左心室(LVFW)四个部位进行急性心律失常。通过S1-S2起搏方案捕获MR数据,并用于创建MR曲线,在每个位点生成恢复时间常数tau。起搏部位之间tau蛋白含量无显著差异。磁共振曲线线性回归分析显示,起搏部位的坡度无显著差异。结论:虽然已经发现起搏部位会影响心室的收缩状态,但这是已知的第一个证明tau在体内制剂中没有变化的研究。这表明MR描述的机电耦合的改变不足以提供对健康心脏起搏部位和心功能的深入了解。
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Effect of pacing site on systolic mechanical restitution curves in the in vivo canine model.

Introduction: Pacing site is known to influence the contractile state of the ventricle. Non-physiologic pacing sites such as the right ventricular apex (RVA) or left ventricular freewall (LVFW) have been shown to decrease the contractile state of normal myocardium, due to abnormal electrical propagation. The impact of pacing at these sites may alter mechanical restitution (MR), a fundamental cardiac property involving the electro-mechanical regulation of contraction. This, in turn, may affect cardiac function. The present study was conducted to determine if pacing site alters the time constant of MR: tau.

Methods and results: Anesthetized canines (n = 6) were acutely paced at four sites: right atrium (RA), RVA, right ventricular septum (RVS), and LVFW. MR data was captured by the S1-S2 pacing protocol and used to create MR curves, generating a restitution time constant, tau, at each site. No significant difference in tau was found between pacing sites. A linear regression analysis of MR curves revealed that there was no significant difference in slope between pacing sites.

Conclusion: Although pacing site has been found to influence the contractile state of the ventricle, this is the first known study to demonstrate no change in tau in an in vivo preparation. This suggests that alteration of electro-mechanical coupling described by MR is not sufficiently robust to provide insight into pacing site and cardiac function in healthy hearts.

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