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Vulnerable window for conduction block in a one-dimensional cable of cardiac cells, 2: Multiple extrasystoles

机译:心脏细胞的一维电缆中传导阻滞的脆弱窗口,2:多个收缩期

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Unidirectional conduction block of premature extrasystoles can lead to initiation of cardiac reentry, causing lethal arrhythmias including ventricular fibrillation. Multiple extrasystoles are often more effective at inducing unidirectional conduction block and reentry than a single extrasystole. Since the substrate for conduction block is spatial dispersion of refractoriness, in this study we investigate how the first extrasystole modulates this dispersion to influence the "vulnerable window'' for conduction block by subsequent extrasystoles, particularly in relation to action potential duration restitution and conduction velocity restitution properties. Using a kinematic model to represent wavefront-waveback interactions and simulations with the Luo-Rudy model in a one-dimensional cable of cardiac cells, we show that in homogeneous tissue, a premature extrasystole can create a large dispersion of refractoriness leading to conduction block of a subsequent extrasystole. In heterogeneous tissue, however, a premature extrasystole can either reduce or enhance the dispersion of refractoriness depending on its propagation direction with respect to the previous beat. With multiple extrasystoles at random coupling intervals, vulnerability to conduction block is proportional to their number. In general, steep action potential duration restitution and broad conduction velocity restitution promote dispersion of refractoriness in response to multiple extrasystoles, and thus enhance vulnerability to conduction block. These restitution properties also promote spatially discordant alternans, a setting which is particularly prone to conduction block. The equivalent dispersion of refractoriness created dynamically in homogeneous tissue by spatially discordant alternans is more likely to cause conduction block than a comparable degree of preexisting dispersion in heterogeneous tissue.
机译:早搏的单向传导阻滞可导致心脏折返的开始,引起致命的心律不齐,包括心室纤颤。多个收缩期通常比单个收缩期更有效地诱导单向传导阻滞和折返。由于传导阻滞的基质是难治性的空间分散,因此在本研究中,我们研究了第一个收缩前期如何通过随后的收缩前期,特别是与动作电位的持续时间恢复和传导速度有关,调节该弥散以影响传导阻滞的“脆弱窗口”使用运动学模型来表示波前-回波相互作用以及使用Luo-Rudy模型在一维心肌细胞电缆中进行的模拟,我们表明,在均质组织中,过早的收缩前期会造成难治性的大范围弥散,从而导致然而,在异质组织中,过早的收缩前期可根据其相对于前一搏动的传播方向来减少或增强难治性的离散度。与他们的n成正比琥珀色。通常,陡峭的动作电位持续时间恢复和广泛的传导速度恢复促进了对多个收缩期的反应,使难治性分散,从而增强了传导阻滞的脆弱性。这些恢复特性还促进了空间不一致的交替变化,这种变化特别容易导致传导阻滞。在空间上不一致的交替体在同质组织中动态产生的等效耐火度色散比在异质组织中存在的同等程度的色散更可能引起传导阻滞。

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