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首页> 外文期刊>Mathematical Biosciences: An International Journal >Modeling ventricular repolarization: Effects of transmural and apex-to-base heterogeneities in action potential durations
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Modeling ventricular repolarization: Effects of transmural and apex-to-base heterogeneities in action potential durations

机译:心室复极化建模:跨壁和根尖异质性对动作电位持续时间的影响

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摘要

Heterogeneities in the densities of membrane ionic currents of myocytes cause regional variations in action potential duration (APD) at various intramural depths and along the apico-basal and circumferential directions in the left ventricle. This work extends our previous study of cartesian slabs to ventricular walls shaped as an ellipsoidal volume and including both transmural and apex-to-base APD heterogeneities. Our 3D simulation study investigates the combined effect on repolarization sequences and APD distributions of: (a) the intrinsic APD heterogeneity across the wall and along the apex-to-base direction, and (b) the electrotonic currents that modulate the APDs when myocytes are embedded in a ventricular wall with fiber rotation and orthotropic anisotropy. our findings show that: (i) the transmural and apex-to-base heterogeneities have only a weak influence on the repolarization patterns on myocardial layers parallel to the epicardium; (ii) the patterns of APD distribution on the epicardial surface are mostly affected by the apex-to-base heterogeneities and do not reveal the APD transmural heterogeneity; (iii) the transmural heterogeneity is clearly discernible in both repolarization and APD patterns only on transmural sections; (iv) the apex-to-base heterogeneity is clearly discernible only in APD patterns on layers parallel to the epicardium. Thus, in our orthotropic ellipsoidal wall, the complex 3D electrotonic modulation of APDs does not fully mix the effects of the transmural and apex-to-base heterogeneity. The intrinsic spatial heterogeneity of the APDs is unmasked in the modulated APD patterns only in the appropriate transmural or intramural sections. These findings are independent of the stimulus location (epicardial, endocardial) and of Purkinje involvement.
机译:心肌细胞膜离子电流密度的异质性会导致各种壁内深度处以及沿左心室的顶基和圆周方向的动作电位持续时间(APD)发生区域变化。这项工作将我们以前对笛卡尔平板的研究扩展到呈椭圆形的心室壁,并且包括跨壁和从基尖到基端的APD异质性。我们的3D模拟研究研究了以下因素对复极化序列和APD分布的综合影响:(a)跨壁并沿顶点到基部方向的固有APD异质性,以及(b)当心肌细胞被激活时调节APD的电声电流嵌入在具有纤维旋转和正交各向异性的心室壁中。我们的研究结果表明:(i)跨壁和根尖异质性对平行于心外膜的心肌层的复极模式影响很小。 (ii)心外膜表面上APD分布的模式主要受根尖到基部的异质性影响,并且没有揭示APD透壁异质性; (iii)透壁异质性在复极化和APD模式中仅在透壁部分明显可见; (iv)仅在与心外膜平行的层上的APD模式中才能清楚地识别出根尖到基部的异质性。因此,在我们的正交各向异性椭圆形壁中,APD的复杂3D电声调制不能完全混合跨壁和根尖至基部异质性的影响。仅在适当的透壁或壁内切片中,APD的固有空间异质性才在调制的APD模式中得以掩盖。这些发现与刺激部位(心外膜,心内膜)和浦肯野受累无关。

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