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异质性缝隙连接重塑稳定愈合期犬梗死心外膜边缘区的折返环路:一项计算研究。

Heterogeneous gap junction remodeling stabilizes reentrant circuits in the epicardial border zone of the healing canine infarct: a computational study.

作者信息

Cabo Candido, Boyden Penelope A

机构信息

Dept. of Pharmacology, Columbia University, New York, NY, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2006 Dec;291(6):H2606-16. doi: 10.1152/ajpheart.00346.2006. Epub 2006 Aug 25.

Abstract

The ventricular tachycardias (VTs) that originate in the 5-day epicardial border zone (EBZ) of the healing canine infarcted heart are due to reentrant excitation. In cells surviving in the EBZ, both sarcolemmal ionic channels and gap junction conductance and distribution are remodeled. We previously showed that the heterogeneities in sodium current (I(Na)) and L-type calcium channel current (I(CaL)) of the center and outer pathway cells result in a homogenization of the refractory period that in turn stabilizes reentrant VTs for approximately 10 beats. To understand how heterogeneities in transverse gap junctional conductance remodeling reported experimentally contribute to the stability of these tachycardias, we studied the dynamics of reentering waves in two-dimensional computer models of the EBZ. First we used a computer model with homogeneous ionic channel properties [infarcted border zone cell model (IZ)]. These simulations show that, in the absence of heterogeneities in ionic channel properties, reentrant waves tend to drift to localized regions of uncoupling and stabilize there. Second, we used a computer model with a more realistic representation of the heterogeneous EBZ, including cellular models for both the center (IZ(c)) and outer (IZ(o)) pathway cells. These simulations show that neither a region of uniform uncoupling nor a step transition between two regions with different side-to-side (transverse) cell coupling stabilizes reentry in this substrate. However, an area of localized uncoupling did stabilize reentry in such a model. We propose that in addition to the heterogeneities in I(Na) and I(CaL) properties, heterogeneities in gap junctional conductance in the EBZ causing regions of localized uncoupling stabilize VT in the EBZ. Previous experimental in situ activation maps of the 5-day EBZ show that the lines of block form in regions of slow transverse propagation. This is consistent with our findings that areas of localized uncoupling stabilize reentry.

摘要

起源于愈合期犬梗死心脏5天的心外膜边缘区(EBZ)的室性心动过速(VTs)是由折返激动引起的。在EBZ存活的细胞中,肌膜离子通道以及缝隙连接电导和分布均发生重塑。我们之前表明,中央和外周径路细胞的钠电流(I(Na))和L型钙通道电流(I(CaL))的异质性导致不应期均匀化,进而使折返性VTs稳定大约10次搏动。为了理解实验报道的横向缝隙连接电导重塑的异质性如何促进这些心动过速的稳定性,我们在EBZ的二维计算机模型中研究了折返波的动力学。首先,我们使用了具有均匀离子通道特性的计算机模型[梗死边缘区细胞模型(IZ)]。这些模拟表明,在离子通道特性不存在异质性的情况下,折返波倾向于漂移至解耦的局部区域并在那里稳定下来。其次,我们使用了一个更真实地反映异质性EBZ的计算机模型,包括中央(IZ(c))和外周(IZ(o))径路细胞的细胞模型。这些模拟表明,无论是均匀解耦区域还是两个具有不同左右(横向)细胞耦联区域之间的阶跃转变,都不能使该基质中的折返稳定。然而,局部解耦区域确实能使这种模型中的折返稳定。我们提出,除了I(Na)和I(CaL)特性的异质性外,EBZ中缝隙连接电导的异质性导致局部解耦区域使EBZ中的VT稳定。先前对5天EBZ的实验性原位激活图显示,阻滞线在横向传播缓慢的区域形成。这与我们关于局部解耦区域使折返稳定的发现一致。

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