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首页> 外文期刊>Circulation research: a journal of the American Heart Association >IK1 heterogeneity affects genesis and stability of spiral waves in cardiac myocyte monolayers.
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IK1 heterogeneity affects genesis and stability of spiral waves in cardiac myocyte monolayers.

机译:IK1异质性会影响心肌细胞单层螺旋波的发生和稳定性。

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Previous studies have postulated an important role for the inwardly rectifying potassium current (I(K1)) in controlling the dynamics of electrophysiological spiral waves responsible for ventricular tachycardia and fibrillation. In this study, we developed a novel tissue model of cultured neonatal rat ventricular myocytes (NRVMs) with uniform or heterogeneous Kir2.1expression achieved by lentiviral transfer to elucidate the role of I(K1) in cardiac arrhythmogenesis. Kir2.1-overexpressed NRVMs showed increased I(K1) density, hyperpolarized resting membrane potential, and increased action potential upstroke velocity compared with green fluorescent protein-transduced NRVMs. Opposite results were observed in Kir2.1-suppressed NRVMs. Optical mapping of uniformly Kir2.1 gene-modified monolayers showed altered conduction velocity and action potential duration compared with nontransduced and empty vector-transduced monolayers, but functional reentrant waves could not be induced. In monolayers with an island of altered Kir2.1 expression, conduction velocity and action potential duration of the locally transduced and nontransduced regions were similar to those of the uniformly transduced and nontransduced monolayers, respectively, and functional reentrant waves could be induced. The waves were anchored to islands of Kir2.1 overexpression and remained stable but dropped in frequency and meandered away from islands of Kir2.1 suppression. In monolayers with an inverse pattern of I(K1) heterogeneity, stable high frequency spiral waves were present with I(K1) overexpression, whereas lower frequency, meandering spiral waves were observed with I(K1) suppression. Our study provides direct evidence for the contribution of I(K1) heterogeneity and level to the genesis and stability of spiral waves and highlights the potential importance of I(K1) as an antiarrhythmia target.
机译:先前的研究假设内向整流钾电流(I(K1))在控制负责室速和心律颤动的电生理螺旋波的动力学中起重要作用。在这项研究中,我们开发了一种新的组织培养的新生大鼠心室肌细胞(NRVM),通过慢病毒转移实现了均匀或异构Kir2.1表达,从而阐明了I(K1)在心律失常中的作用。与绿色荧光蛋白转导的NRVM相比,Kir2.1过度表达的NRVM显示出增加的I(K1)密度,超极化的静息膜电位和上升的动作电位上升速度。在Kir2.1抑制的NRVM中观察到相反的结果。与未转导和空载体转导的单层相比,均匀地Kir2.1基因修饰的单层的光学作图显示了改变的传导速度和动作电位持续时间,但不能诱导功能性折返波。在具有改变的Kir2.1表达岛的单分子层中,局部转导和非转导区域的传导速度和动作电位持续时间分别与均匀转导和非转导的单分子层相似,并且可以诱导功能性折返波。波浪被锚定在Kir2.1过表达的岛上,并保持稳定,但频率下降,并远离Kir2.1抑制的岛。在具有I(K1)异质性反型的单层中,存在稳定的高频螺旋波,且I(K1)过表达,而在较低频率下,观察到蜿蜒的螺旋波,且具有I(K1)抑制。我们的研究为I(K1)异质性和水平对螺旋波的发生和稳定性的贡献提供了直接证据,并强调了I(K1)作为抗心律失常靶标的潜在重要性。

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