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The efficacy of class III anti-arrhythmic drugs in 3D canine atrial models: Is the blockade of IKCa pro- or anti-arrhythmic?

机译:III类抗心律不齐药物在3D犬房模型中的功效:IKCa的阻滞是抗心律失常还是抗心律失常?

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Small conductance calcium-activated potassium channel current, IKCa, has recently been characterized in atrial tissue and linked with atrial arrhythmogenesis. As IKCa does not contribute significantly to the ventricular action potential, there is great interest in developing pharmacological agents targeting these channels. However, experimental data so far have presented conflicting evidence as to whether IKCa inhibition is pro- or anti-arrhythmic. We have created a new formulation for IKCa, which we included in recently developed heterogeneous and anisotropic 3D canine atrial models. These were applied to investigate the effect of IKCa blockade compared to inhibition of other potassium currents: IKr and IKur. Blocking IKCa led to the termination of AF in the 3D atrial model, in contrast to blockades of IKur or IKr. Blocking IKCa prolonged action potential duration, APD, by at least 20 ms in all atrial cell types, whereas IKr or IKur blocks did not increase APD by more than 10 ms, thus explaining IKCa's effectiveness in terminating AF. Nevertheless, the blockade of IKCa also led to an increase in APD dispersion, which is expected to be pro-arrhythmic. In cases when the APD dispersion effects dominate over the APD prolongation, the blockade of IKCa is expected to be pro-arrhythmic, as seen in experimental models of non-remodelled canine atria.
机译:最近在心房组织中发现了小电导的钙激活钾通道电流I KCa ,并与心律失常有关。由于I KCa 对心室动作电位的贡献不大,因此开发针对这些通道的药理学引起了极大的兴趣。然而,到目前为止,关于I KCa 抑制作用是促心律失常还是抗心律失常的实验数据都存在争议。我们为I KCa 创建了新的配方,将其包含在最近开发的异质和各向异性3D犬心房模型中。与抑制其他钾电流:I Kr 和I Kur 相比,这些用于研究I KCa 阻滞的作用。与I Kur 或I Kr 的阻断相反,阻断I KCa 导致3D心房模型中房颤的终止。在所有心房细胞类型中,阻断I KCa 可延长动作电位持续时间APD至少20 ms,而阻断I Kr 或I Kur 不会将APD增加10毫秒以上,因此可以说明I KCa 在终止AF方面的有效性。尽管如此,I KCa 的阻滞也导致APD离散度增加,这有望导致心律失常。如在非重塑犬心房的实验模型中看到的那样,如果APD分散效应在APD延长期间占主导地位,则I KCa 的阻滞预期是促心律失常的。

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