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动作电位时程恢复的心室间差异导致灌注心脏中不同的心室节律。

Interventricular Differences in Action Potential Duration Restitution Contribute to Dissimilar Ventricular Rhythms in Perfused Hearts.

作者信息

Handa Balvinder S, Lawal Saheed, Wright Ian J, Li Xinyang, Cabello-García Javier, Mansfield Catherine, Chowdhury Rasheda A, Peters Nicholas S, Ng Fu Siong

机构信息

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Imperial College Healthcare NHS Trust, London, United Kingdom.

出版信息

Front Cardiovasc Med. 2019 Apr 3;6:34. doi: 10.3389/fcvm.2019.00034. eCollection 2019.

Abstract

Dissimilar ventricular rhythms refer to the occurrence of different ventricular tachyarrhythmias in the right and left ventricles or different rates of the same tachyarrhythmia in the two ventricles. We investigated the inducibility of dissimilar ventricular rhythms, their underlying mechanisms, and the impact of anti-arrhythmic drugs (lidocaine and amiodarone) on their occurrence. Ventricular tachyarrhythmias were induced with burst pacing in 28 Langendorff-perfused Sprague Dawley rat hearts (14 control, 8 lidocaine, 6 amiodarone) and bipolar electrograms recorded from the right and left ventricles. Fourteen (6 control, 4 lidocaine, 4 amiodarone) further hearts underwent optical mapping of transmembrane voltage to study interventricular electrophysiological differences and mechanisms of dissimilar rhythms. In control hearts, dissimilar ventricular rhythms developed in 8/14 hearts (57%). In lidocaine treated hearts, there was a lower cycle length threshold for developing dissimilar rhythms, with 8/8 (100%) hearts developing dissimilar rhythms in comparison to 0/6 in the amiodarone group. Dissimilar ventricular tachycardia (VT) rates occurred at longer cycle lengths with lidocaine vs. control (57.1 ± 7.9 vs. 36.6 ± 8.4 ms, < 0.001). The ratio of LV:RV VT rate was greater in the lidocaine group than control (1.91 ± 0.30 vs. 1.76 ± 0.36, < 0.001). The gradient of the action potential duration (APD) restitution curve was shallower in the RV compared with LV (Control - LV: 0.12 ± 0.03 vs RV: 0.002 ± 0.03, = 0.015), leading to LV-to-RV conduction block during VT. Interventricular differences in APD restitution properties likely contribute to the occurrence of dissimilar rhythms. Sodium channel blockade with lidocaine increases the likelihood of dissimilar ventricular rhythms.

摘要

不同步心室节律是指右心室和左心室出现不同的室性快速性心律失常,或同一快速性心律失常在两个心室中的频率不同。我们研究了不同步心室节律的可诱导性、其潜在机制以及抗心律失常药物(利多卡因和胺碘酮)对其发生的影响。在28个Langendorff灌注的Sprague Dawley大鼠心脏(14个对照、8个利多卡因、6个胺碘酮)中通过短阵刺激诱发室性快速性心律失常,并记录右心室和左心室的双极电图。另外14个心脏(6个对照、4个利多卡因、4个胺碘酮)进行跨膜电压光学标测,以研究心室间电生理差异和不同步节律的机制。在对照心脏中,14个心脏中有8个(57%)出现了不同步心室节律。在利多卡因治疗的心脏中,出现不同步节律的周期长度阈值较低,8/8(100%)的心脏出现了不同步节律,而胺碘酮组为0/6。与对照相比,利多卡因使不同步室性心动过速(VT)的发生率出现在更长的周期长度时(57.1±7.9对36.6±8.4毫秒,P<0.001)。利多卡因组左心室与右心室VT频率之比大于对照组(1.91±0.30对1.76±0.36,P<0.001)。与左心室相比,右心室动作电位时程(APD)恢复曲线的斜率更平缓(对照 - 左心室:0.12±0.03对右心室:0.002±0.03,P = 0.015),导致VT期间左心室向右心室的传导阻滞。APD恢复特性的心室间差异可能导致不同步节律的发生。利多卡因对钠通道的阻滞增加了不同步心室节律发生的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03ae/6456660/80d6044514f7/fcvm-06-00034-g0001.jpg

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