首页> 外文会议>Biomedical Engineering and Biotechnology (iCBEB), 2012 International Conference on >Optical Mapping of the Effect of Pacing Rate and Ikr Blocker, Dofetilide, on Heterogeneity of Action Potential Duration between Rabbit Right and Left Ventricle
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Optical Mapping of the Effect of Pacing Rate and Ikr Blocker, Dofetilide, on Heterogeneity of Action Potential Duration between Rabbit Right and Left Ventricle

机译:起搏速率和Ikr受体阻滞剂多非利特对兔左右心室动作电位持续时间异质性影响的光学映射

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In homogeneity of cardiac electro physiology is existed in both normal and diseased hearts, which would be exacerbated by electrical or structural remodeling. Slow heart rate or decreasing repolarization reserve of action potential can enhance transmural heterogeneity and promote arrhythmia generation. In this study, we used optical mapping technique to investigate how pacing rate changing and Ikr blocker, Dofetilide, influence the heterogeneity of action potential duration between rabbit right and left ventricle simultaneously. The results showed that slowing pacing rate might increase the heterogeneity of inter-ventricles and there were early after depolarization (EAD) happening in right ventricle and inducing trigged activity in left ventricle at BCL of 2000ms. 30 nmol/L Dofetilide could prolong the APD in both right and left ventricle markedly at BCL of 2000, 1000, and 500ms. However, the increment of APD in right ventricle was 226 ± 96ms, and in left ventricle was 213 ± 100ms at BCL of 1000 ms, which demonstrated that Dofetilide did not increase the heterogeneity between two ventricles significantly (P > 0.05). The results suggested Dofetilide inducing Torsades de points (Tdp) because of increasing transmural dispersion of repolarization (TDR), instead of increasing heterogeneity between right and left ventricle.
机译:在正常和患病的心脏中均存在心脏电生理学的同质性,这将因电或结构重塑而加剧。缓慢的心律或动作电位复极储备的减少可增强透壁异质性并促进心律失常的发生。在这项研究中,我们使用光学作图技术研究起搏速率的变化和Ikr阻滞剂多非利特如何同时影响兔左右心室之间动作电位持续时间的异质性。结果表明,慢速起搏可能会增加心室之间的异质性,并且在2000ms的BCL时,右心室发生了去极化(EAD)早期,并诱发了左心室的触发活动。 30 nmol / L多普利特可以在2000、1000和500ms的BCL时显着延长左右心室的APD。然而,在1000 ms的BCL时,右心室的APD增量为226±96ms,而左心室的APD增量为213±100ms,这表明多非利特不会显着增加两个心室之间的异质性(P> 0.05)。结果表明多非利特引起的扭转性室性心动过速(Tdp)是因为增加了跨壁的复极分散(TDR),而不是增加了右心室和左心室之间的异质性。

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