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氟卡尼激发试验中右心室传导敏感性增加的潜在机制。

Mechanisms underlying increased right ventricular conduction sensitivity to flecainide challenge.

作者信息

Veeraraghavan Rengasayee, Poelzing Steven

机构信息

Nora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah, Salt Lake City, UT 84112-5000, USA.

出版信息

Cardiovasc Res. 2008 Mar 1;77(4):749-56. doi: 10.1093/cvr/cvm090. Epub 2007 Dec 4.

Abstract

AIMS

The cardiac sodium current (I(Na)) is a major determinant of conduction. Mechanisms underlying regionally heterogeneous conduction slowing secondary to reduced I(Na) in diseases such as the Brugada syndrome and heart failure remain incompletely understood. Right precordial electrophysiological manifestations during flecainide challenge suggest a decreased right ventricular depolarization reserve. We hypothesized that heterogeneous cardiac sodium channel (Na(v)1.5) distribution between ventricles causes interventricular depolarization heterogeneities.

METHODS AND RESULTS

Western blotting analysis revealed Na(v)1.5, and Kir2.1 protein expressions were 18.2 and 12.0% lower, respectively, in the guinea pig right ventricle (RV) compared with the left ventricle (LV). Conduction velocity (theta) heterogeneities were quantified by optical mapping during LV or RV pacing. Although RV transverse theta((thetaT)) was significantly greater than LV (thetaT) by 33.09 +/- 1.38% under control conditions, there were no differences in longitudinal theta. During partial sodium channel blockade (flecainide, 0.5 microM), RV theta decreased by 35.3 +/- 1.3%, whereas LV theta decreased by 29.2 +/- 1.0%. These data demonstrate that the RV has an increased conduction dependence on sodium channel availability. Partial blockade of the inward rectifier potassium current (I(K1)) by BaCl(2) (10 microm) significantly increased theta in both ventricles under control conditions. However, BaCl(2) only increased conduction dependence on sodium channel availability in the LV. This suggests that the LV may have an increased depolarization reserve compared with the RV, but the larger I(K1) depresses control LV theta.

CONCLUSION

Interventricular I(K1) heterogeneities may underlie conduction heterogeneities observed under control conditions. However, under conditions where I(Na) is functionally reduced in disease or during pharmacological sodium channel blockade, the heterogeneity in Na(v)1.5 expression may become a significant determinant of conduction heterogeneities.

摘要

目的

心脏钠电流(I(Na))是传导的主要决定因素。在诸如 Brugada 综合征和心力衰竭等疾病中,由于 I(Na) 降低导致的局部异质性传导减慢的潜在机制仍未完全阐明。氟卡尼激发试验期间右胸前区的电生理表现提示右心室去极化储备降低。我们推测心室之间心脏钠通道(Na(v)1.5)分布的异质性导致心室间去极化异质性。

方法与结果

蛋白质印迹分析显示,与左心室(LV)相比,豚鼠右心室(RV)中 Na(v)1.5 和 Kir2.1 蛋白表达分别降低了 18.2%和 12.0%。通过在左心室或右心室起搏期间进行光学标测来量化传导速度(theta)异质性。尽管在对照条件下右心室横向 theta(thetaT)比左心室(thetaT)显著大 33.09±1.38%,但纵向 theta 没有差异。在部分钠通道阻滞(氟卡尼,0.5 microM)期间,右心室 theta 降低了 35.3±1.3%,而左心室 theta 降低了 29.2±1.0%。这些数据表明右心室对钠通道可用性的传导依赖性增加。在对照条件下,BaCl(2)(10 微摩尔)对内向整流钾电流(I(K1))的部分阻滞显著增加了两个心室的 theta。然而,BaCl(2)仅增加了左心室对钠通道可用性的传导依赖性。这表明与右心室相比,左心室可能具有增加的去极化储备,但较大的 I(K1) 压低了对照左心室 theta。

结论

心室间 I(K1) 异质性可能是对照条件下观察到的传导异质性的基础。然而,在疾病中 I(Na) 功能降低的情况下或在药理学钠通道阻滞期间,Na(v)1.5 表达的异质性可能成为传导异质性的重要决定因素。

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