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产生 Brugada 综合征或进行性心脏传导系统疾病的钠通道动力学变化。

Sodium channel kinetic changes that produce Brugada syndrome or progressive cardiac conduction system disease.

作者信息

Zhang Zhu-Shan, Tranquillo Joseph, Neplioueva Valentina, Bursac Nenad, Grant Augustus O

机构信息

Duke Univ. Medical Center, Box 3504, Durham, NC 27710, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2007 Jan;292(1):H399-407. doi: 10.1152/ajpheart.01025.2005. Epub 2006 Jul 28.

Abstract

Some mutations of the sodium channel gene Na(V1.5) are multifunctional, causing combinations of LQTS, Brugada syndrome and progressive cardiac conduction system disease (PCCD). The combination of Brugada syndrome and PCCD is uncommon, although they both result from a reduction in the sodium current. We hypothesize that slow conduction is sufficient to cause S-T segment elevation and undertook a combined experimental and theoretical study to determine whether conduction slowing alone can produce the Brugada phenotype. Deletion of lysine 1479 in one of two positively charged clusters in the III/IV inter-domain linker causes both syndromes. We have examined the functional effects of this mutation using heterologous expression of the wild-type and mutant sodium channel in HEK-293-EBNA cells. We show that DeltaK1479 shifts the potential of half-activation, V(1/2m), to more positive potentials (V(1/2m) = -36.8 +/- 0.8 and -24.5 +/- 1.3 mV for the wild-type and DeltaK1479 mutant respectively, n = 11, 10). The depolarizing shift increases the extent of depolarization required for activation. The potential of half-inactivation, V(1/2h), is also shifted to more positive potentials (V(1/2h) = -85 +/- 1.1 and -79.4 +/- 1.2 mV for wild-type and DeltaK1479 mutant respectively), increasing the fraction of channels available for activation. These shifts are quantitatively the same as a mutation that produces PCCD only, G514C. We incorporated experimentally derived parameters into a model of the cardiac action potential and its propagation in a one dimensional cable (simulating endo-, mid-myocardial and epicardial regions). The simulations show that action potential and ECG changes consistent with Brugada syndrome may result from conduction slowing alone; marked repolarization heterogeneity is not required. The findings also suggest how Brugada syndrome and PCCD which both result from loss of sodium channel function are sometimes present alone and at other times in combination.

摘要

钠通道基因Na(V1.5)的一些突变具有多种功能,可导致长QT综合征(LQTS)、 Brugada综合征和进行性心脏传导系统疾病(PCCD)的组合。Brugada综合征和PCCD的组合并不常见,尽管它们都是由钠电流减少引起的。我们假设缓慢传导足以导致S-T段抬高,并进行了一项结合实验和理论的研究,以确定仅传导减慢是否能产生Brugada表型。在III/IV结构域间连接区两个带正电荷簇之一中赖氨酸1479的缺失会导致这两种综合征。我们使用野生型和突变型钠通道在HEK-293-EBNA细胞中的异源表达,研究了这种突变的功能效应。我们发现,DeltaK1479将半激活电位V(1/2m) 移向更正的电位(野生型和DeltaK1479突变体的V(1/2m) 分别为-36.8±0.8和-24.5±1.3 mV,n = 11, 10)。去极化移位增加了激活所需的去极化程度。半失活电位V(1/2h) 也移向更正的电位(野生型和DeltaK1479突变体的V(1/2h) 分别为-85±1.1和-79.4±1.2 mV),增加了可用于激活的通道比例。这些移位在数量上与仅产生PCCD的突变G514C相同。我们将实验得出的参数纳入心脏动作电位及其在一维电缆中传播的模型(模拟内膜、中层心肌和心外膜区域)。模拟结果表明,仅传导减慢可能导致与Brugada综合征一致的动作电位和心电图变化;不需要明显的复极异质性。这些发现还揭示了同样由钠通道功能丧失引起的Brugada综合征和PCCD有时单独出现,有时同时出现的原因。

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