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本文引用的文献

1
Larger late sodium conductance in M cells contributes to electrical heterogeneity in canine ventricle.M细胞中较大的晚钠电流有助于犬心室的电不均一性。
Am J Physiol Heart Circ Physiol. 2001 Aug;281(2):H689-97. doi: 10.1152/ajpheart.2001.281.2.H689.
2
Distribution of a persistent sodium current across the ventricular wall in guinea pigs.豚鼠心室壁持续性钠电流的分布
Circ Res. 2000 Nov 10;87(10):910-4. doi: 10.1161/01.res.87.10.910.
3
Protein kinase C-dependent modulation of Na+ currents increases the excitability of rat neocortical pyramidal neurones.蛋白激酶C依赖性的钠电流调节增加大鼠新皮质锥体神经元的兴奋性。
J Physiol. 2000 Oct 15;528 Pt 2(Pt 2):291-304. doi: 10.1111/j.1469-7793.2000.00291.x.
4
Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome.与长QT综合征相关的钠通道突变D1790G的分子药理学
Circulation. 2000 Aug 22;102(8):921-5. doi: 10.1161/01.cir.102.8.921.
5
Effects of BDF 9198 on action potentials and ionic currents from guinea-pig isolated ventricular myocytes.BDF 9198对豚鼠离体心室肌细胞动作电位和离子电流的影响。
Br J Pharmacol. 2000 Aug;130(8):1753-66. doi: 10.1038/sj.bjp.0703476.
6
Long QT syndrome.长QT综合征
Cardiol Clin. 2000 May;18(2):309-25. doi: 10.1016/s0733-8651(05)70143-0.
7
Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome.复极跨壁离散度与致心律失常性:Brugada综合征与长QT综合征
J Electrocardiol. 1999;32 Suppl:158-65. doi: 10.1016/s0022-0736(99)90074-2.
8
Functional, structural, and dynamic basis of electrical heterogeneity in healthy and diseased cardiac muscle: implications for arrhythmogenesis and anti-arrhythmic drug therapy.健康和患病心肌电不均一性的功能、结构及动态基础:对心律失常发生机制和抗心律失常药物治疗的意义
Pharmacol Ther. 1999 Nov;84(2):207-31. doi: 10.1016/s0163-7258(99)00033-9.
9
Transient outward current, Ito1, is altered in cardiac memory.
Circulation. 1999 Apr 13;99(14):1898-905. doi: 10.1161/01.cir.99.14.1898.
10
Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel.心脏钠通道中一种新型长QT综合征突变(R1623Q)的表型特征
Circulation. 1998 Feb 24;97(7):640-4. doi: 10.1161/01.cir.97.7.640.

成年大鼠心脏左心室壁钠电流梯度

Gradient of sodium current across the left ventricular wall of adult rat hearts.

作者信息

Ashamalla S M, Navarro D, Ward C A

机构信息

Department of Physiology, Queen's University, Kingston, Ontario, Canada K7L 3N6.

出版信息

J Physiol. 2001 Oct 15;536(Pt 2):439-43. doi: 10.1111/j.1469-7793.2001.0439c.xd.

DOI:10.1111/j.1469-7793.2001.0439c.xd
PMID:11600679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2278873/
Abstract
  1. Gradients of ion channels across the left ventricular (LV) wall have been well characterized and it has been shown that disruption of such gradients leads to altered rates of repolarization across the wall, which is associated with the generation of arrhythmias. 2. We have hypothesized that a transmural gradient of I(Na) is present and have directly measured this current in adult rat myocytes isolated from both the epicardial and endocardial layers of the left ventricle. Currents were also recorded in right ventricular (RV) myocytes for comparison. 3. Peak inward I(Na) currents, at -30 mV, were -49.7 +/- 2.5 pA pF(-1) (n = 22), -32.9 +/- 3.2 pA pF(-1) (n = 16) and -49.7 +/- 3.7 pA pF(-1) (n = 24) for RV, LV epicardial and LV endocardial myocytes, respectively. No differences in the voltage dependence of inactivation, the voltage dependence of steady-state inactivation, or reactivation were reported. 4. Our results demonstrate that a gradient of sodium current density is present across the LV wall of adult rat hearts.
摘要
  1. 左心室壁上离子通道的梯度已得到充分表征,并且已经表明这种梯度的破坏会导致整个心室壁复极速率改变,这与心律失常的发生有关。2. 我们推测存在I(Na)的跨壁梯度,并直接测量了从成年大鼠左心室心外膜和心内膜层分离的心肌细胞中的这种电流。还记录了右心室(RV)心肌细胞中的电流以作比较。3. 在-30 mV时,RV、LV心外膜和LV心内膜心肌细胞的内向I(Na)电流峰值分别为-49.7 +/- 2.5 pA pF(-1)(n = 22)、-32.9 +/- 3.2 pA pF(-1)(n = 16)和-49.7 +/- 3.7 pA pF(-1)(n = 24)。未报告失活的电压依赖性、稳态失活的电压依赖性或再激活方面的差异。4. 我们的结果表明,成年大鼠心脏的左心室壁存在钠电流密度梯度。