Literature DB >> 10688323

Cellular basis for long QT, transmural dispersion of repolarization, and torsade de pointes in the long QT syndrome.

W Shimizu1, C Antzelevitch.   

Abstract

Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5). Preliminary clinical studies have reported different phenotypic electrocardiographic patterns and different sensitivity to pacing or pharmacological therapy for each genotype. A transmural electrocardiogram and transmembrane action potentials from epicardial, M, and endocardial cells were simultaneously recorded from an arterially perfused wedge of canine left ventricle. Isoproterenol (100 nmol/L) in the presence of chromanol 293B (30 micromol/L), an I(Ks) blocker (LQT1 model), produced a preferential prolongation of M-cell action potential duration (APD), resulting in an increase in transmural dispersion of repolarization (TDR) and a broad-based T wave, as commonly seen in LQT1 patients. D-Sotalol (100 micromol/L), an I(Kr) blocker (LQT2 model), and ATX-II (20 nmol/L), an agent that augments late I(Na) (LQT3 model), also produced a preferential prolongation of M-cell APD, an increase in TDR, and low-amplitude T wave with a bifurcated appearance (LQT2), and late-appearing T wave (LQT3), respectively. APD-, QT-, and TDR-rate relations were much steeper in the LQT3 model than in either the LQT1 or LQT2 model, whereas the rate relations in the LQT1 and LQT2 models were both steeper than those under control conditions. Spontaneous and programmed electrical stimulation-induced torsade de pointes (TdP) were observed in all 3 models. Propranolol (1 micromol/L), a beta blocker, completely prevented the effect of isoproterenol to persistently or transiently increase TDR and to induce TdP in the LQT1 and LQT2 models, but facilitated TdP in the LQT3 model. Mexiletine, a class IB Na+ channel blocker, dose-dependently (2-20 micromol/L) abbreviated the QT and APD more in the LQT3 model, but decreased TDR and suppressed TdP in the 3 models.

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Year:  1999        PMID: 10688323     DOI: 10.1016/s0022-0736(99)90077-8

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  28 in total

1.  Changes in ventricular repolarization duration during typical daily emotion in patients with Long QT syndrome.

Authors:  Richard D Lane; Wojciech Zareba; Harry T Reis; Derick R Peterson; Arthur J Moss
Journal:  Psychosom Med       Date:  2010-12-23       Impact factor: 4.312

2.  Repolarization gradients and arrhythmogenicity in the murine heart.

Authors:  Matthew J Killeen; Ian N Sabir
Journal:  J Physiol       Date:  2007-07-12       Impact factor: 5.182

3.  Cannabidiol protects against high glucose-induced oxidative stress and cytotoxicity in cardiac voltage-gated sodium channels.

Authors:  Mohamed A Fouda; Mohammad-Reza Ghovanloo; Peter C Ruben
Journal:  Br J Pharmacol       Date:  2020-03-10       Impact factor: 8.739

4.  Inhibition of the late sodium current as a potential cardioprotective principle: effects of the late sodium current inhibitor ranolazine.

Authors:  L Belardinelli; J C Shryock; H Fraser
Journal:  Heart       Date:  2006-07       Impact factor: 5.994

5.  Ionic current basis of electrocardiographic waveforms: a model study.

Authors:  Kazutaka Gima; Yoram Rudy
Journal:  Circ Res       Date:  2002-05-03       Impact factor: 17.367

6.  Dimethyl lithospermate B, an extract of Danshen, suppresses arrhythmogenesis associated with the Brugada syndrome.

Authors:  Jeffrey M Fish; Daniel R Welchons; Young-Sup Kim; Suk-Ho Lee; Won-Kyung Ho; Charles Antzelevitch
Journal:  Circulation       Date:  2006-03-13       Impact factor: 29.690

7.  Bradycardia-induced Torsade de Pointes - An arrhythmia Less Understood.

Authors:  Narayanan Namboodiri
Journal:  Indian Pacing Electrophysiol J       Date:  2010-10-31

8.  Persistent atrial fibrillation is associated with reduced risk of torsades de pointes in patients with drug-induced long QT syndrome.

Authors:  Dawood Darbar; John Kimbrough; Asif Jawaid; Robert McCray; Marylyn D Ritchie; Dan M Roden
Journal:  J Am Coll Cardiol       Date:  2008-02-26       Impact factor: 24.094

9.  Transient Outward K+ Current (Ito) Underlies the Right Ventricular Initiation of Polymorphic Ventricular Tachycardia in a Transgenic Rabbit Model of Long-QT Syndrome Type 1.

Authors:  Bum-Rak Choi; Weiyan Li; Dmitry Terentyev; Anatoli Y Kabakov; Mingwang Zhong; Colin M Rees; Radmila Terentyeva; Tae Yun Kim; Zhilin Qu; Xuwen Peng; Alain Karma; Gideon Koren
Journal:  Circ Arrhythm Electrophysiol       Date:  2018-06

10.  Ionic mechanisms limiting cardiac repolarization reserve in humans compared to dogs.

Authors:  Norbert Jost; László Virág; Philippe Comtois; Balázs Ordög; Viktória Szuts; György Seprényi; Miklós Bitay; Zsófia Kohajda; István Koncz; Norbert Nagy; Tamás Szél; János Magyar; Mária Kovács; László G Puskás; Csaba Lengyel; Erich Wettwer; Ursula Ravens; Péter P Nánási; Julius Gy Papp; András Varró; Stanley Nattel
Journal:  J Physiol       Date:  2013-07-22       Impact factor: 5.182

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