Literature DB >> 2540529

Two molecular transitions influence cardiac sodium channel gating.

D T Yue1, J H Lawrence, E Marban.   

Abstract

Sodium channels from diverse excitable membranes are very similar in their structure, yet surprisingly heterogeneous in their behavior. The processes that govern the opening and closing of sodium channels have appeared difficult to describe in terms of a single, unifying molecular scheme. Now cardiac sodium channels have been analyzed by high-resolution single-channel recordings over a broad range of potentials. Channels exhibited both complex and simple gating patterns at different voltages. Such behavioral diversity can be explained by the balance between two molecular transitions whereby channels can exit the open state.

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Year:  1989        PMID: 2540529     DOI: 10.1126/science.2540529

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  34 in total

1.  Cardiac sodium channel Markov model with temperature dependence and recovery from inactivation.

Authors:  L A Irvine; M S Jafri; R L Winslow
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

2.  Macroscopic and unitary properties of physiological ion flux through T-type Ca2+ channels in guinea-pig heart cells.

Authors:  C W Balke; W C Rose; E Marban; W G Wier
Journal:  J Physiol       Date:  1992-10       Impact factor: 5.182

3.  Exponential activation of the cardiac Na+ current in single guinea-pig ventricular cells.

Authors:  T Mitsuiye; A Noma
Journal:  J Physiol       Date:  1992       Impact factor: 5.182

4.  The quantal gating charge of sodium channel inactivation.

Authors:  N G Greeff; I C Forster
Journal:  Eur Biophys J       Date:  1991       Impact factor: 1.733

5.  Sodium channel inactivation from resting states in guinea-pig ventricular myocytes.

Authors:  J H Lawrence; D T Yue; W C Rose; E Marban
Journal:  J Physiol       Date:  1991-11       Impact factor: 5.182

6.  Inhibition of the fast sodium inward current in ventricular cardiomyocytes of rats and guinea pigs by a novel potent sodium channel blocking agent.

Authors:  B Koidl; W Schreibmayer; P Wolf; H A Tritthart
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1990-11       Impact factor: 3.000

7.  A computational model to predict the effects of class I anti-arrhythmic drugs on ventricular rhythms.

Authors:  Jonathan D Moreno; Z Iris Zhu; Pei-Chi Yang; John R Bankston; Mao-Tsuen Jeng; Chaoyi Kang; Lianguo Wang; Jason D Bayer; David J Christini; Natalia A Trayanova; Crystal M Ripplinger; Robert S Kass; Colleen E Clancy
Journal:  Sci Transl Med       Date:  2011-08-31       Impact factor: 17.956

8.  Coupling between fast and slow inactivation revealed by analysis of a point mutation (F1304Q) in mu 1 rat skeletal muscle sodium channels.

Authors:  H B Nuss; J R Balser; D W Orias; J H Lawrence; G F Tomaselli; E Marban
Journal:  J Physiol       Date:  1996-07-15       Impact factor: 5.182

9.  Inactivation of single cardiac Na+ channels in three different gating modes.

Authors:  T Böhle; M Steinbis; C Biskup; R Koopmann; K Benndorf
Journal:  Biophys J       Date:  1998-10       Impact factor: 4.033

10.  Maximum open probability of single Na+ channels during depolarization in guinea-pig cardiac cells.

Authors:  T Kimitsuki; T Mitsuiye; A Noma
Journal:  Pflugers Arch       Date:  1990-07       Impact factor: 3.657

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