Literature DB >> 7918982

Late Na channels in cardiac cells: the physiological role of background Na channels.

C F Starmer, J Starobin, A O Grant.   

Abstract

Two types of the late Na channels, burst and background, were studied in Purkinje and ventricular cells. In the whole-cell configuration, steady-state Na currents were recorded at potentials (-70 to -80 mV) close to the normal cell resting potential. The question of the contribution of late Na channels to this background Na conductance was investigated. During depolarization, burst Na channels were active for periods (up to approximately 5 s), which exceeded the action potential duration. However, they eventually closed without reopening, indicating the presence of slow and complete inactivation. When, at the moment of burst channel opening, the potential was switched to -80 mV, the channel closed quickly without reopening. We conclude that the burst Na channels cannot contribute significantly to the background Na conductance. Background Na channels undergo incomplete inactivation. After a step depolarization, their activity decreased in time, approaching a steady-state level. Background Na channel openings could be recorded at constant potentials in the range from -120 to 0 mV. After step depolarizations to potentials near -70 mV and more negative, a significant fraction of Na current was carried by the background Na channels. Analysis of the background channel behavior revealed that their gating properties are qualitatively different from those of the early Na channels. We suggest that background Na channels represent a special type of Na channel that can play an important role in the initiation of cardiac action potential and in the TTX-sensitive background Na conductance.

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Year:  1994        PMID: 7918982      PMCID: PMC1225344          DOI: 10.1016/S0006-3495(94)80464-3

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  26 in total

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2.  A source of bias in the analysis of single channel data: assessing the apparent interaction between channel proteins.

Authors:  J L Hurwitz; M A Dietz; C F Starmer; A O Grant
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3.  Mechanisms of closure of cardiac sodium channels in rabbit ventricular myocytes: single-channel analysis.

Authors:  A O Grant; C F Starmer
Journal:  Circ Res       Date:  1987-06       Impact factor: 17.367

4.  Slow inactivation of the sodium current in rabbit cardiac Purkinje fibres.

Authors:  E Carmeliet
Journal:  Pflugers Arch       Date:  1987-01       Impact factor: 3.657

5.  Different conductance states of the bursting Na channel in guinea-pig ventricular myocytes.

Authors:  B Nilius; J Vereecke; E Carmeliet
Journal:  Pflugers Arch       Date:  1989-01       Impact factor: 3.657

6.  Factors related to the low resting membrane potentials of diseased human atrial muscles.

Authors:  S Imanishi; M Arita
Journal:  Jpn J Physiol       Date:  1987

7.  Late sodium current and its contribution to action potential configuration in guinea pig ventricular myocytes.

Authors:  T Kiyosue; M Arita
Journal:  Circ Res       Date:  1989-02       Impact factor: 17.367

8.  Blockade of rabbit atrial sodium channels by lidocaine. Characterization of continuous and frequency-dependent blocking.

Authors:  F R Gilliam; C F Starmer; A O Grant
Journal:  Circ Res       Date:  1989-09       Impact factor: 17.367

Review 9.  Two modes of gating during late Na+ channel currents in frog sartorius muscle.

Authors:  J B Patlak; M Ortiz
Journal:  J Gen Physiol       Date:  1986-02       Impact factor: 4.086

10.  Cardiac Na currents and the inactivating, reopening, and waiting properties of single cardiac Na channels.

Authors:  D L Kunze; A E Lacerda; D L Wilson; A M Brown
Journal:  J Gen Physiol       Date:  1985-11       Impact factor: 4.086

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  15 in total

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Authors:  Victor A Maltsev; Albertas Undrovinas
Journal:  Prog Biophys Mol Biol       Date:  2007-08-10       Impact factor: 3.667

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3.  Chronic heart failure slows late sodium current in human and canine ventricular myocytes: implications for repolarization variability.

Authors:  Victor A Maltsev; Norman Silverman; Hani N Sabbah; Albertas I Undrovinas
Journal:  Eur J Heart Fail       Date:  2006-10-24       Impact factor: 15.534

Review 4.  Pathophysiology of the cardiac late Na current and its potential as a drug target.

Authors:  Jonathan D Moreno; Colleen E Clancy
Journal:  J Mol Cell Cardiol       Date:  2011-12-16       Impact factor: 5.000

5.  Patch-clamp analysis in canine cardiac Purkinje cells of a novel sodium component in the pacemaker range.

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Journal:  J Physiol       Date:  2003-02-14       Impact factor: 5.182

6.  I(Ca(TTX)) channels are distinct from those generating the classical cardiac Na(+) current.

Authors:  Y Chen-Izu; Q Sha; S R Shorofsky; S W Robinson; W G Wier; L Goldman; C W Balke
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

7.  Beta-receptor activation increases sodium current in guinea pig heart.

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8.  Wavelet formation in excitable cardiac tissue: the role of wavefront-obstacle interactions in initiating high-frequency fibrillatory-like arrhythmias.

Authors:  J M Starobin; Y I Zilberter; E M Rusnak; C F Starmer
Journal:  Biophys J       Date:  1996-02       Impact factor: 4.033

9.  Late Na+ current produced by human cardiac Na+ channel isoform Nav1.5 is modulated by its beta1 subunit.

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Journal:  J Physiol Sci       Date:  2009-03-03       Impact factor: 2.781

10.  An antisense oligonucleotide against H1 inhibits the classical sodium current but not ICa(TTX) in rat ventricular cells.

Authors:  Qun Sha; Shawn W Robinson; Stacey L McCulle; Stephen R Shorofsky; Paul A Welling; L Goldman; C William Balke
Journal:  J Physiol       Date:  2003-01-24       Impact factor: 5.182

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