Literature DB >> 6093559

Slow inactivation of Vmax in guinea pig ventricular myocardium.

C W Clarkson, T Matsubara, L M Hondeghem.   

Abstract

Measurements of maximum upstroke velocity (Vmax) of guinea pig ventricular action potentials were used to investigate the effect of prolonged depolarization on the inactivation and recovery kinetics of cardiac sodium channels. Membrane potential before stimulated upstrokes was controlled by passing current across a sucrose gap. Two phases of inactivation ("slow" and "ultra-slow") having kinetics and voltage dependence different from the commonly observed fast inactivation process were observed. Ultra-slow inactivation developed exponentially with a time constant of several minutes between -60 and -20 mV. In contrast, slow inactivation developed with a time constant of 1-6 s between -60 and 40 mV. Under steady-state conditions slow and ultra-slow inactivations were virtually absent at -85 mV, while 50% of Vmax underwent slow inactivation at approximately 10 mV and 50% underwent ultra-slow inactivation at approximately -40 mV. Recovery from slow inactivation occurred exponentially with a time constant of about 2 s at -70 to -85 mV and 0.7 s at -100 mV. Recovery from ultra-slow inactivation was not completely characterized but was complete within 20 s at -85 mV. No significant effect of external [K+] (1-10 mM) on slow inactivation was found. The results suggest the existence of two additional inactivated states of the cardiac sodium channel distinctly different from the fast inactivated state.

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Year:  1984        PMID: 6093559     DOI: 10.1152/ajpheart.1984.247.4.H645

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  14 in total

1.  Block of cardiac sodium channels by amiodarone studied by using Vmax of action potential in single ventricular myocytes.

Authors:  H Honjo; I Kodama; K Kamiya; J Toyama
Journal:  Br J Pharmacol       Date:  1991-03       Impact factor: 8.739

2.  Modification of Na channel inactivation by alpha-chymotrypsin in single cardiac myocytes.

Authors:  C W Clarkson
Journal:  Pflugers Arch       Date:  1990-09       Impact factor: 3.657

3.  Lidocaine blocks open and inactivated cardiac sodium channels.

Authors:  T Matsubara; C Clarkson; L Hondeghem
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1987-08       Impact factor: 3.000

4.  Sodium current kinetics in cat atrial myocytes.

Authors:  C H Follmer; R E ten Eick; J Z Yeh
Journal:  J Physiol       Date:  1987-03       Impact factor: 5.182

5.  Electrophysiological effects of SD-3212, a new antiarrhythmic agent with vasodilator action, on guinea-pig ventricular cells.

Authors:  I Kodama; R Suzuki; K Maruyama; J Toyama
Journal:  Br J Pharmacol       Date:  1995-01       Impact factor: 8.739

6.  Fast and slow blockade of sodium channels by flecainide in rabbit cardiac Purkinje fibres.

Authors:  G Konzen; B Reichardt; O Hauswirth
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1990-06       Impact factor: 3.000

7.  Electrophysiological effects of the combination of mexiletine and flecainide in guinea-pig ventricular fibres.

Authors:  E Delpón; C Valenzuela; J Tamargo
Journal:  Br J Pharmacol       Date:  1991-06       Impact factor: 8.739

8.  Electrophysiological effects of Ro 22-9194, a new antiarrhythmic agent, on guinea-pig ventricular cells.

Authors:  K Maruyama; I Kodama; T Anno; R Suzuki; J Toyama
Journal:  Br J Pharmacol       Date:  1995-01       Impact factor: 8.739

9.  Effects of propafenone on electrical and mechanical activities of single ventricular myocytes isolated from guinea-pig hearts.

Authors:  H Honjo; T Watanabe; K Kamiya; I Kodama; J Toyama
Journal:  Br J Pharmacol       Date:  1989-07       Impact factor: 8.739

10.  Quinidine blocks cardiac sodium channels during opening and slow inactivation in guinea-pig papillary muscle.

Authors:  L M Hondeghem; T Matsubara
Journal:  Br J Pharmacol       Date:  1988-02       Impact factor: 8.739

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