Literature DB >> 1312912

Existence of both fast and slow channel activity during the early stages of ventricular fibrillation.

X Zhou1, P Guse, P D Wolf, D L Rollins, W M Smith, R E Ideker.   

Abstract

Although sodium channels have been reported to be inactive after 5-10 minutes of ventricular fibrillation (VF), their state during early VF is unknown. In 12 open-chest dogs, a floating glass microelectrode was used to record intracellular action potentials from the right ventricle during pacing and during electrically induced VF. Before any drug was administered, an initial episode of VF was continuously recorded for at least 20 seconds followed by defibrillation. Recordings were made during VF episodes after superfusion for 15 minutes around the microelectrode site by low (2.8 x 10(-5) M) and high (10(-4) M) concentrations of tetrodotoxin (TTX) in five dogs, or by low (4 microM) and high (100 microM) concentrations of verapamil in another four dogs. In three dogs, VF was induced without drugs three times to determine if the effects observed in the previous dogs were caused by the drugs or by successive episodes of VF. Ten consecutive action potentials were analyzed at the onset and after 5, 10, 15, and 20 seconds of VF. Action potential amplitude and duration during paced rhythm or VF were not changed by the local perfusion of either TTX or verapamil. In the TTX group, the maximum upstroke rate of depolarization of an action potential (Vmax) during paced rhythm was 104 +/- 14 V/sec for control cycles before any drug was given, 86 +/- 15 V/sec for the low TTX concentration, and 55 +/- 14 V/sec for the high TTX concentration (p less than 0.05 versus other two). Vmax decreased from 55 +/- 32 V/sec at the beginning of VF to 37 +/- 27 V/sec after 20 seconds of VF for predrug VF, from 39 +/- 20 V/sec to 18 +/- 11 V/sec for low-dose TTX VF, and from 18 +/- 13 V/sec to 12 +/- 7 V/sec for high-dose TTX VF (p less than 0.05 among the three groups). In the dogs receiving verapamil, VF was still inducible with Vmax not significantly different from predrug VF at the onset and after 5 or 20 seconds of VF but with Vmax smaller (p less than 0.05) for verapamil than for predrug VF after 10 or 15 seconds of VF. In three dogs, Vmax was not significantly different during three successive episodes of VF when no drug was given between the episodes.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1312912     DOI: 10.1161/01.res.70.4.773

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  5 in total

1.  Spiral waves in two-dimensional models of ventricular muscle: formation of a stationary core.

Authors:  J Beaumont; N Davidenko; J M Davidenko; J Jalife
Journal:  Biophys J       Date:  1998-07       Impact factor: 4.033

2.  Epicardial conductors can lower the defibrillation threshold in rabbit hearts.

Authors:  Jared A Sims; Stephen B Knisley Ast
Journal:  IEEE Trans Biomed Eng       Date:  2008-10-21       Impact factor: 4.538

3.  Verapamil reduces incidence of reentry during ventricular fibrillation in pigs.

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Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-08-29       Impact factor: 4.733

4.  Excito-oscillatory dynamics as a mechanism of ventricular fibrillation.

Authors:  Richard A Gray; Delilah J Huelsing
Journal:  Heart Rhythm       Date:  2008-01-17       Impact factor: 6.343

5.  Sarcolemmal ATP-sensitive potassium channels modulate skeletal muscle function under low-intensity workloads.

Authors:  Zhiyong Zhu; Ana Sierra; Colin M-L Burnett; Biyi Chen; Ekaterina Subbotina; Siva Rama Krishna Koganti; Zhan Gao; Yuejin Wu; Mark E Anderson; Long-Sheng Song; David J Goldhamer; William A Coetzee; Denice M Hodgson-Zingman; Leonid V Zingman
Journal:  J Gen Physiol       Date:  2013-12-16       Impact factor: 4.086

  5 in total

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