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J Vereecke

Publications and source records attributed to J Vereecke.

69 records · Page 4Linked to original sources
PubMed1980

K efflux through inward rectifying K channels in voltage clamped Purkinje fibers.

The 42K efflux was measured in voltage clamped sheep Purkinje fibers. The voltage dependence of the K efflux can be described as N-shaped, showing a negative slope region. At potentials negative to -30mV, the K efflux is largely due to K flowing through a channel which rectifies in the inward direction and which is blocked by external application of 20mM Cs+. At potentials positive to -30mV an outward rectifier dominates the shape of the K efflux-voltage relationship. This component is insensitive to short external application of Cs+. Both components were also found when Na+ was replaced by tetramethylammonium. When the steady-state current-voltage relationship is compared with the K efflux one can conclude that the outward rectifying K flux largely determines the shape of this curve at positive membrane potentials, while the negative slope region of the K efflux correlates with the negative slope of the steady-state current-voltage relation. The K efflux is only slightly enhanced by stimulation of the preparation, corroborating the finding of inward-going rectification of the K channel. A clamp program repetitively activating the positive dynamic current e.g. by alternating the membrane potential between -70 and +10mV, increases the K efflux by about 50% as compared to the efflux measured in steady-state at this positive membrane potential. 4-Aminopyridine suppresses both this extra K efflux and the positive dynamic current. It is concluded that K ions contribute to the positive dynamic current.

Animals↗
PubMed1980

Ionic currents during hypoxia in voltage-clamped cat ventricular muscle.

To explore the mechanisms underlying the shortening of the cardiac action potential in hypoxia, we studied the effect of hypoxia on the ionic currents in cat papillary and trabecular muscles using the single sucrose gap-voltage clamp technique. For potentials positive to -70 mV, hypoxia induces an increase in time-independent outward current. The changes in the tail current suggest that time-dependent outward current is not increased but, rather, reduced. Because the time course of ik remains unchanged, we concluded that the shortening of the action potential is not a result of a change in the time-dependent outward current. In the potential range of the plateau, the amplitude of the slow inward current is not affected by hpoxia. Its time constant of inactivation appears slightly decreased. The prolongation of the action potential by epinephrine during hypoxia is accompanied by an increase in the slow inward current. As a result of these studies, we conclude that the shortening of the cardiac action potential in the early stage of hypoxia results from an increase in K+ outward background current.

Action Potentials↗
PubMedDate not supplied

Effects of the enantiomers of flecainide on action potential characteristics in the guinea-pig papillary muscle.

The enantiomers of flecainide, a Class Ic antiarrhythmic agent, were tested in the guinea-pig papillary muscle using the standard microelectrode technique. In 5.4 mM external K+ and at a stimulation frequency of 1 Hz, significant differences were observed in the effect of the enantiomers on maximal rate of depolarization, action potential amplitude and action potential duration. Maximal rate of depolarization and action potential amplitude were more suppressed in the presence of (+)flecainide. Maximal rate of depolarization was reduced to 54.4 +/- 1.4% (n = 23) (mean +/- S.E.M.) of maximum in the presence of 7.2 microM (+)flecainide and to 60.5 +/- 1.1% (n = 24) in the presence of the same concentration of (-)flecainide. The stimulation interval used had a pronounced influence on maximal rate of depolarization for both enantiomers. At almost all stimulation intervals tested, block was larger for (+)flecainide than for (-)flecainide. When the stimulation interval was shortened from 10 sec to 0.25 sec, the maximal rate of depolarization was reduced from 89.8 +/- 0.8% (n = 13) to 37.4 +/- 2.3% (n = 10) of the control in the presence of 7.2 microM of (+)flecainide and from 91.7 +/- 0.8% (n = 14) to 44.9 +/- 1.6% (n = 12) when the same concentration of (-)flecainide was used. The effect on maximal rate of depolarization was also voltage-dependent. For both enantiomers, inactivation curves, recorded at a frequency of 0.6/min, were shifted to more negative potentials. There was no significant difference in magnitude of shift between the two enantiomers.

Action Potentials↗