4.7 Article

Class III effects of dofetilide and arrhythmias are modulated by [K+]O in an in vitro model of simulated-ischemia and reperfusion in guinea-pig ventricular myocardium

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EUROPEAN JOURNAL OF PHARMACOLOGY
卷 532, 期 3, 页码 279-289

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DOI: 10.1016/j.ejphar.2005.12.083

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dofetilide; potassium; ischemia-reperfusion; delayed outward rectifier; (guinea-pig)

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To evaluate class III effects of clinically relevant concentrations of dofetilide (5 and 10 nmol/l) and the effects of extracellular potassium [K+](o) modulation of arrhythmias onset at the level of the border zone, we used a previously reported in vitro model whereby normoxic and ischemic/reperfused zones were studied. Guinea-pig right ventricular strips (driven at 1 Hz at 36.5 +/- 0.5 degrees C) were superfused with Tyrode's solution in oxygenated (HCO3- 25 mmol/l, K+ 4 mmol/l, pH 7.35 +/- 0.05, glucose 5.5 mmol/l: normal zone) and ischemia-simulating conditions (HCO3- 9 mmol/l, pH 6.90 +/- 0.05, no oxygen and no glucose: altered zone) having either [K+](o) 4 (n=20), 8 (n=20) or 12 (n=20) mmol/l. Action potentials in normal and altered zones were recorded simultaneously during 30 min of simulated-ischemia and after 30 min of reperfusion with oxygenated Tyrode's solution. Each preparation served as control for successive phases of dofetilide studies (at 5 and 10 nmol/l) and action potential values were normalized to those present at the beginning of the experiment. During simulated-ischemia, the higher the [K+](o) the worse were action potential changes, although full recovery was seen upon 30 min of reperfusion in all [K+](o) groups. A high incidence of ischemia/reperfusion arrhythmias was observed in 4 and 12 mmol/l [K+](o) groups as opposed to a low incidence of arrhythmias in 8 mmol/l [K+](o) group. Dofetilide at 5 and 10 nmol/l with all [K+](o) explored: (i) exhibited class III effects, (ii) was effective (or neutral) against ventricular arrhythmias during both simulated-ischemia and reperfusion, and (iii) did not globally increase the dispersion of action potential durations between normal and altered zones. Different arrhythmogenic mechanisms are involved in this model at different [K+](o) with 8 mmol/l providing relative protection. Class III effects of dofetilide are evident in the normal zone when in the ischemic-like zone ranges from 4 to 12 mmol/l. Thus dofetilide did not increase dispersion of repolarization and had either an antiarrhythmic or a neutral effect during ischemia/reperfusion. (c) 2006 Elsevier B.V. All rights reserved.

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