2019
DOI: 10.1007/s00232-019-00098-x
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Prevailing Effects of Ibutilide on Fast Delayed Rectifier K+ Channel

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Cited by 6 publications
(2 citation statements)
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“…The electrophysiological mechanisms of cardioversion are mainly as follows: By inhibiting potassium channels, it speci cally inhibits potassium currents, but the difference is that ibutilide also promotes sodium and calcium in ux in the plateau phase and plays a role in prolonging the plateau phase of action potential in cardiomyocytes; it causes prolongation of action potential duration and prolongation of QTc in cardiomyocytes, and then exerts its antiarrhythmic effect [10][11] . Ibutilide is more effective in inhibiting atrial myocardium than sinus node, atrioventricular node and ventricular myocardium, so it is more effective in inhibiting atrial arrhythmia than ventricular arrhythmia [12] . At present, many domestic and foreign scholars have studied the rational use of ibutilide in atrial brillation ablation.…”
Section: Of Postoperative Maintenance Time Of Normal Sinus Rhythm In ...mentioning
confidence: 99%
“…The electrophysiological mechanisms of cardioversion are mainly as follows: By inhibiting potassium channels, it speci cally inhibits potassium currents, but the difference is that ibutilide also promotes sodium and calcium in ux in the plateau phase and plays a role in prolonging the plateau phase of action potential in cardiomyocytes; it causes prolongation of action potential duration and prolongation of QTc in cardiomyocytes, and then exerts its antiarrhythmic effect [10][11] . Ibutilide is more effective in inhibiting atrial myocardium than sinus node, atrioventricular node and ventricular myocardium, so it is more effective in inhibiting atrial arrhythmia than ventricular arrhythmia [12] . At present, many domestic and foreign scholars have studied the rational use of ibutilide in atrial brillation ablation.…”
Section: Of Postoperative Maintenance Time Of Normal Sinus Rhythm In ...mentioning
confidence: 99%
“…For instance, amiodarone (anti-arrhythmic drug, VGPC channel blocker) can also block L-type calcium, potassium and sodium currents; prolong phase 3 of the cardiac action potential; and reduce pulse rate in humans [174][175][176]. It was also shown that ibutilide (anti-arrhythmic drug, VGPC blocker) inhibited the activity of hERG potassium channels and delayed inward rectifier potassium and L-type calcium channels in Guinea pig cardiomyocytes [177]. The other antiarrhythmic drugs flecainide and quinidine work mainly by blocking the Nav1.5 sodium channel [178,179].…”
Section: Complex Activity Of Ion Channel Regulatorsmentioning
confidence: 99%