2005Unpublished venueRequires access

Electrophysiological Effect of Resveratrol on Pacemaker Cells in Sinoatrial Node of Rabbits

Zheng Liu, Qingshan Wang, Juan Zhao, Liping Zhang, Fuwei Wang, Ming Li

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Abstract

AIM In order to investigate whether resveratrol can he used as a kind of antiarrhythmic drug, the electrophysiological effect of resveratrol on pacemaker cells in sinoatrial node was studied. METHODS Using intracellular microelectrode technique to record the action potential of pacemaker cells in sinoatrial node of rabbits, RESULTS Resveratrol (30-120μmol•L^(-1)) significantly decreased amplitude of action potential, maximal rate of depolarization (V(subscript max)), velocity of diastolic (phase 4) depolarization and rate of pacemaker firing, but did not affect maximal diastolic potential and duration of 90% repolarization of action potential. Pretreatment with L-type calcium channel agonist Bay-K-8644 (0.5μmol•L^(-1)) 10mim antagonized the effect of resveratrol (60μmol•L^(-1)). While applying cesium chloride (2mmol•L^(-1)), a hyper-polarization-activated current blocker, adding tetraethylammonium chloride (20mmol•L^(-1)), a potassium channel antagonist, or applying L-NAME (0.5mmol•L^(-1)), a NO synthase inhibitor, had no significantly influence on the electrophysiological effects of resveratrol. CONCLUSION Resveratrol exerts inhibitory electrophysiological effects on pacemaker cells in sinoatrial node of rabbits, which may be due to reduction in calcium influx via a NO-independent manner.

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AIM In order to investigate whether resveratrol can he used as a kind of antiarrhythmic drug, the electrophysiological effect of resveratrol on pacemaker cells in sinoatrial node was studied. METHODS Using intracellular microelectrode technique to record the action potential of pacemaker cells in sinoatrial node of rabbits, RESULTS Resveratrol (30-120μmol•L^(-1)) significantly decreased amplitude of action potential, maximal rate of depolarization (V(subscript max)), velocity of diastolic (phase 4) depolarization and rate of pacemaker firing, but did not affect maximal diastolic potential and duration of 90% repolarization of action potential. Pretreatment with L-type calcium channel agonist Bay-K-8644 (0.5μmol•L^(-1)) 10mim antagonized the effect of resveratrol (60μmol•L^(-1)). While applying cesium chloride (2mmol•L^(-1)), a hyper-polarization-activated current blocker, adding tetraethylammonium chloride (20mmol•L^(-1)), a potassium channel antagonist, or applying L-NAME (0.5mmol•L^(-1)), a NO synthase inhibitor, had no significantly influence on the electrophysiological effects of resveratrol. CONCLUSION Resveratrol exerts inhibitory electrophysiological effects on pacemaker cells in sinoatrial node of rabbits, which may be due to reduction in calcium influx via a NO-independent manner.

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Available abstract

AIM In order to investigate whether resveratrol can he used as a kind of antiarrhythmic drug, the electrophysiological effect of resveratrol on pacemaker cells in sinoatrial node was studied. METHODS Using intracellular microelectrode technique to record the action potential of pacemaker cells in sinoatrial node of rabbits, RESULTS Resveratrol (30-120μmol•L^(-1)) significantly decreased amplitude of action potential, maximal rate of depolarization (V(subscript max)), velocity of diastolic (phase 4) depolarization and rate of pacemaker firing, but did not affect maximal diastolic potential and duration of 90% repolarization of action potential. Pretreatment with L-type calcium channel agonist Bay-K-8644 (0.5μmol•L^(-1)) 10mim antagonized the effect of resveratrol (60μmol•L^(-1)). While applying cesium chloride (2mmol•L^(-1)), a hyper-polarization-activated current blocker, adding tetraethylammonium chloride (20mmol•L^(-1)), a potassium channel antagonist, or applying L-NAME (0.5mmol•L^(-1)), a NO synthase inhibitor, had no significantly influence on the electrophysiological effects of resveratrol. CONCLUSION Resveratrol exerts inhibitory electrophysiological effects on pacemaker cells in sinoatrial node of rabbits, which may be due to reduction in calcium influx via a NO-independent manner.

Key concepts: Sinoatrial node, Electrophysiology, Diastolic depolarization, Chemistry, Depolarization, Bay K8644, Pacemaker potential, Resveratrol

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