Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation

Introduction: We assessed the effects of pilsicainide, a pure Na+ channel blocker, and nifekalant, a pure rapid delayed rectifier potassium current (IKr) blocker, on the electrophysiological characteristics within the pulmonary vein (PV) and at the PV-left atrial (LA) junction. Methods and Results:...

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Main Authors: Tomoo Yasuda, MD, Koichiro Kumagai, MD, Masahiro Ogawa, MD, Hideko Nakashima, MD, Bo Zhang, PhD, Shin-ichiro Miura, MD, Keijiro Saku, MD
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Journal of Arrhythmia
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1880427610800250
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spelling doaj-a6d5e08d65f84a7fb4f8ea4fa6b2122e2020-11-25T02:34:02ZengWileyJournal of Arrhythmia1880-42762010-01-0126425926610.1016/S1880-4276(10)80025-0Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial FibrillationTomoo Yasuda, MDKoichiro Kumagai, MDMasahiro Ogawa, MDHideko Nakashima, MDBo Zhang, PhDShin-ichiro Miura, MDKeijiro Saku, MDIntroduction: We assessed the effects of pilsicainide, a pure Na+ channel blocker, and nifekalant, a pure rapid delayed rectifier potassium current (IKr) blocker, on the electrophysiological characteristics within the pulmonary vein (PV) and at the PV-left atrial (LA) junction. Methods and Results: We used a basket catheter for PV mapping in 38 patients with paroxysmal atrial fibrillation (AF). Programmed stimulation was performed in the distal PV and PV-LA junction before and after the infusion of pilsicainide (1 mg/kg; n = 24) or nifekalant (0.3 mg/kg; n = 14). Both drugs significantly prolonged the effective refractory period (ERP) of the distal PV and PV-LA junction. Pilsicainide significantly decreased the ERP heterogeneity of the PV and PV-LA junction (36 ± 43 vs. 9 ± 60 ms, P < 0:05). In contrast, nifekalant significantly increased the ERP heterogeneity of the PV and PV-LA junction (from 38 ± 34 to 60 ± 46 ms, P < 0:01). Pilsicainide significantly prolonged the conduction time (S1-A1) from the distal PV to the PV-LA junction (from 42 ± 12 to 63 ± 26 ms, P < 0:001), whereas this did not change with nifekalant. Conclusions: In AF patients, pilsicainide has antiarrhythmic effects mainly on the distal PV by modifying the ERP and conduction properties. In contrast, nifekalant has antiarrhythmic effects mainly on the PV-LA junction by modifying the ERP.http://www.sciencedirect.com/science/article/pii/S1880427610800250NifekalantPulmonary veinAtrial fibrillationPilsicainideElectrophysiology
collection DOAJ
language English
format Article
sources DOAJ
author Tomoo Yasuda, MD
Koichiro Kumagai, MD
Masahiro Ogawa, MD
Hideko Nakashima, MD
Bo Zhang, PhD
Shin-ichiro Miura, MD
Keijiro Saku, MD
spellingShingle Tomoo Yasuda, MD
Koichiro Kumagai, MD
Masahiro Ogawa, MD
Hideko Nakashima, MD
Bo Zhang, PhD
Shin-ichiro Miura, MD
Keijiro Saku, MD
Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
Journal of Arrhythmia
Nifekalant
Pulmonary vein
Atrial fibrillation
Pilsicainide
Electrophysiology
author_facet Tomoo Yasuda, MD
Koichiro Kumagai, MD
Masahiro Ogawa, MD
Hideko Nakashima, MD
Bo Zhang, PhD
Shin-ichiro Miura, MD
Keijiro Saku, MD
author_sort Tomoo Yasuda, MD
title Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
title_short Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
title_full Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
title_fullStr Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
title_full_unstemmed Comparison of the Effects of Na+ and K+ Channel Blockers on the Electrophysiological Properties of the Pulmonary Veins in Patients with Atrial Fibrillation
title_sort comparison of the effects of na+ and k+ channel blockers on the electrophysiological properties of the pulmonary veins in patients with atrial fibrillation
publisher Wiley
series Journal of Arrhythmia
issn 1880-4276
publishDate 2010-01-01
description Introduction: We assessed the effects of pilsicainide, a pure Na+ channel blocker, and nifekalant, a pure rapid delayed rectifier potassium current (IKr) blocker, on the electrophysiological characteristics within the pulmonary vein (PV) and at the PV-left atrial (LA) junction. Methods and Results: We used a basket catheter for PV mapping in 38 patients with paroxysmal atrial fibrillation (AF). Programmed stimulation was performed in the distal PV and PV-LA junction before and after the infusion of pilsicainide (1 mg/kg; n = 24) or nifekalant (0.3 mg/kg; n = 14). Both drugs significantly prolonged the effective refractory period (ERP) of the distal PV and PV-LA junction. Pilsicainide significantly decreased the ERP heterogeneity of the PV and PV-LA junction (36 ± 43 vs. 9 ± 60 ms, P < 0:05). In contrast, nifekalant significantly increased the ERP heterogeneity of the PV and PV-LA junction (from 38 ± 34 to 60 ± 46 ms, P < 0:01). Pilsicainide significantly prolonged the conduction time (S1-A1) from the distal PV to the PV-LA junction (from 42 ± 12 to 63 ± 26 ms, P < 0:001), whereas this did not change with nifekalant. Conclusions: In AF patients, pilsicainide has antiarrhythmic effects mainly on the distal PV by modifying the ERP and conduction properties. In contrast, nifekalant has antiarrhythmic effects mainly on the PV-LA junction by modifying the ERP.
topic Nifekalant
Pulmonary vein
Atrial fibrillation
Pilsicainide
Electrophysiology
url http://www.sciencedirect.com/science/article/pii/S1880427610800250
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