Endothelin-1 modulates the arrhythmogenic activity of pulmonary veins

Ameya R. Udyavar, Yao Chang Chen, Yi Jen Chen, Chen Chuan Cheng, Cheng I. Lin, Shih Ann Chen

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Effect of Endothelin-1 on Pulmonary Veins. Objective: Endothelin-1 has important cardiovascular effects and is activated during atrial fibrillation. Pulmonary veins (PVs) play a critical role in the pathophysiology of atrial fibrillation. The aim of this study was to evaluate whether endothelin-1 affects PV arrhythmogenic activity. Methods: Conventional microelectrodes were used to record the action potentials (APs) and contractility in isolated rabbit PV tissue specimens before and after the administration of endothelin-1 (0.1, 1, 10 nM). The ionic currents of isolated PV cardiomyocytes were investigated before and after the administration of endothelin-1 (10 nM) through whole-cell patch clamps. Results: In the tissue preparation, endothelin-1 (1, 10 nM) concentration dependently shortened the AP duration and decreased the PV firing rates. Endothelin-1 (10 nM) decreased the resting membrane potential. Endothelin-1 (0.1, 1, 10 nM) decreased the contractility and increased the resting diastolic tension. In single PV cardiomyocytes, endothelin-1 (10 nM) decreased the PV firing rates from 2.7 ± 1.0 Hz to 0.8 ± 0.5 Hz (n = 16). BQ-485 (100 μM, endothelin-1 type A receptor blocker) reversed and prevented the chrono-inhibitory effects of endothelin-1 (10 nM). Endothelin-1 (10 nM) reduced the L-type calcium currents, transient outward currents, delayed rectifier currents, transient inward currents, and sodium-calcium exchanger currents in the PV cardiomyocytes with and without pacemaker activity. Endothelin-1 (10 nM) increased the inward rectifier potassium current, hyperpolarization-induced pacemaker current, and the sustained outward potassium current in PV cardiomyocytes with and without pacemaker activity. Conclusion: Endothelin-1 may have an antiarrhythmic potential through its direct electrophysiological effects on the PV cardiomyocytes and its action on multiple ionic currents.

Original languageEnglish
Pages (from-to)285-292
Number of pages8
JournalJournal of Cardiovascular Electrophysiology
Volume19
Issue number3
DOIs
Publication statusPublished - Mar 2008

Fingerprint

Pulmonary Veins
Endothelin-1
Cardiac Myocytes
Atrial Fibrillation
Action Potentials
Potassium
Sodium-Calcium Exchanger
Endothelin A Receptors
Microelectrodes
Membrane Potentials

Keywords

  • Atrial fibrillation
  • Endothelin-1
  • Ion currents
  • Pulmonary veins

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology

Cite this

Endothelin-1 modulates the arrhythmogenic activity of pulmonary veins. / Udyavar, Ameya R.; Chen, Yao Chang; Chen, Yi Jen; Cheng, Chen Chuan; Lin, Cheng I.; Chen, Shih Ann.

In: Journal of Cardiovascular Electrophysiology, Vol. 19, No. 3, 03.2008, p. 285-292.

Research output: Contribution to journalArticle

Udyavar, Ameya R. ; Chen, Yao Chang ; Chen, Yi Jen ; Cheng, Chen Chuan ; Lin, Cheng I. ; Chen, Shih Ann. / Endothelin-1 modulates the arrhythmogenic activity of pulmonary veins. In: Journal of Cardiovascular Electrophysiology. 2008 ; Vol. 19, No. 3. pp. 285-292.
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AB - Effect of Endothelin-1 on Pulmonary Veins. Objective: Endothelin-1 has important cardiovascular effects and is activated during atrial fibrillation. Pulmonary veins (PVs) play a critical role in the pathophysiology of atrial fibrillation. The aim of this study was to evaluate whether endothelin-1 affects PV arrhythmogenic activity. Methods: Conventional microelectrodes were used to record the action potentials (APs) and contractility in isolated rabbit PV tissue specimens before and after the administration of endothelin-1 (0.1, 1, 10 nM). The ionic currents of isolated PV cardiomyocytes were investigated before and after the administration of endothelin-1 (10 nM) through whole-cell patch clamps. Results: In the tissue preparation, endothelin-1 (1, 10 nM) concentration dependently shortened the AP duration and decreased the PV firing rates. Endothelin-1 (10 nM) decreased the resting membrane potential. Endothelin-1 (0.1, 1, 10 nM) decreased the contractility and increased the resting diastolic tension. In single PV cardiomyocytes, endothelin-1 (10 nM) decreased the PV firing rates from 2.7 ± 1.0 Hz to 0.8 ± 0.5 Hz (n = 16). BQ-485 (100 μM, endothelin-1 type A receptor blocker) reversed and prevented the chrono-inhibitory effects of endothelin-1 (10 nM). Endothelin-1 (10 nM) reduced the L-type calcium currents, transient outward currents, delayed rectifier currents, transient inward currents, and sodium-calcium exchanger currents in the PV cardiomyocytes with and without pacemaker activity. Endothelin-1 (10 nM) increased the inward rectifier potassium current, hyperpolarization-induced pacemaker current, and the sustained outward potassium current in PV cardiomyocytes with and without pacemaker activity. Conclusion: Endothelin-1 may have an antiarrhythmic potential through its direct electrophysiological effects on the PV cardiomyocytes and its action on multiple ionic currents.

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