Triggered firing in pulmonary veins initiated by in vitro autonomic nerve stimulation

Heart Rhythm. 2005 Jun;2(6):624-31. doi: 10.1016/j.hrthm.2005.02.012.

Abstract

Background: Rapid firing within pulmonary vein sleeves frequently initiates atrial fibrillation. The role of the autonomic nervous system in facilitating spontaneous firing is unknown.

Objectives: The purpose of this study was to determine if autonomic nerve stimulation within canine atrium and pulmonary vein sleeves initiates arrhythmia formation.

Methods: Extracellular bipolar and intracellular microelectrode recordings were obtained from isolated superfused canine pulmonary veins (N = 28) and right atrium (N = 5) during local autonomic nerve stimulation.

Results: Autonomic nerve stimulation decreased pulmonary vein sleeve action potential duration (APD90 = 160 +/- 17 to 92 +/- 24 ms; P < .01) and initiated rapid (782 +/- 158 bpm) firing from early afterdepolarizations in 22 of 28 pulmonary vein preparations. The initial spontaneous beat had a coupling interval of 97 +/- 26 ms. Failure to induce arrhythmia was associated with a failure to shorten APD90 (151 +/- 18 to 142 +/- 8 ms; P = .39). Muscarinic receptor blockade (atropine: 3.2 x 10(-8) M) prevented APD90 shortening in 8 of 8 preparations and suppressed firing in 6 of 8 preparations, whereas beta1-adrenergic receptor blockade (atenolol: 3.2 x 10(-8) M) suppressed firing in 8 of 8 preparations. Suppression of the Ca transient with ryanodine (10(-5) M) completely suppressed firing in 6 of 6 preparations. Inhibition of forward Na/Ca exchange by a transient increase in [Ca+2]o completely suppressed firing in 4 of 6 preparations. The same stimulus trains produce atropine-suppressed APD90 shortening in superfused right atrial free wall but fail to produce triggered arrhythmia.

Conclusions: The data demonstrate triggered firing within canine pulmonary veins with combined parasympathetic and sympathetic nerve stimulation. Both an enhanced Ca transient and increased Na/Ca exchange may be required for arrhythmia formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atenolol / pharmacology
  • Atrial Fibrillation / physiopathology*
  • Atropine / pharmacology
  • Autonomic Nervous System / physiology*
  • Dogs
  • Electric Stimulation
  • Electrophysiologic Techniques, Cardiac
  • Heart Atria / physiopathology
  • Male
  • Pulmonary Veins / physiology*
  • Ryanodine / pharmacology
  • Tetrodotoxin / pharmacology

Substances

  • Ryanodine
  • Tetrodotoxin
  • Atenolol
  • Atropine