4.5 Article

Attraction of Rotors to the Pulmonary Veins in Paroxysmal Atrial Fibrillation: A Modeling Study

Journal

BIOPHYSICAL JOURNAL
Volume 106, Issue 8, Pages 1811-1821

Publisher

CELL PRESS
DOI: 10.1016/j.bpj.2014.02.030

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Categories

Funding

  1. National Heart, Lung, and Blood Institute [P01-11L039707, P01-HL08722, R01-BL118304]
  2. Coulter Foundation from the Biomedical Engineering Department (University of Michigan)
  3. Gelman Award from the Cardiovascular Division (University of Michigan)
  4. Leducq Foundation
  5. Faro Global MIONN-FGUVa [FG/US/0775/2009]
  6. PROMETEO grant [2010-093]
  7. Generalitat Valenciana [BEST/2011]
  8. Cardiovascular Protection Excellence Research microcluster, VLC-Campus (Spain)

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Maintenance of paroxysmal atrial fibrillation (AF) by fast rotors in the left atrium (LA) or at the pulmonary veins (PVs) is not fully understood. To gain insight into this dynamic and complex process, we studied the role of the heterogeneous distribution of transmembrane currents in the PVs and LA junction (PV-LAJ) in the localization of rotors in the PVs. We also investigated whether simple pacing protocols could be used to predict rotor drift in the PV-LAJ. Experimentally observed heterogeneities in 40, l(K1), l(Ks), l(kr), l(to) and l(caL) in the PV-LAJ were incorporated into two- and pseudo three-dimensional models of Courtemanche-Ramirez-Nattel-Kneller human atrial kinetics to simulate various conditions and investigate rotor drifting mechanisms. Spatial gradients in the currents resulted in shorter action potential duration, minimum diastolic potential that was less negative, and slower upstroke and conduction velocity for rotors in the PV region than in the LA. Rotors under such conditions drifted toward the PV and stabilized at the shortest action potential duration and less-excitable region, consistent with drift direction under intercellular coupling heterogeneities and regardless of the geometrical constraint in the PVs. Simulations with various l(K1) gradient conditions and current-voltage relationships substantiated its major role in the rotor drift. In our 1:1 pacing protocol, we found that among various action potential properties, only the minimum diastolic potential gradient was a rate-independent predictor of rotor drift direction. Consistent with experimental and clinical AF studies, simulations in an electrophysiologically heterogeneous model of the PV-LAJ showed rotor attraction toward the PV. Our simulations suggest that l(k1) heterogeneity is dominant compared to other currents in determining the drift direction through its impact on the excitability gradient. These results provide a believed novel framework for understanding the complex dynamics of rotors in AF.

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