A Regional Reduction in Ito and IKACh in the Murine Posterior Left Atrial Myocardium Is Associated with Action Potential Prolongation and Increased Ectopic Activity

Background The left atrial posterior wall (LAPW) is potentially an important area for the development and maintenance of atrial fibrillation. We assessed whether there are regional electrical differences throughout the murine left atrial myocardium that could underlie regional differences in arrhythmia susceptibility. Methods We used high-resolution optical mapping and sharp microelectrode recordings to quantify regional differences in electrical activation and repolarisation within the intact, superfused murine left atrium and quantified regional ion channel mRNA expression by Taqman Low Density Array. We also performed selected cellular electrophysiology experiments to validate regional differences in ion channel function. Results Spontaneous ectopic activity was observed during sustained 1Hz pacing in 10/19 intact LA and this was abolished following resection of LAPW (0/19 resected LA, P<0.001). The source of the ectopic activity was the LAPW myocardium, distinct from the pulmonary vein sleeve and LAA, determined by optical mapping. Overall, LAPW action potentials (APs) were ca. 40% longer than the LAA and this region displayed more APD heterogeneity. mRNA expression of Kcna4, Kcnj3 and Kcnj5 was lower in the LAPW myocardium than in the LAA. Cardiomyocytes isolated from the LAPW had decreased Ito and a reduced IKACh current density at both positive and negative test potentials. Conclusions The murine LAPW myocardium has a different electrical phenotype and ion channel mRNA expression profile compared with other regions of the LA, and this is associated with increased ectopic activity. If similar regional electrical differences are present in the human LA, then the LAPW may be a potential future target for treatment of atrial fibrillation.

[1]  L. Zon,et al.  Chamber identity programs drive early functional partitioning of the heart , 2015, Nature Communications.

[2]  A. Glukhov,et al.  Electrophysiological Characteristics, Rhythm, Disturbances and Conduction Discontinuities Under Autonomic Stimulation in the Rat Pulmonary Vein Myocardium , 2015, Journal of cardiovascular electrophysiology.

[3]  P. Sanders,et al.  Acute Atrial Stretch Results in Conduction Slowing and Complex Signals at the Pulmonary Vein to Left Atrial Junction: Insights Into the Mechanism of Pulmonary Vein Arrhythmogenesis , 2014, Circulation. Arrhythmia and electrophysiology.

[4]  Hamid Dehghani,et al.  An automated system using spatial oversampling for optical mapping in murine atria. Development and validation with monophasic and transmembrane action potentials , 2014, Progress in biophysics and molecular biology.

[5]  Jussi T. Koivumäki,et al.  Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant. , 2014, American journal of physiology. Heart and circulatory physiology.

[6]  D. Ypey,et al.  Atrium-Specific Kir3.x Determines Inducibility, Dynamics, and Termination of Fibrillation by Regulating Restitution-Driven Alternans , 2013, Circulation.

[7]  M. Buckingham,et al.  Asymmetric Fate of the Posterior Part of the Second Heart Field Results in Unexpected Left/Right Contributions to Both Poles of the Heart , 2012, Circulation research.

[8]  Niels Voigt,et al.  Recent advances in the molecular pathophysiology of atrial fibrillation. , 2011, The Journal of clinical investigation.

[9]  U. Ravens,et al.  Ultra-rapid delayed rectifier channels: molecular basis and therapeutic implications. , 2011, Cardiovascular research.

[10]  Baofeng Yang,et al.  Characterization and Comparison of Na+, K+ and Ca2+ Currents Between Myocytes from Human Atrial Right Appendage and Atrial Septum , 2008, Cellular Physiology and Biochemistry.

[11]  M. Buckingham,et al.  Atrial myocardium derives from the posterior region of the second heart field, which acquires left-right identity as Pitx2c is expressed , 2008, Development.

[12]  Richard P Harvey,et al.  Pitx2c and Nkx2-5 Are Required for the Formation and Identity of the Pulmonary Myocardium , 2007, Circulation research.

[13]  Jason Ng,et al.  Unique autonomic profile of the pulmonary veins and posterior left atrium. , 2007, Journal of the American College of Cardiology.

[14]  Hong Liu,et al.  Sodium-calcium exchange initiated by the Ca2+ transient: an arrhythmia trigger within pulmonary veins. , 2006, Journal of the American College of Cardiology.

[15]  H. Karagueuzian,et al.  Heterogeneous pulmonary vein myocardial cell repolarization implications for reentry and triggered activity. , 2005, Heart rhythm.

[16]  Prashanthan Sanders,et al.  Spectral Analysis Identifies Sites of High-Frequency Activity Maintaining Atrial Fibrillation in Humans , 2005, Circulation.

[17]  OmerBerenfeld,et al.  Spectral Analysis Identifies Sites of High-Frequency Activity Maintaining Atrial Fibrillation in Humans , 2005 .

[18]  W. Giles,et al.  Heterogeneity of action potential durations in isolated mouse left and right atria recorded using voltage-sensitive dye mapping. , 2004, American journal of physiology. Heart and circulatory physiology.

[19]  Stanley Nattel,et al.  The effect of vagally induced dispersion of action potential duration on atrial arrhythmogenesis. , 2004, Heart rhythm.

[20]  Masahiro Ogawa,et al.  Electrophysiologic properties of pulmonary veins assessed using a multielectrode basket catheter. , 2004, Journal of the American College of Cardiology.

[21]  C. Antzelevitch,et al.  Transmembrane action potential heterogeneity in the canine isolated arterially perfused right atrium: effect of IKr and IKur/Ito block. , 2004, American journal of physiology. Heart and circulatory physiology.

[22]  M. Hocini,et al.  Electrical Disconnection of the Coronary Sinus by Radiofrequency Catheter Ablation to Isolate a Trigger of Atrial Fibrillation , 2004, Journal of cardiovascular electrophysiology.

[23]  W. Giles,et al.  Electrophysiological evidence for a gradient of G protein‐gated K+ current in adult mouse atria , 2003, British journal of pharmacology.

[24]  Wei-Shiang Lin,et al.  Catheter Ablation of Paroxysmal Atrial Fibrillation Initiated by Non–Pulmonary Vein Ectopy , 2003, Circulation.

[25]  M. Mansour,et al.  Mother rotors and fibrillatory conduction: a mechanism of atrial fibrillation. , 2002, Cardiovascular research.

[26]  M. Yamada The role of muscarinic K(+) channels in the negative chronotropic effect of a muscarinic agonist. , 2002, The Journal of pharmacology and experimental therapeutics.

[27]  M. Richardson,et al.  Development of the human pulmonary vein and its incorporation in the morphologically left atrium , 2001, Cardiology in the Young.

[28]  S Nattel,et al.  Potential Ionic Mechanism for Repolarization Differences Between Canine Right and Left Atrium , 2001, Circulation research.

[29]  A. Camm,et al.  Left atrial appendage: structure, function, and role in thromboembolism , 1999, Heart.

[30]  S Nattel,et al.  Ionic mechanisms of regional action potential heterogeneity in the canine right atrium. , 1998, Circulation research.

[31]  StanleyNattel,et al.  Ionic Mechanisms of Regional Action Potential Heterogeneity in the Canine Right Atrium , 1998 .

[32]  J Clémenty,et al.  Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. , 1998, The New England journal of medicine.

[33]  M S Spach,et al.  Interaction of Inhomogeneities of Repolarization With Anisotropic Propagation in Dog Atria: Mechanism for Both Preventing and Initiating Reentry , 1989, Circulation research.

[34]  G. Fishman,et al.  Scn1b deletion leads to increased tetrodotoxin-sensitive sodium current, altered intracellular calcium homeostasis and arrhythmias in murine hearts. , 2014, The Journal of physiology.

[35]  Charles Peskin,et al.  Arrhythmogenic consequences of action potential duration gradients in the atria. , 2011, The Canadian journal of cardiology.