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Complex Interactions Between the Sinoatrial Node and Atrium During Reentrant Arrhythmias in the Canine Heart

https://doi.org/10.1161/circulationaha.109.935288

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ar.1091410205openalex-snapshot

Anatomy of the human sinus node

inferredcites →https://doi.org/10.1002/ar.1091590406openalex-snapshot

Reconstruction of the human sinoatrial node

inferredcites →https://doi.org/10.1007/s11936-999-0021-9openalex-snapshot

Disorders of sinus function

inferredcites →https://doi.org/10.1016/0002-8703(83)90516-1openalex-snapshot

Interactions among the critical factors affecting sinus node function: The quantitative effects of the duration and frequency of atrial pacing and of vagal and sympathetic stimulation upon overdrive suppression of the sinus node

inferredcites →https://doi.org/10.1016/0002-9149(88)90945-9openalex-snapshot

Assessment by autonomic blockade of age-related changes of the sinus node function and autonomic regulation in sick sinus syndrome

inferredcites →https://doi.org/10.1016/0735-1097(92)90492-6openalex-snapshot

Sinus automaticity and sinoatrial conduction in severe symptomatic sick sinus syndrome

inferredcites →https://doi.org/10.1016/j.hrthm.2006.12.047openalex-snapshot

Application of blebbistatin as an excitation–contraction uncoupler for electrophysiologic study of rat and rabbit hearts

inferredcites →https://doi.org/10.1016/j.hrthm.2007.07.012openalex-snapshot

Near-infrared voltage-sensitive fluorescent dyes optimized for optical mapping in blood-perfused myocardium

inferredcites →https://doi.org/10.1016/j.jacc.2003.09.030openalex-snapshot

Roles of adrenergic and cholinergic stimulation in spontaneous atrial fibrillation in dogs

inferredcites →https://doi.org/10.1016/s0006-3495(01)76034-1openalex-snapshot

Visualizing Excitation Waves inside Cardiac Muscle Using Transillumination

inferredcites →https://doi.org/10.1016/s0008-6363(00)00135-8openalex-snapshot

The sinoatrial node, a heterogeneous pacemaker structure

inferredcites →https://doi.org/10.1016/s0735-1097(00)01039-1openalex-snapshot

Heart rate variability and early recurrence of atrial fibrillation after electrical cardioversion

inferredcites →https://doi.org/10.1046/j.1540-8167.2003.02229.xopenalex-snapshot

Abnormal Sinus Node Function in Clinical Arrhythmias

inferredcites →https://doi.org/10.1053/pcad.2002.130388openalex-snapshot

Structure and function of the sinus node, AV node and his bundle of the human heart: Part I—Structure

inferredcites →https://doi.org/10.1053/pcad.2003.1openalex-snapshot

Structure and function of the sinus node, AV node and his bundle of the human heart: Part II–function

inferredcites →https://doi.org/10.1097/00005344-199809000-00012openalex-snapshot

Local Cholinergic Suppression of Pacemaker Activity in the Rabbit Sinoatrial Node

inferredcites →https://doi.org/10.1111/j.1540-8167.2005.50145.xopenalex-snapshot

Sinus Node Region as an Ultimate Source Driving Chronic Atrial Fibrillation

inferredcites →https://doi.org/10.1111/j.1749-6632.1965.tb49390.xopenalex-snapshot

COMPARATIVE MORPHOLOGY OF THE CARDIAC CONDUCTION TISSUE IN ANIMALS*

inferredcites →https://doi.org/10.1126/science.275.5301.841openalex-snapshot

Paradoxical Improvement of Impulse Conduction in Cardiac Tissue by Partial Cellular Uncoupling

inferredcites →https://doi.org/10.1152/ajpheart.00022.2006openalex-snapshot

Postganglionic nerve stimulation induces temporal inhibition of excitability in rabbit sinoatrial node

inferredcites →https://doi.org/10.1152/ajpheart.1986.250.4.h630openalex-snapshot

Effect of canine cardiac nerves on heart rate, rhythm, and pacemaker location

inferredcites →https://doi.org/10.1152/ajpheart.1990.258.6.h1632openalex-snapshot

Effect of neurotransmitters on the activation sequence of the isolated atrium

inferredcites →https://doi.org/10.1152/ajpheart.1995.269.3.h877openalex-snapshot

Primary negativity does not predict dominant pacemaker location: implications for sinoatrial conduction

inferredcites →https://doi.org/10.1152/ajplegacy.1914.34.4.368openalex-snapshot

EXPERIMENTS ON THE ORIGIN AND PROPAGATION OF THE IMPULSE IN THE HEART

inferredcites →https://doi.org/10.1161/01.cir.0000121734.47409.aaopenalex-snapshot

Electrophysiological and Electroanatomic Characterization of the Atria in Sinus Node Disease

inferredcites →https://doi.org/10.1161/01.cir.101.2.194openalex-snapshot

Stable Microreentrant Sources as a Mechanism of Atrial Fibrillation in the Isolated Sheep Heart

inferredcites →https://doi.org/10.1161/01.cir.102.15.1807openalex-snapshot

Electrical Remodeling of the Atria Associated With Paroxysmal and Chronic Atrial Flutter

inferredcites →https://doi.org/10.1161/01.cir.16.1.20openalex-snapshot

Disease of the Sinoatrial Node Associated with Bradycardia, Asystole, Syncope, and Paroxysmal Atrial Fibrillation

inferredcites →https://doi.org/10.1161/01.cir.34.1.139openalex-snapshot

Comparative Ultrastructure of the Sinus Node in Man and Dog

inferredcites →https://doi.org/10.1161/01.cir.51.5.797openalex-snapshot

Corrected sinus node recovery time. Experimental physiologic and pathologic determinants.

inferredcites →https://doi.org/10.1161/01.cir.63.1.80openalex-snapshot

Coexistence of sick sinus rhythm and atrial flutter-fibrillation.

inferredcites →https://doi.org/10.1161/01.cir.64.4.832openalex-snapshot

Role of autonomic regulatory mechanism in sinoatrial conduction and sinus node automaticity in sick sinus syndrome.

inferredcites →https://doi.org/10.1161/01.cir.66.4.864openalex-snapshot

The sinus node electrogram in patients with and without sick sinus syndrome: techniques and correlation between directly measured and indirectly estimated sinoatrial conduction time.

inferredcites →https://doi.org/10.1161/01.cir.77.6.1221openalex-snapshot

Demonstration of a widely distributed atrial pacemaker complex in the human heart.

inferredcites →https://doi.org/10.1161/01.cir.86.1.263openalex-snapshot

Sinus node automaticity during atrial fibrillation in isolated rabbit hearts.

inferredcites →https://doi.org/10.1161/01.cir.86.1.334openalex-snapshot

Sinus node during atrial fibrillation. To beat or not to beat?

inferredcites →https://doi.org/10.1161/01.cir.94.11.2953openalex-snapshot

Pacing-Induced Chronic Atrial Fibrillation Impairs Sinus Node Function in Dogs

inferredcites →https://doi.org/10.1161/01.cir.98.1.54openalex-snapshot

High-Resolution, Three-dimensional Fluorescent Imaging Reveals Multilayer Conduction Pattern in the Atrioventricular Node

inferredcites →https://doi.org/10.1161/01.res.0000022854.95998.5copenalex-snapshot

Frequency-Dependent Breakdown of Wave Propagation Into Fibrillatory Conduction Across the Pectinate Muscle Network in the Isolated Sheep Right Atrium

inferredcites →https://doi.org/10.1161/01.res.27.1.129openalex-snapshot

Role of the Sinus Node in the Mechanism of Cholinergic Atrial Fibrillation

inferredcites →https://doi.org/10.1161/01.res.44.4.557openalex-snapshot

Direct demonstration of sinus node reentry in the rabbit heart.

inferredcites →https://doi.org/10.1161/01.res.71.5.1254openalex-snapshot

Cholinergically mediated tachyarrhythmias induced by a single extrastimulus in the isolated canine right atrium.

inferredcites →https://doi.org/10.1161/01.res.77.5.957openalex-snapshot

Relative Densities of Muscarinic Cholinergic and β-Adrenergic Receptors in the Canine Sinoatrial Node and Their Relation to Sites of Pacemaker Activity

inferredcites →https://doi.org/10.1161/circresaha.108.193193openalex-snapshot

Structural and Functional Evidence for Discrete Exit Pathways That Connect the Canine Sinoatrial Node and Atria

inferredcites →https://doi.org/10.1161/circresaha.109.209841openalex-snapshot

Mapping Cardiac Pacemaker Circuits

inferredcites →https://doi.org/10.1161/circulationaha.104.526210openalex-snapshot

Importance of Geometry and Refractory Period in Sustaining Atrial Fibrillation

inferredcites →https://doi.org/10.1161/circulationaha.104.527325openalex-snapshot

Altered Right Atrial Excitation and Propagation in Connexin40 Knockout Mice

inferredcites →https://doi.org/10.1161/circulationaha.107.733147openalex-snapshot

Optical Mapping of the Human Atrioventricular Junction

inferredcites →https://doi.org/10.1161/circulationaha.108.789677openalex-snapshot

Funny Current Downregulation and Sinus Node Dysfunction Associated With Atrial Tachyarrhythmia

inferredcites →https://doi.org/10.1196/annals.1341.029openalex-snapshot

Species‐ and Preparation‐Dependence of Stretch Effects on Sino‐Atrial Node Pacemaking

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4754538openalex-extracted

Sinoatrial Node Function and the Role of Sinoatrial Remodelling in the Typical Atrial Flutter Substrate

inferred← citeshttps://doi.org/10.1002/9781118481585.ch9openalex-snapshot

Optical Mapping of the Sinoatrial Node and Atrioventricular Node

inferred← citeshttps://doi.org/10.1007/978-3-031-33588-4_6openalex-snapshot

Unique Features of the Human Sinoatrial Node Structure, Function, and Arrhythmias: Mechanistic Insights from Integrated 3D Mapping Approaches

inferred← citeshttps://doi.org/10.1007/978-3-319-01643-6_5openalex-snapshot

Autonomic Regulation and Pathophysiological Remodelling

inferred← citeshttps://doi.org/10.1007/978-3-319-01643-6_7openalex-snapshot

Pacemaking and Autonomic Regulation in the 3D Sinoatrial Node and Atria

inferred← citeshttps://doi.org/10.1007/978-3-319-01643-6_9openalex-snapshot

Discussion

inferred← citeshttps://doi.org/10.1007/s00246-012-0249-0openalex-snapshot

Structure–Function Relationship in the Sinus and Atrioventricular Nodes

inferred← citeshttps://doi.org/10.1007/s00380-016-0922-yopenalex-snapshot

Acute ivabradine treatment reduces heart rate without increasing atrial fibrillation inducibility irrespective of underlying vagal activity in dogs

inferred← citeshttps://doi.org/10.1007/s00424-013-1337-6openalex-snapshot

A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00028-6openalex-snapshot

Mechanisms of Normal and Dysfunctional Sinoatrial Nodal Excitability and Propagation

inferred← citeshttps://doi.org/10.1016/b978-0-323-44733-1.00039-0openalex-snapshot

Pulmonary Vein Ganglia and the Neural Regulation of the Heart Rate

inferred← citeshttps://doi.org/10.1016/b978-1-4557-2856-5.00039-xopenalex-snapshot

Pulmonary Vein Ganglia and the Neural Regulation of the Heart Rate

inferred← citeshttps://doi.org/10.1016/j.arcmed.2014.04.005openalex-snapshot

Relationship Between Two Arrhythmias: Sinus Node Dysfunction and Atrial Fibrillation

inferred← citeshttps://doi.org/10.1016/j.bspc.2021.102460openalex-snapshot

Prediction of atrial fibrillation inducibility using spatiotemporal activation analysis combined with network mapping

inferred← citeshttps://doi.org/10.1016/j.cjca.2011.08.119openalex-snapshot

Characteristics of Fibrillatory Activities During Spontaneous Termination of Paroxysmal Atrial Fibrillation: New Insight From High-Density Right Atrium Frequency Mapping

inferred← citeshttps://doi.org/10.1016/j.hrthm.2010.10.018openalex-snapshot

Termination of sustained atrial flutter and fibrillation using low-voltage multiple-shock therapy

inferred← citeshttps://doi.org/10.1016/j.hrthm.2012.09.012openalex-snapshot

Tachy-brady arrhythmias: The critical role of adenosine-induced sinoatrial conduction block in post-tachycardia pauses

inferred← citeshttps://doi.org/10.1016/j.hrthm.2022.08.039openalex-snapshot

Three-dimensional functional anatomy of the human sinoatrial node for epicardial and endocardial mapping and ablation

inferred← citeshttps://doi.org/10.1016/j.hrthm.2024.10.003openalex-snapshot

Sinoatrial node function and the role of sinoatrial conduction in the typical atrial flutter substrate

inferred← citeshttps://doi.org/10.1016/j.ijcard.2015.10.004openalex-snapshot

Renal failure induces atrial arrhythmogenesis from discrepant electrophysiological remodeling and calcium regulation in pulmonary veins, sinoatrial node, and atria

inferred← citeshttps://doi.org/10.1016/j.ijcard.2016.07.027openalex-snapshot

Gap junction modifiers regulate electrical activities of the sinoatrial node and pulmonary vein: Therapeutic implications in atrial arrhythmogenesis

inferred← citeshttps://doi.org/10.1016/j.jacbts.2018.08.004openalex-snapshot

Natriuretic Peptide Receptor-C Protects Against Angiotensin II-Mediated Sinoatrial Node Disease in Mice

inferred← citeshttps://doi.org/10.1016/j.jacep.2020.09.012openalex-snapshot

Evidence of Superior and Inferior Sinoatrial Nodes in the Mammalian Heart

inferred← citeshttps://doi.org/10.1016/j.jacep.2020.11.017openalex-snapshot

Endo-Epicardial Mapping of In Vivo Human Sinoatrial Node Activity

inferred← citeshttps://doi.org/10.1016/j.jtbi.2018.09.023openalex-snapshot

Analysis of heterogeneous cardiac pacemaker tissue models and traveling wave dynamics

inferred← citeshttps://doi.org/10.1016/j.jvc.2018.10.004openalex-snapshot

Canine and human sinoatrial node: differences and similarities in the structure, function, molecular profiles, and arrhythmia

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2015.12.011openalex-snapshot

Human sinoatrial node structure: 3D microanatomy of sinoatrial conduction pathways

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2022.10.008openalex-snapshot

The virtual sinoatrial node: What did computational models tell us about cardiac pacemaking?

inferred← citeshttps://doi.org/10.1016/j.tvjl.2021.105650openalex-snapshot

Optimizing single-chamber pacing in dogs Part 1: Rate determinations, rate interventions and hysteresis

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Insights into sinus arrhythmia of the dog: Acetylcholine perfusion of canine right atrium results in beat-to-beat patterns that mimic sinus arrhythmia supporting exit block in the sinoatrial conduction pathways

inferred← citeshttps://doi.org/10.1016/j.yjmcc.2011.04.016openalex-snapshot

Effects of KATP channel openers diazoxide and pinacidil in coronary-perfused atria and ventricles from failing and non-failing human hearts

inferred← citeshttps://doi.org/10.1038/s41422-021-00499-5openalex-snapshot

Identification of an endogenous glutamatergic transmitter system controlling excitability and conductivity of atrial cardiomyocytes

inferred← citeshttps://doi.org/10.1038/s41598-019-57246-5openalex-snapshot

In silico study of the effects of anti-arrhythmic drug treatment on sinoatrial node function for patients with atrial fibrillation

inferred← citeshttps://doi.org/10.1080/24699322.2016.1240307openalex-snapshot

Activities of the sinus node pacemaking during the simulated atrial reentry

inferred← citeshttps://doi.org/10.1088/1742-6596/1903/1/012062openalex-snapshot

Modelling Study on Acetylcholine Regulation to the Pacemaker Ability of the Sinoatrial Tissue in Hearts

inferred← citeshttps://doi.org/10.1093/eurheartj/ehs391openalex-snapshot

Altered HCN4 channel C-linker interaction is associated with familial tachycardia–bradycardia syndrome and atrial fibrillation

inferred← citeshttps://doi.org/10.1093/eurheartj/eht452openalex-snapshot

Calsequestrin 2 deletion causes sinoatrial node dysfunction and atrial arrhythmias associated with altered sarcoplasmic reticulum calcium cycling and degenerative fibrosis within the mouse atrial pacemaker complex1

inferred← citeshttps://doi.org/10.1101/2024.12.18.629224openalex-snapshot

Sinoatrial node impulses emerge from incessant, unique, kinetic transitions in disordered local calcium dynamics

inferred← citeshttps://doi.org/10.1109/cic.2015.7411049openalex-snapshot

Simulation of the pacemaker created from the cardiomyocytes by reducing inward-rectifier K+ current

inferred← citeshttps://doi.org/10.1111/jvim.17071openalex-snapshot

Use of machine learning and Poincaré density grid in the diagnosis of sinus node dysfunction caused by sinoatrial conduction block in dogs

inferred← citeshttps://doi.org/10.1113/jp272979openalex-snapshot

The impacts of age and frailty on heart rate and sinoatrial node function

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Effects of natriuretic peptides on electrical conduction in the sinoatrial node and atrial myocardium of the heart

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Impaired sinoatrial node function and increased susceptibility to atrial fibrillation in mice lacking natriuretic peptide receptor C

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Quantification of fiber orientation in the canine atrial pacemaker complex using optical coherence tomography

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Redundant and diverse intranodal pacemakers and conduction pathways protect the human sinoatrial node from failure

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Adverse Cardiac Structural Remodelling Induced by Cholinergic Atrial Fibrillation Regardless of Estrogen Deficiency in Rats

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Onset of atrial arrhythmias elicited by autonomic modulation of rabbit sinoatrial node activity: a modeling study

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Chronotropic Modulation of the Source-Sink Relationship of Sinoatrial-Atrial Impulse Conduction and Its Significance to Initiation of AF: A One-Dimensional Model Study

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Computational Modeling of Electrical Cell-to-cell Interactions in Cardiac Tissue: Applications to Model Parameter Selection and Pacemaker Function

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Fibrosis, Electrics and Genetics

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Mechanistic insight into the functional role of human sinoatrial node conduction pathways and pacemaker compartments heterogeneity: A computer model analysis

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Association of Sick Sinus Syndrome with Incident Cardiovascular Disease and Mortality: The Atherosclerosis Risk in Communities Study and Cardiovascular Health Study

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Computational assessment of the functional role of sinoatrial node exit pathways in the human heart

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Regional heterogeneity of right atrial repolarization. Monophasic action potential mapping in swine

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Ca2+ Signaling and Heart Rhythm

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Fibrosis: a structural modulator of sinoatrial node physiology and dysfunction

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The involvement of TRPC3 channels in sinoatrial arrhythmias

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