Related Experiment Video
Updated: May 29, 2026

Laser-Induced Action Potential-Like Measurements of Cardiomyocytes on Microelectrode Arrays for Increased Predictivity of Safety Pharmacology
Published on: September 13, 2022
Distinct pharmacologic substrate in lidocaine-sensitive, repetitive atrial tachycardia
Pablo A Chiale1, Luciano Faivelis, Hugo A Garro
1Centro de Arritmias Cardíacas, Goverment of Buenos Aires City, Buenos Aires, Argentina. pablochiale@fibertel.com.ar
Abstract:
Lidocaine-sensitive, repetitive atrial tachycardia is an uncommon arrhythmia. The electrophysiologic substrate is still unknown, and the pharmacologic responses have not been fully explored. The aim of this study was to investigate the effects of intravenous adenosine and verapamil in patients with lidocaine-sensitive atrial tachycardia. In 9 patients with repetitive uniform atrial tachycardia, the response to intravenous adenosine (12 mg), lidocaine (1 mg/kg body weight), and verapamil (10 mg) were sequentially investigated. Simultaneous 12-lead electrocardiogram (ECG) was recorded at baseline and continuously monitored thereafter. Tracings were obtained at regularly timed intervals right after the administration of each drug to evaluate changes in the arrhythmia characteristics. Repetitive atrial tachycardia was abolished by intravenous lidocaine in the 9 patients within the first 2 minutes after the end of injection. Adenosine suppressed the arrhythmia in 2 patients and shortened the runs of atrial ectopic activity in 1 patient, while verapamil was effective in 2 patients, 1 of them insensitive to adenosine and the other 1 sensitive to this agent. In 5 patients, the arrhythmia was abolished by radiofrequency ablation at different sites of the right atrium. Lidocaine-sensitive atrial tachycardia may eventually be also suppressed by adenosine and/or verapamil. This suggests that this enigmatic arrhythmia may be caused by different underlying electrophysiologic substrates and that at least in some cases, delayed afterdepolarizations seem to play a determining role.
Insights
Lidocaine effectively treats repetitive atrial tachycardia. Adenosine and verapamil show varied responses, suggesting diverse electrophysiologic substrates and a role for delayed afterdepolarizations in this uncommon arrhythmia.
Area of Science:
- Cardiology
- Electrophysiology
- Pharmacology
Background:
- Repetitive atrial tachycardia (RAT) is an uncommon arrhythmia with an unknown electrophysiologic substrate.
- Pharmacologic responses of RAT have not been fully explored.
Purpose of the Study:
- To investigate the effects of intravenous adenosine and verapamil in patients with lidocaine-sensitive atrial tachycardia.
- To explore potential underlying electrophysiologic mechanisms of RAT.
Main Methods:
- Sequential administration of intravenous adenosine (12 mg), lidocaine (1 mg/kg), and verapamil (10 mg) in 9 patients with RAT.
- Simultaneous 12-lead electrocardiogram (ECG) monitoring and analysis of arrhythmia characteristics post-drug administration.
- Radiofrequency ablation was performed in 5 patients.
Main Results:
- Lidocaine abolished RAT in all 9 patients within 2 minutes.
- Adenosine suppressed RAT in 2 patients; verapamil was effective in 2 patients.
- Radiofrequency ablation successfully abolished the arrhythmia in 5 patients.
Conclusions:
- Lidocaine-sensitive RAT can be suppressed by adenosine and/or verapamil, indicating diverse electrophysiologic substrates.
- Delayed afterdepolarizations may play a significant role in the pathogenesis of some RAT cases.
- Further research is needed to fully elucidate the mechanisms of RAT.
More Related Videos
10:53Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents
Published on: July 3, 2013
07:42Contractions of Human-iPSC-derived Cardiomyocyte Syncytia Measured with a Ca-sensitive Fluorescent Dye in Temperature-controlled 384-well Plates
Published on: October 18, 2018
Related Concept Videos
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers
Cardiopulmonary Resuscitation IV: Pharmacological Management
Depolarizing Blockers: Mechanism of Action
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because succinylcholine...