© 2001 by European Society of Cardiology
Copyright © 2001, European Society of Cardiology
Induction of atrial tachycardia and fibrillation in the mouse heart
aDepartment of Cardiology, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA
bDepartment of Pediatrics, Harvard Medical School, Boston, MA 02115, USA
* Corresponding author. Tel.: +1-617-355-6432; fax: +1-617-739-9058 berul{at}cardio.tch.harvard.edu
Background: Atrial tachycardia and fibrillation in humans may be partly consequent to vagal stimulation. Induction of fibrillation in the small heart is considered to be impossible due to lack of a critical mass of >100–200 mm2. Even with the recent progression of the technology of in vivo and in vitro mouse electrophysiological studies, few reports describe atrial tachycardia or fibrillation in mice. The purpose of this study was to attempt provocation of atrial tachyarrhythmia in mice using transvenous pacing following cholinergic stimulation. Methods and results: In vivo electrophysiology studies were performed in 14 normal mice. A six-lead ECG was recorded from surface limb leads, and an octapolar electrode catheter was inserted via jugular vein cutdown approach for simultaneous atrial and ventricular endocardial recording and pacing. Atrial tachycardia and fibrillation were inducible in one mouse at baseline electrophysiology study and eleven of fourteen mice after carbamyl choline injection. The mean duration of atrial tachycardia was 126±384 s. The longest episode lasted 35 min and only terminated after atropine injection. Reinduction of atrial tachycardia after administration of atropine was not possible. Conclusion: Despite the small mass of the normal mouse atria, sustained atrial tachycardia and fibrillation can be easily and reproducibly inducible with endocardial pacing after cholinergic agonist administration. This finding may contribute to our understanding of the classical theories of arrhythmogenesis and critical substrates necessary for sustaining microreentrant circuits. The techniques of transcatheter parasympathetic agonist-mediated atrial tachycardia induction may be valuable in further murine electrophysiological studies, especially mutant models with potential atrial arrhythmia phenotypes.
KEYWORDS Arrhythmia (mechanisms); Autonomic nervous system; Supraventr. arrhythmia
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