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Vagal Stimulation Promotes Atrial Electrical Remodeling Induced by Rapid Atrial Pacing in Dogs: Evidence of a Noncholinergic Effect
Author(s) -
YANG DONGHUI,
XI YUTAO,
AI TOMOHIKO,
WU GERU,
SUN JUNPING,
RAZAVI MEHDI,
DELAPASSE SCOTT,
SHURAIL MOSSAIB,
GAO LIANJUN,
MATHURIA NILESH,
ELAYDA MACARTHUR,
CHENG JIE
Publication year - 2011
Publication title -
pacing and clinical electrophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.686
H-Index - 101
eISSN - 1540-8159
pISSN - 0147-8389
DOI - 10.1111/j.1540-8159.2011.03133.x
Subject(s) - atropine , medicine , antagonist , atrial fibrillation , vagus nerve stimulation , stimulation , anesthesia , vagus nerve , endocrinology , carnivora , cardiology , receptor
Background: Atrial electrical remodeling (AER) is one of the mechanisms by which atrial fibrillation (AF) begets AF. It is known that vagal activity increases the propensity for AF. However, vagal effects on AER have not been fully investigated.Methods: Adult mongrel dogs were divided in four groups: group I, rapid atria pacing (RAP); group II, RAP plus vagal nerve stimulation (VNS); group III, RAP and VNS with atropine (0.2 mg/kg/h, intravenous), and group IV, group III plus vasoactive intestinal polypeptide (VIP) antagonist ([D‐p‐Cl‐Phe 6 , Leu 17 ]‐VIP, 0.125 μg/kg/h). VNS was performed bilaterally through vagosympathetic trunks to achieve second‐degree AV block or sinus rate slowing of >30 beats per minute. Atrial effective refractory periods (AERPs) were determined in the coronary sinus and right atrial appendage every hour at drive cycle lengths (DCLs) 350 ms, 300 ms, and 250 ms.Results: During 5 hours RAP with or without VNS, AERP shortened progressively from baseline at both pacing sites and at all DCLs (P < 0.01). Furthermore, RAP‐induced AERP shortening was more pronounced with VNS (P < 0.01). With atropine, the AERP shortening during VNS was blunted (P < 0.01), but was still significantly more pronounced than that in group I (P < 0.05). However, VNS effect on AERP shortening was eliminated completely with the combination of atropine and VIP antagonist (P = 0.15 vs group I).Conclusion: Increased vagal activity promotes RAP‐induced AER, which could not be totally accounted for by cholinergic effect but could be blocked by the combination of atropine and VIP antagonist. Vagally released VIP may have important role in the vagal promotion of AER. (PACE 2011; 34:1092–1099)