PMID- 20962102 OWN - NLM STAT- MEDLINE DCOM- 20110613 LR - 20110217 IS - 1755-3245 (Electronic) IS - 0008-6363 (Linking) VI - 89 IP - 4 DP - 2011 Mar 1 TI - The role of pulmonary veins vs. autonomic ganglia in different experimental substrates of canine atrial fibrillation. PG - 825-33 LID - 10.1093/cvr/cvq332 [doi] AB - AIMS: Pulmonary vein (PV)-encircling ablation, which is effective in suppressing atrial fibrillation (AF), damages autonomic ganglia near the PV ostia. This study examined the effects of PV isolation (PVI) vs. peri-PV ganglionic plexus ablation (GPA) in two discrete canine AF models: ventricular tachypacing (240 bpm, 2 weeks)-induced congestive heart failure (CHF), and atrial tachypacing (400 bpm, 1 week)-induced atrial tachycardia remodeling (ATR). METHODS AND RESULTS: All PVs were isolated with an epicardial radiofrequency clamp in nine CHF and eight ATR dogs. Peri-PV ganglionic plexi (identified by bradycardic responses to high-frequency stimulation) were ablated in six CHF and five ATR dogs with an epicardial radiofrequency-ablation pen. Electrophysiologic measurements, including 240-electrode AF mapping, were obtained and dominant frequencies (DFs) determined. Atrial growth associated protein-43 (GAP-43) and neurofilament-M (NF-M) expression were determined immunohistologically. In CHF, neither PVI nor GPA affected AF duration, DF or the already low AF vulnerability. In ATR, PVI reduced AF vulnerability (75 +/- 6% to 55 +/- 11%, P< 0.05) but did not alter AF duration or DF. In contrast, GPA prolonged atrial refractory period and decreased AF vulnerability (75 +/- 8 to 30 +/- 10%, P< 0.05), AF duration (617 +/- 246 to 39 +/- 23 s, **P< 0.01), and DF (11.4 +/- 0.6 to 8.6 +/- 0.3** Hz, left atrium) in ATR dogs. Both GAP-43 and NF-M expression were decreased in CHF (by 63.1** and 60.0%**) and increased in ATR (by 65.5** and 92.1%, P< 0.001) compared with control. CONCLUSIONS: PVs play a minor role in experimental AF due to CHF or ATR, but autonomic ganglia are important in AF related to ATR. Differential neural remodelling may contribute to varying effects of GPA in discrete AF substrates. FAU - Nishida, Kunihiro AU - Nishida K AD - Research Center and Department of Medicine, Montreal Heart Institute and Universite de Montreal, 5000 Belanger Street, Montreal, QC, Canada H1T 1C8. FAU - Maguy, Ange AU - Maguy A FAU - Sakabe, Masao AU - Sakabe M FAU - Comtois, Philippe AU - Comtois P FAU - Inoue, Hiroshi AU - Inoue H FAU - Nattel, Stanley AU - Nattel S LA - eng GR - MGP 6957/Canadian Institutes of Health Research/Canada GR - MOP44365/Canadian Institutes of Health Research/Canada PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20101020 PL - England TA - Cardiovasc Res JT - Cardiovascular research JID - 0077427 SB - IM MH - Animals MH - Atrial Fibrillation/*etiology/physiopathology MH - Dogs MH - Ganglia, Autonomic/*physiology MH - Heart Failure/complications/pathology/physiopathology MH - Pulmonary Veins/*physiology MH - Refractory Period, Electrophysiological MH - Tachycardia/complications EDAT- 2010/10/22 06:00 MHDA- 2011/06/15 06:00 CRDT- 2010/10/22 06:00 PHST- 2010/10/22 06:00 [entrez] PHST- 2010/10/22 06:00 [pubmed] PHST- 2011/06/15 06:00 [medline] AID - cvq332 [pii] AID - 10.1093/cvr/cvq332 [doi] PST - ppublish SO - Cardiovasc Res. 2011 Mar 1;89(4):825-33. doi: 10.1093/cvr/cvq332. Epub 2010 Oct 20.