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PMID: 11325877 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Dynamics of intramural and transmural reentry during ventricular fibrillation in isolated swine ventricles.

Circulation research ·Vol. 88 ·No. 8 ·2001-04-27 ·Pages 839-48

Valderrábano M, Lee MH, Ohara T, Lai AC, Fishbein MC, Lin SF, Karagueuzian HS, Chen PS

Abstract

The intramural dynamics of ventricular fibrillation (VF) remain poorly understood. Recent investigations have suggested that stable intramural reentry may underlie the mechanisms of VF. We performed optical mapping studies of VF in isolated swine right ventricles (RVs) and left ventricles (LVs). Nine RV walls were cut obliquely in their distal edge exposing the transmural surface. Six LV wedge preparations were also studied. Results showed that intramural reentry was present. In RV, 28 of 44 VF episodes showed reentry; 15% of the activation pathways were reentrant. Except for 4 episodes, reentry was transmural, involving subendocardial structures as the papillary muscle (PM) or trabeculae. In LV, reentry was observed in 27 of 27 VF episodes; 23% of the activations were part of reentrant pathways (P<0.05 compared with RV). All LV reentrant pathways were truly intramural (confined to the wall) and were frequently located at the PM insertion. In both ventricles, reentry was spatially and temporally unstable. Histological studies showed abrupt changes in fiber orientation at sites of reentry and wave splitting. Connexin 40 immunostaining demonstrated intramyocardial Purkinje fibers at sites of reentry in the PM root and around endocardial trabeculae. Our results confirm that reentry is frequent-but unstable-in the myocardial wall during VF. In RV, reentry is mostly transmural and requires participation of subendocardial structures. The LV has a greater incidence of reentry and is intramural. Anisotropic anatomic structures played key roles in the generation of wave splitting and in the maintenance of reentry.

MeSH Terms
Animals Anisotropy Body Surface Potential Mapping Connexins/metabolism Electrophysiologic Techniques, Cardiac Heart Conduction System/physiopathology Heart Ventricles/physiopathology In Vitro Techniques Myocardium/metabolism Optics and Photonics Papillary Muscles/physiopathology Purkinje Fibers/metabolism Swine Ventricular Dysfunction, Left/physiopathology Ventricular Dysfunction, Right/physiopathology Ventricular Fibrillation/physiopathology
Chemicals
Connexins connexin 40
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Valderrábano M
Division of Cardiology, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Lee M H
Ohara T
Lai A C
Fishbein M C
Lin S F
Karagueuzian H S
Chen P S
Article Info
Journal
Circulation research
Abbr.
Circ Res
ISSN
1524-4571
Published
2001-04-27
Pages
839-48
Language
English
Region
United States
NLM ID
0047103
Subset
IM
Grants
NHLBI NIH HHS · P50-HL-52319 · United States
NHLBI NIH HHS · R01 HL-66389 · United States
Corrections
CommentIn
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