Effects of sterile pericarditis on connexins 40 and 43 in the atria: correlation with abnormal conduction and atrial arrhythmias
Authors:
- Li LiLLLi Li
- Celeen M. KhrestianCKCeleen M. Khrestian
- Naomichi MatsumotoNMNaomichi Matsumoto
- Jayakumar SahadevanJSJayakumar Sahadevan
- Mary L. RuehrMRMary L. Ruehr
- David R. Van WagonerDWDavid R. Van Wagoner
- Igor R. EfimovIEIgor R. Efimov
- Albert L. WaldoAWAlbert L. Waldo
- 1 August 2007
- journal article
- Published by American Physiological Society in American Journal of Physiology-Heart and Circulatory Physiology
- Vol. 293 (2) , H1231-H1241
Abstract
The canine sterile pericarditis model is characterized by impaired conduction and atrial arrhythmia vulnerability. Electrical and structural remodeling processes caused by the inflammatory response likely promote these abnormalities. In the present study, we tested the hypothesis that altered distribution of atrial connexins is associated with markedly abnormal atrial conduction, thereby contributing to vulnerability to atrial flutter (AFL) and atrial fibrillation (AF) induction and maintenance. During rapid pacing and induced, sustained AFL or AF in five sterile pericarditis (SP) and five normal (NL) dogs, epicardial atrial electrograms were recorded simultaneously from both atria (380 electrodes) or from the right atrium (RA) and Bachmann's bundle (212 electrodes). Tissues from RA sites were subjected to immunostaining and immunoblotting to assess connexin (Cx) 40 and Cx43 distribution and expression. Transmural myocyte (α-actinin) and fibroblast (vimentin) volume were also assessed by immunostaining. RA pacing maps showed markedly abnormal conduction in SP, with uniform conduction in NL. Total RA activation time was significantly prolonged in SP vs. NL at 300-ms and 200-ms pacing-cycle lengths. Sustained arrhythmias were only inducible in SP [total: 4/5 (AFL: 3/5; AF: 1/5)]. In NL, Cx40, Cx43, α-actinin, and vimentin were homogeneously distributed transmurally. In SP, Cx40, Cx43, and α-actinin were absent epicardially, decreased midmyocardially, and normal endocardially. SP increased epicardial vimentin expression, suggesting fibroblast proliferation. Immunoblot analysis confirmed reduced expression of Cx40 and Cx43 in SP. The transmural gradient in the volume fraction of Cx40 and Cx43 in SP is associated with markedly abnormal atrial conduction and is likely an important factor in the vulnerability to induction and maintenance of AFL/AF in SP.Keywords
This publication has 25 references indexed in Scilit:
- Spatially and temporally distinct expression of fibroblast connexins after sheep ventricular infarctionCardiovascular Research, 2004
- Relationship Between Connexins and Atrial Activation During Human Atrial FibrillationJournal of Cardiovascular Electrophysiology, 2004
- Reverse Structural and Gap-Junctional Remodeling After Prolonged Atrial Fibrillation in the GoatCirculation, 2003
- Structural correlate of atrial fibrillation in human patientsCardiovascular Research, 2002
- Anisotropic Conduction Properties in Canine Atria Analyzed by High-Resolution Optical MappingCirculation, 2002
- The Gap-Junctional Protein Connexin40 Is Elevated in Patients Susceptible to Postoperative Atrial FibrillationCirculation, 2001
- Conduction Disturbances and Increased Atrial Vulnerability in Connexin40-Deficient Mice Analyzed by Transesophageal StimulationCirculation, 1999
- Reduced cardiac conduction velocity and predisposition to arrhythmias in connexin40-deficient miceCurrent Biology, 1998
- Simultaneous Multisite Mapping Studies During Induced Atrial Fibrillation in the Sterile Pericarditis ModelCirculation, 1997
- The effects on atrial electrophysiology and structure of surgically induced right atrial enlargement in dogs.Circulation Research, 1981