Gap junctional remodeling in relation to stabilization of atrial fibrillation in the goat

• Published in: Cardiovascular research 2000-06, Vol.46 (3), p.476-486
• Main Authors: VAN DER VELDEN, Huub M. W, AUSMA, Jannie, ROOK, Martin B, HELLEMONS, Anita J. C. G. M, VAN VEEN, Toon A. A. B, ALLESSIE, Maurits A, JONGSMA, Habo J
• Format: Article
• Language: English
• Subjects: Animals; Atrial Appendage - chemistry; Atrial Appendage - metabolism; Atrial Fibrillation - metabolism; Biological and medical sciences; Blotting, Western; Cardiac dysrhythmias; Cardiac Pacing, Artificial; Cardiology. Vascular system; Connexin 43 - analysis; Connexin 43 - metabolism; Connexins - analysis; Connexins - metabolism; Female; Gap Junction alpha-5 Protein; Goats; Heart; Immunohistochemistry; Medical sciences; Microscopy, Confocal; Reverse Transcriptase Polymerase Chain Reaction; Time Factors
• ISSN: 0008-6363; 1755-3245
• DOI: 10.1016/s0008-6363(00)00026-2

It has been postulated that high atrial rate induced changes at the level of the gap junctions ('gap junctional remodeling', i.e. changes in distribution, intercellular orientation and expression of gap junction proteins), could be part of the vicious circle of electrophysiologic and structural changes leading to sustained atrial fibrillation (AF). To obtain experimental evidence in favour of such a postulate the timing of this remodeling process was studied in relation to the development of sustained AF in a goat model. Thin sections from the left (LAA) and right atrial appendage (RAA) from goats in sinus rhythm (SR) or AF, induced through programmed endocardial burst pacing for time periods between 0 and 16 weeks, were immunolabeled with antibodies against connexin(Cx)40 and Cx43 and analysed by immunofluorescence and confocal laser scanning microscopy. During SR the distribution pattern for Cx43 was completely homogeneous (LAA and RAA) and for Cx40 mostly homogeneous (LAA: all five goats, RAA: three out of five goats). The distribution pattern for Cx43 remained stable during AF, while the Cx40 distribution pattern became increasingly heterogeneous, both in the LAA and RAA, with increasing duration of pacing. This increase in heterogeneity in Cx40 distribution correlated (Spearman rank order) with an increase in stability of AF and the occurrence of structural changes (myolysis) in atrial myocytes. The Cx40/Cx43 immunofluorescence signal ratio in both the LAA and RAA appeared to be significantly lower in AF (1-16 weeks) as compared to SR (0 weeks); going from 0 to 16 weeks average ratios decreased 54.5% (n=5; P=0.026) in the LAA and 35.8 (n=5; P=0.034) in the RAA. Western blot analyses revealed similar decreases in the total Cx40/Cx43 protein ratio, on average 50.0% (n=5; P=0.008) and 47.8% (n=5; P=0.02) in the LAA and RAA, respectively. No changes were measured in the levels of Cx40 or Cx43 mRNA, as was assessed through RT-PCR. The time course of changes in the distribution and content of Cx40 gap junctions as observed during endocardial burst pacing of the goat atrium suggests that Cx40 gap junctional remodeling might be involved in the pathogenesis of sustained atrial fibrillation.