Expression of connexins 40 and 43 in human left atrium in atrial fibrillation of different aetiologies

被引:68
作者
Wetzel, U
Boldt, A
Lauschke, J
Weigl, J
Schirdewahn, P
Dorszewski, A
Doll, N
Hindricks, G
Dhein, S
Kottkamp, H
机构
[1] Univ Leipzig, Ctr Heart, Dept Electrophysiol, D-04289 Leipzig, Germany
[2] Univ Leipzig, Ctr Heart, Dept Cardiovasc Surg, D-04289 Leipzig, Germany
关键词
D O I
10.1136/hrt.2003.024216
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To test the hypothesis that atrial fibrillation (AF) is associated with changes in the expression of connexins 40 and 43 in the left atrium with more pronounced changes in mitral valve disease than in lone AF. Methods: Protein concentrations of connexin 40 and connexin 43 were analysed in left atrial tissue of patients undergoing cardiac surgery. One group of patients had lone AF (n = 41), one group had AF and mitral valve repair ( n = 36), and one group in sinus rhythm served as controls ( n = 15). Results: Western blot analysis of connexin 40 and connexin 43 expression showed an increase of both gap junctional proteins ( connexin 43. connexin 40) in patients with AF of all forms compared with patients in sinus rhythm ( p = 0.01 and p = 0.011, respectively). Subgroup analysis showed increased concentrations of connexin 40 in lone AF and AF with mitral valve disease compared with sinus rhythm ( p = 0.06 and p = 0.029, respectively), whereas the same analysis for connexin 43 reached significance only in the mitral valve disease group ( p = 0.031). No differences in connexin 40 and connexin 43 expression were detectable between lone AF and AF with mitral valve disease. Within the groups connexin 40 and connexin 43 expression did not differ between patients with paroxysmal AF and patients with chronic AF. Conclusion: The present study shows for the first time that AF can induce changes in the left atrium with increased connexin expression. Furthermore, no systematic differences between patients with paroxysmal and chronic AF were detected.
引用
收藏
页码:166 / 170
页数:5
相关论文
共 39 条
[1]   Reverse structural and gap-junctional remodeling after prolonged atrial fibrillation in the goat [J].
Ausma, J ;
van der Velden, HMW ;
Lenders, MH ;
van Ankeren, EP ;
Jongsma, HJ ;
Ramaekers, FCS ;
Borgers, M ;
Allessie, MA .
CIRCULATION, 2003, 107 (15) :2051-2058
[2]   A gap in understanding the connection between connexins and cardiac conduction [J].
Berul, CI .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1999, 10 (10) :1376-1379
[3]   Expression of angiotensin II receptors in human left and right atrial tissue in atrial fibrillation with and without underlying mitral valve disease [J].
Boldt, A ;
Wetzel, U ;
Welgl, J ;
Garbade, J ;
Lauschkel, J ;
Hindricks, G ;
Kottkamp, H ;
Gummert, JF ;
Dhein, S .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 42 (10) :1785-1792
[4]   Altered connexin expression in human congestive heart failure [J].
Dupont, E ;
Matsushita, T ;
Kaba, RA ;
Vozzi, C ;
Coppen, SR ;
Khan, N ;
Kaprielian, R ;
Yacoub, MH ;
Severs, NJ .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (02) :359-371
[5]   The gap-junctional protein connexin40 is elevated in patients susceptible to postoperative atrial fibrillation [J].
Dupont, E ;
Ko, YS ;
Rothery, S ;
Coppen, SR ;
Baghai, M ;
Haw, M ;
Severs, NJ .
CIRCULATION, 2001, 103 (06) :842-849
[6]   Radiofrequency catheter ablation of the atria eliminates pacing-induced sustained atrial fibrillation and reduces connexin 43 in dogs [J].
Elvan, A ;
Huang, XD ;
Pressler, ML ;
Zipes, DP .
CIRCULATION, 1997, 96 (05) :1675-1685
[7]   Gap junction remodeling in hypertrophied left ventricles of aortic-banded rats: Prevention by angiotensin II type 1 receptor blockade [J].
Emdad, L ;
Uzzaman, M ;
Takagishi, Y ;
Honjo, H ;
Uchida, T ;
Severs, NJ ;
Kodama, I ;
Murata, Y .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (02) :219-231
[8]   Electrical remodeling in atrial fibrillation - Time course and mechanisms [J].
Goette, A ;
Honeycutt, C ;
Langberg, JJ .
CIRCULATION, 1996, 94 (11) :2968-2974
[9]   Conduction disturbances and increased atrial vulnerability in connexin40-deficient mice analyzed by transesophageal stimulation [J].
Hagendorff, A ;
Schumacher, B ;
Kirchhoff, S ;
Lüderitz, B ;
Willecke, K .
CIRCULATION, 1999, 99 (11) :1508-1515
[10]   Heterogeneous loss of connexin43 protein in ischemic dog hearts [J].
Huang, XD ;
Sandusky, GE ;
Zipes, DP .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1999, 10 (01) :79-91