Angiotensin II-induced changes of calcium sparks and ionic currents in human atrial myocytes: Potential role for early remodeling in atrial fibrillation

被引:69
作者
Gassanov, N
Brandt, MC
Michels, G
Lindner, M
Er, F
Hoppe, UC
机构
[1] Univ Cologne, Dept Internal Med 3, D-50937 Cologne, Germany
[2] Univ Cologne, CMMC, Ctr Mol Med, D-5000 Cologne 41, Germany
关键词
angiotensin; atrial fibrillation; ionic currents; calcium sparks; remodeling;
D O I
10.1016/j.ceca.2005.10.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: Atrial angiotensin II (ANG II) levels have been shown to be increased in atrial fibrillation (AF). The purpose of the study was to evaluate a potential role of ANG II in the early remodeling and susceptibility to chronicization of AF. Methods and results: Isolated human atrial myocytes were incubated in ANG II and/or angiotensin type 1 receptor blocker candesartan. ANG II markedly increased the frequency of spontaneous Ca2+ sparks, spark full duration, time to peak Ca2+ fluorescence and decay time measured by confocal imaging. Sarcoplasmic reticulum calcium content estimated by caffeine-evoked calcium release did not differ between ANG II-treated cells and controls. Patch-clamp recordings revealed that ANG II significantly decreased I-to and increased I-Ca,I-L current densities. Candesartan blocked these ANG II-mediated alterations. ANG II exhibited no effect on I-KI, I-Kur and I-f current size. Expression of connexin 40 and connexin 43 was not significantly changed by ANG II as assessed by immunohistochemistry and Western blot analysis. Conclusion: ANG II-induced alterations of calcium handling and electrophysiological changes inhuman atrial cells similar to those previously observed in the onset of AF. Prevention of these alterations by candesartan might constitute a useful pharmacological strategy for the treatment of AF. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:175 / 186
页数:12
相关论文
共 62 条
[21]   Electrical, morphological, and ultrastructural remodeling and reverse remodeling in a canine model of chronic atrial fibrillation [J].
Everett, TH ;
Li, H ;
Mangrum, JM ;
McRury, ID ;
Mitchell, MA ;
Redick, JA ;
Haines, DE .
CIRCULATION, 2000, 102 (12) :1454-1460
[22]   Endothelin induces differentiation of ANP-EGFP expressing embryonic stem cells towards a pacemaker phenotype [J].
Gassanov, N ;
Er, F ;
Zagidullin, N ;
Hoppe, UC .
FASEB JOURNAL, 2004, 18 (12) :1710-+
[23]   Regulation of angiotensin II receptor subtypes during atrial fibrillation in humans [J].
Goette, A ;
Arndt, M ;
Röcken, C ;
Spiess, A ;
Staack, T ;
Geller, JC ;
Huth, C ;
Ansorge, S ;
Klein, HU ;
Lendeckel, U .
CIRCULATION, 2000, 101 (23) :2678-2681
[24]   Increased expression of extracellular signal-regulated kinase and angiotensin-converting enzyme in human atria during atrial fibrillation [J].
Goette, A ;
Staack, T ;
Röcken, C ;
Arndt, M ;
Geller, JC ;
Huth, C ;
Ansorge, S ;
Klein, HU ;
Lendeckel, U .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 35 (06) :1669-1677
[25]   Electrical remodeling in atrial fibrillation - Time course and mechanisms [J].
Goette, A ;
Honeycutt, C ;
Langberg, JJ .
CIRCULATION, 1996, 94 (11) :2968-2974
[26]   Characterization of the hyperpolarization-activated inward current in isolated human atrial myocytes [J].
Hoppe, UC ;
Beuckelmann, DJ .
CARDIOVASCULAR RESEARCH, 1998, 38 (03) :788-801
[27]   Molecular dissection of cardiac repolarization by in vivo Kv4.3 gene transfer [J].
Hoppe, UC ;
Marbán, E ;
Johns, DC .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (08) :1077-1084
[28]   Distinct gene-specific mechanisms of arrhythmia revealed by cardiac gene transfer of two long QT disease genes, HERG and KCNE1 [J].
Hoppe, UC ;
Marbán, E ;
Johns, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (09) :5335-5340
[29]   Atrial fibrillation is associated with increased spontaneous calcium release from the sarcoplasmic reticulum in human atrial myocytes [J].
Hove-Madsen, L ;
Llach, A ;
Bayes-Genís, A ;
Roura, S ;
Font, ER ;
Arís, A ;
Cinca, J .
CIRCULATION, 2004, 110 (11) :1358-1363
[30]   Intracellular Ca2+ release contributes to automaticity in cat atrial pacemaker cells [J].
Hüser, J ;
Blatter, LA ;
Lipsius, SL .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 524 (02) :415-422