Enhanced Activity of Inositol-1,4,5-Trisphosphate Receptors in Atrial Myocytes of Atrial Fibrillation Patients

被引:22
作者
Liang, Xin [3 ]
Xie, Hong [4 ]
Zhu, Pei-Hong [4 ]
Hu, Jun [2 ,3 ]
Zhao, Qiang [1 ]
Wang, Chun-Sheng [1 ]
Yang, Cheng [1 ]
机构
[1] Fu Dan Univ, Zhong Shan Hosp, Dept Cardiac Surg, Shanghai Inst Cardiovasc Dis, Shanghai 200032, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Shanghai 200030, Peoples R China
[4] Shanghai Inst Biol Sci, Unit Cell Signal Transduct, Shanghai, Peoples R China
关键词
Atrial fibrillation; Inositol-1,4,5-trisphosphate receptor; Ca2+ sparks; Ca2+ waves; Ryanodine receptor; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; RAT VENTRICULAR MYOCYTES; CARDIAC MYOCYTES; RYANODINE RECEPTORS; CALCIUM-RELEASE; MESSENGER-RNA; CA2+ RELEASE; SPARKS; ARRHYTHMIAS; EXPRESSION;
D O I
10.1159/000228584
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The roles of inositol-1,4,5-trisphosphate receptors (IP(3)Rs) in arrhythmia are not fully understood, especially in human beings. Recently, the reported upregulated expression of IP(3)Rs in atrial myocytes of atrial fibrillation (AF) subjects suggested that IP(3)Rs might be associated with AF. To directly understand the roles of IP(3)Rs in AF, we have investigated the IP3R-dependent Ca2+ events as well as the cross-talk between IP(3)Rs and ryanodine receptors (RyRs) in permeabilized atrial myocytes of AF and normal sinus rhythm (NSR) patients by Ca2+ imaging. In the presence of tetracaine, IP3R-dependent Ca2+ events in AF atrial myocytes showed increased frequency, delayed termination and broadened width, compared with NSR myocytes. Moreover, when RyRs were not inhibited, IP3 or adenophostin induced an outburst of RyR-dependent spontaneous Ca2+ sparks with the altered spatial-temporal characteristics. The activation of IP(3)Rs also enhanced Ca2+ waves. These effects on RyR-dependent Ca2+ signaling were significantly stronger in AF myocytes than in NSR cells and were completely blocked by 2-aminoethoxydiphenyl borate. Thus, our results suggested not only an enhanced activity of IP(3)Rs but also an elevated cross-talk between IP3R- and RyR-mediated Ca2+ signaling in atrial myocytes of human AF patients, a reflection of altered function of IP(3)Rs in AF. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:180 / 191
页数:12
相关论文
共 38 条
[1]   THE NOREPINEPHRINE-STIMULATED INOSITOL PHOSPHATE RESPONSE IN HUMAN ATRIA [J].
ANDERSON, KE ;
LAMBERT, KA ;
WOODCOCK, EA .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1995, 27 (10) :2415-2419
[2]   ACE-inhibitor treatment attenuates atrial structural remodeling in patients with lone chronic atrial fibrillation [J].
Boldt, A ;
Scholl, A ;
Garbade, J ;
Resetar, ME ;
Mohr, FW ;
Gummert, JF ;
Dhein, S .
BASIC RESEARCH IN CARDIOLOGY, 2006, 101 (03) :261-267
[3]   Amplitude distribution of calcium sparks in confocal images:: Theory and studies with an automatic detection method [J].
Cheng, H ;
Song, LS ;
Shirokova, N ;
González, A ;
Lakatta, EG ;
Ríos, E ;
Stern, MD .
BIOPHYSICAL JOURNAL, 1999, 76 (02) :606-617
[4]   Calcium signaling between sarcolemmal calcium channels and ryanodine receptors in heart cells [J].
Cheng, HP ;
Wang, SQ .
FRONTIERS IN BIOSCIENCE, 2002, 7 :D1867-D1878
[5]   Endothelin and cardiac arrhythmias:: do endothelin antagonists have a therapeutic potential as antiarrhythmic drugs? [J].
Duru, F ;
Barton, M ;
Lüscher, TF ;
Candinas, R .
CARDIOVASCULAR RESEARCH, 2001, 49 (02) :272-280
[6]   INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR-MEDIATED CA2+ SIGNALING IN THE BRAIN [J].
FURUICHI, T ;
MIKOSHIBA, K .
JOURNAL OF NEUROCHEMISTRY, 1995, 64 (03) :953-960
[7]   Immunolocalization of type 2 inositol 1,4,5-trisphosphate receptors in cardiac myocytes from newborn mice [J].
García, KD ;
Shah, T ;
García, J .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (04) :C1048-C1057
[8]   Ca2+ diffusion and sarcoplasmic reticulum transport both contribute to [Ca2+](i) decline during Ca2+ sparks in rat ventricular myocytes [J].
Gomez, AM ;
Cheng, HP ;
Lederer, WJ ;
Bers, DM .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 496 (02) :575-581
[9]  
Guo Ji-hong, 2004, Zhonghua Yi Xue Za Zhi, V84, P1196
[10]  
Gutstein DE, 1997, HEART VESSELS, P53