Characterization of effects of endothelin-1 on the L-type Ca2+ current in human atrial myocytes

被引:17
作者
Boixel, C
Dinanian, S
Lang-Lazdunski, L
Mercadier, JJ
Hatem, SN
机构
[1] Fac Med Xavier Bichat, INSERM, U460, F-75018 Paris, France
[2] Hop Antoine Beclere, Serv Cardiol, F-92141 Clamart, France
[3] Assistance Publ Hop Paris, Grp Hosp Bichat Claude Bernard, Serv Physiol Explorat Fonct, F-75018 Paris, France
[4] Assistance Publ Hop Paris, Grp Hosp Bichat Claude Bernard, Serv Chirurg Cardiaque, F-75018 Paris, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2001年 / 281卷 / 02期
关键词
human cardiac cells; whole cell patch clamp;
D O I
10.1152/ajpheart.2001.281.2.H764
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effects of endothelin-1 (ET-1) on the L-type Ca2+ current (I-Ca) were examined in whole cell patch-clamped human atrial myocytes. Depending on the initial current density, ET-1 (10 nM) increased the amplitude of I-Ca by 99 +/- 7% or decreased it by 33 +/- 2%. The stimulatory effect predominated on current of low density (2.3 +/- 0.2 pA/ pF), whereas I-Ca of higher density (5.8 +/- 0.3 pA/ pF) was inhibited by ET-1. After I-Ca stimulation by 1 muM isoproterenol, ET-1 always inhibited the current by 32 +/- 7% (P< 0.05), an effect that was suppressed by pretreating myocytes with pertussis toxin. Atrial natriuretic peptide (ANP) inhibited I-Ca (41 +/- 3%) by reducing intracellular cAMP concentration. In ANP-treated myocytes, the stimulatory effect of ET-1 on I-Ca predominated (52 +/- 7%). The inhibitory effect of ET-1 on I-Ca was blocked by the ETA antagonist BQ-123, whereas the stimulatory effect was suppressed by the ETB agonist BQ-788. We conclude that ET-1 has opposite effects on I-Ca depending on the baseline amplitude of current, and both subtype ET receptors are implicated in the signal transduction pathways.
引用
收藏
页码:H764 / H773
页数:10
相关论文
共 43 条
[1]  
BKAILY G, 1995, J CARDIOVASC PHARM, V26, pS293
[2]   Tyrosine kinase and protein kinase C regulate L-type Ca2+ current cooperatively in human atrial myocytes [J].
Boixel, C ;
Tessier, S ;
Pansard, Y ;
Lang-Lazdunski, L ;
Mercadier, JJ ;
Hatem, SN .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (02) :H670-H676
[3]   alpha(1)-adrenergic activation inhibits beta-adrenergic-stimulated unitary Ca2+ currents in cardiac ventricular myocytes [J].
Chen, L ;
ElSherif, N ;
Boutjdir, M .
CIRCULATION RESEARCH, 1996, 79 (02) :184-193
[4]   ROLE OF CA2+ CHANNEL IN CARDIAC EXCITATION-CONTRACTION COUPLING IN THE RAT - EVIDENCE FROM CA2+ TRANSIENTS AND CONTRACTION [J].
CLEEMANN, L ;
MORAD, M .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 432 :283-312
[5]  
DAMRON DS, 1993, J BIOL CHEM, V268, P27335
[6]   ATRIAL NATRIURETIC FACTOR REGULATES THE CALCIUM CURRENT IN FROG ISOLATED CARDIAC-CELLS [J].
GISBERT, MP ;
FISCHMEISTER, R .
CIRCULATION RESEARCH, 1988, 62 (04) :660-667
[7]   Different compartments of sarcoplasmic reticulum participate in the excitation-contraction coupling process in human atrial myocytes [J].
Hatem, SN ;
Benardeau, A ;
RuckerMartin, C ;
Marty, I ;
deChamisso, P ;
Villaz, M ;
Mercadier, JJ .
CIRCULATION RESEARCH, 1997, 80 (03) :345-353
[8]   Endothelin ETA receptor regulates signaling and ANF gene expression via multiple G protein-linked pathways [J].
HilalDandan, R ;
Ramirez, MT ;
Villegas, S ;
Gonzalez, A ;
EndoMochizuki, Y ;
Brown, JH ;
Brunton, LL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (01) :H130-H137
[9]   POSITIVE CHRONOTROPIC EFFECTS OF ENDOTHELIN, A NOVEL ENDOTHELIUM-DERIVED VASOCONSTRICTOR PEPTIDE [J].
ISHIKAWA, T ;
YANAGISAWA, M ;
KIMURA, S ;
GOTO, K ;
MASAKI, T .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1988, 413 (01) :108-110
[10]   ENDOTHELIN ENHANCES THE CONTRACTILE RESPONSIVENESS OF ADULT-RAT VENTRICULAR MYOCYTES TO CALCIUM BY A PERTUSSIS TOXIN-SENSITIVE PATHWAY [J].
KELLY, RA ;
EID, H ;
KRAMER, BK ;
ONEILL, M ;
LIANG, BT ;
REERS, M ;
SMITH, TW .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) :1164-1171