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
[21]   NEGATIVE CHRONOTROPIC EFFECT OF ENDOTHELIN-1 MEDIATED THROUGH ET(A) RECEPTORS IN GUINEA-PIG ATRIA [J].
ONO, K ;
ETO, K ;
SAKAMOTO, A ;
MASAKI, T ;
SHIBATA, K ;
SADA, T ;
HASHIMOTO, K ;
TSUJIMOTO, G .
CIRCULATION RESEARCH, 1995, 76 (02) :284-292
[22]   ENDOTHELIN-A RECEPTOR MEDIATES CARDIAC INHIBITION BY REGULATING CALCIUM AND POTASSIUM CURRENTS [J].
ONO, K ;
TSUJIMOTO, G ;
SAKAMOTO, A ;
ETO, K ;
MASAKI, T ;
OZAKI, Y ;
SATAKE, M .
NATURE, 1994, 370 (6487) :301-304
[23]   Positive inotropic responses mediated by endothelin ETA and ETB receptors in human myocardial trabeculae [J].
Opgaard, OS ;
Möller, S ;
de Vries, R ;
Edvinsson, L ;
Saxena, PR .
CLINICAL SCIENCE, 2000, 99 (03) :161-168
[24]  
OUADID H, 1992, MOL PHARMACOL, V41, P346
[25]  
PEREZREYES E, 1992, J BIOL CHEM, V267, P1792
[26]   Differential effects of subunit interactions on protein kinase A- and C-mediated phosphorylation of L-type calcium channels [J].
Puri, TS ;
Gerhardstein, BL ;
Zhao, XL ;
Ladner, MB ;
Hosey, MM .
BIOCHEMISTRY, 1997, 36 (31) :9605-9615
[27]   cGMP-stimulated cyclic nucleotide phosphodiesterase regulates the basal calcium current in human atrial myocytes [J].
RivetBastide, M ;
Vandecasteele, G ;
Hatem, S ;
Verde, I ;
Benardeau, A ;
Mercadier, JJ ;
Fischmeister, R .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (11) :2710-2718
[28]  
RUBANYI GM, 1994, PHARMACOL REV, V46, P325
[29]   Endogenous endothelin-1 participates in the maintenance of cardiac function in rats with congestive heart failure marked increase in endothelin-1. Production in the failing heart [J].
Sakai, S ;
Miyauchi, T ;
Sakurai, T ;
Kasuya, Y ;
Ihara, M ;
Yamaguchi, I ;
Goto, K ;
Sugishita, Y .
CIRCULATION, 1996, 93 (06) :1214-1222
[30]  
SOKOLOVSKY M, 1993, RECEPTOR CHANNEL, V1, P295