The peptide ''FRCRCFa'', dialysed intracellularly, inhibits the Na/Ca exchange in rabbit ventricular myocytes with high affinity

被引:38
作者
Hobai, IA
Khananshvili, D
Levi, AJ
机构
[1] UNIV BRISTOL,SCH MED SCI,DEPT PHYSIOL,BRISTOL BS8 1TD,AVON,ENGLAND
[2] TEL AVIV UNIV,SCH MED,DEPT PHYSIOL & PHARMACOL,IL-69978 TEL AVIV,ISRAEL
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1997年 / 433卷 / 04期
基金
英国惠康基金;
关键词
FRCRCFa; Na/Ca exchange; Na/Ca exchange inhibition; myocyte; patch clamp;
D O I
10.1007/s004240050300
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We investigated the effect in rabbit ventricular myocytes of ''FRCRCFa'', a newly developed peptide inhibitor of the Na/Ca exchange. Myocytes were whole cell patch clamped and experiments were carried out at 36 degrees C. The Na/Ca exchange was measured selectively, by blocking interfering ion channel currents and the Na/K pump, as the membrane current which could be inhibited by 5 mM nickel (Ni; a known blocker of the Na/Ca exchange). Increasing concentrations of FRCRCFa dialysed into the cell from the patch-pipette inhibited the Na/Ca exchange current. The dose/response curve could be fitted by a function for co-operative ligand binding, which predicted a KD for FRCRCFa-mediated inhibition of 22.7 +/- 3.7 nM, with a Hill coefficient of 0.61 +/- 0.06. Pipette FRCRCFa concentrations of 1 mu M and above were sufficient to cause complete inhibition of Na/Ca exchange current. The inhibitory effect of FRCRCFa was independent of membrane potential and relatively selective: IO CIM FRCRCFa dialysed into the cell had no effect on the L-type Ca current and delayed rectifier and inward rectifier K currents. Thus FRCRCFa appears to be a potent and relatively selective inhibitor of the Na/Ca exchange in intact cardiac myocytes, and may be of value for studies of the Na/Ca exchange.
引用
收藏
页码:455 / 463
页数:9
相关论文
共 41 条
[1]   MITOCHONDRIAL AND SARCOLEMMAL CA2+ TRANSPORT REDUCE [CA2+](I) DURING CAFFEINE CONTRACTURES IN RABBIT CARDIAC MYOCYTES [J].
BASSANI, RA ;
BASSANI, JWM ;
BERS, DM .
JOURNAL OF PHYSIOLOGY-LONDON, 1992, 453 :591-608
[2]   COMPETITION AND REDISTRIBUTION AMONG CALCIUM-TRANSPORT SYSTEMS IN RABBIT CARDIAC MYOCYTES [J].
BERS, DM ;
BASSANI, JWM ;
BASSANI, RA .
CARDIOVASCULAR RESEARCH, 1993, 27 (10) :1772-1777
[3]  
BERS DM, 1991, EXCITATION CONTRACTI
[4]  
BOYETT MR, 1992, BOWDITCH REVISITED, P111
[5]  
BROWN AM, 1981, J PHYSIOL-LONDON, V318, P479
[6]   THE EFFECT OF EXCHANGER INHIBITORY PEPTIDE (XIP) ON SODIUM CALCIUM EXCHANGE CURRENT IN GUINEA-PIG VENTRICULAR CELLS [J].
CHIN, TK ;
SPITZER, KW ;
PHILIPSON, KD ;
BRIDGE, JHB .
CIRCULATION RESEARCH, 1993, 72 (03) :497-503
[7]   ANTIARRHYTHMIC ACTIVITY OF AMILORIDE - MECHANISMS [J].
DUFF, HJ ;
BROWN, CE ;
CRAGOE, EJ ;
RAHMBERG, M .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1991, 17 (06) :879-888
[8]   THE DEPENDENCE OF SODIUM PUMPING AND TENSION ON INTRACELLULAR SODIUM ACTIVITY IN VOLTAGE-CLAMPED SHEEP PURKINJE-FIBERS [J].
EISNER, DA ;
LEDERER, WJ ;
VAUGHANJONES, RD .
JOURNAL OF PHYSIOLOGY-LONDON, 1981, 317 (AUG) :163-187
[9]   NA-CA EXCHANGE - STOICHIOMETRY AND ELECTROGENICITY [J].
EISNER, DA ;
LEDERER, WJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (03) :C189-C202
[10]  
ENYEDI A, 1993, J BIOL CHEM, V268, P17120