Profile and kinetics of L-type calcium current during the cardiac ventricular action potential compared in guinea-pigs, rats and rabbits

被引:71
作者
Linz, KW [1 ]
Meyer, R [1 ]
机构
[1] Univ Bonn, Inst Physiol, D-53111 Bonn, Germany
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2000年 / 439卷 / 05期
关键词
L-type calcium channel; action potential clamp; channel inactivation; guinea-pig; rabbit; rat;
D O I
10.1007/s004240050982
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The substantial interspecies differences in mammalian cardiac action potentials (APs) are attributed primarily to variations in K+ currents. In a comparative study On isolated ventricular myocytes from guinea-pigs, rabbits and rats, we investigated the influence of the species-based AP differences on the time course of the L-type Ca2+ current (I-Ca.L). In addition, we tested whether also species-dependent properties of the I-Ca.L contribute to its time course during the AP. In patch-clamp measurements, I-Ca.L was characterised using conventional square pulses and digitised APs as command voltages. Special interest was directed to the analysis of the actual time courses of I-Ca.L, and L-type channel activation and inactivation during APs. Although species-specific differences in AP shape strongly influence the amplitude and the time course of I-Ca.L, divergence in L-type channel inactivation was found as well. In each species I-Ca.L inactivation was related to Ca2+ influx via L-type channels. However, while L-type channels showed similar Ca2+ dependency in the rabbit and the rat. a 2-times higher Ca2+ influx was necessary to achieve a given degree of inactivation in the guinea-pig. Thus, inactivation of I-Ca.L is delayed in the guinea-pig, thereby contributing to the prolonged AP plateau in this species. Comparing the actual time course of I-Ca.L, and L-type channel activation and inactivation revealed that, in each species. fading of I-Ca.L during final repolarisation was caused by deactivation (i.e. closure of the channel's d-gate) rather than inactivation.
引用
收藏
页码:588 / 599
页数:12
相关论文
共 33 条
[21]   The late component of L-type calcium current during guinea-pig cardiac action potentials and its contribution to contraction [J].
Linz, KW ;
Meyer, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1998, 436 (05) :679-688
[22]   A DYNAMIC-MODEL OF THE CARDIAC VENTRICULAR ACTION-POTENTIAL .1. SIMULATIONS OF IONIC CURRENTS AND CONCENTRATION CHANGES [J].
LUO, CH ;
RUDY, Y .
CIRCULATION RESEARCH, 1994, 74 (06) :1071-1096
[23]   REGULATION AND MODULATION OF CALCIUM CHANNELS IN CARDIAC, SKELETAL, AND SMOOTH-MUSCLE CELLS [J].
MCDONALD, TF ;
PELZER, S ;
TRAUTWEIN, W ;
PELZER, DJ .
PHYSIOLOGICAL REVIEWS, 1994, 74 (02) :365-507
[24]   ELECTRICAL-ACTIVITY AND CONTRACTION IN CELLS ISOLATED FROM RAT AND GUINEA-PIG VENTRICULAR MUSCLE - A COMPARATIVE-STUDY [J].
MITCHELL, MR ;
POWELL, T ;
TERRAR, DA ;
TWIST, VW .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 391 :527-544
[25]   THE RELATIVE CONTRIBUTIONS OF DIFFERENT INTRACELLULAR AND SARCOLEMMAL SYSTEMS TO RELAXATION IN RAT VENTRICULAR MYOCYTES [J].
NEGRETTI, N ;
ONEILL, SC ;
EISNER, DA .
CARDIOVASCULAR RESEARCH, 1993, 27 (10) :1826-1830
[26]  
Noble D, 1998, CAN J CARDIOL, V14, P123
[27]  
Nygren A, 1998, CIRC RES, V82, P63
[28]   ROLE OF AN INWARDLY RECTIFYING POTASSIUM CURRENT IN RABBIT VENTRICULAR ACTION-POTENTIAL [J].
SHIMONI, Y ;
CLARK, RB ;
GILES, WR .
JOURNAL OF PHYSIOLOGY-LONDON, 1992, 448 :709-727
[29]   THE CELL-SURFACE OF ISOLATED CARDIAC MYOCYTES - A LIGHT-MICROSCOPE STUDY WITH USE OF FLUOROCHROME-COUPLED LECTINS [J].
STEGEMANN, M ;
MEYER, R ;
HAAS, HG ;
ROBERTNICOUD, M .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1990, 22 (07) :787-803
[30]   ROLE OF POTASSIUM CHANNELS IN CYCLE LENGTH DEPENDENT REGULATION OF ACTION-POTENTIAL DURATION IN MAMMALIAN CARDIAC PURKINJE AND VENTRICULAR MUSCLE-FIBERS [J].
SURAWICZ, B .
CARDIOVASCULAR RESEARCH, 1992, 26 (11) :1021-1029