Single-channel properties of L-type calcium channels from failing human ventricle

被引:29
作者
Handrock, R
Schröder, F
Hirt, S
Haverich, A
Mittmann, C
Herzig, S
机构
[1] Univ Cologne, Dept Pharmacol, D-50931 Cologne, Germany
[2] Univ Kiel, Dept Cardiothorac Surg, Kiel, Germany
[3] Hannover Med Sch, Dept Cardiothorac Surg, D-3000 Hannover, Germany
[4] Univ Hamburg, Dept Pharmacol, Hamburg, Germany
关键词
calcium channel; L type; single-channel recording; heart failure; human ventricular myocyte;
D O I
10.1016/S0008-6363(97)00257-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The aim of our study was to analyse the single-channel properties of L-type calcium channels from failing human heart and to compare them to the respective animal data. Furthermore, we intended to evaluate the feasibility of future single-channel studies on the role of calcium channels in the pathophysiology of heart failure, Methods: Single L-type calcium channels were recorded in ventricular myocytes from explanted failing human heart, using the cell-attached configuration of the patch-clamp technique. Results: One or more successful registrations of calcium channels could be obtained in 11 of 19 cell isolations. Determination of single-channel conductance yielded a mean value of 16.6 +/- 1.2 pS (70 mM Ba2+ as the charge carrier) under control conditions and 23.7 +/- 2.8 pS in presence of the calcium-channel agonist FPL 64176. The rapid gating process could be described by a C <-> C <-> O gating scheme. Slow gating analysis revealed a highly significant clustering of active and non-active sweeps. Conclusion: Single-channel measurements of L-type calcium channels in human failing ventricle are feasible and reproducible despite the varying patient characteristics. Their channel properties are qualitatively comparable to those found in other mammals. Whether there are quantitative differences due to the underlying heart failure can be elucidated in further studies. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:445 / 455
页数:11
相关论文
共 50 条
[31]   MODULATION OF SLOW GATING PROCESS OF CALCIUM CHANNELS BY ISOPRENALINE IN GUINEA-PIG VENTRICULAR CELLS [J].
OCHI, R ;
KAWASHIMA, Y .
JOURNAL OF PHYSIOLOGY-LONDON, 1990, 424 :187-204
[32]   2 PHOSPHATASE SITES ON THE CA2+ CHANNEL AFFECTING DIFFERENT KINETIC FUNCTIONS [J].
ONO, K ;
FOZZARD, HA .
JOURNAL OF PHYSIOLOGY-LONDON, 1993, 470 :73-84
[33]  
PELZER D, 1985, RECENT ASPECTS CALCI, P3
[34]   Voltage-gated calcium channel currents in human coronary myocytes - Regulation by cyclic GMP and nitric oxide [J].
Quignard, JF ;
Frapier, JM ;
Harricane, MC ;
Albat, B ;
Nargeot, J ;
Richard, S .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (02) :185-193
[35]  
RAMPE D, 1991, J PHARMACOL EXP THER, V259, P982
[36]   Cardiac Na+/Ca2+ exchange activity in patients with end-stage heart failure [J].
Reinecke, H ;
Studer, R ;
Vetter, R ;
Holtz, J ;
Drexler, H .
CARDIOVASCULAR RESEARCH, 1996, 31 (01) :48-54
[37]   PROPERTIES OF SINGLE CALCIUM CHANNELS IN CARDIAC CELL-CULTURE [J].
REUTER, H ;
STEVENS, CF ;
TSIEN, RW ;
YELLEN, G .
NATURE, 1982, 297 (5866) :501-504
[38]   MACROSCOPIC AND UNITARY PROPERTIES OF PHYSIOLOGICAL ION FLUX THROUGH L-TYPE CA2+ CHANNELS IN GUINEA-PIG HEART-CELLS [J].
ROSE, WC ;
BALKE, CW ;
WIER, WG ;
MARBAN, E .
JOURNAL OF PHYSIOLOGY-LONDON, 1992, 456 :267-284
[39]   MODULATION OF L-TYPE CA CHANNEL ACTIVITY BY P-2-PURINERGIC AGONIST IN CARDIAC-CELLS [J].
SCAMPS, F ;
NILIUS, B ;
ALVAREZ, J ;
VASSORT, G .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 422 (05) :465-471
[40]   EVIDENCE FOR AN INTERACTION OF HALOTHANE WITH THE L-TYPE CA-2+ CHANNEL IN HUMAN MYOCARDIUM [J].
SCHMIDT, U ;
SCHWINGER, RHG ;
BOHM, S ;
UBERFUHR, P ;
KREUZER, E ;
REICHART, B ;
VONMEYER, L ;
ERDMANN, E ;
BOHM, M .
ANESTHESIOLOGY, 1993, 79 (02) :332-339