Cardiac contractility modulation by non-excitatory currents: Studies in isolated cardiac muscle

被引:75
作者
Brunckhorst, CB
Shemer, I
Mika, Y
Ben-Haim, SA
Burkhoff, D
机构
[1] Technion Israel Inst Technol, Bruce Rappaport Fac Med, Dept Physiol & Biophys, IL-31096 Haifa, Israel
[2] Univ Zurich Hosp, Inst Cardiol, CH-8091 Zurich, Switzerland
[3] Impulse Dynam, Orangeburg, NY USA
关键词
inotropy; sarcoplasmic reticulum; papillary muscle; EC coupling; membrane potential;
D O I
10.1016/j.ejheart.2005.05.011
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: Myocardial contractility can be altered using voltage clamp techniques by modulating amplitude and duration of the action potential resulting in enhanced calcium entry in the cell of isolated muscle strips (Non-Excitatory Currents; NEC). Extracellular electrical stimuli delivered during the absolute refractory period (Cardiac Contractility Modulation; CCM) have recently been shown to produce inotropic effects in-vivo. Aim: Understanding the cellular mechanism, underlying the CCM effect, is essential for evaluating its clinical potential. We tested the hypothesis that NEC and CCM modulate contractility via similar cellular mechanisms. Methods: Square wave electric currents were applied in the organ bath to isometrically contracting rabbit RV papillary muscle and human failing trabecular muscle during the absolute refractory period (ARP). Results: These currents, which did not initiate new action potentials or contractions, modulated action potential duration (shortened or lengthened) and contractility (enhanced or depressed) in a manner that depended upon their amplitude, duration and delay from the pacing stimulus. The contractility modulation effect in the rabbit RV papillary muscle was markedly blunted after exposure to ryanodine, indicating that the sarcoplasmic reticulum plays an important role in the contractility modulation. Conclusion: Like voltage clarnping, extracellular currents applied during the ARP can similarly modulate action potential duration in-vitro and modulate myocardial contractility by similar intracellular mechanisms. This concept provides the potential of a therapeutic strategy in patients with heart failure to enhance contractility. (c) 2005 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
相关论文
共 36 条
[1]
Cardiac resynchronization in chronic heart failure [J].
Abraham, WT ;
Fisher, WG ;
Smith, AL ;
Delurgio, DB ;
Leon, AR ;
Loh, E ;
Kocovic, DZ ;
Packer, M ;
Clavell, AL ;
Hayes, DL ;
Ellestad, M ;
Messenger, J ;
Trupp, RJ ;
Underwood, J ;
Pickering, F ;
Truex, C ;
McAtee, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (24) :1845-1853
[2]
REFRACTORY PERIOD FIELD STIMULATION OF RIGHT ATRIA - A METHOD FOR STUDYING PRESYNAPTIC RECEPTORS IN CARDIAC AUTONOMIC TRANSMISSION [J].
ANGUS, JA ;
HARVEY, K .
JOURNAL OF PHARMACOLOGICAL METHODS, 1981, 6 (01) :51-64
[3]
MECHANICAL RESPONSE OF FROGS AND MAMMALIAN MYOCARDIUM TO MODIFICATIONS OF ACTION POTENTIAL DURATION BY CONSTANT CURRENT PULSES [J].
ANTONI, H ;
JACOB, R ;
KAUFMANN, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1969, 306 (01) :33-&
[5]
BLINKS JR, 1966, J PHARMACOL EXP THER, V151, P221
[6]
EFFECTS OF ACTION-POTENTIAL DURATION ON EXCITATION-CONTRACTION COUPLING IN RAT VENTRICULAR MYOCYTES - ACTION-POTENTIAL VOLTAGE-CLAMP MEASUREMENTS [J].
BOUCHARD, RA ;
CLARK, RB ;
GILES, WR .
CIRCULATION RESEARCH, 1995, 76 (05) :790-801
[7]
Electric Currents Applied During the Refractory Period Can Modulate Cardiac Contractility In Vitro and In Vivo [J].
Daniel Burkhoff ;
Itzik Shemer ;
Bella Felzen ;
Juichiro Shimizu ;
Yuval Mika ;
Marc Dickstein ;
David Prutchi ;
Nissim Darvish ;
Shlomo A. Ben-Haim .
Heart Failure Reviews, 2001, 6 (1) :27-34
[8]
*CARE HF STUD INV, 2005, NEW ENGL J MED, V352, P1539
[9]
POSTEXTRASYSTOLIC POTENTIATION - DO WE REALLY KNOW WHAT IT MEANS AND HOW TO USE IT [J].
COOPER, MW .
CIRCULATION, 1993, 88 (06) :2962-2971
[10]
The sarcoplasmic reticulum and the Na+Ca2+ exchanger both contribute to the Ca2+ transient of failing human ventricular myocytes [J].
Dipla, K ;
Mattiello, JA ;
Margulies, KB ;
Jeevanandam, V ;
Houser, SR .
CIRCULATION RESEARCH, 1999, 84 (04) :435-444