Multiscale modelling of drug-induced effects on cardiac electrophysiological activity

被引:90
作者
Brennan, T. [2 ]
Fink, M. [3 ]
Rodriguez, B. [1 ]
机构
[1] Univ Oxford, Comp Lab, Oxford OX1 3QD, England
[2] Univ Oxford, Dept Engn Sci, Oxford OX1 3PJ, England
[3] Univ Oxford, Dept Physiol, Oxford OX1 3QX, England
基金
英国工程与自然科学研究理事会;
关键词
Electrophysiology; Pharmacology; Mathematical modelling; ACTION-POTENTIAL DURATION; ION-CHANNEL BLOCKADE; RECTIFIER K+-CURRENT; LONG-QT SYNDROME; COMPUTATIONAL BIOLOGY; PARAMETER-ESTIMATION; POTASSIUM CHANNEL; LOCAL-ANESTHETICS; SODIUM-CHANNELS; DEPENDENT BLOCK;
D O I
10.1016/j.ejps.2008.09.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many drugs fail in the clinical trials and therefore do not reach the market due to adverse effects on cardiac electrical function. This represents a growing concern for both regulatory and pharmaceutical agencies as it translates into important socio-economic costs. Drugs affecting cardiac activity come from diverse pharmacological groups and their interaction with cardiac electrophysiology can result in increased risk of potentially life threatening arrhythmias, such as Torsade de Pointes. The mechanisms of drug interaction with the heart are very complex and the effects span from the ion channel to the whole organ level. This makes their investigation Using solely experimental in vitro and in vivo techniques very difficult. Computational modelling of cardiac electrophysiological behaviour has provided insight into the mechanisms of cardiac arrhythmogenesis, with high spatio-temporal resolution, from the ion channel to the whole organ level. it therefore represents a powerful tool in investigating mechanisms of drug-induced changes in cardiac behaviour and in their pro-arrhythmic potential. This article presents a comprehensive review of the recent advances in detailed models of drug action on cardiac electrophysiological activity. (C) 2008 Elsevier B.V All rights reserved.
引用
收藏
页码:62 / 77
页数:16
相关论文
共 91 条
[31]   Role of the calcium-independent transient outward current Ito1 in shaping action potential morphology and duration [J].
Greenstein, JL ;
Wu, R ;
Po, S ;
Tomaselli, GF ;
Winslow, RL .
CIRCULATION RESEARCH, 2000, 87 (11) :1026-1033
[32]   Alteration of HERG current profile during the cardiac ventricular action potential, following a pore mutation [J].
Hancox, JC ;
Witchel, HJ ;
Varghese, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 253 (03) :719-724
[33]  
Hill A. V., 1910, Journal of Physiology, V40, P4, DOI DOI 10.1113/JPHYSIOL.1910.SP001386
[35]  
Hille B., 2001, Ion Channels of Excitable Membranes, V3rd
[36]   A QUANTITATIVE DESCRIPTION OF MEMBRANE CURRENT AND ITS APPLICATION TO CONDUCTION AND EXCITATION IN NERVE [J].
HODGKIN, AL ;
HUXLEY, AF .
JOURNAL OF PHYSIOLOGY-LONDON, 1952, 117 (04) :500-544
[37]   TIME-DEPENDENT AND VOLTAGE-DEPENDENT INTERACTIONS OF ANTIARRHYTHMIC DRUGS WITH CARDIAC SODIUM CHANNELS [J].
HONDEGHEM, LM ;
KATZUNG, BG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 472 (3-4) :373-398
[38]  
Hondeghem LM, 2001, CIRCULATION, V103, P2004
[39]   FREQUENCY-DEPENDENT EFFECTS OF D-SOTALOL AND AMIODARONE ON THE ACTION-POTENTIAL DURATION OF THE HUMAN RIGHT VENTRICLE [J].
HUIKURI, HV ;
YLIMAYRY, S .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 1992, 15 (11) :2103-2107
[40]   RECTIFYING PROPERTIES OF HEART MUSCLE [J].
HUTTER, OF ;
NOBLE, D .
NATURE, 1960, 188 (4749) :495-495