High-throughput screening of drug-binding dynamics to HERG improves early drug safety assessment

被引:58
作者
Di Veroli, Giovanni Y. [1 ]
Davies, Mark R.
Zhang, Henggui
Abi-Gerges, Najah
Boyett, Mark R. [1 ]
机构
[1] Univ Manchester, Inst Cardiovasc Sci, Manchester M13 9NT, Lancs, England
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2013年 / 304卷 / 01期
关键词
computational modeling; human ether-a-go-go-related gene ion channel; drug-binding kinetics; QT prolongation; Torsades de Pointes arrhythmia; QT INTERVAL PROLONGATION; POTASSIUM CHANNEL; I-KR; VENTRICULAR ARRHYTHMIA; PROARRHYTHMIC RISK; ION CHANNELS; REPOLARIZATION; ELECTROPHYSIOLOGY; CISAPRIDE; BLOCK;
D O I
10.1152/ajpheart.00511.2012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Di Veroli GY, Davies MR, Zhang H, Abi-Gerges N, Boyett MR. High-throughput screening of drug-binding dynamics to HERG improves early drug safety assessment. Am J Physiol Heart Circ Physiol 304: H104-H117, 2013. First published October 26, 2012; doi:10.1152/ajpheart.00511.2012.-The use of computational models to predict drug-induced changes in the action potential (AP) is a promising approach to reduce drug safety attrition but requires a better representation of more complex drug-target interactions to improve the quantitative prediction. The blockade of the human ether-a-go-go-related gene (HERG) channel is a major concern for QT prolongation and Torsade de Pointes risk. We aim to develop quantitative in-silico AP predictions based on a new electrophysiological protocol (suitable for high-throughput HERG screening) and mathematical modeling of ionic currents. Electrophysiological recordings using the IonWorks device were made from HERG channels stably expressed in Chinese hamster ovary cells. A new protocol that delineates inhibition over time was applied to assess dofetilide, cisapride, and almokalant effects. Dynamic effects displayed distinct profiles for these drugs compared with concentration-effects curves. Binding kinetics to specific states were identified using a new HERG Markov model. The model was then modified to represent the canine rapid delayed rectifier K+ current at 37 degrees C and carry out AP predictions. Predictions were compared with a simpler model based on conductance reduction and were found to be much closer to experimental data. Improved sensitivity to concentration and pacing frequency variables was obtained when including binding kinetics. Our new electrophysiological protocol is suitable for high-throughput screening and is able to distinguish drug-binding kinetics. The association of this protocol with our modeling approach indicates that quantitative predictions of AP modulation can be obtained, which is a significant improvement compared with traditional conductance reduction methods.
引用
收藏
页码:H104 / H117
页数:14
相关论文
共 43 条
  • [21] Evaluation of drug-induced QT interval prolongation - Implications for drug approval and labelling
    Malik, M
    Camm, AJ
    [J]. DRUG SAFETY, 2001, 24 (05) : 323 - 351
  • [22] The utility of hERG and repolarization assays in evaluating delayed cardiac repolarization: Influence of multi-channel block
    Martin, RL
    McDermott, JS
    Salmen, HJ
    Palmatier, J
    Cox, BF
    Gintant, GA
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2004, 43 (03) : 369 - 379
  • [23] Molecular interactions between two long-QT syndrome gene products, HERG and KCNE2, rationalized by in vitro and in silico analysis
    Mazhari, R
    Greenstein, JL
    Winslow, RL
    Marbán, E
    Nuss, HB
    [J]. CIRCULATION RESEARCH, 2001, 89 (01) : 33 - 38
  • [24] Investigating dynamic protocol-dependence of hERG potassium channel inhibition at 37 °C: Cisapride versus dofetilide
    Milnes, James T.
    Witchel, Harry J.
    Leaney, Joanne L.
    Leishman, Derek J.
    Hancox, Jules C.
    [J]. JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2010, 61 (02) : 178 - 191
  • [25] Simulation of multiple ion channel block provides improved early prediction of compounds' clinical torsadogenic risk
    Mirams, Gary R.
    Cui, Yi
    Sher, Anna
    Fink, Martin
    Cooper, Jonathan
    Heath, Bronagh M.
    McMahon, Nick C.
    Gavaghan, David J.
    Noble, Denis
    [J]. CARDIOVASCULAR RESEARCH, 2011, 91 (01) : 53 - 61
  • [26] hERG potassium channels and the structural basis of drug-induced arrhythmias
    Mitcheson, John S.
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 2008, 21 (05) : 1005 - 1010
  • [27] Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate
    Mitcheson, JS
    Chen, J
    Sanguinetti, MC
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2000, 115 (03) : 229 - 239
  • [28] Automated electrophysiology makes the pace for cardiac ion channel safety screening
    Moeller, Clemens
    Witchel, Harry
    [J]. FRONTIERS IN PHARMACOLOGY, 2011, 2
  • [29] Collation, assessment and analysis of literature in vitro data on hERG receptor blocking potency for subsequent modeling of drugs' cardiotoxic properties
    Polak, Sebastian
    Wisniowska, Barbara
    Brandys, Jerzy
    [J]. JOURNAL OF APPLIED TOXICOLOGY, 2009, 29 (03) : 183 - 206
  • [30] RISK OF DEVELOPING LIFE-THREATENING VENTRICULAR ARRHYTHMIA ASSOCIATED WITH TERFENADINE IN COMPARISON WITH OVER-THE-COUNTER ANTIHISTAMINES, IBUPROFEN AND CLEMASTINE
    PRATT, CM
    HERTZ, RP
    ELLIS, BE
    CROWELL, SP
    LOUV, W
    MOYE, L
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1994, 73 (05) : 346 - 352