Effects of Common Antitussive Drugs on the hERG Potassium Channel Current

被引:20
|
作者
Deisemann, Heike [1 ]
Ahrens, Nadine [1 ]
Schlobohm, Irene [1 ]
Kirchhoff, Christian [1 ]
Netzer, Rainer [1 ]
Moeller, Clemens [1 ]
机构
[1] Evotec AG, D-22525 Hamburg, Germany
关键词
antitussive; clobutinol; hERG; QT prolongation; torsade de pointes;
D O I
10.1097/FJC.0b013e31818eec8d
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A common over-the-counter (OTC) non-opioid antitussive drug, clobutinol, was recently withdrawn from the market due to its potential to induce cardiac arrhythmias by a blockade of the potassium channel coded by the human ether-a-go-go-related gene (hERG). In this study, we investigated the effects of a number of antitussive compounds on the hERG ion channel current using patch-clamp electrophysiology, and compared the effects to that of clobutinol. The compounds clobutinol, pentoxyverine, dextromethorphan, and codeine inhibited the outward current in hERG transfected cells with half-maximal inhibition concentrations (IC50) of 1-9 mu M, 3.0 mu M, 5.1 mu M, and 97 mu M, respectively. For the obromine, no significant effect on the hERG current at a concentration up to 100 mu M was detected. Safety margins between the effects of the drugs on the hERG ion channel current and their calculated maximal free therapeutic plasma concentration were calculated. These results were compared to assess potential risks of the compounds to induce torsade de pointes-type arrhythmias.
引用
收藏
页码:494 / 499
页数:6
相关论文
共 50 条
  • [21] Inhibition of HERG potassium channel current by the Class 1a antiarrhythmic agent disopyramide
    Paul, AA
    Witchel, HJ
    Hancox, JC
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (05) : 1243 - 1250
  • [22] Ion Conduction through the hERG Potassium Channel
    Ceccarini, Luisa
    Masetti, Matteo
    Cavalli, Andrea
    Recanatini, Maurizio
    PLOS ONE, 2012, 7 (11):
  • [23] The Interactions Between hERG Potassium Channel and Blockers
    Du, Lupei
    Li, Minyong
    You, Qidong
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2009, 9 (04) : 330 - 338
  • [24] Predictive models for hERG potassium channel blockers
    Cianchetta, G
    Li, Y
    Kang, JS
    Rampe, D
    Fravolini, A
    Cruciani, G
    Vaz, RJ
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (15) : 3637 - 3642
  • [25] Mechanism of inward rectification in the HERG potassium channel
    Smith, PL
    Baukrowitz, T
    Yellen, G
    BIOPHYSICAL JOURNAL, 1996, 70 (02) : WAMA3 - WAMA3
  • [26] Block of the Cardiac Potassium Channel HERG by Cations
    Adrian, Jeremy
    Ng, Jacky
    Khawaja, Huzaifa
    Asadollahi, Zahra
    Miller, Alan
    BIOPHYSICAL JOURNAL, 2020, 118 (03) : 261A - 262A
  • [27] Toward a Consensus Model of the hERG Potassium Channel
    Stary, Anna
    Wacker, Soeren J.
    Boukharta, Lars
    Zachariae, Ulrich
    Karimi-Nejad, Yasmin
    Aqvist, Johan
    Vriend, Gert
    de Groot, Bert L.
    CHEMMEDCHEM, 2010, 5 (03) : 455 - 467
  • [28] Mechanism of hERG potassium channel block by tolterodine
    Wang, Na
    Ma, Jihua
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2015, 66 (16) : C101 - C102
  • [29] Mapping the block of dofetilide in the HERG potassium channel
    Kiehn, J
    Ficker, E
    Jarolimek, W
    Brown, AM
    CIRCULATION, 1997, 96 (08) : 2377 - 2377
  • [30] Blockade of HERG potassium channel by sibutramine HCl
    Kim, E.
    Park, S.
    Kim, K.
    Lee, H.
    FEBS JOURNAL, 2007, 274 : 233 - 233