Literature DB >> 15132818

Inactivation gating determines drug potency: a common mechanism for drug blockade of HERG channels.

Bao-feng Yang1, Dong-hui Xu, Chao-qian Xu, Zhe Li, Zhi-min Du, Hui-zhen Wang, De-li Dong.   

Abstract

AIM: To determine the mechanisms of interactions between different drugs and HERG channels.
METHODS: Various antiarrhythmic (dofetilide, quinidine, azimilide, RP58866) and non-antiarrhythmic (terfenadine, nicotine) agents were used on HERG channels expressed in Xenopus oocyte. Whole-cell voltage-clamp techniques were used.
RESULTS: All drugs produced concentration-dependent block of HERG current. The inhibition was markedly facilitated with voltage protocols favoring channel inactivation (eg, less negative holding potentials). Maneuvers that weakened channel inactivation (eg, elevation of external K+), relieved HERG blockade by all drugs. Moreover, the inhibitory potency was reduced by at least 20-300 fold with varying compounds when rapid C-type inactivation was removed by a mutation located between the transmembrane domains 5 and 6 (S631A).
CONCLUSION: The inactivation gating of HERG channels determines the blocking potency of drugs. This mechanism might be common to drugs of various classes.

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Year:  2004        PMID: 15132818

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  7 in total

1.  Pharmacology of the short QT syndrome N588K-hERG K+ channel mutation: differential impact on selected class I and class III antiarrhythmic drugs.

Authors:  M J McPate; R S Duncan; J C Hancox; H J Witchel
Journal:  Br J Pharmacol       Date:  2008-08-25       Impact factor: 8.739

Review 2.  Translational toxicology and rescue strategies of the hERG channel dysfunction: biochemical and molecular mechanistic aspects.

Authors:  Kai-ping Zhang; Bao-feng Yang; Bao-xin Li
Journal:  Acta Pharmacol Sin       Date:  2014-11-24       Impact factor: 6.150

Review 3.  The ERG1 K+ Channel and Its Role in Neuronal Health and Disease.

Authors:  Francisco G Sanchez-Conde; Eric N Jimenez-Vazquez; David S Auerbach; David K Jones
Journal:  Front Mol Neurosci       Date:  2022-05-03       Impact factor: 6.261

4.  The 5-HT2 antagonist ketanserin is an open channel blocker of human cardiac ether-à-go-go-related gene (hERG) potassium channels.

Authors:  Q Tang; Z-Q Li; W Li; J Guo; H-Y Sun; X-H Zhang; C-P Lau; H-F Tse; S Zhang; G-R Li
Journal:  Br J Pharmacol       Date:  2008-06-23       Impact factor: 8.739

5.  Probing the molecular basis of hERG drug block with unnatural amino acids.

Authors:  Logan C Macdonald; Robin Y Kim; Harley T Kurata; David Fedida
Journal:  Sci Rep       Date:  2018-01-10       Impact factor: 4.379

6.  Investigating the state dependence of drug binding in hERG channels using a trapped-open channel phenotype.

Authors:  Samrat Thouta; Garman Lo; Lukas Grajauskas; Tom Claydon
Journal:  Sci Rep       Date:  2018-03-21       Impact factor: 4.379

7.  Inhibition of the HERG potassium channel by the tricyclic antidepressant doxepin.

Authors:  R S Duncan; M J McPate; J M Ridley; Z Gao; A F James; D J Leishman; J L Leaney; H J Witchel; J C Hancox
Journal:  Biochem Pharmacol       Date:  2007-05-03       Impact factor: 5.858

  7 in total

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