Literature DB >> 15817095

Blocking characteristics of hERG, hNav1.5, and hKvLQT1/hminK after administration of the novel anti-arrhythmic compound AZD7009.

Frida Persson1, Leif Carlsson, Göran Duker, Ingemar Jacobson.   

Abstract

INTRODUCTION: AZD7009 is a novel anti-arrhythmic compound under development for short- and long-term management of atrial fibrillation and flutter. Electrophysiological studies in animals have shown high anti-arrhythmic efficacy, predominant action on atrial electrophysiology, and low proarrhythmic activity. The main aim of this study was to characterize the blocking effects of AZD7009 on the human ether-a-go-go-related gene (hERG), the hNav1.5, and the hKvLQT1/hminK currents. METHODS AND
RESULTS: hERG, hKvLQT1/hminK, and hNav1.5 were expressed in CHO K1 cells. Currents were measured using the whole-cell configuration of the voltage-clamp technique. AZD7009 inhibited the hERG current with an IC50 of 0.6 +/- 0.07 microM (n = 6). AZD7009 1 microM hyperpolarized the potential for half-maximal activation from -8.2 +/- 0.1 mV to -18.0 +/- 0.6 mV (P < 0.001, n = 14) and induced pre-pulse potentiation at potentials near the activation threshold. The hNav1.5 current was blocked with an IC50 of 4.3 +/- 1.20 microM at 10 Hz (n = 6) and block developed use-dependently. Recovery from use-dependent block was slow, tau= 131 seconds. AZD7009 inhibited the hKvLQT1/hminK current only at high concentrations (IC50= 193 +/- 20 microM, n = 6).
CONCLUSION: AZD7009 inhibits both the hERG and the hNav1.5 current, and it is most likely this combined current block that underlies the prolongation of the refractoriness and the low proarrhythmic activity demonstrated in animals in vivo.

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Year:  2005        PMID: 15817095     DOI: 10.1046/j.1540-8167.2005.40427.x

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN: 1045-3873


  8 in total

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Authors:  Charles Antzelevitch; Alexander Burashnikov
Journal:  Ann N Y Acad Sci       Date:  2010-02       Impact factor: 5.691

5.  Tolterodine reduces veratridine-augmented late INa, reverse-INCX and early afterdepolarizations in isolated rabbit ventricular myocytes.

Authors:  Chao Wang; Lei-Lei Wang; Chi Zhang; Zhen-Zhen Cao; An-Tao Luo; Pei-Hua Zhang; Xin-Rong Fan; Ji-Hua Ma
Journal:  Acta Pharmacol Sin       Date:  2016-08-29       Impact factor: 6.150

6.  NF-kappaB-dependent transcriptional regulation of the cardiac scn5a sodium channel by angiotensin II.

Authors:  Lijuan L Shang; Shamarendra Sanyal; Arnold E Pfahnl; Zhe Jiao; Jon Allen; Hong Liu; Samuel C Dudley
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7.  Can inhibition of IKur promote atrial fibrillation?

Authors:  Alexander Burashnikov; Charles Antzelevitch
Journal:  Heart Rhythm       Date:  2008-08-06       Impact factor: 6.343

Review 8.  Do we need pharmacological therapy for atrial fibrillation in the ablation era?

Authors:  Samuel Lévy
Journal:  J Interv Card Electrophysiol       Date:  2007-03-06       Impact factor: 1.759

  8 in total

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