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首页> 外文期刊>Journal of cardiovascular electrophysiology >Blocking characteristics of hERG, hNav1.5, and hKvLQT1/hminK after administration of the novel anti-arrhythmic compound AZD7009.
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Blocking characteristics of hERG, hNav1.5, and hKvLQT1/hminK after administration of the novel anti-arrhythmic compound AZD7009.

机译:新型抗心律失常化合物AZD7009给药后,hERG,hNav1.5和hKvLQT1 / hminK的阻断特性。

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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.
机译:简介:AZD7009是一种正在研发的新型抗心律不齐化合物,可用于短期和长期管理房颤和扑动。动物的电生理研究表明,抗心律不齐的功效高,对心房电生理的主要作用以及低的心律失常活性。这项研究的主要目的是表征AZD7009对人类以太相关基因(hERG),hNav1.5和hKvLQT1 / hminK电流的阻断作用。方法和结果:在CHO K1细胞中表达了hERG,hKvLQT1 / hminK和hNav1.5。使用电压钳技术的全电池配置测量电流。 AZD7009以0.6 +/- 0.07 microM(n = 6)的IC50抑制hERG电流。 AZD7009 1 microM将最大激活的半电势从-8.2 +/- 0.1 mV极化到-18.0 +/- 0.6 mV(P <0.001,n = 14),并在接近激活阈值的电势下诱导了脉冲前增强作用。 hNav1.5电流在10 Hz(n = 6)时被IC50抑制为4.3 +/- 1.20 microM,并因用途而异。从与使用有关的块中恢复很慢,tau = 131秒。 AZD7009仅在高浓度(IC50 = 193 +/- 20 microM,n = 6)下抑制hKvLQT1 / hminK电流。结论:AZD7009抑制hERG和hNav1.5电流,并且最有可能是这种结合的电流阻滞奠定了在动物体内表现出的难治性延长和低心律失常活性的基础。

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