Persson Frida, Carlsson Leif, Duker Göran, Jacobson Ingemar
AstraZeneca R&D Mölndal, Integrative Pharmacology, Mölndal, Sweden.
J Cardiovasc Pharmacol. 2005 Jul;46(1):7-17. doi: 10.1097/01.fjc.0000161405.37198.c1.
AZD7009 is a novel antiarrhythmic compound in early clinical development for management of atrial fibrillation. Electrophysiological studies in animals have shown high antiarrhythmic efficacy, predominant action on atrial electrophysiology, and low proarrhythmic activity. AZD7009 has previously been shown to inhibit hERG and hNav1.5 currents. The main objective of the present study was to characterize the effects of AZD7009 on hKv1.5 and hKv4.3/hKChIP2.2 currents to get a deeper understanding of the ion channel-blocking properties of the compound. hKv1.5 and hKv4.3/hKChIP2.2 currents were expressed in CHO cells. Currents were measured using the whole-cell configuration of the voltage-clamp technique. AZD7009 inhibited hKv1.5 and hKv4.3/hKChIP2.2 currents with equal potency: the IC50 for hKv1.5 block was 27.0 +/- 1.6 muM (n = 6), and the IC50 for hKv4.3/hKChIP2.2 block was 23.7 +/- 4.4 muM (n = 5). Block of the hKv4.3/hKChIP2.2 current was frequency dependent with larger block at higher frequency, whereas block of the hKv1.5 current was slightly decreased at higher frequency. In conclusion, AZD7009 inhibits both the hKv1.5 and the hKv4.3/hKChIP2.2 currents. These effects likely contribute to the effects described in animals in vivo.
AZD7009是一种处于房颤治疗早期临床开发阶段的新型抗心律失常化合物。动物电生理研究表明其具有高抗心律失常疗效、对心房电生理有主要作用且促心律失常活性低。此前已证明AZD7009可抑制hERG和hNav1.5电流。本研究的主要目的是表征AZD7009对hKv1.5和hKv4.3/hKChIP2.2电流的影响,以更深入了解该化合物的离子通道阻断特性。hKv1.5和hKv4.3/hKChIP2.2电流在CHO细胞中表达。使用电压钳技术的全细胞配置测量电流。AZD7009以同等效力抑制hKv1.5和hKv4.3/hKChIP2.2电流:hKv1.5阻断的IC50为27.0±1.6μM(n = 6),hKv4.3/hKChIP2.2阻断的IC50为23.7±4.4μM(n = 5)。hKv4.3/hKChIP2.2电流的阻断呈频率依赖性,频率越高阻断越大,而hKv1.5电流的阻断在较高频率时略有降低。总之,AZD7009抑制hKv1.5和hKv4.3/hKChIP2.2电流。这些作用可能有助于解释其在动物体内的作用。