Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Biochem Pharmacol. 2012 Aug 15;84(4):498-506. doi: 10.1016/j.bcp.2012.05.002. Epub 2012 May 11.
The natural flavones and polymethylflavone have been reported to have cardiovascular protective effects. In the present study, we determined whether quecertin, apigenin and their methylated compounds (3,7,3',4'-tetramethylquecertin, 3,5,7,3',4'-pentamethylquecertin, 7,4'-dimethylapigenin, and 5,7,4'-trimethylapigenin) would block the atrial specific potassium channel hKv1.5 using a whole-cell patch voltage-clamp technique. We found that only trimethylapigenin showed a strong inhibitory effect on hKv1.5 channel current. This compound suppressed hKv1.5 current in HEK 293 cell line (IC₅₀=6.4 μM), and the ultra-rapid delayed rectify K⁺ current I(Kur) in human atrial myocytes (IC₅₀=8.0 μM) by binding to the open channels and showed a use- and frequency-dependent manner. In addition, trimethylapigenin decreased transient outward potassium current (I(to)) in human atrial myocytes, inhibited acetylcholine-activated K⁺ current (IC₅₀=6.8μM) in rat atrial myocytes. Interestingly, trimethylapigenin had a weak inhibition of hERG channel current. Our results indicate that trimethyapigenin significantly inhibits the atrial potassium currents hKv1.5/I(Kur) and I(KACh), which suggests that trimethylapigenin may be a potential candidate for anti-atrial fibrillation.
天然类黄酮和多甲氧基黄酮已被报道具有心血管保护作用。在本研究中,我们使用全细胞膜片钳电压钳技术,确定了洋芹素、芹菜素及其甲基化化合物(3,7,3',4'-四甲基洋芹素、3,5,7,3',4'-五甲基洋芹素、7,4'-二甲基金丝桃苷和 5,7,4'-三甲基金丝桃苷)是否会阻断心房特异性钾通道 hKv1.5。我们发现只有三甲基金丝桃苷对 hKv1.5 通道电流表现出强烈的抑制作用。该化合物抑制 HEK 293 细胞系中的 hKv1.5 电流(IC₅₀=6.4 μM),以及人心房肌细胞中的超快延迟整流钾电流 I(Kur)(IC₅₀=8.0 μM),通过与开放通道结合表现出使用和频率依赖性。此外,三甲基金丝桃苷降低人心房肌细胞中的瞬间外向钾电流(I(to)),抑制大鼠心房肌细胞中乙酰胆碱激活的钾电流(IC₅₀=6.8μM)。有趣的是,三甲基金丝桃苷对 hERG 通道电流的抑制作用较弱。我们的结果表明,三甲基金丝桃苷显著抑制心房钾电流 hKv1.5/I(Kur)和 I(KACh),这表明三甲基金丝桃苷可能是抗心房颤动的潜在候选药物。