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天然黄酮刺槐素可阻断在HEK 293细胞中稳定表达的小电导钙激活钾通道。

The Natural Flavone Acacetin Blocks Small Conductance Ca-Activated K Channels Stably Expressed in HEK 293 Cells.

作者信息

Chen Kui-Hao, Liu Hui, Sun Hai-Ying, Jin Man-Wen, Xiao Guo-Sheng, Wang Yan, Li Gui-Rong

机构信息

Department of Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, Hong Kong.

Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Pharmacol. 2017 Oct 10;8:716. doi: 10.3389/fphar.2017.00716. eCollection 2017.

Abstract

The natural flavone acacetin inhibits several voltage-gated potassium currents in atrial myocytes, and has anti-atrial fibrillation (AF) effect in experimental AF models. The present study investigates whether acacetin inhibits the Ca-activated potassium (K) currents, including small conductance (SK1, SK2, and SK3), intermediate conductance (IK), and large-conductance (BK) channels stably expressed in HEK 293 cells. The effects of acacetin on these K channels were determined with a whole-cell patch voltage-clamp technique. The results showed that acacetin inhibited the three subtype SK channel currents in concentration-dependent manner with IC of 12.4 μM for SK1, 10.8 μM for SK2, and 11.6 μM for SK3. Site-directed mutagenesis of SK3 channels generated the mutants H490N, S512T, H521N, and A537V. Acacetin inhibited the mutants with IC of 118.5 μM for H490N, 275.2 μM for S512T, 15.3 μM for H521N, and 10.6 μM for A537V, suggesting that acacetin interacts with the P-loop helix of SK3 channel. However, acacetin at 3-10 μM did not decrease, but induced a slight increase of BK (+70 mV) by 8% at 30 μM. These results demonstrate the novel information that acacetin remarkably inhibits SK channels, but not IK or BK channels, which suggests that blockade of SK by acacetin likely contributes to its anti-AF property previously observed in experimental AF.

摘要

天然黄酮刺槐素可抑制心房肌细胞中的多种电压门控钾电流,并在实验性房颤模型中具有抗房颤(AF)作用。本研究调查刺槐素是否抑制钙激活钾(K)电流,包括在HEK 293细胞中稳定表达的小电导(SK1、SK2和SK3)、中电导(IK)和大电导(BK)通道。采用全细胞膜片电压钳技术测定刺槐素对这些钾通道的影响。结果表明,刺槐素以浓度依赖性方式抑制三种亚型的SK通道电流,对SK1的半数抑制浓度(IC)为12.4 μM,对SK2为10.8 μM,对SK3为11.6 μM。对SK3通道进行定点诱变产生了H490N、S512T、H521N和A537V突变体。刺槐素对这些突变体的抑制作用中,H490N的IC为118.5 μM,S512T为275.2 μM,H521N为15.3 μM,A537V为10.6 μM,表明刺槐素与SK3通道的孔环螺旋相互作用。然而,3 - 10 μM的刺槐素不会降低,而是在30 μM时使BK(+70 mV)轻微增加8%。这些结果证明了新的信息,即刺槐素显著抑制SK通道,但不抑制IK或BK通道,这表明刺槐素对SK通道的阻断可能有助于其先前在实验性房颤中观察到的抗房颤特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fe8/5646423/3431f0037fb0/fphar-08-00716-g001.jpg

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