The Natural Flavone Acacetin Blocks Small Conductance Ca2+-Activated K+ Channels Stably Expressed in HEK 293 Cells

被引:15
作者
Chen, Kui-Hao [1 ,2 ]
Liu, Hui [1 ,2 ]
Sun, Hai-Ying [1 ]
Jin, Man-Wen [2 ]
Sheng, Xiao-Guo [3 ]
Wang, Yan [3 ]
Li, Gui-Rong [1 ,3 ]
机构
[1] Univ Hong Kong, Li Ka Shing Fac Med, Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Pharmacol, Wuhan, Hubei, Peoples R China
[3] Xiamen Univ, Xiamen Cardiovasc Hosp, Xiamen, Peoples R China
关键词
acacetin; ion channels; potassium channels; small conductance Ca2+-activated potassium channels; ACTIVATED POTASSIUM CHANNELS; ATRIAL-FIBRILLATION; SK CHANNELS; REPOLARIZATION; RATS; PHARMACOLOGY; INHIBITION; MIGRATION; COMPLEX; ROLES;
D O I
10.3389/fphar.2017.00716
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 Ca2+-activated potassium (K-Ca) currents, including small conductance (SK(Ca)1, SK(Ca)2, and SK(Ca)3), intermediate conductance (IKCa), and large-conductance (BKCa) channels stably expressed in HEK 293 cells. The effects of acacetin on these K-Ca channels were determined with a whole-cell patch voltage-clamp technique. The results showed that acacetin inhibited the three subtype SKCa channel currents in concentration-dependent manner with IC50 of 12.4 mu M for SK(Ca)1, 10.8 mu M for SK(Ca)2, and 11.6 mu M for SK(Ca)3. Site-directed mutagenesis of SK(Ca)3 channels generated the mutants H490N, S512T, H521N, and A537V. Acacetin inhibited the mutants with IC50 of 118.5 mu M for H490N, 275.2 mu M for S512T, 15.3 mu M for H521N, and 10.6 mu M for A537V, suggesting that acacetin interacts with the P-loop helix of SK(Ca)3 channel. However, acacetin at 3-10 mu M did not decrease, but induced a slight increase of BKCa (+70 mV) by 8% at 30 mu M. These results demonstrate the novel information that acacetin remarkably inhibits SKCa channels, but not IKCa or BKCa channels, which suggests that blockade of SKCa by acacetin likely contributes to its anti-AF property previously observed in experimental AF.
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页数:9
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