Comparative Effects of Guanfu Base A and Guanfu Base G on HERG K+ Channel

被引:14
作者
Huang, Xingfu [1 ,2 ,3 ]
Yang, Yanmin [2 ,3 ]
Zhu, Jun [2 ,3 ]
Xu, Dingli [1 ]
Peng, Jian [1 ]
Liu, Jinghan [4 ]
机构
[1] So Med Univ, Dept Cardiol, Nanfang Hosp, Guangzhou, Guangdong, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll, Emergency Ctr, Cardiovasc Inst, Beijing 100037, Peoples R China
[3] Chinese Acad Med Sci, Peking Union Med Coll, Fuwai Hosp, Beijing 100730, Peoples R China
[4] China Pharmaceut Univ, Ctr Drug Metab & Pharmacokinet, Nanjing 210009, Peoples R China
关键词
Guanfu base A; acehytisine hydrochloride; Guanfu base G; HERG; K+ channel; cardiac arrhythmia; ion channels; POTASSIUM CHANNEL; ACEHYTISINE HYDROCHLORIDE; MOLECULAR DETERMINANTS; CARDIAC-ARRHYTHMIA; DE-POINTES; I-KR; TRAFFICKING; CISAPRIDE; BLOCK; DRUG;
D O I
10.1097/FJC.0b013e318236e380
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Guanfu base A (GFA) and Guanfu base G (GFG) are chemicals isolated from Aconitum coreanum. The potassium channel encoded by the human ether-a-go-go related gene (HERG) plays an important role in repolarization of the cardiac action potential. The purpose of the present study was to investigate the effects of GFA and GFG on the HERG channel and its structure-function relationship. Methods: The effects of GFA and GFG were investigated in human embryonic kidney 293 (HEK293) cells transiently transfected with HERG complementary DNA using a whole-cell patch clamp technique. Results: GFA and GFG inhibited HERG channel current in concentration-, voltage-, and time-dependent manners. The IC50 for GFA and GFG was 1.64 mM and 17.9 mu M, respectively. Both GFA and GFG shifted the activation curve in a negative direction and accelerated channel inactivation but showed no effect on the inactivation curve. Moreover, GFG also accelerated channel recovery from inactivation. Conclusions: Both GFA and GFG blocked HERG channel current. This effect was stronger after GFG treatment rather than GFA treatment. This blockade was dependent on open and inactivated channel states. These results indicate that GFA could be a rather promising antiarrhythmic drug without severe side effects, whereas GFG could cause QT prolongation and requires further research.
引用
收藏
页码:77 / 83
页数:7
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