期刊文献+

乌头碱阻断表达在卵母细胞上的HERG通道的电药理特性 被引量:4

Electropharmacological properties of acontine while blocking HERG potassium channels expressed on Xenopus laevis oocytes
下载PDF
导出
摘要 目的观察乌头碱对表达在卵母细胞上的HERG电流的影响。方法HERG通道表达在非洲爪蟾卵母细胞上,利用双电极电压钳技术测量其电流。结果①HERG通道可以稳定表达在卵母细胞上;②乌头碱以浓度和电压依赖性方式阻断表达在卵母细胞上的野生型HERG通道,阻断的半数抑制浓度值是1.801±0.332μmol/L;③乌头碱对HERG电流的阻断呈时间依赖性;④峰电流幅值被1μmol/L乌头碱显著降低,而稳态失活的半数失活电压(-39.10±1.04 mV vs-41.61±2.66 mV,P>0.05,n=6)没有被乌头碱的阻断显著改变,而斜率k(32.37±1.04 mV vs 41.05±4.19 mV,P<0.05,n=6)出现正向移动。结论乌头碱对HERG电流呈浓度、电压和时间依赖性阻断,而其对失活状态下的HERG通道无明显阻断作用,HERG通道可能是乌头碱致心律失常的关键离子靶点之一。 Objective To investigate the inhibitory effect of acontine on human ether-a-go-go-related gene (HERG) channels expressed on Xenopus laevis ooeytes. Methods HERG channels were expressed on Xenopus laevis ooeytes and studied using two microelectrode voltage clamp technique. Results In HERG channels, acontine carried on a voltageand concentration-dependent inhibition with IC50 of were 1. 801 ±0. 332 μmol/L. Acontine preferentially blocked the current of open-state HERG channel with a time-dependent way. On the other hand, the peak current was inhibited significantly by 1 μmol/L of aconitine ,but the half voltage( V1/2 )of stable inactivation was not be impacted with a positive shift of the slope (k) of the stable inactive curve( -39.10±1.04 mVvs -41.61±2.66 mV, P〉0.05, n=6). Conclusions Aconitine blocks HERG channel with a voltage- and concentration-and time-dependent pattern, but it does not inhibit the inactive channels. It can be conferred that HERG channel may be one of the key target sites of which aconitine effects on and accordingly induces arrhythmias.
出处 《中国心脏起搏与心电生理杂志》 北大核心 2009年第6期528-532,共5页 Chinese Journal of Cardiac Pacing and Electrophysiology
关键词 电生理学 乌头碱 HERG 心律失常 钾通道 电压钳技术 Electrophysiology Acontine Human ether-a-go-go-related gene (HERG) Arrhythmias Potassium chan- nels Voltage clamp technique
  • 相关文献

参考文献5

二级参考文献47

  • 1赵庆桃.乌头碱中毒45例分析[J].中国误诊学杂志,2004,4(1):121-121. 被引量:7
  • 2张瑞英,富路,张蕾,孟繁超.乌头碱中毒致恶性心律失常及心源性休克抢救成功1例[J].中国实用内科杂志,2005,25(2):192-192. 被引量:5
  • 3[1]Ruffolo HR, Jr Boyle P, Venuit RP. Carvedilol(Kredex): A novel multiple action cardiovascular agent[J]. Drug Today, 1991, 27(3):465
  • 4[2]Ruffolo RR Jr, Bril A, Feuerstein GZ. Cardioprotective potential of carvedilol[J]. Cardiology,1993,82(3):S24
  • 5[3]Xie J, Dunn A, Tsikouris JP, et al. A placebo controlled evalution of the antifibrillatory effects of carvedilol[J]. J Electrocardiol, 2001,34(1):25
  • 6[4]Raos, Sikdar SK. Modification of alpha subunit of RⅡA sodium channels by aconitine[J]. Pflugers Arch, 2000,439(3):349
  • 7[5]Takusagawa M, Komori S, Matsumura K, et al. The inhibitory effects of carvedilol against arrhythmias induced by coronary reperfusion in anesthetized rats[J]. J Cardiovasc Pharmacol Ther,2000, 5(2):105
  • 8[6]Hoher M, Friedrich M, Sommer T, et al. Effects of carvedilol on left ventricular function and arrhythmias during repeated short-time myocardial ischemia in experimental pigs[J]. Z Cardiol, 1998, 78 (suppl 3):7
  • 9雷载权,张廷横.中华临床中药学[M].第1版.北京:人民卫生出版社,1998:723-732.
  • 10周斌.乌头碱致心律失常1例[J].中华医学丛刊,2003,3(10):54-54.

共引文献104

同被引文献72

引证文献4

二级引证文献66

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部