首页 | 本学科首页   官方微博 | 高级检索  
     

KCNQ2/3钾通道电流特征及M_1受体的调节作用
引用本文:贾庆忠 贾占峰 张英俊 刘伯一 张海林. KCNQ2/3钾通道电流特征及M_1受体的调节作用[J]. 中国药理学通报, 2005, 21(10): 1199-1203
作者姓名:贾庆忠 贾占峰 张英俊 刘伯一 张海林
作者单位:河北医科大学药理学教研室 河北石家庄050017(贾庆忠,贾占峰,刘伯一),河北医科大学第三医院麻醉科 河北石家庄050051(张英俊),河北医科大学药理学教研室 河北石家庄050017(张海林)
基金项目:国家自然科学基金资助项目(No.30270361);科技部重大基础研究前期研究专项资助项目(No.2003CCA00300)
摘    要:目的观察KCNQ2/3通道电流特征及M1受体激活对该电流的调节作用。方法以CHO细胞作为表达体系,用脂质体共转染KCNQ2、KCNQ3钾离子通道及毒蕈碱型M1受体。全细胞膜片钳方法,观察KCNQ2/3电流特征,药理学阻断剂的作用及M1受体激活对电流的调节。结果KC-NQ2/3电流呈现慢激活、低阈值、非失活、电压依赖性的外向钾离子电流特点,其激活电压的阈值在-60 mV,半数激活电压值(-26.8±1.2)mV,其去活曲线可用双指数方程拟合,fτast约101 m s;sτlow约为309 m s。该电流对4-AP,Ba2+,TEA不敏感,L inop ird ine抑制KCNQ2/3电流IC50为(6.5±0.83)μmol.L-1。乙酰胆碱激活M1受体后会可逆性地抑制KCNQ2/3电流,其抑制的IC50为(0.7±0.05)μmol.L-1。结论KCNQ2/3通道作为神经细胞M通道的分子基础,其电流特征与M电流一致,L inop ird ine对其有较强阻断作用,神经递质乙酰胆碱通过激活M1受体明显抑制该通道电流。研究KCNQ2/3通道电流特征及受体调节规律,对于理解与中枢兴奋性有关的疾病如:惊厥、癫痫、阿尔采末病等发生机制有重要指导意义。

关 键 词:KCNQ2/3电流  M电流  阻断剂  M1受体  调节
文章编号:1001-1978(2005)10-1199-05
收稿时间:2005-05-09
修稿时间:2005-07-29

Characteristics of KCNQ2/3 potassium channel current and its modulation by M1 receptor
JIA Qing-zhong,JIA Zhan-feng,ZHANG Ying-jun,LIU Bo-yi,ZHANG Hai-lin. Characteristics of KCNQ2/3 potassium channel current and its modulation by M1 receptor[J]. Chinese Pharmacological Bulletin, 2005, 21(10): 1199-1203
Authors:JIA Qing-zhong  JIA Zhan-feng  ZHANG Ying-jun  LIU Bo-yi  ZHANG Hai-lin
Abstract:Aim To study the characteristics of KCNQ2/3 potassium channel expressed in CHO cells and its modulation by M_1 receptor.Methods KCNQ2 and KCNQ3 potassium channels and M_1 receptor were co-expressed in CHO cells.Whole cell patch-clamp techniques was used to observe the characteristics of KCNQ2/3 current,its modulation by the M_1 receptor,and the effects of the common potassium channel blockers.Results KCNQ2/3 current recorded in CHO cells was a slow-activation low-threshold non-inactivating,voltage-dependent outward potassium current.KCNQ2/3 current was elicited at about-60 mV,V_(1/2)(-26.8±1.2) mV and the deactivation current fitted two exponential function,with τ_(fast) of 101ms and τ_(slow) of 309 ms.The channel was not sensitive to common pharmacological blockers such as 4-AP,Ba~(2+) and TEA,but was inhibited significantly by linopirdine,with a IC_(50) of(6.5±0.83) μmol·L~(-1).Acetylcholine suppressed the KCNQ2/3 current reversibly via M_1 receptor,with a IC_(50) of(0.7±0.05) μmol·L~(-1).Conclusion KCNQ2 and KCNQ3 channels are the molecular basis of M-current observed in neuronal cells.KCNQ2/Q3 current expressed in CHO cells has similar characteristics as that seen in neuronal M-current.Linopirdine is a powerful blocker of KCNQ2/3 channel and acetylcholine inhibits the current by muscarinic M_1 receptor.This experiment has laid a solid basis for further study of M-current and KCNQ2/3 current,and is important for the study of neurological diseases relating to alteration of M-current,such as convulsion,epilepsy and Alzheimers disease.
Keywords:KCNQ2/3 current   M-current   blockers   M1 receptor   modulation
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号