VERAPAMIL BLOCKS A RAPIDLY ACTIVATING DELAYED RECTIFIER K+ CHANNEL CLONED FROM HUMAN HEART

被引:0
|
作者
RAMPE, D
WIBLE, B
FEDIDA, D
DAGE, RC
BROWN, AM
机构
[1] BAYLOR COLL MED,DEPT MOLEC PHYSIOL & BIOPHYS,HOUSTON,TX 77030
[2] QUEENS UNIV,DEPT PHYSIOL,KINGSTON K7L 3N6,ONTARIO,CANADA
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中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Verapamil is an antagonist of L-type Ca2+ channels, and part of its binding site is located in the sixth transmembrane segment (S6) in the fourth repeat of the protein. Verapamil also blocks K+ channels, which are members of the same supergene family as Ca2+ channels. We examined the effects of verapamil on a rapidly activating delayed rectifier K+ channel (designated fHK) cloned from human heart. Verapamil inhibited Rb-86+ efflux from fHK-transfected human embryonic kidney cells with an EC50 of 4.5 x 10(-5) m. Whole-cell patch-clamp experiments revealed that verapamil induced a rapid component of fHK current inactivation but was without effect on activation. The effect was concentration and voltage dependent and was attributed to open channel blockade. The apparent association and dissociation rate constants measured at +50 mV were about 1.65 x 10(5) m-1 sec-1 and 3.48 sec-1, respectively. S6 of fHK has significant homology to that portion of the verapamil binding site identified in Ca2+ channels, and S6 is thought to form part of the inner mouth of K+ channel pores. The data support a role for verapamil as a blocker of the inner pore of voltage-dependent K+ channels in human myocardium.
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页码:642 / 648
页数:7
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