Large-conductance, calcium-activated potassium channels: Structural and functional implications

被引:263
作者
Ghatta, S [1 ]
Nimmagadda, D
Xu, XP
O'Rourke, ST
机构
[1] N Dakota State Univ, Coll Pharm, Dept Pharmaceut Sci, Fargo, ND 58105 USA
[2] GlaxoSmithKline, CVU, CEDD, King Of Prussia, PA 19406 USA
关键词
BK; calcium; voltage sensitivity; BK openers; BK blockers;
D O I
10.1016/j.pharmthera.2005.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The large-conductance, calcium-activated potassium channels (BK, also termed BKCa, Slo, or MaxiK) distributed in both excitable and nonexcitable cells are involved in many cellular functions such as action potential repolarization; neuronal excitability; neurotransmitter release; hormone secretion; tuning of cochlear hair cells; innate immunity; and modulation of the tone of vascular, airway, uterine, gastrointestinal, and urinary bladder smooth muscle tissues. Because of their high conductance, activation of BK channels has a strong effect on membrane potential. BK channels differ from all other potassium (K) channels due to their high sensitivity to both intracellular calcium (Ca2+) concentrations and voltage. These features make BK channels ideal negative feedback regulators in many cell types by decreasing voltage-dependent Ca2+ entry through membrane potential hyperpolarization. The current review aims to give a comprehensive understanding of the structure and molecular biology of BK channels and their relevance to various pathophysiological conditions. The review will also focus on the therapeutic potential and pharmacology of the various BK channel activators and blockers. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:103 / 116
页数:14
相关论文
共 167 条
[1]   CALCIUM-ACTIVATED POTASSIUM CHANNELS EXPRESSED FROM CLONED COMPLEMENTARY DNAS [J].
ADELMAN, JP ;
SHEN, KZ ;
KAVANAUGH, MP ;
WARREN, RA ;
WU, YN ;
LAGRUTTA, A ;
BOND, CT ;
NORTH, RA .
NEURON, 1992, 9 (02) :209-216
[2]  
Ahn Duck Sun, 1994, Yonsei Medical Journal, V35, P10
[3]   PKG-I-ALPHA PHOSPHORYLATES THE ALPHA-SUBUNIT AND UP-REGULATES RECONSTITUTED GK(CA) CHANNELS FROM TRACHEAL SMOOTH-MUSCLE [J].
ALIOUA, A ;
HUGGINS, JP ;
ROUSSEAU, E .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 268 (06) :L1057-L1063
[4]   Modulation of the molecular composition of large conductance, Ca2+activated K+ channels in vascular smooth muscle during hypertension [J].
Amberg, GC ;
Bonev, AD ;
Rossow, CF ;
Nelson, MT ;
Santana, LF .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (05) :717-724
[5]   Downregulation of the BK channel β1 subunit in genetic hypertension [J].
Amberg, GC ;
Santana, LF .
CIRCULATION RESEARCH, 2003, 93 (10) :965-971
[6]   Endothelium-derived hyperpolarizing factor in human internal mammary artery is 11,12-epoxyeicosatrienoic acid and causes relaxation by activating smooth muscle BKCa channels [J].
Archer, SL ;
Gragasin, FS ;
Wu, XC ;
Wang, SH ;
McMurtry, S ;
Kim, DH ;
Platonov, M ;
Koshal, A ;
Hashimoto, K ;
Campbell, WB ;
Falck, JR ;
Michelakis, ED .
CIRCULATION, 2003, 107 (05) :769-776
[7]   AN ENZYMATIC MECHANISM FOR POTASSIUM CHANNEL STIMULATION THROUGH PERTUSSIS-TOXIN-SENSITIVE G-PROTEINS [J].
ARMSTRONG, DL ;
WHITE, RE .
TRENDS IN NEUROSCIENCES, 1992, 15 (10) :403-408
[8]   A COMPONENT OF CALCIUM-ACTIVATED POTASSIUM CHANNELS ENCODED BY THE DROSOPHILA-SLO LOCUS [J].
ATKINSON, NS ;
ROBERTSON, GA ;
GANETZKY, B .
SCIENCE, 1991, 253 (5019) :551-555
[9]   17β-estradiol induces L-type Ca2+ channel activation and regulates redox function in macrophages [J].
Azenabor, AA ;
Chaudhry, AU .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2003, 59 (01) :17-28
[10]   MOLECULAR-BASIS OF GATING CHARGE IMMOBILIZATION IN SHAKER POTASSIUM CHANNELS [J].
BEZANILLA, F ;
PEROZO, E ;
PAPAZIAN, DM ;
STEFANI, E .
SCIENCE, 1991, 254 (5032) :679-683