Vascular large conductance calcium-activated potassium channels: Functional role and therapeutic potential

被引:87
作者
Eichhorn, Birgit [1 ]
Dobrev, Dobromir [1 ]
机构
[1] Tech Univ Dresden, Fak Med, Inst Pharmakol & Toxikol, D-01307 Dresden, Germany
关键词
calcium-activated potassium channel (BKCa channel maxiK channel); endothelial cells; vascular smooth muscle cells; hypertension; atherosclerosis; diabetes;
D O I
10.1007/s00210-007-0193-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Large-conductance Ca2+-activated K+ channels (BKCa or maxiK channels) are expressed in different cell types. They play an essential role in the regulation of various cell functions. In particular, BKCa channels have been extensively studied in vascular smooth muscle cells, where they contribute to the control of vascular tone. They facilitate the feedback regulation against the rise of intracellular Ca2+, membrane depolarization and vasoconstriction. BKCa channels promote a K+ outward current and lead to membrane hyperpolarization. In endothelial cells expression and function of BKCa channels play an important role in the regulation of the vascular smooth muscle activity. Endothelial BKCa channels modulate the biosyntheses and release of various vasoactive modulators and regulate the membrane potential. Because of their regulatory role in vascular tone, endothelial BKCa channels have been suggested as therapeutic targets for the treatment of cardiovascular diseases. Hypertension, atherosclerosis, and diabetes are associated with altered current amplitude, open probability, and Ca2+-sensing of BKCa channels. The properties of BKCa channels and their role in endothelial and vascular smooth muscle cells would address them as potential therapeutic targets. Further studies are necessary to identify the detailed molecular mechanisms of action and to investigate selective BKCa channels openers as possible therapeutic agents for clinical use.
引用
收藏
页码:145 / 155
页数:11
相关论文
共 147 条
[41]   Endothelial cell pathway for conduction of hyperpolarization and vasodilation along hamster feed artery [J].
Emerson, GG ;
Segal, SS .
CIRCULATION RESEARCH, 2000, 86 (01) :94-100
[42]   ENHANCED SINGLE-CHANNEL K+ CURRENT IN ARTERIAL MEMBRANES FROM GENETICALLY HYPERTENSIVE RATS [J].
ENGLAND, SK ;
WOOLDRIDGE, TA ;
STEKIEL, WJ ;
RUSCH, NJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :H1337-H1345
[43]  
ESSIN K, 2007, J PHYSL, V9
[44]  
Félétou M, 2000, ACTA PHARMACOL SIN, V21, P1
[45]   Endothelium-derived hyperpolarizing factor -: Where are we now? [J].
Feletou, Michel ;
Vanhoutte, Paul M. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (06) :1215-1225
[46]   Gain-of-function mutation in the KCNMB1 potassium channel subunit is associated with low prevalence of diastolic hypertension [J].
Fernández-Fernández, JM ;
Tomás, M ;
Vázquez, E ;
Orio, P ;
Latorre, R ;
Sentí, M ;
Marrugat, J ;
Valverde, MA .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (07) :1032-1039
[47]   Nitric oxide-dependent β2-adrenergic dilatation of rat aorta is mediated through activation of both protein kinase A and Akt [J].
Ferro, A ;
Coash, M ;
Yamamoto, T ;
Rob, J ;
Ji, Y ;
Queen, L .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 143 (03) :397-403
[48]   Activation of nitric oxide synthase by β2-adrenoceptors in human umbilical vein endothelium in vitro [J].
Ferro, A ;
Queen, LR ;
Priest, RM ;
Xu, BA ;
Ritter, JM ;
Poston, L ;
Ward, JPT .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 126 (08) :1872-1880
[49]   β-adrenoceptors and potassium channels [J].
Ferro, Albert .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2006, 373 (03) :183-185
[50]   Subplasmalemmal ryanodine-sensitive Ca2+ release contributes to Ca2+-dependent K+ channel activation in a human umbilical vein endothelial cell line [J].
Frieden, M ;
Graier, WF .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 524 (03) :715-724