Natural bile acids and synthetic analogues modulate large conductance Ca2+-activated K+ (BKCa) channel activity in smooth muscle cells

被引:85
作者
Dopico, AM
Walsh, JV
Singer, JJ
机构
[1] Univ Tennessee, Coll Med, Dept Pharmacol, Hlth Sci Ctr, Memphis, TN 38163 USA
[2] Univ Massachusetts, Sch Med, Dept Physiol, Worcester, MA 01655 USA
关键词
bile salts; maxi-K channels; smooth muscle; liver disease;
D O I
10.1085/jgp.119.3.251
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Bile acids have been reported to produce relaxation Of smooth muscle both in vitro and in vivo. The cellular mechanisms underlying bile acid-induced relaxation are largely unknown. Here we demonstrate, rising patch-clamp techniques, that natural bile acids and synthetic analogues reversibly increase BKCa channel activity in rabbit mesenteric artery smooth muscle cells. In excised inside-out patches bile acid-induced increases in channel activity acre characterized by a parallel leftward shift in the activity-voltage relationship. This increase in BKCa channel activity is not due to Ca2+-dependent mechanism(s) or changes in freely diffusible messengers, but to a direct action of the bile acid on the channel protein itself or some closely, associated component in the cell membrane. For naturally occurring bile acids, the magnitude of bile acid-induced increase in BKCa channel activity is inversely related to the number of hydroxyl groups in the bile acid molecule. By using synthetic analogues, we demonstrate that such increase in activin, is not affected by several chemical modifications in the lateral chain of the molecule, but is markedly favored by polar groups in the side of the steroid rings opposite to the side where the methyl groups are located, which stresses the importance of the planar polarity of the molecule. Bile acid-induced increases in BKCa channel activity are also observed in Smooth muscle cells freshly, dissociated from rabbit main pulmonary artery and gallbladder, raising the possibility that a direct activation of BKCa channels by these planar steroids is a widespread phenomenon in many smooth muscle cell types. Bile acid concentrations that increase BKCa channel activity in mesenteric artery smooth muscle cells are found in the systemic circulation under a variety of human pathophysiological conditions, and their ability to enhance BKCa channel activity may explain their relaxing effect on smooth muscle.
引用
收藏
页码:251 / 273
页数:23
相关论文
共 91 条
[51]  
LAWRENCE DK, 1975, MOL PHARMACOL, V11, P280
[52]  
LEWIS B, 1969, LANCET, V1, P219
[53]   Membrane stiffness and channel function [J].
Lundbaek, JA ;
Birn, P ;
Girshman, J ;
Hansen, AJ ;
Andersen, OS .
BIOCHEMISTRY, 1996, 35 (12) :3825-3830
[54]   LYSOPHOSPHOLIPIDS MODULATE CHANNEL FUNCTION BY ALTERING THE MECHANICAL-PROPERTIES OF LIPID BILAYERS [J].
LUNDBAEK, JA ;
ANDERSEN, OS .
JOURNAL OF GENERAL PHYSIOLOGY, 1994, 104 (04) :645-673
[55]   ROLE OF SURFACE ELECTROSTATICS IN THE OPERATION OF A HIGH-CONDUCTANCE CA-2+-ACTIVATED K+ CHANNEL [J].
MACKINNON, R ;
LATORRE, R ;
MILLER, C .
BIOCHEMISTRY, 1989, 28 (20) :8092-8099
[56]   FUNCTIONAL MODIFICATION OF A CA-2+-ACTIVATED K+ CHANNEL BY TRIMETHYLOXONIUM [J].
MACKINNON, R ;
MILLER, C .
BIOCHEMISTRY, 1989, 28 (20) :8087-8092
[57]   CALCIUM-ACTIVATED POTASSIUM CHANNELS - REGULATION BY CALCIUM [J].
MCMANUS, OB .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1991, 23 (04) :537-560
[58]   Characteristics of single, large-conductance calcium-dependent potassium channels (BKCa) from smooth muscle cells isolated from the rabbit mesenteric artery [J].
Mistry, DK ;
Garland, CJ .
JOURNAL OF MEMBRANE BIOLOGY, 1998, 164 (02) :125-138
[59]   CORRELATION BETWEEN THE HYDROPHOBIC NATURE OF MONOSACCHARIDES AND CHOLATES, AND THEIR HYDROPHOBIC INDEXES [J].
MIYAJIMA, K ;
MACHIDA, K ;
TAGA, T ;
KOMATSU, H ;
NAKAGAKI, M .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1988, 84 :2537-2544
[60]   CHARACTERIZATION OF THE ILEAL NA+/BILE SALT COTRANSPORTER IN BRUSH-BORDER MEMBRANE-VESICLES AND FUNCTIONAL EXPRESSION IN XENOPUS-LAEVIS OOCYTES [J].
MULLINS, JGL ;
BEECHEY, RB ;
GOULD, GW ;
CAMPBELL, FC ;
SHIRAZIBEECHEY, SP .
BIOCHEMICAL JOURNAL, 1992, 285 :785-790