Nifedipine block of capacitative calcium entry in cultured human uterine smooth-muscle cells

被引:38
作者
Young, RC [1 ]
Schumann, R [1 ]
Zhang, PS [1 ]
机构
[1] Med Univ S Carolina, Dept Obstet & Gynecol, Charleston, SC 29425 USA
关键词
myometrium; capacitative calcium entry; mechanisms of action of nifedipine;
D O I
10.1016/S1071-5576(01)00109-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To determine whether nifedipine inhibits capacitative calcium entry at clinically relevant concentrations using human myocytes as a model for human myometrium. Methods: Myocyte cultures were initiated from the myometrium of term pregnant women who underwent cesarean deliver. Paired cells were chosen for study. The cell of interest was stimulated by an intercellular calcium wave from the adjacent cell. In this fashion, release of sarcoplasmic reticulum (SR) calcium was accomplished with minimal disturbance of the plasma membrane and the subplasmalemmal space (SPS) of the cell studied. Depletion of the SR calcium stores by the calcium wave activated the capacitative calcium current, elevated calcium in the SPS, and activated calcium-activated potassium channels. A cell-attached patch clamp was used to monitor the outward current resulting from the calcium activation of these potassium channels. Calcium green-1 fluorescence was used to simultaneously monitor changes of the deep cytosolic calcium concentration. Experiments were performed at varying concentration of nifedipine (0-10 mu mol/L). Results: Nifedipine reduced outward potassium currents in a dose-dependent manner. Nifedipine at 100 nmol/L resulted in greater than a 50% reduction of outward current, indicating a significant inhibition of capacitative calcium entry at that concentration. Higher concentrations of nifedipine abolished outward current. Experiments designed to detect indirect effects of nifedipine on capacitative calcium entry were negative. Conclusions: Nifedipine block of capacitative calcium entry occurred at concentrations similar to those required to block L-type voltage-activated calcium channels. These data suggest that block of capacitative calcium entry may be an important mechanism of action when nifedipine is clinically used for tocolysis of preterm labor. (J Soc gynecol Investig 2001; 8:210-5) Copyright (C) 2001 by the Society for Gynecologic Investigation.
引用
收藏
页码:210 / 215
页数:6
相关论文
共 16 条
[1]   A capacitative calcium current in cultured skeletal muscle cells is mediated by the calcium-specific leak channel and inhibited by dihydropyridine compounds [J].
Hopf, FW ;
Reddy, P ;
Hong, J ;
Steinhard, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (37) :22358-22367
[2]   PHARMACOKINETICS OF ORAL NIFEDIPINE - RELEVANCE OF THE DISTRIBUTION PHASE [J].
HOYOVADILLO, C ;
CASTANEDAHERNANDEZ, G ;
HERRERA, JE ;
VIDALGARATE, J ;
SALAZAR, LA ;
MORENORAMOS, A ;
CHAVEZ, F ;
TENA, I ;
HONG, E .
JOURNAL OF CLINICAL PHARMACOLOGY, 1989, 29 (03) :251-256
[3]   Functional interaction between InsP3 receptors and store-operated Htrp3 channels [J].
Kiselyov, K ;
Xu, X ;
Mozhayeva, G ;
Kuo, T ;
Pessah, I ;
Mignery, G ;
Zhu, X ;
Birnbaumer, L ;
Muallem, S .
NATURE, 1998, 396 (6710) :478-482
[4]   Gating of store-operated channels by conformational coupling to ryanodine receptors [J].
Kiselyov, KI ;
Shin, DM ;
Wang, YM ;
Pessah, IN ;
Allen, PD ;
Muallem, S .
MOLECULAR CELL, 2000, 6 (02) :421-431
[5]   Requirement of the inositol trisphosphate receptor for activation of store-operated Ca2+ channels [J].
Ma, HT ;
Patterson, RL ;
van Rossum, DB ;
Birnbaumer, L ;
Mikoshiba, K ;
Gill, DL .
SCIENCE, 2000, 287 (5458) :1647-1651
[6]   Oxytocin-stimulated capacitative calcium entry in human myometrial cells [J].
Monga, M ;
Campbell, DF ;
Sanborn, BM .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1999, 181 (02) :424-429
[7]   Nifedipine versus ritodrine for suppression of preterm labor;: a meta-analysis [J].
Oei, SG ;
Mol, BWJ ;
de Kleine, MJK ;
Brölmann, HAM .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1999, 78 (09) :783-788
[8]   Relationship of ion channel activity to control of myometrial calcium [J].
Sanborn, BM .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2000, 7 (01) :4-11
[9]   The role of the sarcoplasmic reticulum as a Ca2+ sink in rat uterine smooth muscle cells [J].
Shmigol, AV ;
Eisner, DA ;
Wray, S .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 520 (01) :153-163
[10]  
TAKEMURA H, 1989, J BIOL CHEM, V264, P12266