EFFECT OF CA2+ AGONIST BAY K-8644 IN HUMAN PLACENTAL ARTERIES

被引:6
|
作者
BARRUS, MT
REVIRIEGO, J
MARIN, J
机构
[1] UNIV AUTONOMA MADRID,FAC MED,DEPT FARMACOL & TERAPEUT,E-28029 MADRID,SPAIN
[2] UNIV AUTONOMA MADRID,FAC MED,DEPT FISIOL,E-28029 MADRID,SPAIN
来源
GENERAL PHARMACOLOGY | 1995年 / 26卷 / 05期
关键词
HUMAN PLACENTAL ARTERIES; BAY K 8644; NIFEDIPINE; DILTIAZEM; CALCIUM CHANNELS;
D O I
10.1016/0306-3623(94)00289-Y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Bay K 8644 (0.1 mu M) induced weak contractions in human placental artery segments that were increased in the presence of 7.5 mM K+. K+ and serotonin (5-HT) induced contractions that were enhanced by preincubation of segments with Bay K 8644. These enhancements were reduced by nifedipine (0.1 mu M) and diltiazem (1 mu M). 2. Bay K 8644 induced a Ca-45(2+) uptake increase which was potentiated by depolarization with K+ (less than 30 mM) and antagonized by nifedipine. K+ (15 and 30 mM) and 5-HT (1 mu M) induced Ca-45(2+) uptake that was enhanced by Bay K 8644. 3. These results suggest that Bay K 8644: (1) is unable to activate the quiescent potential-operated Ca2+ channels (POCs) of these arteries, and (2) activates receptor (5-HT)-operated Ca2+ channels or facilitates Ca2+ influx through POCs activated by 5-HT.
引用
收藏
页码:989 / 996
页数:8
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