Slow association of positively charged Ca2+ channel antagonist amlodipine to dihydropyridine receptor sites in rat brain membranes

被引:4
作者
Qu, YL
Sugiyama, K
Hattori, K
Yamamoto, A
Watanabe, K
Nagatomo, T
机构
[1] NIIGATA COLL PHARM,DEPT PHARMACOL,NIIGATA 96021,JAPAN
[2] TSUBAME ROSAI HOSP,RES LABS,DIV CARDIOVASC,TSUBAME,NIIGATA 95912,JAPAN
来源
GENERAL PHARMACOLOGY | 1996年 / 27卷 / 01期
关键词
amlodipine; Ca2+ antagonists; H-3-PN200-110; pH dependence; rat brain; slow association; slow onset;
D O I
10.1016/0306-3623(95)00085-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. No significant differences were observed in K-d and B-max values between pH 7.2 (0.16 +/- 0.01 nM and 155.36 +/- 16.07 fmol/mg protein) and pH 10.0(0.15 +/- 0.01 nM and 158.63 +/- 13.80 fmol/mg protein) in rat brain membranes. 2. The IC50 ratios at 0- and 270-min preincubations of amlodipine and manidipine at pH 7.2 were 23.09 and 10.25, respectively, whereas these ratios for these two drugs at pH 10.0 mere 2.63 and 1.34, respectively. 3. In contrast, on treatment with nisoldipine, benidipine, SM-6586 and nifedipine, no significant differences were observed in the IC50 ratios between 0- and 270-min preincubations at pH 7.2 and 10.0.
引用
收藏
页码:137 / 140
页数:4
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