Venodilator effects of pranidipine, a 1,4-dihydropyridine Ca2+ channel antagonist, in rats: Comparison with nifedipine and amlodipine

被引:11
|
作者
Hirano, T
Ohura, M
Orito, K
Fujiki, H
Miyakoda, G
Mori, T
机构
[1] 2Nd Tokushima Inst. of New Drug Res., Otsuka Pharmaceutical Co., Ltd., Tokushima 771-01, 463-10 Kagasuno, Kawauchi-cho
关键词
pranidipine (OPC-13340); Ca2+ channel antagonist; circulatory filling pressure; mean; venodilator effect; (rat); DIHYDROPYRIDINE CALCIUM-ANTAGONIST; CONSCIOUS RATS; OPC-13340; PRESSURE; POTENT; CAPACITANCE; BLOCKER; DOGS;
D O I
10.1016/S0014-2999(97)10007-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of pranidipine, a dihydropyridine Ca2+ channel antagonist, on mean circulatory filling pressure, an index of body venous tone, were compared with those of other dihydropyridines (nifedipine and amlodipine) and nitroglycerin in anaesthetized hexamethonium-and norepinephrine-treated rats. In this study, the compounds were used at doses having a equi-hypotensive effect. Intravenous bolus injection of pranidipine (10 and 30 mu g/kg) significantly decreased mean circulatory filling pressure in a dose-dependent manner, as did nitroglycerin (30 and 100 mu g/kg). Nifedipine (30 and 100 mu g/kg), however, did not affect mean circulatory filling pressure. Amlodipine (1000 and 3000 mu g/kg) decreased mean circulatory filling pressure only at the higher dose. These results suggest that pranidipine has a greater venodilator effect than nifedipine and amlodipine.
引用
收藏
页码:201 / 204
页数:4
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