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左旋千金藤立定对血压和对α—肾上腺素受体...
引用本文:沈德莉,鲁映青.左旋千金藤立定对血压和对α—肾上腺素受体...[J].中国药理学报,1991,12(6):514-518.
作者姓名:沈德莉  鲁映青
摘    要:

关 键 词:千金藤立定  降压剂  胸主动脉  血压

Effect of (-)-stepholidine on blood pressure and alpha-adrenoceptor agonists-, KCl- and CaCl2-evoked contractions of aortic strips]
D L Shen,G Z Jin,Y F He,Z D Zhang,Z Sun,Y Q Lu,Z C Yang.Effect of (-)-stepholidine on blood pressure and alpha-adrenoceptor agonists-, KCl- and CaCl2-evoked contractions of aortic strips][J].Acta Pharmacologica Sinica,1991,12(6):514-518.
Authors:D L Shen  G Z Jin  Y F He  Z D Zhang  Z Sun  Y Q Lu  Z C Yang
Institution:Shanghai Institute of Materia Medica, Chinese Academy of Sciences.
Abstract:Iv (-)-SPD lowered the blood pressure in anesthetized rat, the ED50 value was 5.1 +/- 2.5 mg.kg-1. In the experiments of rat and rabbit aortic strips, (-)-SPD 0.3-100.0 mumol.L-1 inhibited the contraction initiated by clonidine (alpha 2) and phenylephrine (alpha 1) and shifted the dose-response curve to the right parallely without change in maximum response. The inhibitory ratio of (-)-SPD acting on alpha 2/alpha 1 adrenergic receptors was about 7.2, and (-)-SPD thus was predominant inhibition on alpha 2 adrenergic receptors. In the experiment of aortic strips from reserpinized rabbits, the inhibition of (-)-SPD on contraction evoked by clonidine was diminished markedly. The results suggest that (-)-SPD stimulated mainly the alpha 2-adrenergic receptors of presynaptic nerve endings. Moreover (-)-SPD 1 mumol.L-1 inhibited the release of intracellular Ca2+ initiated by NE. (-)-SPD 3-30 mumol.L-1 blocked the voltage-dependent Ca2+ channel.
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