Wilffert B, van Heiningen P N, Mathy M J, Batink H D, de Jonge A, Thoolen M J, Timmermans P B, van Zwieten P A
Naunyn Schmiedebergs Arch Pharmacol. 1984 Aug;327(1):90-2. doi: 10.1007/BF00504998.
Following i.v. bolus injections into pithed normotensive rats, the maximal diastolic pressor responses to B-HT 920 and B-HT 958 amounted to 115 and 35 mm Hg, respectively. Prazosin (0.1 mg/kg, i.v., -15 min) was without effect on the log dose-pressor effect curve of B-HT 958, whereas yohimbine (1 mg/kg, i.v., -15 min) shifted this curve about 30-fold to the right, showing the exclusive participation of alpha 2-adrenoceptors in the vasoconstrictor response to B-HT 958. In doses of 10 and 30 mg/kg, B-HT 958 displaced the log dose-vasoconstrictor effect curve of B-HT 920 approximately 6- and 30-fold, respectively, to the right, illustrating the partial agonism of B-HT 958 at postjunctional vascular alpha 2-adrenoceptors. Despite the marked difference in intrinsic activity of B-HT 920 and B-HT 958, the calcium entry blocker nifedipine exhibited a comparable inhibitory action on the vasopressor responses to both agonists. This finding indicates that partial and full agonism at vascular alpha 2-adrenoceptors are not related to the susceptibility of the initiated pressor response to inhibition by calcium entry blockade.
在向脊髓横断的正常血压大鼠静脉推注给药后,B-HT 920和B-HT 958的最大舒张压升压反应分别达到115和35 mmHg。哌唑嗪(0.1 mg/kg,静脉注射,-15分钟)对B-HT 958的对数剂量-升压效应曲线无影响,而育亨宾(1 mg/kg,静脉注射,-15分钟)使该曲线右移约30倍,表明α2-肾上腺素受体在对B-HT 958的血管收缩反应中起唯一作用。B-HT 958剂量为10和30 mg/kg时,分别使B-HT 920的对数剂量-血管收缩效应曲线右移约6倍和30倍,说明B-HT 958对节后血管α2-肾上腺素受体具有部分激动作用。尽管B-HT 920和B-HT 958的内在活性存在显著差异,但钙通道阻滞剂硝苯地平对两种激动剂引起的升压反应表现出相当的抑制作用。这一发现表明,血管α2-肾上腺素受体的部分激动和完全激动与起始升压反应对钙通道阻滞抑制的敏感性无关。