Llenas J, Massingham R
Eur J Pharmacol. 1983 Jan 28;87(1):53-9. doi: 10.1016/0014-2999(83)90049-3.
In an attempt to extend the hypothesis that activation of vascular postsynaptic alpha 2-adrenoceptors requires an influx of Ca2+ ions, the effects of 2 calcium entry blocking drugs verapamil and cinnarizine have been examined as inhibitors of the pressor responses to methoxamine and B-HT 920 in autoperfused dog hindlimb preparations. Verapamil (0.1-1 mg i.a.) selectively antagonized responses to B-HT 920 and had little or no effect upon responses to methoxamine, thus supporting this hypothesis. However cinnarizine, over the dose range studied (0.1-1 mg/kg i.a.) produced quantitatively similar inhibitions of the hindlimb responses to B-HT 920 and methoxamine. These results suggest that cinnarizine may have a different site of action to verapamil in resistance vessels of the dog hindlimb.
为了拓展血管突触后α2 - 肾上腺素能受体激活需要Ca2+离子内流这一假说,研究了两种钙通道阻滞剂维拉帕米和桂利嗪对自灌注犬后肢制剂中对甲氧明和B - HT 920升压反应的抑制作用。维拉帕米(0.1 - 1毫克,动脉内注射)选择性地拮抗对B - HT 920的反应,而对甲氧明的反应几乎没有影响,从而支持了这一假说。然而,在所研究的剂量范围内(0.1 - 1毫克/千克,动脉内注射),桂利嗪对后肢对B - HT 920和甲氧明的反应产生了数量上相似的抑制作用。这些结果表明,在犬后肢阻力血管中,桂利嗪的作用位点可能与维拉帕米不同。