Bou J, Massingham R
Eur J Pharmacol. 1986 Mar 4;121(3):319-25. doi: 10.1016/0014-2999(86)90252-9.
Diltiazem (10 microM) did not significantly affect concentration-response curves to the full, relatively selective alpha 1-adrenoceptor agonists phenylephrine and cirazoline in rabbit aorta and dog saphenous vein preparations. The effects of these 2 agonists remained resistant to diltiazem even in tissues pretreated with phenoxybenzamine (0.03 or 0.1 microM, 20 min) to reduce the alpha-adrenoceptor reserve. Sgd 101/75 and St 587 were partial agonists in both vascular preparations. The concentration-response curves to these relatively selective alpha 1-adrenoceptor agonists were also unaffected, or only slightly attenuated, by diltiazem. B-HT 920 at low concentrations preferentially stimulated the dog saphenous vein preparation and only at high concentrations elicited small contractions of the rabbit aorta. The responses to B-HT 920 were mediated by alpha 2-adrenoceptors in the vein and by alpha 1-adrenoceptors in the aorta yet concentration-response curves to this agonist were significantly attenuated by diltiazem in both tissues. The results indicate that the resistance of certain alpha-adrenoceptor-mediated responses in vascular preparations to calcium entry blockers need not be associated with the presence of a significant receptor reserve and that calcium dependency of a response may be determined by the agonist.
地尔硫䓬(10微摩尔)对兔主动脉和犬隐静脉标本中对完全性、相对选择性α1 - 肾上腺素能受体激动剂去氧肾上腺素和西拉唑啉的浓度 - 反应曲线无显著影响。即使在预先用酚苄明(0.03或0.1微摩尔,20分钟)处理以减少α - 肾上腺素能受体储备的组织中,这两种激动剂的作用对地尔硫䓬仍有抗性。Sgd 101/75和St 587在两种血管标本中均为部分激动剂。地尔硫䓬对这些相对选择性α1 - 肾上腺素能受体激动剂的浓度 - 反应曲线也无影响,或仅略有减弱。低浓度的B - HT 920优先刺激犬隐静脉标本,仅在高浓度时引起兔主动脉的小收缩。对B - HT 920的反应在静脉中由α2 - 肾上腺素能受体介导,在主动脉中由α1 - 肾上腺素能受体介导,但该激动剂的浓度 - 反应曲线在两种组织中均被地尔硫䓬显著减弱。结果表明,血管标本中某些α - 肾上腺素能受体介导的反应对钙通道阻滞剂的抗性不一定与显著的受体储备的存在相关,并且反应的钙依赖性可能由激动剂决定。