Konno F, Takayanagi I
Naunyn Schmiedebergs Arch Pharmacol. 1986 Jul;333(3):271-6. doi: 10.1007/BF00512940.
Interactions of several alpha-adrenoceptor agonists and antagonists with their receptors were studied in rabbit and guinea pig iris dilator smooth muscle and rabbit aortic strips using pharmacological procedures. In rabbit iris dilators and aortic strips, noradrenaline acted as a full agonist, while oxymetazoline, clonidine and tizanidine acted as partial agonists. The dissociation constants of full and partial agonists in the dilators, calculated after irreversible blockade of a proportion of the active receptors with phenoxybenzamine, were similar to those in the aortic strips. Furthermore, the relative intrinsic efficacies of partial agonists were practically equal in the two tissues, suggesting that these drugs act on the same alpha-adrenoceptors. Since the alpha 2-agonists clonidine and tizanidine had low affinity in the rabbit dilators, the alpha-adrenoceptors in this tissue appear to be of alpha 1-type. These results were further supported by the fact that the pA2-value of prazosin, an alpha 1-antagonist, was approximately 2 log units higher than that of yohimbine, an alpha 2-antagonist. However, pA2-values of four quinazolines (prazosin, bunazosin, SM911 and SM2470) and two yohimbine alkaloids (yohimbine and corynanthine) were significantly lower in the rabbit dilator muscle than in rabbit aortic strips. Two imidazoline antagonists (phentolamine and tolazoline) and a phenethanolamine (labetalol) acted on the alpha 1-adrenoceptors in the two tissues nonselectively. These results suggest that alpha 1-adrenoceptors in the rabbit dilator muscle and aortic strips may not be identical and that both selective and nonselective antagonists which act on these receptor sites exist.(ABSTRACT TRUNCATED AT 250 WORDS)
采用药理学方法,研究了几种α - 肾上腺素能受体激动剂和拮抗剂与兔和豚鼠虹膜开大肌平滑肌以及兔主动脉条中受体的相互作用。在兔虹膜开大肌和主动脉条中,去甲肾上腺素作为完全激动剂起作用,而羟甲唑啉、可乐定和替扎尼定作为部分激动剂起作用。在用苯氧苄胺不可逆地阻断一定比例的活性受体后,计算出的完全和部分激动剂在虹膜开大肌中的解离常数与在主动脉条中的相似。此外,部分激动剂在这两种组织中的相对内在活性实际上是相等的,这表明这些药物作用于相同的α - 肾上腺素能受体。由于α₂激动剂可乐定和替扎尼定在兔虹膜开大肌中的亲和力较低,该组织中的α - 肾上腺素能受体似乎是α₁型。哌唑嗪(一种α₁拮抗剂)的pA₂值比育亨宾(一种α₂拮抗剂)的pA₂值高约2个对数单位,这一事实进一步支持了这些结果。然而,四种喹唑啉类药物(哌唑嗪、布那唑嗪、SM911和SM2470)和两种育亨宾生物碱(育亨宾和柯楠因)在兔虹膜开大肌中的pA₂值明显低于兔主动脉条中的pA₂值。两种咪唑啉拮抗剂(酚妥拉明和妥拉唑啉)和一种苯乙醇胺(拉贝洛尔)对这两种组织中的α₁ - 肾上腺素能受体均无选择性作用。这些结果表明,兔虹膜开大肌和主动脉条中的α₁ - 肾上腺素能受体可能不相同,并且存在作用于这些受体位点的选择性和非选择性拮抗剂。(摘要截短至250字)