Pittner H
Arch Int Pharmacodyn Ther. 1987 Feb;285(2):199-210.
The beta 1-adrenoceptor blocking agent celiprolol was tested for alpha 2-adrenoceptor blocking properties in different pharmacological models. In radioligand binding studies celiprolol shows a tenfold higher affinity to alpha 2- in comparison to alpha 1-adrenoceptors; however, the affinity of celiprolol to alpha-adrenoceptors is at least 100 times lower than that to beta-adrenoceptors. Celiprolol enhances the inhibitory effect of the alpha 2-adrenoceptor agonist clonidine in the electrically stimulated rat vas deferens in vitro; this celiprolol effect is abolished, but not reversed by propranolol. In pithed rats celiprolol inhibits the tachycardia induced by spinal electrical stimulation; the inhibitory effect of clonidine on the same parameter is augmented by celiprolol, but reversed by rauwolscine. Also in pithed rats celiprolol does not affect the pressor effect of the alpha 2-adrenoceptor agonist B-HT 920. From these results it is concluded that celiprolol does not possess any relevant alpha 2-adrenoceptor blocking properties which could explain the broncho- and vasodilating actions of that substance.
在不同的药理模型中对β1 -肾上腺素受体阻滞剂塞利洛尔的α2 -肾上腺素受体阻断特性进行了测试。在放射性配体结合研究中,与α1 -肾上腺素受体相比,塞利洛尔对α2 -肾上腺素受体的亲和力高10倍;然而,塞利洛尔对α -肾上腺素受体的亲和力比对β -肾上腺素受体的亲和力至少低100倍。塞利洛尔可增强α2 -肾上腺素受体激动剂可乐定对体外电刺激大鼠输精管的抑制作用;普萘洛尔可消除但不能逆转塞利洛尔的这种作用。在脊髓麻醉大鼠中,塞利洛尔可抑制脊髓电刺激诱发的心动过速;可乐定对同一参数的抑制作用可被塞利洛尔增强,但可被萝芙木碱逆转。同样在脊髓麻醉大鼠中,塞利洛尔不影响α2 -肾上腺素受体激动剂B-HT 920的升压作用。从这些结果可以得出结论,塞利洛尔不具有任何相关的α2 -肾上腺素受体阻断特性,而这些特性可以解释该物质的支气管扩张和血管舒张作用。