McGrath J C
Br J Pharmacol. 1984 Aug;82(4):769-81. doi: 10.1111/j.1476-5381.1984.tb16473.x.
alpha-Adrenoceptor antagonism of several test drugs was assessed against adrenergic contractile responses to field stimulation in rat vas deferens and anococcygeus, the prejunctional inhibitory effect of xylazine in vas deferens and the contractile effects of alpha-adrenoceptor agonists in anococcygeus. Against the adrenergic nerve-induced contraction in vas deferens, the potency series was WB 4101 greater than prazosin greater than apoyohimbine greater than corynanthine greater than yohimbine greater than rauwolscine. Against the inhibitory effect of xylazine in vas deferens the potency series was apoyohimbine greater than rauwolscine = yohimbine greater than WB 4101 much greater than prazosin and corynanthine. In anococcygeus, against the contractile responses to adrenergic nerve stimulation or to the agonists amidephrine, noradrenaline and xylazine, the potency series was apoyohimbine greater than corynanthine greater than rauwolscine. These results show that apoyohimbine is more potent than the yohimbine sterioisomers as an antagonist at alpha 1- and alpha 2-adrenoceptors but is not more selective. The assay methods employed confirm the current classification of 'alpha'-receptors and drugs.
评估了几种受试药物对大鼠输精管和肛尾肌中电场刺激引起的肾上腺素能收缩反应的α-肾上腺素受体拮抗作用、赛拉嗪在输精管中的突触前抑制作用以及α-肾上腺素受体激动剂在肛尾肌中的收缩作用。在输精管中,对抗肾上腺素能神经诱导的收缩,效价顺序为WB 4101>哌唑嗪>阿朴育亨宾>育亨宾碱>育亨宾>萝芙辛。在输精管中,对抗赛拉嗪的抑制作用,效价顺序为阿朴育亨宾>萝芙辛 = 育亨宾>WB 4101>>哌唑嗪和育亨宾碱。在肛尾肌中,对抗肾上腺素能神经刺激或激动剂酰胺福林、去甲肾上腺素和赛拉嗪的收缩反应,效价顺序为阿朴育亨宾>育亨宾碱>萝芙辛。这些结果表明,作为α1和α2肾上腺素受体拮抗剂,阿朴育亨宾比育亨宾立体异构体更有效,但选择性并不更高。所采用的测定方法证实了目前对“α”受体和药物的分类。