Andersson P, Olsson O A, Waldeck B
Acta Pharmacol Toxicol (Copenh). 1982 Oct;51(4):358-64. doi: 10.1111/j.1600-0773.1982.tb01037.x.
A series of phenylethanolamine derivatives were examined with respect to their bronchospasmolytic effect and their ability to depress the contractions of the soleus muscle in cat and guinea-pig. One group of compounds including D2343 (1-(4-hydroxyphenyl)-2-[1,1-dimethyl-3-(2-methoxyphenyl) propylamino]-ethanol HCl), a new beta 2-adrenoceptor agonist, appeared to be more effective in combating bronchospasm induced by histamine than in depressing the contractions of the soleus muscle in anaesthetized cat. This difference disappeared when serotonin was used to induce bronchospasm. Terbutaline antagonized histamine and serotonin equally well. Experiments in vivo and in vitro with guinea-pigs gave ambiguous results. Slowly developing effects was a common feature of the compounds showing the apparent effect separation. None of the available beta-adrenoceptor agonists appears to distinguish between the adrenoceptors in the airway smooth muscle mediating bronchial relaxation and those in the skeletal muscle associated with tremor.
研究了一系列苯乙醇胺衍生物的支气管解痉作用以及抑制猫和豚鼠比目鱼肌收缩的能力。包括新型β2 -肾上腺素能受体激动剂D2343(1 -(4 - 羟基苯基)- 2 - [1,1 - 二甲基 - 3 -(2 - 甲氧基苯基)丙基氨基] - 乙醇盐酸盐)在内的一组化合物,在对抗组胺诱导的支气管痉挛方面似乎比抑制麻醉猫的比目鱼肌收缩更有效。当使用血清素诱导支气管痉挛时,这种差异消失。特布他林对抗组胺和血清素的效果同样良好。豚鼠体内和体外实验结果不明确。作用缓慢出现是显示出明显效应分离的化合物的共同特征。现有的β -肾上腺素能受体激动剂似乎都无法区分介导支气管舒张的气道平滑肌中的肾上腺素能受体和与震颤相关的骨骼肌中的肾上腺素能受体。