Dabiré H, Mouillé P, Schmitt H
Eur J Pharmacol. 1982 Dec 17;86(1):83-6. doi: 10.1016/0014-2999(82)90400-9.
In the vas deferens of the rat, (-)-170 150 (imidazolinyl-2)-benzodioxane-1-4 or 2-(2-(1,4-benzodioxanyl))-2-imidazoline appeared to be more selective than (+)-170 150 for antagonizing the inhibitory effects of clonidine on the twitch response. In contrast, (+)-170 150 was the most potent of the two isomers for antagonizing the centrally mediated clonidine- or azepexole-induced sleep in chickens. These unexpected results seem to indicate that there are several subpopulations of alpha 2-adrenoceptors.
在大鼠的输精管中,(-)-170 150(咪唑啉基-2)-苯并二恶烷-1,4或2-(2-(1,4-苯并二恶烷基))-2-咪唑啉在拮抗可乐定对抽搐反应的抑制作用方面似乎比(+)-170 150更具选择性。相比之下,(+)-170 150是这两种异构体中拮抗可乐定或阿泽哌唑诱导的鸡中枢介导睡眠作用最强的。这些意外结果似乎表明存在几种α2-肾上腺素能受体亚群。