Colpaert F C, Janssen P A
Eur J Pharmacol. 1984 Aug 3;103(1-2):169-71. doi: 10.1016/0014-2999(84)90206-1.
The study used the loss of the righting reflex in response to the alpha 2-agonist xylazine in an in vivo rat assay to determine possible effects of the LSD antagonist pirenperone at alpha 2-adrenoceptors. Pirenperone antagonized the response and was more potent (ED50: 0.32 mg/kg) than yohimbine (1.25 mg/kg) and piperoxan (3.30 mg/kg). The data suggest that pirenperone may act at alpha 2-adrenoceptors in vivo.
该研究在体内大鼠试验中利用对α2-激动剂赛拉嗪的翻正反射丧失来确定LSD拮抗剂匹泮哌隆对α2-肾上腺素能受体可能产生的影响。匹泮哌隆可拮抗该反应,且比育亨宾(1.25mg/kg)和哌泊昔生(3.30mg/kg)更有效(半数有效剂量:0.32mg/kg)。数据表明匹泮哌隆可能在体内作用于α2-肾上腺素能受体。