Cunningham K A, Callahan P M, Craigmyle N A, Appel J B
Eur J Pharmacol. 1985 Dec 17;119(3):225-9. doi: 10.1016/0014-2999(85)90299-7.
Bromocriptine, lergotrile and lisuride but not apomorphine, ergonovine or lysergic acid diethylamide (LSD) mimicked clonidine in rats trained to discriminate this compound (0.02 mg/kg) from saline. BC 105, ketanserin and haloperidol failed to block the clonidine cue. Yohimbine was an effective antagonist of clonidine but not of the lisuride substitution for clonidine. Since dopamine does not appear to be involved in the stimulus effects of clonidine, the behavioral similarities between clonidine and some ergots may be related to alpha-adrenoceptor stimulation; however, the role of blood pressure changes in the stimulus effects of all of these compounds should not be overlooked.
在经过训练能区分可乐定(0.02毫克/千克)和生理盐水的大鼠中,溴隐亭、麦角腈和麦角异胺能模拟可乐定的作用,但阿扑吗啡、麦角新碱或麦角酸二乙酰胺(LSD)则不能。BC 105、酮色林和氟哌啶醇未能阻断可乐定的提示作用。育亨宾是可乐定的有效拮抗剂,但不是麦角异胺替代可乐定的拮抗剂。由于多巴胺似乎不参与可乐定的刺激作用,可乐定与某些麦角生物碱之间的行为相似性可能与α-肾上腺素能受体刺激有关;然而,不应忽视血压变化在所有这些化合物刺激作用中的作用。