McKearney J W
Neuropharmacology. 1983 Jun;22(6):775-9. doi: 10.1016/0028-3908(83)90102-8.
Squirrel monkeys were studied under fixed-interval schedules in which responding was maintained either by food presentation or by termination of stimuli correlated with electric shock delivery, or under a schedule in which responses decreased the intensity of electric shock, which periodically increased in intensity (shock titration). Clonidine-HCl (0.01-1.7 mg/kg) decreased responding under the fixed-interval schedules and increased the intensity at which shock was maintained under the titration schedule. Pretreatment with the alpha 2-adrenoreceptor antagonist yohimbine-HCl (0.1-1.0 mg/kg) resulted in a 3-10-fold shift to the right in the clonidine dose-response curve. Similar antagonism was seen after pretreatment with small doses of the less selective alpha-adrenoreceptor antagonist, tolazoline-HCl (3.0, 5.6 mg/kg), but not with the alpha 1 antagonist prazosin (0.1, 0.3 mg/kg). The effects of clonidine on behavior under these conditions were apparently due to actions at alpha 2-adrenoreceptor sites.
松鼠猴在固定间隔时间表下接受研究,在该时间表中,反应通过食物呈现或与电击释放相关的刺激终止来维持,或者在一种反应会降低电击强度(电击强度会周期性增加,即电击滴定)的时间表下接受研究。盐酸可乐定(0.01 - 1.7毫克/千克)在固定间隔时间表下减少了反应,并在滴定时间表下提高了维持电击的强度。用α2 - 肾上腺素能受体拮抗剂盐酸育亨宾(0.1 - 1.0毫克/千克)预处理导致可乐定剂量 - 反应曲线向右移动3至10倍。用小剂量选择性较低的α - 肾上腺素能受体拮抗剂盐酸妥拉唑啉(3.0、5.6毫克/千克)预处理后也观察到类似的拮抗作用,但用α1拮抗剂哌唑嗪(0.1、0.3毫克/千克)预处理则未观察到。在这些条件下,可乐定对行为的影响显然是由于其作用于α2 - 肾上腺素能受体部位。