Wettstein J G, Spealman R D
Department of Psychiatry, Harvard Medical School, Boston, MA.
Pharmacol Biochem Behav. 1988 Apr;29(4):741-5. doi: 10.1016/0091-3057(88)90196-7.
The behavioral effects of the pyrazoloquinoline CGS 8216 were studied in squirrel monkeys trained to respond under a fixed-interval (FI) schedule of food presentation. Dose-effect curves were determined by administering cumulative doses IV during timeout periods that preceded sequential components of the FI schedule. CGS 8216 (0.1-3.0 mg/kg) produced dose-related decreases in the rate of FI responding. In comparison, diazepam (0.1-3.0 mg/kg) had biphasic effects under identical conditions: intermediate doses increased the rate, whereas high doses decreased the rate of FI responding. Pretreatment with the benzodiazepine antagonist Ro 15-1788 (3.0 or 5.6 mg/kg) attenuated the decreases in response rate normally produced by high doses of CGS 8216. The behavioral effects of CGS 8216 were not altered systematically by pretreatment with either diazepam (0.3-3.0 mg/kg) or the alpha 2-adrenergic agonist clonidine (0.01-0.03 mg/kg). The results suggest that CGS 8216 has benzodiazepine inverse agonist effects on schedule-controlled behavior of squirrel monkeys. CGS 8216 can, however, be distinguished from inverse agonists of the beta-carboline type on the basis of its effects in the presence of diazepam or clonidine.
在接受固定间隔(FI)食物呈现时间表训练的松鼠猴中研究了吡唑并喹啉CGS 8216的行为效应。通过在FI时间表的连续部分之前的超时期间静脉注射累积剂量来确定剂量效应曲线。CGS 8216(0.1 - 3.0毫克/千克)使FI反应率产生剂量相关的降低。相比之下,地西泮(0.1 - 3.0毫克/千克)在相同条件下具有双相效应:中等剂量增加反应率,而高剂量降低FI反应率。用苯二氮䓬拮抗剂Ro 15 - 1788(3.0或5.6毫克/千克)预处理可减弱高剂量CGS 8216通常产生的反应率降低。用要么地西泮(0.3 - 3.0毫克/千克)要么α2 - 肾上腺素能激动剂可乐定(0.01 - 0.03毫克/千克)预处理,CGS 8216的行为效应没有系统性改变。结果表明,CGS 8216对松鼠猴的时间表控制行为具有苯二氮䓬反向激动剂作用。然而,根据其在地西泮或可乐定存在时的效应,CGS 8216可与β - 咔啉类型的反向激动剂区分开来。