Gardner C R, Budhram P, Parker F L
Roussel Laboratories Limited, Swindon, Wiltshire, UK.
Pharmacol Biochem Behav. 1992 Oct;43(2):583-8. doi: 10.1016/0091-3057(92)90194-k.
Rats were trained to discriminate the low-efficacy benzodiazepine receptor inverse agonist RU 33965 from vehicle in a two-lever discrimination task on a fixed ratio (FR) 20 schedule. Consistent discrimination was obtained at 0.5 mg/kg PO RU 33965. Both leptazol and stronger inverse agonists (FG7142, S-135, RU 34000) substituted for the cue. The weak inverse agonists/antagonists RU 33094, RU 34030, Ro 15-1788, and ZK 93426 also substituted for the cue with the latter two compounds being particularly potent. The agonist and partial agonists diazepam, RU 33203, and RU 39419 did not substitute for the RU 33965 cue but RU 39419 antagonised it. The full agonists diazepam and loprazolam only consistently antagonised the cue when given IP 5 min pretest. These data suggest that the RU 33965 cue results from its weak inverse agonist activity at benzodiazepine receptors, but kinetic factors must be considered when interpreting drug effects in discrimination studies.
在固定比率(FR)20的双杠杆辨别任务中,训练大鼠区分低效价苯二氮䓬受体反向激动剂RU 33965和赋形剂。口服0.5mg/kg的RU 33965时能获得稳定的辨别。戊四氮和更强效的反向激动剂(FG7142、S - 135、RU 34000)可替代该线索。弱反向激动剂/拮抗剂RU 33094、RU 34030、Ro 15 - 1788和ZK 93426也可替代该线索,后两种化合物尤为有效。激动剂和部分激动剂地西泮、RU 33203和RU 39419不能替代RU 33965线索,但RU 39419可拮抗它。完全激动剂地西泮和氯普唑仑仅在预测试前5分钟腹腔注射时能持续拮抗该线索。这些数据表明,RU 33965线索源于其在苯二氮䓬受体上的弱反向激动剂活性,但在辨别研究中解释药物作用时必须考虑动力学因素。