Eisenberg R M
University of Minnesota, School of Medicine, Department of Pharmacology, Duluth 55812.
Psychopharmacology (Berl). 1993;110(4):467-70. doi: 10.1007/BF02244654.
Rats, subjected to sound-vibration stress, showed an abrupt increase in plasma corticosterone (CS). This stimulation was reliably produced using a Burgess brand "vibro-graver," a standard tool used for engraving. With the tool set at "8" or coarse, the barrel of the tool was placed on the animal's flank and the point held against the side of the metal cage for 15 s. Plasma CS increased to 29.3 +/- 4.7 micrograms/dl at 15 min and 15.7 +/- 1.8 micrograms/dl at 30 min. These levels were significantly higher than animals pretreated with diazepam, 5 mg/kg i.v., 2 h prior to stimulation (9.2 +/- 2.0 and 7.4 +/- 1.5 micrograms/dl, respectively). Animals which were pretreated with CGS-8216 (a mixed agonist/antagonist at the benzodiazepine receptor), 2 mg/kg i.v., 30 min prior to diazepam had the protective effects of diazepam abolished. Sound/vibration produced a significant elevation in plasma CS in animals given CGS-8216 alone; but, this elevation was significantly lower than in vehicle-treated controls. This comparatively lower plasma CS level suggests a partial-agonist, diazepam-like effect by CGS-8216. Experiments were done in conscious unrestrained male Sprague-Dawley rats with chronic i.v. catheters. Except for 15 s stimulation exposure, all animals remained isolated in sound-attenuated one-way vision boxes for the duration of the serial blood sampling. Control stimulation exposure involved similar handling without turning on the engraving tool. These results demonstrate: 1) the usefulness of this tool to provide a repeatable stress stimulus; 2) the ability of diazepam to abolish the stress response; 3) that CGS-8216 can antagonize the action of diazepam; and 4) a demonstration of the partial agonist effects of CGS-8216.
遭受声振应激的大鼠血浆皮质酮(CS)水平急剧升高。使用Burgess品牌的“振动雕刻器”(一种用于雕刻的标准工具)可可靠地产生这种刺激。将工具设置为“8”档或粗档,把工具的杆部放在动物胁腹上,尖端抵住金属笼的侧面持续15秒。血浆CS在15分钟时升至29.3±4.7微克/分升,30分钟时为15.7±1.8微克/分升。这些水平显著高于在刺激前2小时静脉注射5毫克/千克地西泮预处理的动物(分别为9.2±2.0和7.4±1.5微克/分升)。在静脉注射地西泮前30分钟静脉注射CGS - 8216(一种苯二氮䓬受体混合激动剂/拮抗剂)2毫克/千克预处理的动物,地西泮的保护作用被消除。单独给予CGS - 8216的动物中,声音/振动使血浆CS显著升高;但是,这种升高显著低于赋形剂处理的对照组。这种相对较低的血浆CS水平表明CGS - 8216具有部分激动剂、类似地西泮的作用。实验在清醒、未束缚的慢性静脉插管雄性Sprague - Dawley大鼠中进行。除了15秒的刺激暴露外,所有动物在连续采血期间都单独饲养在隔音的单向观察箱中。对照刺激暴露包括类似的操作,但不开启雕刻工具。这些结果表明:1)该工具用于提供可重复应激刺激的有效性;2)地西泮消除应激反应的能力;3)CGS - 8216可拮抗地西泮的作用;4)证明了CGS - 8216的部分激动剂作用。