Lister R G
Laboratory of Clinical Studies, NIAAA, Bethesda, MD 20892.
Pharmacol Biochem Behav. 1988 Jul;30(3):701-6. doi: 10.1016/0091-3057(88)90087-1.
The effects of RO 15-4513, RO 15-3505 and FG 7142 on the anxiolytic properties of ethanol in mice were investigated using the plus-maze test of anxiety. Before being tested on the plus-maze, the mice were tested in a holeboard apparatus. All three inverse agonists attenuated the reduction in exploration caused by ethanol in the holeboard test. In the plus-maze, only RO 15-4513 and FG 7142, which possess anxiogenic properties when administered alone, attenuated ethanol's anxiolytic effect. RO 15-3505, which alone had no effect on anxiety, failed to significantly reduce ethanol's anxiolytic effect. Neither RO 15-4513 nor FG 7142 reduced the increase in the total number of arm entries caused by ethanol. These data indicate that the interaction between ethanol and benzodiazepine receptor ligands depends both on the intrinsic properties of the ligands and the behavior under investigation.
使用焦虑加迷宫试验研究了RO 15 - 4513、RO 15 - 3505和FG 7142对小鼠乙醇抗焦虑特性的影响。在加迷宫试验之前,先在洞板装置中对小鼠进行测试。在洞板试验中,所有这三种反向激动剂都减弱了乙醇引起的探索行为减少。在加迷宫试验中,只有单独给药时具有致焦虑特性的RO 15 - 4513和FG 7142减弱了乙醇的抗焦虑作用。单独使用时对焦虑无影响的RO 15 - 3505未能显著降低乙醇的抗焦虑作用。RO 15 - 4513和FG 7142均未减少乙醇引起的进入臂总数的增加。这些数据表明,乙醇与苯二氮䓬受体配体之间的相互作用既取决于配体的内在特性,也取决于所研究的行为。