Hilakivi L A, Lister R G
Laboratory of Clinical Studies, National Institute of Alcohol Abuse and Alcoholism, Bethesda, MD 20892.
Eur J Pharmacol. 1988 Sep 1;154(1):109-13. doi: 10.1016/0014-2999(88)90372-x.
Ethanol (2 g/kg) reduces the time spent in social interaction and increases locomotor activity of pairs of NIH Swiss mice. This study examined whether two benzodiazepine receptor inverse agonists, RO 15-4513 (3 mg/kg) and FG 7142 (30 mg/kg) are able to reverse these effects. Neither drug alone altered social behavior, but both significantly attenuated the effect of ethanol on social interaction. They did not affect the ethanol-induced increase in motor activity. Benzodiazepine receptor inverse agonists thus appear capable of antagonizing some, but not all of the behavioral effects of ethanol in this paradigm.
乙醇(2克/千克)会减少NIH瑞士小鼠对的社交互动时间,并增加其运动活性。本研究检测了两种苯二氮䓬受体反向激动剂RO 15 - 4513(3毫克/千克)和FG 7142(30毫克/千克)是否能够逆转这些效应。单独使用这两种药物均未改变社交行为,但二者均显著减弱了乙醇对社交互动的影响。它们并未影响乙醇诱导的运动活性增加。因此,在这一范例中,苯二氮䓬受体反向激动剂似乎能够拮抗乙醇的部分而非全部行为效应。