Lister R G
Laboratory of Clinical Studies, NIAAA, Bethesda, MD 20892.
Life Sci. 1988;42(14):1385-93. doi: 10.1016/0024-3205(88)90168-3.
The intrinsic effects of two imidazodiazepines RO 15-3505 and RO 17-1812 on the behavior of mice in a holeboard test were investigated. The interactions of these two drugs with ethanol were also studied. RO 15-3505 (0.75-6.0 mg/kg) failed to significantly alter either exploratory head-dipping or locomotor activity when administered alone but doses of 0.75 and 1.5 mg/kg reversed the reduction in the number of head-dips caused by ethanol (2 g/kg) and partially reversed ethanol's locomotor stimulant action. In contrast, RO 17-1812 (0.75-6.0 mg/kg) increased locomotor activity when administered alone, and enhanced the reduction in exploration caused by ethanol. Neither RO 15-3505 nor RO 17-1812 altered blood alcohol concentrations suggesting a pharmacodynamic basis for these interactions. The results suggest that in the holeboard test the interactions of imidazodiazepines with ethanol are related to the nature of their interaction with benzodiazepine receptors, inverse agonists antagonising and agonists enhancing ethanol's effects on exploration.
研究了两种咪唑并二氮杂䓬RO 15 - 3505和RO 17 - 1812在洞板试验中对小鼠行为的内在影响。还研究了这两种药物与乙醇的相互作用。单独给予RO 15 - 3505(0.75 - 6.0毫克/千克)时,未能显著改变探索性探头或运动活性,但0.75和1.5毫克/千克的剂量可逆转乙醇(2克/千克)引起的探头次数减少,并部分逆转乙醇的运动兴奋作用。相比之下,单独给予RO 17 - 1812(0.75 - 6.0毫克/千克)会增加运动活性,并增强乙醇引起的探索减少。RO 15 - 3505和RO 17 - 1812均未改变血液酒精浓度,提示这些相互作用存在药效学基础。结果表明,在洞板试验中,咪唑并二氮杂䓬与乙醇的相互作用与其与苯二氮䓬受体的相互作用性质有关,反向激动剂拮抗而激动剂增强乙醇对探索的影响。