Duka T, Stephens D N
Pharmacol Biochem Behav. 1986 Sep;25(3):595-8. doi: 10.1016/0091-3057(86)90147-4.
The ability of naltrexone (NTX) to potentiate the propunishment and convulsant properties of DMCM, a benzodiazepine receptor inverse agonist, was studied in mice. Doses (0.39 and 1.56 mg/kg) of DMCM which were below the threshold for propunishment effects showed a marked ability to enhance the suppressive effects of punishment on locomotor activity in the presence of naltrexone (0.5 or 2.5 mg/kg IP), higher doses of DMCM and NTX (3.13 mg/kg and 10 mg/kg, respectively) had a depressant effect of their own on both punished and unpunished locomotor activity. DMCM given alone induced clonic convulsions (ED50: 5.7 mg/kg IP) but this activity was not changed in the presence of naltrexone. These results suggest an interaction of BZ receptors and opioid systems in the control of anxiety.
在小鼠中研究了纳曲酮(NTX)增强苯二氮䓬受体反向激动剂DMCM的抗惩罚和惊厥特性的能力。低于抗惩罚效应阈值的DMCM剂量(0.39和1.56mg/kg)显示出在存在纳曲酮(0.5或2.5mg/kg腹腔注射)时显著增强惩罚对运动活动抑制作用的能力,更高剂量的DMCM和NTX(分别为3.13mg/kg和10mg/kg)自身对受惩罚和未受惩罚的运动活动均有抑制作用。单独给予DMCM可诱发阵挛性惊厥(半数有效剂量:5.7mg/kg腹腔注射),但在存在纳曲酮时该活性未改变。这些结果提示在焦虑控制中苯二氮䓬受体与阿片系统存在相互作用。