Kehne J H, Cassella J V, Davis M
Yale University School of Medicine, Ribicoff Research Facilities of the Connecticut Mental Health Center, New Haven 06508.
Psychopharmacology (Berl). 1988;94(1):8-13. doi: 10.1007/BF00735872.
Fear potentiation of the acoustic startle reflex was produced by eliciting startle responses in the presence of a light that had been previously paired with a shock. Buspirone (0.6-5.0 mg/kg) and gepirone (1.25-10.0 mg/kg), but not their common metabolite, 1-PP (0.5-40 mg/kg), produced a dose-dependent reduction of fear-potentiated startle. These doses of buspirone and gepirone slightly increased baseline startle levels. Reduction of fear-potentiated startle appears to involve supraspinal sites of action, since intraventricular but not intrathecal administration of buspirone (200 micrograms) reduced fear-enhanced startle. Both buspirone and gepirone were highly efficacious in this model compared to other animal tests that are used to study anxiolytic compounds.
在先前与电击配对过的灯光存在的情况下引发惊吓反应,从而产生恐惧增强的听觉惊吓反射。丁螺环酮(0.6 - 5.0毫克/千克)和吉哌隆(1.25 - 10.0毫克/千克),但不是它们的共同代谢物1 - PP(0.5 - 40毫克/千克),产生了剂量依赖性的恐惧增强惊吓反应的降低。这些剂量的丁螺环酮和吉哌隆略微提高了基线惊吓水平。恐惧增强惊吓反应的降低似乎涉及脊髓上的作用部位,因为脑室内注射丁螺环酮(200微克)而非鞘内注射可降低恐惧增强的惊吓反应。与用于研究抗焦虑化合物的其他动物试验相比,丁螺环酮和吉哌隆在该模型中都具有高效性。