Holmes P V, Drugan R C
Department of Psychology, Brown University, Providence, RI 02912.
Psychopharmacology (Berl). 1991;104(2):249-54. doi: 10.1007/BF02244187.
Previous research has demonstrated that low doses of anxiogenic central benzodiazepine receptor (CBR) ligands, the beta-carbolines, improve performance in various learning and memory tests in animals if administered prior to training. The present experiments compared the effect of a beta-carboline (FG 7142) with that of a pharmacologically distinct anxiogenic compound, a peripheral benzodiazepine receptor (PBR) ligand, 4'-chlorodiazepam (Ro5-4864), in two tests of learning and memory in rats. As expected, FG 7142 significantly improved performance in a passive avoidance test. Ro5-4864 was without effect. In a shuttlebox escape test, Ro5-4864 significantly impaired performance while FG 7142 had no effect. The effect of Ro5-4864 was antagonized by the specific peripheral benzodiazepine receptor antagonist, PK 11195. These results indicate that the differential impact of CBR and PBR anxiogenic ligands on performance in aversively-motivated learning tests may be a reflection of their distinct pharmacologies.
先前的研究表明,低剂量的焦虑ogenic中枢苯二氮䓬受体(CBR)配体,即β-咔啉,如果在训练前给药,可改善动物在各种学习和记忆测试中的表现。本实验在大鼠的两项学习和记忆测试中,比较了一种β-咔啉(FG 7142)与一种药理学上不同的焦虑ogenic化合物,一种外周苯二氮䓬受体(PBR)配体,4'-氯地西泮(Ro5-4864)的效果。正如预期的那样,FG 7142在被动回避测试中显著改善了表现。Ro5-4864没有效果。在穿梭箱逃避测试中,Ro5-4864显著损害了表现,而FG 7142没有效果。Ro5-4864的作用被特异性外周苯二氮䓬受体拮抗剂PK 11195拮抗。这些结果表明,CBR和PBR焦虑ogenic配体对厌恶动机学习测试表现的不同影响可能反映了它们不同的药理学特性。