Bicuculline administered into the amygdala after training blocks benzodiazepine-induced amnesia

被引:39
作者
DickinsonAnson, H
McGaugh, JL
机构
[1] UNIV CALIF IRVINE, CTR NEUROBIOL LEARNING & MEMORY, IRVINE, CA 92697 USA
[2] UNIV CALIF IRVINE, DEPT PSYCHOBIOL & PHARMACOL, IRVINE, CA 92697 USA
[3] SALK INST BIOL STUDIES, GENET LAB, LA JOLLA, CA 92037 USA
关键词
amygdala; benzodiazepine; midazolam; aversive learning; post-training; memory; amnesia; inhibitory avoidance;
D O I
10.1016/S0006-8993(96)01449-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Male Sprague-Dawley rats were injected (i.p.) with either midazolam (MDZ, 2.0 mg/kg) or vehicle (1.0 ml/kg) 10 min before they were trained on a multiple-trial inhibitory avoidance task. Immediately following the training, bicuculline methiodide (BMI; 2.0, 5.6, 56.0 or 197.0 pmol/0.5 mu l) or vehicle (0.5 mu l) was infused bilaterally into the amygdala. On a 48 h retention test the performance of the MDZ-treated animals was significantly poorer than that of controls. The retention of MDZ-treated animals given intra-amygdala injections of the lowest dose of BMI (2.0 pmol) was comparable to that of controls, whereas higher doses of BMI impaired retention. The present results are consistent with other findings indicating that the amygdala mediates the amnestic effects of benzodiazepines on aversive learning. Furthermore, these data suggest that benzodiazepines impair memory by disrupting post-training processes underlying memory consolidation. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:197 / 202
页数:6
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