(±)-α-Methyl-4-carboxyphenylglycine, a metabotropic glutamate receptor blocker, impairs retention of an inhibitory avoidance task in rats when infused into the basolateral nucleus of the amygdala

被引:22
作者
Bianchin, MM
Spanis, CW
Roesler, R
McGaugh, JL
Izquierdo, I [1 ]
机构
[1] UFRGS, Inst Ciencias Basicas Saude, Dept Bioquim, BR-90035003 Porto Alegre, RS, Brazil
[2] Univ Calif Irvine, Ctr Neurobiol Learning & Memory, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
[4] Univ Fed Santa Maria, Dept Neuropsiquiatria, Santa Maria, RS, Brazil
[5] Univ San Diego, Dept Biol, San Diego, CA 92110 USA
关键词
emotionally motivated learning; memory modulation; glutamatergic system; nociception;
D O I
10.1016/S0006-8993(99)02220-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The amygdala is important for memory processes of emotionally motivated learning and the amygdala glutamatergic system may play a key role in this process. In this study we assessed the effect of the infusion of (+/-)-alpha-methyl-4-carboxyphenylglycine (MCPG), a metabotropic glutamate receptor (mGluR) antagonist, into the basolateral complex of the amygdala (BLA) on the learning and retention of an emotionally motivated task. Rats received either vehicle or three different doses of MCPG (0.2, or 1.0, or 5.0 mu g/0.2 mu l/side, respectively) bilaterally into the BLA, 5 min before they were trained in a continuous multiple-trial inhibitory avoidance (CMIA) task. Response latencies during the training were recorded. Retention was assessed 8 days later. MCPG in the doses given did not significantly affect the acquisition of the CMIA task. However, MCPG at a dose of 5.0 mu g/0.2 mu l/side impaired the long-term retention test performance. Additionally, a nociception test indicated that dose of MCPG infused into the BLA did not affect the footshock sensitivity. Our results indicate that MCPG, when infused into the BLA of rats prior to the training, impaired long-term memory of aversive training without affecting acquisition. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:436 / 443
页数:8
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