Inducible repression of CREB function disrupts amygdala-dependent memory

被引:109
|
作者
Josselyn, SA
Kida, S
Silva, AJ
机构
[1] Univ Calif Los Angeles, Brain Res Inst, Dept Neurobiol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Brain Res Inst, Dept Psychol & Psychiat, Los Angeles, CA 90095 USA
[3] Hosp Sick Children, Program Integrat Biol Brain & Behav, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[5] Tokyo Univ Agr, Fac Appl Biosci, Dept Agr Chem & Biosci, Setagaya Ku, Tokyo 1568502, Japan
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.nlm.2004.05.008
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Evidence from Aplysia, Drosophila, mice, and rats indicates that the CREB (cAMP/Ca2+ responsive element binding protein) family of transcription factors is critical for long-term memory. Recent findings, however, suggest that performance abnormalities may contribute to the memory deficits attributed to CREB manipulations in mammals. To clarify the role of CREB in memory, we used a paradigm, conditioned taste avoidance, that places few performance demands on the subject. We show that lesioning or blocking protein synthesis in the basolateral amygdala of mice disrupts conditioned taste aversion. Furthermore, either chronically or acutely disrupting CREB function in two different. types of genetically modified mice blocks memory for conditioned taste aversion measured 24 h following training. Together, these findings indicate that CREB-mediated transcription and protein synthesis are required for conditioned taste aversion memory. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:159 / 163
页数:5
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