Schema-Dependent Gene Activation and Memory Encoding in Neocortex

被引:414
作者
Tse, Dorothy [1 ]
Takeuchi, Tomonori [1 ]
Kakeyama, Masaki [2 ]
Kajii, Yasushi [3 ]
Okuno, Hiroyuki [4 ]
Tohyama, Chiharu [2 ]
Bito, Haruhiko [4 ]
Morris, Richard G. M. [1 ]
机构
[1] Univ Edinburgh, Ctr Cognit & Neural Syst, Edinburgh EH8 9JZ, Midlothian, Scotland
[2] Univ Tokyo, Grad Sch Med, Lab Environm Hlth Sci, Ctr Dis Biol & Integrat Med,Bunkyo Ku, Tokyo 1130033, Japan
[3] Mitsubishi Tanabe Pharma Corp, Pharmacol Res Labs 1, Aoba Ku, Yokohama, Kanagawa 2270033, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Neurochem, Bunkyo Ku, Tokyo 1130033, Japan
基金
日本科学技术振兴机构; 英国医学研究理事会;
关键词
LONG-TERM-MEMORY; SPATIAL MEMORY; ASSOCIATIVE MEMORY; EPISODIC MEMORY; RAT HIPPOCAMPUS; CONSOLIDATION; EXPRESSION; PLASTICITY; EXPERIENCE; NEURONS;
D O I
10.1126/science.1205274
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
When new learning occurs against the background of established prior knowledge, relevant new information can be assimilated into a schema and thereby expand the knowledge base. An animal model of this important component of memory consolidation reveals that systems memory consolidation can be very fast. In experiments with rats, we found that the hippocampal-dependent learning of new paired associates is associated with a striking up-regulation of immediate early genes in the prelimbic region of the medial prefrontal cortex, and that pharmacological interventions targeted at that area can prevent both new learning and the recall of remotely and even recently consolidated information. These findings challenge the concept of distinct fast (hippocampal) and slow (cortical) learning systems, and shed new light on the neural mechanisms of memory assimilation into schemas.
引用
收藏
页码:891 / 895
页数:5
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