The role of protein synthesis in memory consolidation: Progress amid decades of debate

被引:177
作者
Hernandez, Pepe J. [1 ]
Abel, Ted [1 ]
机构
[1] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
关键词
protein synthesis; RNA synthesis; consolidation; memory; amnesia; reconsolidation; protein synthesis inhibitor; sleep; gene expression; transcription; translation; knockout; synaptic; systems; side effects; rescue; hippocampus; learning; LTP; CAMP; CREB; NMDA; tagging; post-translational modification;
D O I
10.1016/j.nlm.2007.09.010
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
A major component of consolidation theory holds that protein synthesis is required to produce the synaptic modification needed for long-term memory storage. Protein synthesis inhibitors have played a pivotal role in the development of this theory. However, these commonly used drugs have unintended effects that have prompted some to reevaluate the role of protein synthesis in memory consolidation. Here we review the role of protein synthesis in memory formation as proposed by consolidation theory calling special attention to the controversy involving the non-specific effects of a group of protein synthesis inhibitors commonly used to study memory formation in vivo. We argue that molecular and genetic approaches that were subsequently applied to the problem of memory formation confirm the results of less selective pharmacological studies. Thus, to a certain extent, the debate over the role of protein synthesis in memory based on interpretational difficulties inherent to the use of protein synthesis inhibitors may be somewhat moot. We conclude by presenting avenues of research we believe will best provide answers to both long-standing and more recent questions facing field of learning and memory. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:293 / 311
页数:19
相关论文
共 302 条
[32]   Sleep to remember [J].
Born, Jan ;
Rasch, Bjorn ;
Gais, Steffen .
NEUROSCIENTIST, 2006, 12 (05) :410-424
[33]   A mouse model of Rubinstein-Taybi syndrome: Defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4 [J].
Bourtchouladze, R ;
Lidge, R ;
Catapano, R ;
Stanley, J ;
Gossweiler, S ;
Romashko, D ;
Scott, R ;
Tully, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10518-10522
[34]  
Bourtchouladze R, 1998, LEARN MEMORY, V5, P365
[35]   DEFICIENT LONG-TERM-MEMORY IN MICE WITH A TARGETED MUTATION OF THE CAMP-RESPONSIVE ELEMENT-BINDING PROTEIN [J].
BOURTCHULADZE, R ;
FRENGUELLI, B ;
BLENDY, J ;
CIOFFI, D ;
SCHUTZ, G ;
SILVA, AJ .
CELL, 1994, 79 (01) :59-68
[36]   HIPPOCAMPAL LONG-TERM DEPRESSION AND DEPOTENTIATION ARE DEFECTIVE IN MICE CARRYING A TARGETED DISRUPTION OF THE GENE ENCODING THE RI-BETA SUBUNIT OF CAMP-DEPENDENT PROTEIN-KINASE [J].
BRANDON, EP ;
ZHUO, M ;
HUANG, YY ;
QI, M ;
GERHOLD, KA ;
BURTON, KA ;
KANDEL, ER ;
MCKNIGHT, GS ;
IDZERDA, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8851-8855
[37]   2-STAGE MODEL OF MEMORY TRACE FORMATION - A ROLE FOR NOISY BRAIN STATES [J].
BUZSAKI, G .
NEUROSCIENCE, 1989, 31 (03) :551-570
[38]   DEFECT IN CYCLIC-AMP PHOSPHODIESTERASE DUE TO THE DUNCE MUTATION OF LEARNING IN DROSOPHILA-MELANOGASTER [J].
BYERS, D ;
DAVIS, RL ;
KIGER, JA .
NATURE, 1981, 289 (5793) :79-81
[39]   Sleep deprivation impairs long-term potentiation in rat hippocampal slices [J].
Campbell, IG ;
Guinan, MJ ;
Horowitz, JM .
JOURNAL OF NEUROPHYSIOLOGY, 2002, 88 (02) :1073-1076
[40]   Serotonin increases phosphorylation of synaptic 4EBP through TOR, but eukaryotic initiation factor 4E levels do not limit somatic cap-dependent translation in Aplysia neurons [J].
Carroll, Matthew ;
Dyer, John ;
Sossin, Wayne S. .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (22) :8586-8598