Different molecular cascades in different sites of the brain control memory consolidation

被引:348
作者
Izquierdo, Ivan
Bevilaqua, Lia R. M.
Rossato, Janine I.
Bonini, Juliana S.
Medina, Jorge H.
Cammarota, Martin
机构
[1] Pontifica Univ Catolica Rio Grande Sul, Hosp Sao Lucas, Ctr Mem, Inst Pesquisas Biomed, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Buenos Aires, Fac Med, Inst Biol Celular & Neurociencias, RA-1121 Buenos Aires, DF, Argentina
关键词
D O I
10.1016/j.tins.2006.07.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To understand cognition, it is important to understand how a learned response becomes a long-lasting memory. This process of memory consolidation has been modeled extensively using one-trial avoidance learning, in which animals (or humans) establish a conditioned response by learning to avoid danger in just one trial. This relies on molecular events in the CA1 region of the hippocampus that resemble those involved in CA1 long-term potentiation (LTP), and it also requires equivalent events to occur with different timings in the basolateral amygdala and the entorhinal, parietal and cingulate cortex. Many of these steps are modulated by monoaminergic pathways related to the perception of and reaction to emotion, which at least partly explains why strong and resistant consolidation is typical of emotion-laden memories. Thus memory consolidation involves a complex network of brain systems and serial and parallel molecular events, even for a task as deceptively simple as one-trial avoidance. We propose that these molecular events might also be involved in many other memory types in animals and humans.
引用
收藏
页码:496 / 505
页数:10
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共 109 条
[71]  
MATTHIES H, 1982, NEURONAL PLASTICITY, P1
[72]   Control of memory formation through regulated expression of a CaMKII transgene [J].
Mayford, M ;
Bach, ME ;
Huang, YY ;
Wang, L ;
Hawkins, RD ;
Kandel, ER .
SCIENCE, 1996, 274 (5293) :1678-1683
[73]   WHY THERE ARE COMPLEMENTARY LEARNING-SYSTEMS IN THE HIPPOCAMPUS AND NEOCORTEX - INSIGHTS FROM THE SUCCESSES AND FAILURES OF CONNECTIONIST MODELS OF LEARNING AND MEMORY [J].
MCCLELLAND, JL ;
MCNAUGHTON, BL ;
OREILLY, RC .
PSYCHOLOGICAL REVIEW, 1995, 102 (03) :419-457
[74]   Emotional arousal and enhanced amygdala activity: New evidence for the old perseveration-consolidation hypothesis [J].
McGaugh, JL .
LEARNING & MEMORY, 2005, 12 (02) :77-79
[75]   Neuroscience - Memory - a century of consolidation [J].
McGaugh, JL .
SCIENCE, 2000, 287 (5451) :248-251
[76]   Retrograde messengers, long-term potentiation and memory [J].
Medina, JH ;
Izquierdo, I .
BRAIN RESEARCH REVIEWS, 1995, 21 (02) :185-194
[77]   Protein kinases: which one is the memory molecule? [J].
Micheau, J ;
Riedel, G .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (04) :534-548
[78]   Elements of a neurobiological theory of the hippocampus: the role of activity-dependent synaptic plasticity in memory [J].
Morris, RGM ;
Moser, EI ;
Riedel, G ;
Martin, SJ ;
Sandin, J ;
Day, M ;
O'Carroll, C .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2003, 358 (1432) :773-786
[79]   SELECTIVE IMPAIRMENT OF LEARNING AND BLOCKADE OF LONG-TERM POTENTIATION BY AN N-METHYL-D-ASPARTATE RECEPTOR ANTAGONIST, AP5 [J].
MORRIS, RGM ;
ANDERSON, E ;
LYNCH, GS ;
BAUDRY, M .
NATURE, 1986, 319 (6056) :774-776
[80]   Complex roles of glutamate in the Gibbs-Ng model of one-trial aversive learning in the new-born chick [J].
Ng, KT ;
ODowd, BS ;
Rickard, NS ;
Robinson, SR ;
Gibbs, ME ;
Rainey, C ;
Zhao, WQ ;
Sedman, GL ;
Hertz, L .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1997, 21 (01) :45-54