Scopolamine prevents retrograde memory interference between two different learning tasks

被引:35
作者
Blake, M. G. [1 ]
Boccia, M. M. [1 ]
Krawczyk, M. C. [1 ]
Baratti, C. M. [1 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, Catedra Farmacol, Lab Neurofarmacol Proc Memoria, RA-1053 Buenos Aires, DF, Argentina
关键词
Acetylcholine; Learning interference; Memory consolidation; Memory reconsolidation; Scopolamine; Novelty; INHIBITORY AVOIDANCE-RESPONSE; PROTEIN-SYNTHESIS; WORKING-MEMORY; CONSOLIDATION; MICE; RECONSOLIDATION; RATS; REACTIVATION; HABITUATION; MECHANISMS;
D O I
10.1016/j.physbeh.2010.11.026
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Subjects exposed to learning experiences could store the new information through memory consolidation process. If consolidation is interfered by exposing the experimental subjects to another novel stimulus, memory of the first learning situation is sometimes disrupted. The cholinergic system is critically involved in acquisition of new information. Here, we use low doses of the muscarinic cholinergic receptor antagonist scopolamine (SCOP) to disrupt acquisition of new information, but sparing memory consolidation of previous memories. Mice were consecutively exposed to two learning situations: the inhibitory avoidance (IA) and the nose-poke habituation (NPH) tasks. The exposure of mice to the NPH task, after being trained in the IA apparatus, impairs consolidation of the avoidance memory in a manner related to the duration of the exposure to the NPH task. If the exposure to the NPH task occurred after reactivation of the avoidance memory, reconsolidation was impaired. Blockade of acquisition of the NPH task by SCOP allowed consolidation and reconsolidation of the avoidance memory. Results indicate that cholinergic system blockade by SCOP impairs acquisition but is less able to affect memory consolidation. The mere exposure and perception of a novel situation are not sufficient conditions to cause impairment of retention performance about previously learned information, but effective processing leading to acquisition of the NPH task information is necessary to cause the interference between both learning situations. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:332 / 337
页数:6
相关论文
共 38 条
[11]   PROTEIN-SYNTHESIS AND MEMORY - A REVIEW [J].
DAVIS, HP ;
SQUIRE, LR .
PSYCHOLOGICAL BULLETIN, 1984, 96 (03) :518-559
[12]   EFFECTS OF CONCURRENT MANIPULATIONS OF CHOLINERGIC AND NORADRENERGIC FUNCTION ON LEARNING AND RETENTION IN MICE [J].
DECKER, MW ;
MCGAUGH, JL .
BRAIN RESEARCH, 1989, 477 (1-2) :29-37
[13]   NF-κB transcription factor is required for inhibitory avoidance long-term memory in mice [J].
Freudenthal, R ;
Boccia, MM ;
Acosta, GB ;
Blake, MG ;
Merlo, E ;
Baratti, CM ;
Romano, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2005, 21 (10) :2845-2852
[14]   Effects of novelty and habituation on acetylcholine, GABA, and glutamate release from the frontal cortex and hippocampus of freely moving rats [J].
Giovannini, MG ;
Rakovska, A ;
Benton, RS ;
Pazzagli, M ;
Bianchi, L ;
Pepeu, G .
NEUROSCIENCE, 2001, 106 (01) :43-53
[15]   Cholinergic modulation of cortical function [J].
Hasselmo, M. E. ;
Giocomo, L. M. .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2006, 30 (1-2) :133-135
[16]   Neuromodulation: acetylcholine and memory consolidation [J].
Hasselmo, ME .
TRENDS IN COGNITIVE SCIENCES, 1999, 3 (09) :351-359
[17]   Mechanisms underlying working memory for novel information [J].
Hasselmo, Michael E. ;
Stern, Chantal E. .
TRENDS IN COGNITIVE SCIENCES, 2006, 10 (11) :487-493
[18]   Behavioural pharmacology and its contribution to the molecular basis of memory consolidation [J].
Izquierdo, I ;
McGaugh, JL .
BEHAVIOURAL PHARMACOLOGY, 2000, 11 (7-8) :517-534
[19]   Novelty causes time-dependent retrograde amnesia for one-trial avoidance in rats through NMDA receptor- and CaMKII-dependent mechanisms in the hippocampus [J].
Izquierdo, I ;
Schröder, N ;
Netto, CA ;
Medina, JH .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (09) :3323-3328
[20]   Enhanced cholinergic suppression of previously strengthened synapses enables the formation of self-organized representations in olfactory cortex [J].
Linster, C ;
Maloney, M ;
Patil, M ;
Hasselmo, ME .
NEUROBIOLOGY OF LEARNING AND MEMORY, 2003, 80 (03) :302-314