5-HT1B receptor knock-out mice exhibit increased exploratory activity and enhanced spatial memory performance in the Morris water maze

被引:179
作者
Malleret, G
Hen, R
Guillou, JL
Segu, L
Buhot, MC
机构
[1] Univ Bordeaux 1, Lab Neurosci Comportementales & Cognit, CNRS, Unite Mixte Rech 5807, F-33405 Talence, France
[2] Columbia Univ, Ctr Neurobiol & Behav, New York, NY 10032 USA
关键词
knock-out mice; serotonin 1B receptors (5-HT1B); learning and memory; anxiety; Morris water maze; receptor autoradiography;
D O I
10.1523/JNEUROSCI.19-14-06157.1999
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In an attempt to characterize the contribution of the 5-HT1B receptor to behavior, 5-HT1B knock-out (KO) mice were subjected to a battery of behavioral paradigms aimed at differentiating various components of cognitive and emotional behaviors. In an object exploration task, wild-type (WT) and 5-HT1B KO mice did not differ in locomotor activity. 5-HT1B KO mice, however, displayed lower thigmotaxis (an index of anxiety) associated with a higher level of object exploratory activity, but no genotype differences were observed in the elevated plus maze. 5-HT1B KO mice also displayed a lack of exploratory habituation. In the spatial version of the Morris water maze, 5-HT1B KO mice showed higher performances in acquisition and transfer test, which was not observed in the visual version of the task. No genotype differences were found in contextual fear conditioning, because both WT and 5-HT1B KO mice were able to remember the context where they had received the aversive stimulus. The deletion of the 5-HT1B receptor, associated with appropriate behavioral paradigms, thus allowed us to dissociate anxiety from response to novelty, and perseverative behavior (lack of habituation) from adaptive behavioral inhibition underlying cognitive flexibility (transfer stage in the water maze). The deletion of the 5-HT1B receptor did not result in significant developmental plasticities for other major 5-HT receptor types but may have influenced other neurotransmission systems. The 5-HT1B receptor may be a key target for serotonin in the modulation of cognitive behavior, particularly in situations involving a high cognitive demand.
引用
收藏
页码:6157 / 6168
页数:12
相关论文
共 47 条
[1]   SEROTONIN 1B RECEPTOR REGULATION AFTER DORSAL SUBICULUM DEAFFERENTATION [J].
AMARA, DA ;
SEGU, L ;
NAILI, S ;
BUHOT, MC .
BRAIN RESEARCH BULLETIN, 1995, 38 (01) :17-23
[2]   HIPPOCAMPAL FUNCTION IN THE RAT - COGNITIVE MAPPING OR VICARIOUS TRIAL AND ERROR [J].
AMSEL, A .
HIPPOCAMPUS, 1993, 3 (03) :251-256
[3]   IMPAIRMENT OF SPATIAL BUT NOT CONTEXTUAL MEMORY IN CAMKII MUTANT MICE WITH A SELECTIVE LOSS OF HIPPOCAMPAL LTP IN THE RANGE OF THE THETA-FREQUENCY [J].
BEACH, ME ;
HAWKINS, RD ;
OSMAN, M ;
KANDEL, ER ;
MAYFORD, M .
CELL, 1995, 81 (06) :905-915
[4]   The effect of nonspatial water maze pretraining in rats subjected to serotonin depletion and muscarinic receptor antagonism: a detailed behavioural assessment of spatial performance [J].
Beiko, J ;
Candusso, L ;
Cain, DP .
BEHAVIOURAL BRAIN RESEARCH, 1997, 88 (02) :201-211
[5]   Activation of 5-HT1B receptors suppresses low but not high frequency synaptic transmission in the rat subicular cortex in vitro [J].
Boeijinga, PH ;
Boddeke, HWGM .
BRAIN RESEARCH, 1996, 721 (1-2) :59-65
[6]   THE MOUSE 5-HYDROXYTRYPTAMINE(1B) RECEPTOR IS LOCALIZED PREDOMINANTLY ON AXON TERMINALS [J].
BOSCHERT, U ;
AMARA, DA ;
SEGU, L ;
HEN, R .
NEUROSCIENCE, 1994, 58 (01) :167-182
[7]   EFFECTS OF RETINAL DEAFFERENTATION ON SEROTONIN RECEPTOR TYPES IN THE SUPERFICIAL GRAY LAYER OF THE SUPERIOR COLLICULUS OF THE RAT [J].
BOULENGUEZ, P ;
ABDELKEFI, J ;
PINARD, R ;
CHRISTOLOMME, A ;
SEGU, L .
JOURNAL OF CHEMICAL NEUROANATOMY, 1993, 6 (03) :167-175
[8]  
Boulenguez P, 1996, SYNAPSE, V24, P203, DOI 10.1002/(SICI)1098-2396(199611)24:3<203::AID-SYN1>3.0.CO
[9]  
2-I
[10]   DISTRACTIBILITY AND LOCOMOTOR-ACTIVITY IN RAT FOLLOWING INTRA-COLLICULAR INJECTION OF A SEROTONIN 1B-1D AGONIST [J].
BOULENGUEZ, P ;
FOREMAN, N ;
CHAUVEAU, J ;
SEGU, L ;
BUHOT, MC .
BEHAVIOURAL BRAIN RESEARCH, 1995, 67 (02) :229-239