Repeated treatment with N-methyl-D-aspartate antagonists in neonatal, but not adult, rats causes long-term deficits of radial-arm maze learning

被引:35
作者
Kawabe, Kouichi
Iwasaki, Tsuneo
Ichitani, Yukio [1 ]
机构
[1] Univ Tsukuba, Inst Psychol & Behav Neurosci, Tsukuba, Ibaraki 3058577, Japan
[2] Mejiro Univ, Fac Human & Social Sci, Shinjuku Ku, Tokyo 1618539, Japan
[3] Osaka City Univ, Grad Sch Literature & Human Sci, Sumiyoshi Ku, Osaka 5588585, Japan
基金
日本学术振兴会;
关键词
NMDA receptor; neonatal and adult repeated; treatment; hippocampus; spatial working memory; radial-arm maze learning; open-field; rat;
D O I
10.1016/j.brainres.2007.06.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain glutamatergic system is involved in synaptic plasticity as a base for learning and neural development. This study investigated the effects of neonatal and adult chronic antagonism of N-methyl-D-aspartate (NMDA) receptors, a subtype of glutamate receptors, on learning and/or memory. Rats were trained in the radial-maze learning, which is known as a measure of spatial working memory capacities, in adulthood after neonatal or adult repeated treatment of MK-801 (dizocilpine; 5-methyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5,10-imine), a non-competitive antagonist, or neonatal repeated treatment of CGS 19755 (cis-4-phosphonomethyl-2-piperadine carboxilic acid), a competitive antagonist. Neonatal repeated treatment of MK-801 or CGS 19755 markedly impaired the radial-arm maze learning. In addition, the treatment altered activities differently in the radial-maze and in the open-field. On the other hand, adult repeated treatment with MK-801 affected neither the radial-maze learning nor activities. Results suggest that chronic blockade of NMDA receptors in a neonatal stage may produce long-lasting deteriorative effects on spatial working memory in adulthood. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 86
页数:10
相关论文
共 48 条
[1]   EFFECTS OF THE NMDA RECEPTOR CHANNEL ANTAGONISTS CPP AND MK801 ON HIPPOCAMPAL FIELD POTENTIALS AND LONG-TERM POTENTIATION IN ANESTHETIZED RATS [J].
ABRAHAM, WC ;
MASON, SE .
BRAIN RESEARCH, 1988, 462 (01) :40-46
[2]   Distinct contributions of glutamate and dopamine receptors to temporal aspects of rodent working memory using a clinically relevant task [J].
Aultman, JM ;
Moghaddam, B .
PSYCHOPHARMACOLOGY, 2001, 153 (03) :353-364
[3]   Hypothesis: Is infantile autism a hypoglutamatergic disorder? Relevance of glutamate-serotonin interactions for pharmacotherapy [J].
Carlsson, ML .
JOURNAL OF NEURAL TRANSMISSION, 1998, 105 (4-5) :525-535
[4]   Animal models of working memory: insights for targeting cognitive dysfunction in schizophrenia [J].
Castner, SA ;
Goldman-Rakic, PS ;
Williams, GV .
PSYCHOPHARMACOLOGY, 2004, 174 (01) :111-125
[5]   LONG-LASTING EFFECTS OF CHRONIC NEONATAL BLOCKADE OF N-METHYL-D-ASPARTATE RECEPTOR THROUGH THE COMPETITIVE ANTAGONIST CGP-39551 IN RATS [J].
FACCHINETTI, F ;
DALLOLIO, R ;
CIANI, E ;
SPARAPANI, M ;
VIRGILI, M ;
CONTESTABILE, A .
NEUROSCIENCE, 1994, 60 (02) :343-353
[6]   STRUCTURAL, NEUROCHEMICAL AND BEHAVIORAL CONSEQUENCES OF NEONATAL BLOCKADE OF NMDA RECEPTOR THROUGH CHRONIC TREATMENT WITH CGP-39551 OR MK-801 [J].
FACCHINETTI, F ;
CIANI, E ;
DALLOLIO, R ;
VIRGILI, M ;
CONTESTABILE, A ;
FONNUM, F .
DEVELOPMENTAL BRAIN RESEARCH, 1993, 74 (02) :219-224
[7]  
Floresco SB, 1997, J NEUROSCI, V17, P1880
[8]   Neurofunctional deficits and potentiated apoptosis by neonatal NMDA antagonist administration [J].
Fredriksson, A ;
Archer, T ;
Alm, H ;
Gordh, T ;
Eriksson, P .
BEHAVIOURAL BRAIN RESEARCH, 2004, 153 (02) :367-376
[9]  
GOLDMANRAKIC PS, 1994, J NEUROPSYCH CLIN N, V6, P348
[10]   HIPPOCAMPAL NEURONAL RESPONSIVENESS TO NMDA AGONISTS AND ANTAGONISTS IN THE ADULT-RAT NEONATALLY TREATED WITH MK-801 [J].
GORTER, JA ;
VEERMAN, M ;
MIRMIRAN, M .
BRAIN RESEARCH, 1992, 572 (1-2) :176-181