Dose-response characteristics of ketamine effect on locomotion, cognitive function and central neuronal activity

被引:104
作者
Imre, G [1 ]
Fokkema, DS [1 ]
Den Boer, JA [1 ]
Ter Horst, GJ [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Psychiat, NL-9700 RB Groningen, Netherlands
关键词
ketamine; light/dark cycle; hyperlocomotion; c-fos; PPI; working memory; schizophrenia; limbic system;
D O I
10.1016/j.brainresbull.2006.01.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present dose-response study sought to determine the effects of subanesthetic dosages (4-16 mg/kg) of ketamine on locomotion, sensorimotor gating (PP1), working memory, as well as c-fos expression in various limbic regions implicated in the pathogenesis of schizophrenia. In addition, we examined whether ketamine-induced locomotion was influenced by the dark/light cycle. We found that ketamine increased locomotor activity in a dose dependent manner, but found no influence of the dark-light cycle. Additionally, ketamine dose-dependently interrupted PP1, resulting in prepulse facilitation at doses of 8 and 12 mg/kg. The dose of 12 mg/kg also induced impairments in working memory assessed by the discrete-trial delayed-alternation task. C-fos expression indicated that the dose-dependent behavioral effects of ketamine might be related to changes in the activity of limbic regions, notably hippocampus and amygdala. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:338 / 345
页数:8
相关论文
共 36 条
[1]   Effects of MK-801 and electroconvulsive shock on c-Fos expression in the rat hippocampus and frontal cortex [J].
Ahn, YM ;
Kang, UG ;
Park, JB ;
Kim, YS .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2002, 26 (03) :513-517
[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]  
Bakshi VP, 1998, J NEUROSCI, V18, P8394
[4]   Differential effects of ketamine on gating of auditory evoked potentials and prepulse inhibition in rats [J].
de Bruin, NMWJ ;
Ellenbroek, BA ;
Cools, AR ;
Coenen, AML ;
van Luijtelaar, ELJM .
PSYCHOPHARMACOLOGY, 1999, 142 (01) :9-17
[5]   Locomotor activity induced by the non-competitive N-methyl-D-aspartate antagonist, MK-801:: Role of nucleus accumbens efferent pathways [J].
De Leonibus, E ;
Mele, A ;
Oliverio, A ;
Pert, A .
NEUROSCIENCE, 2001, 104 (01) :105-116
[6]   Metabolic mapping of the rat brain after subanesthetic doses of ketamine: potential relevance to schizophrenia [J].
Duncan, GE ;
Moy, SS ;
Knapp, DJ ;
Mueller, RA ;
Breese, GR .
BRAIN RESEARCH, 1998, 787 (02) :181-190
[7]  
Gao XM, 1998, SYNAPSE, V29, P14, DOI 10.1002/(SICI)1098-2396(199805)29:1<14::AID-SYN2>3.0.CO
[8]  
2-E
[9]   INDUCTION AND SUPPRESSION OF IMMEDIATE EARLY GENES IN SPECIFIC RAT-BRAIN REGIONS BY THE NONCOMPETITIVE N-METHYL-D-ASPARTATE RECEPTOR ANTAGONIST MK-801 [J].
GASS, P ;
HERDEGEN, T ;
BRAVO, R ;
KIESSLING, M .
NEUROSCIENCE, 1993, 53 (03) :749-758
[10]   STARTLE RESPONSE MODELS OF SENSORIMOTOR GATING AND HABITUATION DEFICITS IN SCHIZOPHRENIA [J].
GEYER, MA ;
SWERDLOW, NR ;
MANSBACH, RS ;
BRAFF, DL .
BRAIN RESEARCH BULLETIN, 1990, 25 (03) :485-498