The puzzle box as a simple and efficient behavioral test for exploring impairments of general cognition and executive functions in mouse models of schizophrenia

被引:92
作者
Ben Abdallah, Nada M-B [1 ]
Fuss, Johannes [1 ]
Trusel, Massimo [2 ]
Galsworthy, Michael J. [3 ]
Bobsin, Kristin [4 ]
Colacicco, Giovanni [3 ]
Deacon, Robert M. J. [5 ]
Riva, Marco A. [2 ]
Kellendonk, Christoph [6 ]
Sprengel, Rolf [4 ]
Lipp, Hans-Peter [3 ]
Gass, Peter [1 ]
机构
[1] Heidelberg Univ, RG, Cent Inst Mental Hlth Mannheim CIMH, RG Behav Biol, Mannheim, Germany
[2] Univ Milan, Dept Pharmacol Sci, Ctr Neuropharmacol, Milan, Italy
[3] Univ Zurich, Inst Anat, CH-8006 Zurich, Switzerland
[4] Max Planck Inst Med Res, Inst Neurobiol, Heidelberg, Germany
[5] Univ Oxford, Dept Expt Psychol, Oxford OX1 3UD, England
[6] Columbia Univ, Dept Pharmacol & Psychiat, New York, NY USA
基金
瑞士国家科学基金会; 英国惠康基金;
关键词
Hippocampus; Medial prefrontal cortex; MK-801; GluA1; Dopamine D2-receptor; Problem solving; SPECIES-TYPICAL BEHAVIORS; ANIMAL-MODELS; SELECTIVE OVEREXPRESSION; CORTEX; MICE; LESIONS; MK-801; PHENCYCLIDINE; HYPOTHESIS; RECEPTORS;
D O I
10.1016/j.expneurol.2010.09.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Deficits in executive functions are key features of schizophrenia. Rodent behavioral paradigms used so far to find animal correlates of such deficits require extensive effort and time. The puzzle box is a problem-solving test in which mice are required to complete escape tasks of increasing difficulty within a limited amount of time. Previous data have indicated that it is a quick but highly reliable test of higher-order cognitive functioning. We evaluated the use of the puzzle box to explore executive functioning in five different mouse models of schizophrenia: mice with prefrontal cortex and hippocampus lesions, mice treated sub-chronically with the NMDA-receptor antagonist MK-801, mice constitutively lacking the GluA1 subunit of AMPA-receptors, and mice over-expressing dopamine D2 receptors in the striatum. All mice displayed altered executive functions in the puzzle box, although the nature and extent of the deficits varied between the different models. Deficits were strongest in hippocampus-lesioned and GluA1 knockout mice, while more subtle deficits but specific to problem solving were found in the medial prefrontal-lesioned mice, MK-801-treated mice, and in mice with striatal overexpression of D2 receptors. Data from this study demonstrate the utility of the puzzle box as an effective screening tool for executive functions in general and for schizophrenia mouse models in particular. Published by Elsevier Inc.
引用
收藏
页码:42 / 52
页数:11
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