Exploratory, anxiety and spatial memory impairments are dissociated in mice lacking the LPA1 receptor

被引:69
|
作者
Castilla-Ortega, Estela [1 ]
Sanchez-Lopez, Jorge [1 ]
Hoyo-Becerra, Carolina [2 ]
Matas-Rico, Elisa [2 ]
Zambrana-Infantes, Emma [1 ]
Chun, Jerold [3 ]
Rodriguez De Fonseca, Fernando [2 ]
Pedraza, Carmen [1 ]
Estivill-Torrus, Guillermo [2 ]
Santin, Luis J. [1 ]
机构
[1] Univ Malaga, Dept Psicobiol & Metodol CC, E-29071 Malaga, Spain
[2] Hosp Reg Univ Carlos Haya, Fdn IMABIS, Unidad Invest, E-29010 Malaga, Spain
[3] Scripps Res Inst, Dept Mol Biol, Helen L Dorris Child & Adolescent Neuropsychiat D, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
Lysophosphatidic acid; Knockout mice; Hole-board; Principal components factorial analysis; Spatial reference memory; Spatial working memory; Habituation; HOLE-BOARD TEST; WORKING-MEMORY; LYSOPHOSPHOLIPID RECEPTORS; PLUS-MAZE; MINERALOCORTICOID RECEPTORS; COGNITIVE PERFORMANCE; HIPPOCAMPAL-NEURONS; PREFRONTAL CORTEX; NERVOUS-SYSTEM; DEFICIENT MICE;
D O I
10.1016/j.nlm.2010.04.003
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Lysophosphatidic acid (LPA) is a new, intercellular signalling molecule in the brain that has an important role in adult hippocampal plasticity. Mice lacking the LPA, receptor exhibit motor, emotional and cognitive alterations. However, the potential relationship among these concomitant impairments was unclear. Wild-type and maLPA(1)-null mice were tested on the hole-board for habituation and spatial learning. MaLPA(1)-null mice exhibited reduced exploration in a novel context and a defective intersession habituation that also revealed increased anxiety-like behaviour throughout the hole-board testing. In regard to spatial memory, maLPA(1) nulls failed to reach the controls' performance at the end of the reference memory task. Moreover, their defective working memory on the first training day suggested a delayed acquisition of the task's working memory rule, which is also a long term memory component. The temporal interval between trials and the task's difficulty may explain some of the deficits found in these mice. Principal components analysis revealed that alterations found in each behavioural dimension were independent. Therefore, exploratory and emotional impairments did not account for the cognitive deficits that may be attributed to maLPA(1) nulls' hippocampal malfunction. (c) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:73 / 82
页数:10
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