Animal models of mental retardation: from gene to cognitive function

被引:35
作者
Branchi, I
Bichler, Z
Berger-Sweeney, J
Ricceri, L
机构
[1] Ist Super Sanita, Lab Fisiopatol Organo & Sistema, Sect Behav Pathophysiol, I-00161 Rome, Italy
[2] CNRS, Inst Transgenose, FRE 2358, Orleans, France
[3] Wellesley Coll, Dept Sci Biol, Wellesley, MA 02481 USA
[4] Ist Super Sanita, Lab Fisiopatol Organo & Sistema, Sect Comparat Psychol, Rome, Italy
关键词
genetically modified; neurodevelopmental disorders; mental retardation; mouse; behavior; development; neuropathology; genetic disorders;
D O I
10.1016/S0149-7634(03)00016-2
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
About 2-3% of all children are affected by mental retardation, and genetic conditions rank among the leading causes of mental retardation. Alterations in the information encoded by genes that regulate critical steps of brain development can disrupt the normal course of development, and have profound consequences on mental processes. Genetically modified mouse models have helped to elucidate the contribution of specific gene alterations and gene-environment interactions to the phenotype of several forms of mental retardation. Mouse models of several neurodevelopmental pathologies, such as Down and Rett syndromes and X-linked forms of mental retardation, have been developed. Because behavior is the ultimate output of brain, behavioral phenotyping of these models provides functional information that may not be detectable using molecular, cellular or histological evaluations. In particular, the study of ontogeny of behavior is recommended in mouse models of disorders having a developmental onset. Identifying the role of specific genes in neuropathologies provides a framework in which to understand key stages of human brain development, and provides a target for potential therapeutic intervention. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:141 / 153
页数:13
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