Behavioral insights from mouse models of forebrain- and amygdala-specific glucocorticoid receptor genetic disruption

被引:35
作者
Arnett, Melinda G. [1 ]
Kolber, Benedict J. [2 ]
Boyle, Maureen P. [3 ]
Muglia, Louis J. [4 ]
机构
[1] Vanderbilt Univ, Dept Pediat, Div Endocrinol, Nashville, TN 37232 USA
[2] Washington Univ, Pain Ctr, Dept Anesthesiol, St Louis, MO 63110 USA
[3] Washington Univ, Dept Pediat, St Louis, MO 63110 USA
[4] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
关键词
Glucocorticoid receptor genetic disruption; Forebrain; Amygdala; Anxiety; Depression; TRANSGENIC MICE; ADRENAL AXIS; ANTISENSE RNA; DEPRESSION; ACTIVATION; ANXIETY; STRESS; BRAIN;
D O I
10.1016/j.mce.2010.11.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genetic modulation of glucocorticoid receptor (GR) function in the brain using transgenic and gene knockout mice has yielded important insights into many aspects of GR effects on behavior and neuroendocrine responses, but significant limitations regarding interpretation of region-specific and temporal requirements remain. Here, we summarize the behavioral phenotype associated with two knockout mouse models to define the role of GRs specifically within the forebrain and amygdala. We report that forebrain-specific GR knockout mice exhibit impaired negative feedback regulation of the hypothalamic-pituitary-adrenal (HPA) axis and increased despair- and anxiety-like behaviors. In addition, mice with a disruption of GR specifically within the central nucleus of the amygdala (CeA) are deficient in conditioned fear behavior. Overall, these models serve as beneficial tools to better understand the biology of GR signaling in the normal stress response and in mood disorders. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:2 / 5
页数:4
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