Department of Pediatrics, Vanderbilt University, Nashville, TN 37232, United States.
Mol Cell Endocrinol. 2011 Apr 10;336(1-2):2-5. doi: 10.1016/j.mce.2010.11.011. Epub 2010 Nov 20.
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.
利用转基因和基因敲除小鼠对脑内糖皮质激素受体(GR)功能进行遗传调控,为 GR 对行为和神经内分泌反应的影响的许多方面提供了重要的见解,但在解释区域特异性和时间需求方面仍存在重大限制。在这里,我们总结了与两种敲除小鼠模型相关的行为表型,以确定 GR 在前脑和杏仁核内的特定作用。我们报告说,前脑特异性 GR 敲除小鼠表现出下丘脑-垂体-肾上腺(HPA)轴负反馈调节受损和绝望和焦虑样行为增加。此外,杏仁核中央核(CeA)内 GR 破坏的小鼠在条件性恐惧行为中存在缺陷。总的来说,这些模型是更好地理解正常应激反应和情绪障碍中 GR 信号生物学的有益工具。