Effects of RU486 treatment after single prolonged stress depend on the post-stress interval

被引:5
|
作者
Ding, Jinlan [1 ,2 ,3 ]
Chen, Xinzhao [3 ]
da Silva, Marcia Santos [1 ,2 ]
Lingeman, Jolanthe [1 ,2 ]
Han, Fang [3 ]
Meijer, Onno C. [1 ,2 ]
机构
[1] Leiden Univ, Leiden Univ Med Ctr, Div Endocrinol, Dept Internal Med, Leiden, Netherlands
[2] Leiden Univ, Leiden Univ Med Ctr, Einthoven Lab Expt Vasc Med, Leiden, Netherlands
[3] China Med Univ, Dept Histol & Embryol, Basic Med Coll, PTSD Lab, Shenyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Single prolonged stress; Behaviour; Mifepristone; Sgk1; FKBP5; GLUCOCORTICOID-RECEPTORS; MIFEPRISTONE TREATMENT; HIPPOCAMPAL STRUCTURE; PTSD; INHIBITION; FKBP5; FEAR; CORTICOSTERONE; MECHANISMS; EXPRESSION;
D O I
10.1016/j.mcn.2020.103541
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Single Prolonged Stress protocol is considered a model for PTSD, as it induces long lasting changes in rat behaviour and endocrine regulation. Previous work demonstrated that some of these changes can be prevented by treatment with the glucocorticoid receptor antagonist RU486, administered a week after the stressor. The current study evaluated the effects of an earlier intervention with RU486, as evaluated 1 week after SPS-exposure. Most RU486 effects occurred independent of prior stress, except for the reversal of a stress-induced increase in locomotor behaviour. The accompanying changes in gene expression depended on gene, brain region, and time. DNA methylation of the robustly down-regulated Fkbp5 gene was dissociated of changes in mRNA expression. The findings reinforce the long term effects of GR antagonist treatment, but also emphasize the need to evaluate changes over time to allow the identification of robust correlates between gene expression and behavioural/endocrine outcome of stressful experiences.
引用
收藏
页数:12
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