Differential effects of antidepressants on dexamethasone-induced nuclear translocation and expression of glucocorticoid receptor

被引:28
|
作者
Funato, Hiromasa [1 ]
Kobayashi, Ayumi [1 ]
Watanabe, Yoshifumi [1 ]
机构
[1] Yamaguchi Univ, Div Neuropsychiat, Dept Neurosci, Sch Med, Ube, Yamaguchi 7558505, Japan
关键词
antidepressant; glucocorticoid receptor; SRp30c; nuclear translocation; alternative splicing;
D O I
10.1016/j.brainres.2006.08.029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The glucocorticoid receptor (GR) is a key regulator of the hypothalamic-pituitary-adrenal (HPA) axis. Mood disorder patients often exhibit abnormalities in this axis. Although the clinical benefit of antidepressants is associated with the normalization of the disturbed HPA activity by enhanced negative feedback of the HPA axis, the precise mechanism remains unknown. In order to examine the effect of antidepressants on the translocation of GR into the nucleus, we performed time-lapse observation on SY5Y cells that had been transiently transfected with plasmids expressing the green fluorescence protein (GFP)-tagged GR alpha. Clornipramine and desipramine facilitated dexamethasone (Dex)-induced GFP-GR alpha nuclear translocation. Coincubation of verapamil, an inhibitor of membrane steroid transporters, showed little or no additive effect on GFP-GR alpha nuclear translocation induced by both Dex and clomipramine. In the absence of Dex, antidepressants did not induce the translocation of GFP-GR alpha into the nucleus. Using real-time PCR, we examined the effect of antidepressants on splicing isoform. of GR, GR alpha, and GR beta in SY5Y and jurkat cells. Incubation with paroxetine and desipramine for 48 h and 7 days increased GR alpha expression, whereas the expression of GR beta remained stable. Antidepressants did not alter the expression of SRp30c that is associated with alternative splicing of GR transcript. Thus, antidepressants exert differential effects on the translocation and expression of GR to enhance GR signaling. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 134
页数:10
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