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抗抑郁化合物对人糖皮质激素受体功能的调节

Modulation of the human glucocorticoid receptor function by antidepressive compounds.

作者信息

Okuyama-Tamura Miho, Mikuni Masahiko, Kojima Itaru

机构信息

Department of Psychiatry, Gunma University School of Medicine, Maebashi, Japan.

出版信息

Neurosci Lett. 2003 May 22;342(3):206-10. doi: 10.1016/s0304-3940(03)00261-1.

Abstract

Hyperactivity of the hypothalamic-pituitary-adrenal axis is associated with depression. We investigated the effect of various types of antidepressant agents in vitro on the function of glucocorticoid receptor (GR). Desipramine, clomiplamine, fluoxetine, milnacipran and clorgyline all induced rapid and sustained translocation of GR into the nucleus of human lymphocytes. In contrast, major and minor tranquilizers, lithium and verapamil, a blocker of membrane steroid transporter, were without effect. These antidepressants did not affect GR-mediated transcription by themselves, but significantly inhibited dexamethasone-induced transcription. These results indicate that structurally different antidepressants induce translocation of GR and inhibit GR-mediated transcription.

摘要

下丘脑-垂体-肾上腺轴功能亢进与抑郁症有关。我们在体外研究了各类抗抑郁药对糖皮质激素受体(GR)功能的影响。地昔帕明、氯米帕明、氟西汀、米那普明和氯吉兰均能诱导GR快速且持续地转位至人淋巴细胞的细胞核中。相比之下,主要和次要的镇静剂、锂盐以及膜类固醇转运体阻滞剂维拉帕米则没有效果。这些抗抑郁药本身并不影响GR介导的转录,但能显著抑制地塞米松诱导的转录。这些结果表明,结构不同的抗抑郁药可诱导GR转位并抑制GR介导的转录。

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