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In vitro modulation of the glucocorticoid receptor by antidepressants.

机译:抗抑郁药对糖皮质激素受体的体外调节。

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Clinical studies have demonstrated an impairment of glucocorticoid receptor (GR)-mediated negative feedback on the hypothalamus-pituitary-adrenal (HPA) axis in patients with major depression (GR resistance), and its resolution by antidepressant treatment. Accordingly, reduced GR function has also been demonstrated in vitro, in peripheral tissues of depressed patients, as shown by reduced sensitivity to the effects of glucocorticoids on immune and metabolic functions. We and others have shown that antidepressants in vitro are able to modulate GR mRNA expression, GR protein level and GR function. This paper reviews the in vitro studies that have examined the effect of antidepressants on GR expression, number and function in human and animal cell lines, and the possible molecular mechanisms underlying these effects. Antidepressants are shown to both increase and decrease GR function in vitro, based on different experimental conditions. Specifically, increased GR function is likely to be mediated by an increased intracellular concentration of glucocorticoids, while decreased GR function seems to be the consequence of GR downregulation. We suggest that the study of the effects of antidepressants on glucocorticoid function might help clarify the therapeutic action of these drugs.
机译:临床研究表明,患有重度抑郁症(GR耐药)的患者的下丘脑-垂体-肾上腺(HPA)轴上糖皮质激素受体(GR)介导的负反馈受到损害,并通过抗抑郁药治疗得以缓解。因此,在抑郁症患者的外周组织中,还证明了体外GR功能降低,这是由于对糖皮质激素对免疫和代谢功能的影响的敏感性降低。我们和其他人已经表明,体外抗抑郁药能够调节GR mRNA表达,GR蛋白水平和GR功能。本文回顾了体外研究,这些研究检查了抗抑郁药对人和动物细胞系GR表达,数量和功能的影响,以及潜在的分子机制。根据不同的实验条件,抗抑郁药在体外显示出增加和减少GR功能的作用。具体而言,增加的GR功能可能是由细胞内糖皮质激素浓度的增加介导的,而降低的GR功能似乎是GR下调的结果。我们建议研究抗抑郁药对糖皮质激素功能的影响可能有助于阐明这些药物的治疗作用。

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