米氮平对 BDNF 翻译的选择性去甲肾上腺素能激活作用

IF 4.6 2区 医学 Q1 NEUROSCIENCES Molecular Neurobiology Pub Date : 2024-11-18 DOI:10.1007/s12035-024-04619-1
Viviana Ciraci, Letizia Santoni, Enrico Tongiorgi
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引用次数: 0

摘要

众所周知,抗抑郁药具有神经营养作用,特别是通过调节脑源性神经营养因子(BDNF)的表达。米氮平是一种四环去甲肾上腺素能和特异性血清素能抗抑郁药(NaSSA),已被观察到能上调 BDNF,但其潜在机制仍不清楚。在本研究中,我们使用人神经母细胞瘤 SH-SY5Y 细胞系研究米氮平是否能通过调节血清素和/或去甲肾上腺素及其受体来增强 BDNF 翻译。用 1 µM 或 10 µM 的米氮平刺激 1 小时后,血清素能受体 5HT1A 下调,而 ADRA2A 和 ADRB2 受体增加。10 µM的米氮平能在刺激3小时后上调内源性BDNF,但不能在刺激1小时后上调内源性BDNF。为了研究主要 BDNF 转录本的翻译,我们使用了带有未翻译 5'UTR 外显子 I、IIc、IV 或 VI 和长版 3'UTR 的嵌合 BDNF 荧光素酶构建体。荧光素酶测定和 Western 印迹显示,米氮平选择性地增强了外显子 IIc-BDNF 长 3'UTR 荧光素酶的翻译。这种增加与去甲肾上腺素的释放有关,阻断ADRA2A或ADRB2肾上腺素受体可抑制外显子-IIc-BDNF-长3'UTR-荧光素酶,阻断ADR2B可抑制内源性BDNF。这些发现从一个新的角度说明了去甲肾上腺素能系统在介导米氮平对 BDNF 翻译的影响中的关键作用。我们提出了一种新的作用机制,其中米氮平通过上调 ADRA2A 和 ADRB2,同时下调血清素能受体,促进去甲肾上腺素的释放和去甲肾上腺素能反应。
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Selective Noradrenergic Activation of BDNF Translation by Mirtazapine.

Antidepressants are known for their neurotrophic effects, particularly through the regulation of brain-derived neurotrophic factor (BDNF) expression. Mirtazapine, a tetracyclic noradrenergic and specific serotonergic antidepressant (NaSSA) has been observed to upregulate BDNF, though its underlying mechanism remains unclear. In this study, we used the human neuroblastoma SH-SY5Y cell line to investigate whether mirtazapine could enhance BDNF translation by modulating serotonin and/or norepinephrine and their receptors. A 1-h stimulation with 1 or 10 µM mirtazapine led to downregulation of serotonergic receptors 5HT1A, while increasing ADRA2A and ADRB2 receptors. Mirtazapine at 10 µM upregulated endogenous BDNF after 3h, but not 1h stimulation. To investigate the translation of major BDNF transcripts, we used chimeric BDNF-luciferase constructs with the untranslated 5'UTR exons I, IIc, IV, or VI, and the long version of the 3'UTR. Luciferase assays and Western blotting revealed that mirtazapine selectively enhanced exon-IIc-BDNF-long3'UTR-Luciferase translation. This increase was associated with norepinephrine release and was inhibited by blocking ADRA2A or ADRB2 adrenoceptors for the exon-IIc-BDNF-long3'UTR-Luciferase, and ADR2B for endogenous BDNF. These findings provide a new perspective on the critical role of the noradrenergic system in mediating mirtazapine's effects on BDNF translation. We propose a novel mechanism of action in which mirtazapine promotes norepinephrine release and noradrenergic responses by upregulating ADRA2A and ADRB2 while downregulating serotonergic receptors.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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