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抗抑郁药具有增加终纹床核儿茶酚胺输出的能力:在抗抑郁治疗中的可能作用?

Antidepressants share the ability to increase catecholamine output in the bed nucleus of stria terminalis: a possible role in antidepressant therapy?

机构信息

Department of Biomedical Sciences, University of Cagliari, Via Ospedale 72, 09124, Cagliari, Italy.

出版信息

Psychopharmacology (Berl). 2014 May;231(9):1925-33. doi: 10.1007/s00213-013-3335-y. Epub 2013 Nov 13.

Abstract

RATIONALE

Antidepressants include a relatively wide spectrum of drugs that increase the synaptic concentration of monoamines, mostly through neurotransmitter reuptake blockade. The bed nucleus of stria teminalis (BNST) is considered a relay station in mediating the activation of stress response but also in the acquisition and expression of emotions. BNST is richly innervated by monoamines and sends back projections to the nucleus of origin. We previously showed that the administration of selective blockers of norepinephrine transporter (NET) increases the extracellular concentration (output) of dopamine, suggesting that dopamine could be captured by NET in the BNST.

OBJECTIVES

The aim of this study, carried out by means of in vivo microdialysis, was to ascertain the acute effects that antidepressants with varying mechanisms of action have on dopamine and norepinephrine output in the BNST.

RESULTS

We observed that all the antidepressants tested (5-20 mg/kg i.p.) increased the output of catecholamines, dose dependently. In particular, the maximum increases (as a percent of basal) for norepinephrine and dopamine respectively, were as follows: desipramine, 239 and 137; reboxetine, 185 and 128; imipramine, 512 and 359; citalopram, 95 and 122; fluoxetine, 122 and 68; bupropion, 255 and 164.

CONCLUSIONS

These results suggest that catecholamine transmission in the BNST may be part of a common downstream pathway that is involved in the action mechanism of antidepressants. Consequently, it is hypothesized that a dysfunction of neuronal transmission in this brain area may have a role in the etiology of affective disorders.

摘要

背景

抗抑郁药包括相对较宽谱的药物,这些药物通过抑制神经递质再摄取来增加单胺的突触浓度。终纹床核(BNST)被认为是介导应激反应激活的中继站,但也是情绪的获得和表达的中继站。BNST 富含单胺能神经支配,并向起源核发送回投射。我们之前的研究表明,选择性去甲肾上腺素转运体(NET)抑制剂的给药会增加多巴胺的细胞外浓度(输出),这表明多巴胺可能在 BNST 中被 NET 捕获。

目的

本研究通过在体微透析技术,旨在确定具有不同作用机制的抗抑郁药对 BNST 中多巴胺和去甲肾上腺素输出的急性影响。

结果

我们观察到所有测试的抗抑郁药(5-20mg/kg 腹腔注射)均剂量依赖性地增加儿茶酚胺的输出。特别是,去甲肾上腺素和多巴胺的最大增加(分别为基础值的百分比)如下:去甲丙咪嗪,239 和 137;瑞波西汀,185 和 128;丙咪嗪,512 和 359;西酞普兰,95 和 122;氟西汀,122 和 68;安非他酮,255 和 164。

结论

这些结果表明,BNST 中的儿茶酚胺传递可能是参与抗抑郁药作用机制的共同下游途径的一部分。因此,假设该脑区神经元传递功能障碍可能与情感障碍的病因有关。

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