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重复给药后,布雷哌唑改变单胺能系统:一项体内电生理学研究。

Brexpiprazole Alters Monoaminergic Systems following Repeated Administration: an in Vivo Electrophysiological Study.

作者信息

Oosterhof Chris A, El Mansari Mostafa, Bundgaard Christoffer, Blier Pierre

机构信息

Institute of Mental Health Research (Dr Oosterhof, Dr El Mansari, and Dr Blier), and Department of Cellular and Molecular Medicine (Dr Oosterhof and Dr Blier), University of Ottawa, Ottawa, Ontario, Canada; Neuroscience Drug Discovery, H. Lundbeck A/S, Valby, Denmark (Dr Bundgaard).

出版信息

Int J Neuropsychopharmacol. 2015 Oct 1;19(3):pyv111. doi: 10.1093/ijnp/pyv111.

Abstract

BACKGROUND

Brexpiprazole was recently approved as adjunctive therapy for depression and treatment of schizophrenia in adults. To complement results from a previous study in which its acute effects were characterized, the present study assessed the effect of repeated brexpiprazole administration on monoaminergic systems.

METHODS

Brexpiprazole (1mg/kg, subcutaneous) or vehicle was administered once daily for 2 and 14 days. Single-unit electrophysiological recordings from noradrenaline neurons in the locus coeruleus, serotonin neurons in the dorsal raphe nucleus, dopaminergic neurons in the ventral tegmental area, and pyramidal neurons in the hippocampus CA3 region were obtained in adult male Sprague-Dawley rats under chloral hydrate anesthesia within 4 hours after final dosing.

RESULTS

Brexpiprazole blunted D2 autoreceptor responsiveness, while firing activity of ventral tegmental area dopaminergic neurons remained unaltered. Brexpiprazole increased the firing rate of locus coeruleus noradrenaline neurons and increased noradrenaline tone on α2-adrenergic receptors in the hippocampus. Administration of brexpiprazole for 2 but not 14 days increased the firing rate of serotonin neurons in the dorsal raphe nucleus. In the hippocampus, serotonin1A receptor blockade significantly disinhibited pyramidal neurons after 2- and 14-day brexpiprazole administration. In contrast, no significant disinhibition occurred after 24-hour washout or acute brexpiprazole.

CONCLUSIONS

Repeated brexpiprazole administration resulted in a marked occupancy of D2 autoreceptors, while discharge activity of ventral tegmental area dopaminergic neurons remained unaltered. Brexpiprazole enhanced serotonergic and noradrenergic tone in the hippocampus, effects common to antidepressant agents. Together, these results provide further insight in the neural mechanisms by which brexpiprazole exerts antidepressant and antipsychotic effects.

摘要

背景

布雷哌唑最近被批准作为成人抑郁症的辅助治疗药物和精神分裂症的治疗药物。为补充先前一项对其急性效应进行特征描述的研究结果,本研究评估了重复给予布雷哌唑对单胺能系统的影响。

方法

将布雷哌唑(1毫克/千克,皮下注射)或赋形剂每天给药一次,持续2天和14天。在水合氯醛麻醉下,于成年雄性斯普拉格-道利大鼠末次给药后4小时内,从蓝斑中的去甲肾上腺素能神经元、中缝背核中的5-羟色胺能神经元、腹侧被盖区中的多巴胺能神经元以及海马CA3区中的锥体神经元进行单单位电生理记录。

结果

布雷哌唑减弱了D2自身受体反应性,而腹侧被盖区多巴胺能神经元的放电活动保持不变。布雷哌唑增加了蓝斑去甲肾上腺素能神经元的放电频率,并增加了海马中α2肾上腺素能受体上的去甲肾上腺素张力。给予布雷哌唑2天而非14天可增加中缝背核中5-羟色胺能神经元的放电频率。在海马中,给予布雷哌唑2天和14天后,5-羟色胺1A受体阻断显著解除了锥体神经元的抑制。相比之下,在24小时洗脱或急性给予布雷哌唑后未发生显著的去抑制作用。

结论

重复给予布雷哌唑导致D2自身受体明显被占据,而腹侧被盖区多巴胺能神经元的放电活动保持不变。布雷哌唑增强了海马中的5-羟色胺能和去甲肾上腺素能张力,这是抗抑郁药常见的效应。总之,这些结果为布雷哌唑发挥抗抑郁和抗精神病作用的神经机制提供了进一步的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a619/4815476/0bfab69788e1/ijnppy_pyv111_f0004.jpg

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