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新型5-羟色胺和去甲肾上腺素再摄取抑制剂071031B对小鼠和大鼠单胺系统的影响。

Effects of 071031B, a novel serotonin and norepinephrine reuptake inhibitor, on monoamine system in mice and rats.

作者信息

Xue Rui, He Xin-Hua, Yuan Li, Chen Hong-Xia, Zhang Li-Ming, Yong Zheng, Yu Gang, Fan Shi-Yong, Li Yun-Feng, Zhong Bo-Hua, Zhang You-Zhi

机构信息

Department of New Drug Evaluation, Beijing Institute of Pharmacology and Toxicology, Beijing, PR China.

Department of Drug Synthesis, Beijing Institute of Pharmacology and Toxicology, Beijing, PR China.

出版信息

J Pharmacol Sci. 2016 Jan;130(1):1-7. doi: 10.1016/j.jphs.2015.07.043. Epub 2015 Aug 10.

DOI:10.1016/j.jphs.2015.07.043
PMID:26318675
Abstract

Our previous study indicated that 071031B, a novel potential serotonin and norepinephrine reuptake inhibitor, showed robust antidepressant activity in multiple depression models, and could simultaneously inhibit 5-HT and NE reuptake in vitro. The present study was to evaluate the effects of 071031B on monoamine system in vivo, by using pharmacological models, including 5-HTP induced head-twitch test, yohimbine toxicity potentiation test, and reserpine induced hypothermia test, and determining monoamine transmitter levels in reserpine induced monoamine depletion model or chronic unpredictable stress (CUS) model. Results in pharmacological models indicated that acute administration of 071031B at 5-20 mg/kg significantly enhanced 5-HTP induced head-twitch behavior, potentiated yohimbine induced lethal rate, and reversed reserpine induced hypothermia. Further monoamine assays demonstrated that acute or chronic administration of 071031B at 10 or 20 mg/kg increased 5-HT and/or NE levels in various brain regions in reserpine or CUS induced monoamine depletion models, respectively, without effect on DA and its metabolites. Our results revealed that 071031B produces potent inhibition of 5-HT and NE reuptake in vivo.

摘要

我们之前的研究表明,新型潜在血清素和去甲肾上腺素再摄取抑制剂071031B在多种抑郁症模型中显示出强大的抗抑郁活性,并且在体外能够同时抑制5-羟色胺(5-HT)和去甲肾上腺素(NE)的再摄取。本研究旨在通过使用药理学模型,包括5-羟色氨酸(5-HTP)诱导的头部抽搐试验、育亨宾毒性增强试验和利血平诱导的体温过低试验,并测定利血平诱导的单胺耗竭模型或慢性不可预测应激(CUS)模型中的单胺递质水平,来评估071031B在体内对单胺系统的影响。药理学模型的结果表明,以5-20mg/kg的剂量急性给予071031B可显著增强5-HTP诱导的头部抽搐行为,增强育亨宾诱导的致死率,并逆转利血平诱导的体温过低。进一步的单胺测定表明,在利血平或CUS诱导的单胺耗竭模型中,以10或20mg/kg的剂量急性或慢性给予071031B分别增加了各个脑区的5-HT和/或NE水平,而对多巴胺(DA)及其代谢产物没有影响。我们的结果表明,071031B在体内对5-HT和NE的再摄取具有强效抑制作用。

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