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萘呋胺(萘基丙戊酸):在 Wistar 大鼠中的药代动力学、行为效应和体温调节。

Naphyrone (naphthylpyrovalerone): Pharmacokinetics, behavioural effects and thermoregulation in Wistar rats.

机构信息

Department of Experimental Neurobiology, National Institute of Mental Health, Klecany, Czech Republic.

Third Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.

出版信息

Addict Biol. 2021 Mar;26(2):e12906. doi: 10.1111/adb.12906. Epub 2020 May 7.

DOI:10.1111/adb.12906
PMID:32378298
Abstract

Naphthylpyrovalerone (naphyrone) is a pyrovalerone cathinone that potently inhibits monoamine transporters and provides stimulatory-entactogenic effects. Little is known about the safety of naphyrone or its effects in vivo, and more research is needed to acquire knowledge about its fundamental effects on physiology and behaviour. Our objective was to investigate naphyrone's pharmacokinetics, acute toxicity, hyperthermic potential and stimulatory and psychotomimetic properties in vivo in male Wistar rats. Pharmacokinetics after 1 mg/kg subcutaneous (sc.) naphyrone were measured over 6 h in serum, the brain, liver and lungs. Rectal temperature (degree Celsius) was measured over 10 h in group-versus individually housed rats after 20 mg/kg sc. In the behavioural experiments, 5, 10 or 20 mg/kg of naphyrone was administered 15 or 60 min prior to testing. Stimulation was assessed in the open field, and sensorimotor processing in a prepulse inhibition (PPI) task. Peak concentrations of naphyrone in serum and tissue were reached at 30 min, with a long-lasting elevation in the brain/serum ratio, consistent with observations of lasting hyperlocomotion in the open field and modest increases in body temperature. Administration of 20 mg/kg transiently enhanced PPI. Naphyrone crosses the blood-brain barrier rapidly and is eliminated slowly, and its long-lasting effects correspond to its pharmacokinetics. No specific signs of acute toxicity were observed; therefore, clinical care and harm-reduction guidance should be in line with that available for other stimulants and cathinones.

摘要

萘基吡咯烷酮(萘呋酮)是一种吡咯烷酮类去甲伪麻黄碱,能强烈抑制单胺转运体,并具有刺激和致快感作用。目前对萘呋酮的安全性或其体内作用知之甚少,需要更多的研究来获取关于其对生理和行为的基本影响的知识。我们的目的是研究萘呋酮在雄性 Wistar 大鼠体内的药代动力学、急性毒性、致热潜能以及刺激和致幻特性。在血清、大脑、肝脏和肺脏中,测量了皮下给予 1 毫克/千克萘呋酮后 6 小时的药代动力学。在 20 毫克/千克皮下注射后,将群居和独居大鼠的直肠温度(摄氏度)测量了 10 小时。在行为实验中,在测试前 15 或 60 分钟给予 5、10 或 20 毫克/千克的萘呋酮。在开放场中评估刺激,在预脉冲抑制(PPI)任务中评估感觉运动处理。萘呋酮在血清和组织中的峰值浓度在 30 分钟达到,大脑/血清比值持续升高,与开放场中持久的过度活跃和体温适度升高一致。给予 20 毫克/千克可短暂增强 PPI。萘呋酮迅速穿过血脑屏障并缓慢消除,其持久作用与其药代动力学相符。未观察到急性毒性的特定迹象;因此,临床护理和减少伤害的指导应与其他兴奋剂和去甲伪麻黄碱一致。

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