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The 5-HT2C receptor agonist lorcaserin reduces cocaine self-administration, reinstatement of cocaine-seeking and cocaine induced locomotor activity

机译:5-HT2C受体激动剂lorcaserin减少可卡因的自我给药,可卡因的恢复和可卡因诱导的运动活动

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摘要

Lorcaserin (Lorqess, Belviq (R)) is a selective 5-HT2C receptor agonist that has received FDA approval for the treatment of obesity. 5-HT2C receptor agonists are also efficacious in decreasing multiple aspects of cocaine motivation and reward in preclinical models. This would suggest that lorcaserin is a clinically available therapeutic with the potential to treat cocaine addiction. Here we report the effects of lorcaserin (0.1 mg/kg-1.0 mg/kg) on multiple aspects of cocaine-related behaviours in rats. We find that lorcaserin dose-dependently decreases cocaine self-administration on progressive and fixed ratio schedules of reinforcement. Lorcaserin also reduces reinstatement of cocaine-seeking behaviour in response to priming injections of cocaine and/or reintroduction of cocaine-associated cues. Finally, lorcaserin dose-dependently decreases cocaine-induced hyperlocomotion. Our results, when considered in concert with similar emergent findings in non-human primates, strongly support continued research into the potential of lorcaserin as a clinical treatment for cocaine addiction. (C) 2015 Elsevier Ltd. All rights reserved.
机译:Lorcaserin(Lorqess,Belviq(R))是一种选择性5-HT2C受体激动剂,已获得FDA批准用于治疗肥胖症。 5-HT2C受体激动剂在减少临床前模型中可卡因动机和奖励的多个方面方面也是有效的。这表明氯卡色林是一种临床可用的治疗剂,具有治疗可卡因成瘾的潜力。在这里,我们报告了氯卡色林(0.1 mg / kg-1.0 mg / kg)对大鼠可卡因相关行为的多个方面的影响。我们发现,lorcaserin剂量依赖性地减少可卡因的自我管理,逐步进行和固定比率的强化治疗。响应于初次注射可卡因和/或可卡因相关提示的重新引入,洛卡西林还降低了可卡因寻求行为的恢复。最后,lorcaserin剂量依赖性地降低可卡因诱导的运动过度。我们的研究结果与非人类灵长类动物的类似新兴发现相结合时,强烈支持继续研究氯卡色林作为可卡因成瘾的临床治疗方法的潜力。 (C)2015 Elsevier Ltd.保留所有权利。

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