Department of Psychology, Western Michigan University, Kalamazoo, MI 49008, United States.
Department of Psychiatry and Behavioral Neuroscience, Wayne State University, Detroit, MI 38677, United States.
Neuropharmacology. 2018 May 15;134(Pt A):22-27. doi: 10.1016/j.neuropharm.2017.10.019. Epub 2017 Oct 16.
Synthetic cathinones, known as "bath salts" on the illicit drug market, pose a significant public health concern. 3,4-Methylenedioxypyrovalerone (MDPV), one of several popular constituents of illicit bath salts, produces similar pharmacological actions to cocaine, albeit with greater potency and efficacy. The present study sought to characterize behavioral and neurochemical effects of repeated exposure to MDPV alone and in combination with cocaine. Male Sprague-Dawley rats were randomly assigned to one the following four treatments, administered once daily for seven days: 1 mg/kg MDPV, 5 mg/kg cocaine, 1 mg/kg MDPV +5 mg/kg cocaine, or saline. Locomotor activity was assessed for 1 h immediately before and 1 h immediately after injections on days 1 and 6. Brains were harvested 20 min after the final injection on day 7 and brain tissue punches were obtained to determine monoamine content within the anterior striatum, medial prefrontal cortex, and nucleus accumbens using High-Performance Liquid Chromatography (HPLC). Drug-induced increases in horizontal activity were significantly greater on treatment day 6 compared to treatment day 1 in all three drug treatment groups in comparison to the saline control group. MDPV produced significantly higher increases in activity compared to either saline or cocaine, although concurrent treatment with MDPV and cocaine produced sub-additive effects. Neurochemical analyses provided no evidence of alterations in total monoamine content following repeated administration of MDPV, cocaine, or the MDPV + COC mixture. Further investigations targeting possible changes in DA receptor sensitivity following repeated exposure to MDPV may help elucidate the mechanistic changes responsible for MDPV-induced behavioral sensitization. This article is part of the Special Issue entitled 'Designer Drugs and Legal Highs.'
合成卡西酮,在非法毒品市场上被称为“浴盐”,对公共健康构成重大威胁。3,4-亚甲基二氧吡咯戊酮(MDPV)是几种流行的非法浴盐成分之一,其产生的药理学作用与可卡因相似,但效力和效果更强。本研究旨在描述重复暴露于 MDPV 单独和与可卡因联合时的行为和神经化学效应。雄性 Sprague-Dawley 大鼠随机分为以下四组之一,每天一次给药,共七天:1mg/kg MDPV、5mg/kg 可卡因、1mg/kg MDPV+5mg/kg 可卡因或生理盐水。在第 1 天和第 6 天注射前 1 小时和注射后 1 小时立即评估运动活动。在第 7 天最后一次注射后 20 分钟采集大脑,并使用高效液相色谱法(HPLC)测定前纹状体、内侧前额叶皮层和伏隔核中的单胺含量。与生理盐水对照组相比,所有三种药物治疗组在治疗第 6 天的药物诱导的水平活动增加均明显大于治疗第 1 天。与生理盐水或可卡因相比,MDPV 导致的活动增加明显更高,尽管 MDPV 和可卡因的联合治疗产生了亚相加作用。神经化学分析未提供重复给予 MDPV、可卡因或 MDPV+COC 混合物后总单胺含量改变的证据。针对重复暴露于 MDPV 后可能发生的 DA 受体敏感性变化的进一步研究可能有助于阐明导致 MDPV 诱导的行为敏化的机制变化。本文是特刊“设计药物和合法兴奋剂”的一部分。