Department of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Molecular Targets and Medications Discovery Branch, National Institute on Drug Abuse, National Institute on Alcohol Abuse and Alcoholism, Bethesda, MD 20852, USA.
Neuropharmacology. 2018 May 15;134(Pt A):28-35. doi: 10.1016/j.neuropharm.2017.08.018. Epub 2017 Aug 12.
"Bath salts" preparations contain synthetic cathinones which interact with monoamine transporters and function as either monoamine uptake inhibitors or releasers. 3,4-Methylenedioxypyrovalerone (MDPV), 3,4-methylenedioxymethcathinone (methylone), and 4-methylmethcathinone (mephedrone) were three of the most common cathinones (i.e., "first-generation" cathinones); however, after the US Drug Enforcement Administration placed them under Schedule I regulations, they were replaced with structurally related cathinones that were not subject to regulations (i.e., "second-generation" cathinones). Although the reinforcing effects of some second-generation cathinones have been described (e.g., α-pyrrolidinopentiophenone [α-PVP]), little is known about how structural modifications, particularly those involving the methylenedioxy moiety and α-alkyl side chain, impact the abuse liability of other second-generation cathinones (e.g., α-pyrrolidinopropiophenone [α-PPP], 3,4-methylenedioxy-α-pyrrolidinobutiophenone [MDPBP], and 3,4-methylenedioxy-α-pyrrolidinopropiophenone [MDPPP]). The present study used male Sprague-Dawley rats (n = 12 per drug) to directly compare: (1) the acquisition of responding for α-PVP (0.032 mg/kg/inf), α-PPP (0.32 mg/kg/inf), MDPBP (0.1 mg/kg/inf), and MDPPP (0.32 mg/kg/inf) under a fixed ratio (FR) 1 schedule of reinforcement; and (2) full dose-response curves for each drug to maintain responding under an FR5 schedule of reinforcement. The average number of days (∼4 days) and percentage (100%) of rats that acquired self-administration was similar for each drug. The observed rank order potency to maintain responding under an FR5 schedule of reinforcement (α-PVP ≈ MDPBP>α-PPP > MDPPP) is consistent with their potencies to inhibit dopamine uptake. These are the first studies to report on the reinforcing effects of the unregulated second-generation cathinones MDPBP, MDPPP, and α-PPP and indicate all three compounds are readily self-administered, suggesting each possesses high potential for abuse. This article is part of the Special Issue entitled 'Designer Drugs and Legal Highs.'
“浴盐”制剂含有合成的去甲伪麻黄碱,可与单胺转运蛋白相互作用,并作为单胺摄取抑制剂或释放剂发挥作用。3,4-亚甲二氧基吡咯戊酮(MDPV)、3,4-亚甲二氧基甲卡西酮(甲基酮)和 4-甲基甲卡西酮(甲卡西酮)是最常见的去甲伪麻黄碱(即“第一代”去甲伪麻黄碱)中的三种;然而,在美国缉毒署将它们列入附表 I 管制之后,它们被结构相似但不受管制的去甲伪麻黄碱所取代(即“第二代”去甲伪麻黄碱)。虽然一些第二代去甲伪麻黄碱的强化作用已经被描述(例如,α-吡咯烷戊基苯酮[α-PVP]),但对于结构修饰如何影响其他第二代去甲伪麻黄碱(例如,α-吡咯烷丙基苯酮[α-PPP]、3,4-亚甲二氧基-α-吡咯烷丁基苯酮[MDPBP]和 3,4-亚甲二氧基-α-吡咯烷丙基苯酮[MDPPP])的滥用倾向,人们知之甚少。本研究使用雄性 Sprague-Dawley 大鼠(每种药物 12 只)直接比较:(1)在固定比率(FR)1 强化方案下,α-PVP(0.032mg/kg/inf)、α-PPP(0.32mg/kg/inf)、MDPBP(0.1mg/kg/inf)和 MDPPP(0.32mg/kg/inf)的获取反应;和(2)每种药物在 FR5 强化方案下维持反应的全剂量反应曲线。每种药物获得自我给药的平均天数(约 4 天)和百分比(100%)相似。在 FR5 强化方案下维持反应的观察到的效价顺序(α-PVP≈MDPBP>α-PPP>MDPPP)与它们抑制多巴胺摄取的效价一致。这些是首次报道不受管制的第二代去甲伪麻黄碱 MDPBP、MDPPP 和 α-PPP 的强化作用的研究,表明这三种化合物都很容易被自我给药,表明它们都具有很高的滥用潜力。本文是特刊“设计药物和合法兴奋剂”的一部分。