Department of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Molecular Targets and Medications Discovery Branch, NIDA and NIAAA, Bethesda, MD, USA.
Neuropsychopharmacology. 2018 Mar;43(4):761-769. doi: 10.1038/npp.2017.141. Epub 2017 Jul 5.
Bath salts use is associated with high rates of abuse, toxicity, and death. Bath salt preparations often contain mixtures of drugs including multiple synthetic cathinones (eg, 3,4-methylenedioxypyrovalerone (MDPV) or 3,4-methylenedioxymethcathinone (methylone)) or synthetic cathinones and caffeine; however, little is known about whether interactions among bath salt constituents contribute to the abuse-related effects of bath salts preparations. This study used male Sprague-Dawley rats responding under a progressive ratio schedule to quantify the reinforcing effectiveness of MDPV, methylone, and caffeine, administered alone and as binary mixtures (n=12 per mixture). Each mixture was evaluated at four ratios (10 : 1, 3 : 1, 1 : 1, and 1 : 3) relative to the mean ED for each drug alone. Dose-addition analyses were used to determine the predicted, additive effect for each dose pair within each drug mixture. MDPV, methylone, and caffeine maintained responding in a dose-dependent manner, with MDPV being the most potent and effective, and caffeine being the least potent and effective of the three bath salts constituents. High levels of responding were also maintained by each of the bath salts mixtures. Although the nature of the interactions tended toward additivity for most bath salts mixtures, supra-additive (3 : 1 MDPV : caffeine, and 3 : 1 and 1 : 1 methylone : caffeine) and sub-additive (3 : 1, 1 : 1, and 1 : 3 MDPV : methylone) interactions were also observed. Together, these findings demonstrate that the composition of bath salts preparations can have an impact on both their reinforcing potency and effectiveness, and suggest that such interactions among constituent drugs could contribute to the patterns of use and effects reported by human bath salts users.
浴盐的使用与滥用、毒性和死亡的高发生率有关。浴盐制剂通常含有多种药物的混合物,包括多种合成卡西酮(例如,3,4-亚甲基二氧吡咯戊酮(MDPV)或 3,4-亚甲基二氧甲卡西酮(甲基酮))或合成卡西酮和咖啡因;然而,对于浴盐成分之间的相互作用是否会导致浴盐制剂的滥用相关影响知之甚少。本研究使用雄性 Sprague-Dawley 大鼠在递增比例方案下进行反应,以量化 MDPV、甲基酮和咖啡因单独给药以及作为二元混合物给药时的强化效力(每组混合物 12 只)。每个混合物在四个比例(10∶1、3∶1、1∶1 和 1∶3)相对于每种药物的平均 ED 进行评估。剂量相加分析用于确定每个药物混合物内每个剂量对的预测、相加效应。MDPV、甲基酮和咖啡因以剂量依赖性方式维持反应,MDPV 是最有效和有效的,而咖啡因是三种浴盐成分中最无效和有效的。每种浴盐混合物也维持了高水平的反应。尽管大多数浴盐混合物的相互作用性质趋于相加,但也观察到超加性(3∶1 MDPV∶咖啡因,以及 3∶1 和 1∶1 甲基酮∶咖啡因)和亚加性(3∶1、1∶1 和 1∶3 MDPV∶甲基酮)相互作用。这些发现表明,浴盐制剂的组成会影响其强化效力和有效性,并且表明成分药物之间的这种相互作用可能导致人类浴盐使用者报告的使用模式和影响。