Lucchetti Jacopo, Marzo Claudio M, Passoni Alice, Di Clemente Angelo, Moro Federico, Bagnati Renzo, Gobbi Marco, Cervo Luigi
Departments of Molecular Biochemistry and Pharmacology (J.L., M.G.), Neuroscience (C.M.M., A.D.C., F.M., L.C.), and Environmental Health Science (A.P., R.B.), IRCCS-Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy
Departments of Molecular Biochemistry and Pharmacology (J.L., M.G.), Neuroscience (C.M.M., A.D.C., F.M., L.C.), and Environmental Health Science (A.P., R.B.), IRCCS-Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
J Pharmacol Exp Ther. 2017 Jun;361(3):492-500. doi: 10.1124/jpet.117.240788. Epub 2017 Apr 12.
-Methyl-4-methylaminorex (4,4'-DMAR) is a phenethylamine derivative with psychostimulant activity whose abuse has been associated with several deaths and a wide range of adverse effects. We recently validated a high-performance liquid chromatography-tandem mass spectrometry method to measure the compound's concentrations in plasma, and we applied it to describe the pharmacokinetic properties of 4,4'-DMAR after a single dose in rats. In this study, we investigated the brain disposition and metabolism of 4,4'-DMAR after intraperitoneal injection as well as its central behavioral effects. Locomotor activity increased after a single injection of 10 mg/kg, peaking at 2 hours and disappearing at 5 hours; in these conditions, brain absorption was very rapid, ( = 30-60 minutes) and large (brain-to-plasma ratio = 24); the half-life was approximately 50 minutes. After 14 daily doses, the compound's effect on locomotor activity was greater (approximately 20% compared with the effect after the first dose), but not for pharmacokinetic reasons. Using high-resolution mass spectrometry, we also identified four metabolites of 4,4'-DMAR in the plasma and brain of treated rats. Semiquantitative analysis indicated low brain permeability and very low brain concentrations, suggesting that these metabolites do not contribute to central behavioral effects; however, the metabolite originating from oxidation of the -methyl group (M2) persisted in the plasma longer and at higher concentrations than the parent molecule and could be used to evaluate drug intake in human consumers. Finally, we describe the rewarding effect of -4,4'-DMAR in the conditioning place preference test, suggesting a high risk of addiction in humans.
4-甲基-4-甲基氨基苯丙胺(4,4'-DMAR)是一种具有精神兴奋活性的苯乙胺衍生物,其滥用已导致数人死亡,并引发了一系列不良反应。我们最近验证了一种高效液相色谱-串联质谱法,用于测量血浆中该化合物的浓度,并将其应用于描述大鼠单次给药后4,4'-DMAR的药代动力学特性。在本研究中,我们研究了腹腔注射后4,4'-DMAR在脑内的分布和代谢及其对中枢的行为影响。单次注射10mg/kg后,运动活性增加,在2小时达到峰值,5小时消失;在此条件下,脑吸收非常迅速(Tmax = 30 - 60分钟)且量大(脑-血浆比 = 24);半衰期约为50分钟。每日给药14次后,该化合物对运动活性的影响更大(与首次给药后的影响相比约增加20%),但并非出于药代动力学原因。使用高分辨率质谱法,我们还在给药大鼠的血浆和脑中鉴定出4,4'-DMAR的四种代谢产物。半定量分析表明,这些代谢产物的脑通透性低且脑内浓度极低,表明它们对中枢行为影响没有贡献;然而,源自α-甲基氧化的代谢产物(M2)在血浆中持续存在的时间比母体分子更长,浓度更高,可用于评估人类使用者的药物摄入情况。最后,我们描述了α-4,4'-DMAR在条件性位置偏爱试验中的奖赏效应,提示其在人类中有很高的成瘾风险。