Anchondo Olivia, Shetty Ritu A, Gatch Michael B
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas.
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas.
J Pharmacol Exp Ther. 2025 Jul;392(7):103617. doi: 10.1016/j.jpet.2025.103617. Epub 2025 May 27.
The prevalence of fluorinated amphetamine and methamphetamine analogs on the illicit market has continued to increase in the past decade. The perceived ability of these compounds to bypass legal regulation has resulted in an increasing popularity among drug users; however, their use produces significant adverse effects, including heart failure, cerebral hemorrhage, and death. This study aimed to investigate the effects of phenyl ring fluorination on the abuse potential of 5 synthetic stimulant compounds: 2- and 3-fluoroamphetamine (FA) and 2-, 3-, and 4-fluoromethamphetamine (FMA). The open-field assay was used to observe the locomotor effects of the compounds and to evaluate effective dose ranges and time courses for psychoactive effects in male Swiss-Webster mice. Discriminative stimulus effects were evaluated using male Sprague-Dawley rats trained to discriminate methamphetamine from saline using an fixed-ratio 10 food-maintained reinforcement schedule in a 2-lever operant box. The compounds tested all resulted in time- and dose-dependent stimulation of locomotor activity. Potencies (ED) ranged from 0.38 to 7.38 mg/kg, with rank-order potency of 2-FMA > methamphetamine > 3-FMA = 3-FA = 2-FMA > 4-FMA. Peak effects varied, with 2-FA, 3-FA, and 3-FMA showing peak effects similar to methamphetamine (5905-7758 counts), while 2-FMA and 4-FMA were weak stimulants with lower peak effects (2200-3980 counts). All fluorinated compounds elicited dose-dependent full substitution for methamphetamine with comparable potencies (ED values = 0.32-0.71 mg/kg). The present study indicates that these analogs may have a potential for abuse comparable to that of methamphetamine, although self-administration studies need to be conducted to confirm this, and the locomotor activity data highlight possible mechanistic differences between the positional analogs through the contrasting potencies and efficacies. SIGNIFICANCE STATEMENT: Fluorinated amphetamine analogs have appeared on the illicit market and produce significant adverse effects. The present study shows that these analogs produce methamphetamine-like locomotor stimulant and discriminative stimulus effects and so may have a potential for abuse comparable to that of methamphetamine and other psychostimulants.
在过去十年中,非法市场上含氟苯丙胺和甲基苯丙胺类似物的流行程度持续上升。这些化合物被认为能够规避法律监管,这使得它们在吸毒者中越来越受欢迎;然而,使用这些化合物会产生严重的不良反应,包括心力衰竭、脑出血和死亡。本研究旨在调查苯环氟化对5种合成兴奋剂化合物滥用潜力的影响:2-氟苯丙胺和3-氟苯丙胺(FA)以及2-、3-和4-氟甲基苯丙胺(FMA)。旷场试验用于观察这些化合物的运动效应,并评估雄性瑞士韦伯斯特小鼠中精神活性效应的有效剂量范围和时程。使用雄性斯普拉格-道利大鼠进行辨别刺激效应评估,这些大鼠在双杠杆操作性实验箱中通过固定比率10食物维持强化程序接受训练,以辨别甲基苯丙胺和生理盐水。所测试的化合物均导致运动活动的时间和剂量依赖性刺激。效价(ED)范围为0.38至7.38mg/kg,效价顺序为2-FMA>甲基苯丙胺>3-FMA = 3-FA = 2-FMA>4-FMA。峰值效应各不相同,2-FA、3-FA和3-FMA的峰值效应与甲基苯丙胺相似(5905 - 7758次计数),而2-FMA和4-FMA是较弱的兴奋剂,峰值效应较低(2200 - 3980次计数)。所有含氟化合物均以相当的效价(ED值 = 0.32 - 0.71mg/kg)引发对甲基苯丙胺的剂量依赖性完全替代。本研究表明,这些类似物可能具有与甲基苯丙胺相当的滥用潜力,尽管需要进行自我给药研究来证实这一点,并且运动活动数据通过对比效价和效力突出了位置类似物之间可能存在的机制差异。意义声明:含氟苯丙胺类似物已出现在非法市场上,并产生严重的不良反应。本研究表明,这些类似物产生类似甲基苯丙胺的运动刺激和辨别刺激效应,因此可能具有与甲基苯丙胺和其他精神兴奋剂相当的滥用潜力。