Nadal-Gratacós Núria, Mata Sandra, Puigseslloses Pol, De Macedo Morgane, Lardeux Virginie, Pain Stephanie, Wang Fu-Hua, Källsten Liselott, Pubill David, Berzosa Xavier, Kehr Jan, Solinas Marcello, Camarasa Jordi, Escubedo Elena, López-Arnau Raul
Department of Pharmacology, Toxicology and Therapeutic Chemistry, Pharmacology Section and Institute of Biomedicine (IBUB), Faculty of Pharmacy, Universitat de Barcelona, 08028, Barcelona, Spain.
Chemical Reactions for Innovative Solutions (CRISOL), IQS School of Engineering, Universitat Ramon Llull, 08017, Barcelona, Spain.
Neuropharmacology. 2025 Jul 1;272:110425. doi: 10.1016/j.neuropharm.2025.110425. Epub 2025 Mar 19.
Synthetic cathinones are emerging psychoactive substances designed to mimic the effects of classical psychostimulants. Among them, α-D2PV, a novel pyrrolidine-containing cathinone characterized by a phenyl group on the α-carbon atom, has gained significant attention. This study investigates the in vitro and in silico mechanism of action as well as the abuse liability of α-D2PV using rodent models. Dopamine (DA), noradrenaline (NE), and serotonin (5-HT) uptake inhibition assays were conducted in HEK293 cells expressing the corresponding human monoamine transporter, complemented by molecular docking studies at the DA transporter (DAT). Behavioral studies in male Swiss CD-1 mice assessed locomotor activity and conditioned place preference, while microdialysis and self-administration experiments were performed in male Sprague-Dawley rats. The findings reveal that α-D2PV is a potent DA and NE uptake inhibitor, with minimal activity at the 5-HT transporter (SERT). Docking studies showed that the benzene rings of α-PVP and α-D2PV align precisely in their most stable conformations at DAT. In vivo, α-D2PV elicited dose-dependent hyperlocomotion, thigmotaxis, and rewarding effects in mice, alongside increased extracellular DA levels in the nucleus accumbens of awake rats. Self-administration experiments confirmed α-D2PV's high reinforcing efficacy, indicating a significant risk of abuse in humans. Finally, these results underscore the necessity for continued surveillance of α-D2PV within the illicit drug market. Furthermore, novel synthetic cathinones incorporating a phenyl ring at the α-carbon side chain warrant proactive monitoring due to their potential to retain dopaminergic activity and evade initial legal controls.
合成卡西酮是一类新型精神活性物质,旨在模拟经典精神兴奋剂的作用。其中,α-D2PV是一种新型含吡咯烷的卡西酮,其α碳原子上有一个苯基,已受到广泛关注。本研究使用啮齿动物模型研究了α-D2PV的体外和计算机模拟作用机制以及滥用可能性。在表达相应人类单胺转运蛋白的HEK293细胞中进行了多巴胺(DA)、去甲肾上腺素(NE)和5-羟色胺(血清素,5-HT)摄取抑制试验,并辅以对DA转运蛋白(DAT)的分子对接研究。在雄性瑞士CD-1小鼠中进行行为学研究,评估运动活性和条件性位置偏爱,同时在雄性Sprague-Dawley大鼠中进行微透析和自我给药实验。研究结果表明,α-D2PV是一种强效的DA和NE摄取抑制剂,对5-HT转运蛋白(SERT)的活性最小。对接研究表明,α-PVP和α-D2PV的苯环在DAT的最稳定构象中精确对齐。在体内,α-D2PV在小鼠中引起剂量依赖性的运动亢进、趋触性和奖赏效应,同时清醒大鼠伏隔核中的细胞外DA水平升高。自我给药实验证实了α-D2PV的高强化效力,表明其在人类中有显著的滥用风险。最后,这些结果强调了在非法药物市场中持续监测α-D2PV的必要性。此外,由于在α-碳侧链含有苯环的新型合成卡西酮有可能保留多巴胺能活性并规避最初的法律管制,因此有必要对其进行主动监测。