Department of Translational Medicine, Section of Legal Medicine and LTTA Centre, University of Ferrara, Via Fossato Di Mortara 70, 44121, Ferrara, Italy.
Department of Scientific Investigation (RIS), Carabinieri, 00191, Rome, Italy.
Psychopharmacology (Berl). 2024 Mar;241(3):489-511. doi: 10.1007/s00213-024-06526-8. Epub 2024 Jan 12.
The 5-methoxy-N-methyl-N-isopropyltryptamine (5-MeO-MiPT, known online as "Moxy") is a new psychedelic tryptamine first identified on Italian national territory in 2014. Its hallucinogen effects are broadly well-known; however, only few information is available regarding its pharmaco-toxicological effects.
Following the seizure of this new psychoactive substances by the Arm of Carabinieri and the occurrence of a human intoxication case, in the current study we had the aim to characterize the in vivo acute effects of systemic administration of 5-MeO-MiPT (0.01-30 mg/kg i.p.) on sensorimotor (visual, acoustic, and overall tactile) responses, thermoregulation, and stimulated motor activity (drag and accelerod test) in CD-1 male mice. We also evaluated variation on sensory gating (PPI, prepulse inhibition; 0.01-10 mg/kg i.p.) and on cardiorespiratory parameters (MouseOx and BP-2000; 30 mg/kg i.p.). Lastly, we investigated the in silico ADMET (absorption, distribution, metabolism, excretion, toxicity) profile of 5-MeO-MiPT compared to 5-methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT) and N,N-dimethyltryptamine (DMT).
This study demonstrates that 5-MeO-MiPT dose-dependently inhibits sensorimotor and PPI responses and, at high doses, induces impairment of the stimulated motor activity and cardiorespiratory changes in mice. In silico prediction shows that the 5-MeO-MiPT toxicokinetic profile shares similarities with 5-MeO-DIPT and DMT and highlights a cytochrome risk associated with this compound.
Consumption of 5-MeO-MiPT can affect the ability to perform activities and pose a risk to human health status, as the correspondence between the effects induced in mice and the symptoms occurred in the intoxication case suggests. However, our findings suggest that 5-MeO-MiPT should not be excluded from research in the psychiatric therapy field.
5-甲氧基-N-甲基-N-异丙基色胺(5-MeO-MiPT,在网上称为“Moxy”)是一种新型迷幻色胺,于 2014 年首次在意大利领土上被发现。其致幻作用广为人知;然而,关于其药物毒理学效应的信息却很少。
在武装宪兵队缴获这种新的精神活性物质并发生人类中毒事件后,在本研究中,我们的目的是描述系统性给予 5-MeO-MiPT(0.01-30mg/kg,ip)对 CD-1 雄性小鼠的感觉运动(视觉、听觉和整体触觉)反应、体温调节和受刺激的运动活动(拖拽和加速试验)的体内急性作用。我们还评估了感觉门控(PPI,预脉冲抑制;0.01-10mg/kg,ip)和心肺参数(MouseOx 和 BP-2000;30mg/kg,ip)的变化。最后,我们研究了 5-MeO-MiPT 与 5-甲氧基-N,N-二异丙基色胺(5-MeO-DIPT)和 N,N-二甲基色胺(DMT)相比的体内 ADMET(吸收、分布、代谢、排泄、毒性)概况。
这项研究表明,5-MeO-MiPT 剂量依赖性地抑制感觉运动和 PPI 反应,并在高剂量下,导致小鼠受刺激的运动活动受损和心肺变化。体内预测表明,5-MeO-MiPT 的毒代动力学特征与 5-MeO-DIPT 和 DMT 相似,并突出了与该化合物相关的细胞色素风险。
5-MeO-MiPT 的消费会影响到进行活动的能力,并对人类健康状况构成风险,因为这与在小鼠中诱导的作用和在中毒病例中出现的症状相符。然而,我们的研究结果表明,5-MeO-MiPT 不应从精神病治疗领域的研究中排除。