Department of Translational Medicine, Section of Legal Medicine and LTTA Center, University of Ferrara, 44121 Ferrara, Italy.
Department of Environmental Sciences and Prevention, University of Ferrara, 44121 Ferrara, Italy.
Int J Mol Sci. 2023 Jan 18;24(3):1882. doi: 10.3390/ijms24031882.
Drug forums are considered as the main platform sources that have contributed to the increase in NPS popularity, especially for those not yet known to law enforcement and therefore not yet illegal. An example is the new synthetic stimulant NM2AI, which has a very short history of human use and abuse. Little is known regarding this compound, but some information from internet forums and the scientific literature indicates NM2AI as a structural derivate of MDAI, which is known for its entactogenic activity. Indeed, the purpose of this study is to evaluate, for the first time, the in vivo acute effect induced by the intraperitoneal injection of NM2AI (1-10-30-100 mg/kg) in mice. We demonstrate the sensory (by visual placing and object tests) and physiological (core temperature measurement) function variations, nociceptor (by tail pinch test) and strength (grip test) alterations, and sensorimotor (time on rod and mobility) decrease. Moreover, we verify the mild hallucinogenic effect of NM2AI (by startle/prepulse inhibition test). Lastly, we perform a pharmacokinetic study on mice blood samples, highlighting that the main active metabolite of NM2AI is 2-aminoindane (2AI). Taken together, our data confirm the suspected entactogenic activity of NM2AI; however, these in vivo effects appear atypical and less intense with respect to those induced by the classic stimulants, in surprising analogy with what is reported by networked users.
药物论坛被认为是导致 NPS 流行的主要平台来源,尤其是对于那些尚未为执法部门所知、因此尚未非法的 NPS。一个例子是新的合成兴奋剂 NM2AI,它在人类使用和滥用方面的历史非常短。关于这种化合物知之甚少,但来自互联网论坛和科学文献的一些信息表明,NM2AI 是 MDAI 的结构衍生物,MDAI 以其致兴奋活性而闻名。事实上,本研究的目的是首次评估 NM2AI(1-10-30-100mg/kg)腹腔注射在小鼠体内引起的急性效应。我们证明了 NM2AI 对感觉(通过视觉放置和物体测试)和生理(核心温度测量)功能变化、伤害感受器(通过尾巴捏测试)和力量(握力测试)改变以及感觉运动(棒上时间和移动性)下降的影响。此外,我们验证了 NM2AI 的轻度致幻作用(通过惊吓/预备脉冲抑制测试)。最后,我们对小鼠血液样本进行了药代动力学研究,突出了 NM2AI 的主要活性代谢物是 2-氨基茚满(2AI)。总之,我们的数据证实了 NM2AI 被怀疑的致兴奋活性;然而,这些体内效应与经典兴奋剂引起的效应相比,似乎是非典型的,且强度较弱,与网络用户报告的情况惊人地相似。