Botanas Chrislean Jun, Yoon Seong Shoon, de la Peña June Bryan, Dela Peña Irene Joy, Kim Mikyung, Woo Taeseon, Seo Joung-Wook, Jang Choon-Gon, Park Kyung-Tae, Lee Young Hun, Lee Yong Sup, Kim Hee Jin, Cheong Jae Hoon
Uimyung Research Institute for Neuroscience, Department of Pharmacy, Sahmyook University, Seoul 01795, Republic of Korea.
Center for Safety Pharmacology, Korea Institute of Toxicology, Daejeon 34114, Republic of Korea.
Biomol Ther (Seoul). 2017 Mar 1;25(2):122-129. doi: 10.4062/biomolther.2016.241.
A diversity of synthetic cathinones has flooded the recreational drug marketplace worldwide. This variety is often a response to legal control actions for one specific compound (e.g. methcathinone) which has resulted in the emergence of closely related replacement. Based on recent trends, the nitrogen atom is one of the sites in the cathinone molecule being explored by designer type modifications. In this study, we designed and synthesized two new synthetic cathinones, (1) α-piperidinopropiophenone (PIPP) and (2) α-piperidinopentiothiophenone (PIVT), which have piperidine ring substituent on their nitrogen atom. Thereafter, we evaluated whether these two compounds have an abuse potential through the conditioned place preference (CPP) in mice and self-administration (SA) in rats. We also investigated whether the substances can induce locomotor sensitization in mice following 7 days daily injection and challenge. qRT-PCR analyses were conducted to determine their effects on dopamine-related genes in the striatum. PIPP (10 and 30 mg/kg) induced CPP in mice, but not PIVT. However, both synthetic cathinones were not self-administered by the rats and did not induce locomotor sensitization in mice. qRT-PCR analyses showed that PIPP, but not PIVT, reduced dopamine transporter gene expression in the striatum. These data indicate that PIPP, but not PIVT, has rewarding effects, which may be attributed to its ability to affect dopamine transporter gene expression. Altogether, this study suggests that PIPP may have abuse potential. Careful monitoring of this type of cathinone and related drugs are advocated.
各种各样的合成卡西酮充斥着全球的娱乐性毒品市场。这种多样性往往是对针对某一种特定化合物(如甲卡西酮)的法律管控行动的回应,这导致了密切相关的替代物的出现。基于最近的趋势,氮原子是卡西酮分子中通过设计类修饰进行探索的位点之一。在本研究中,我们设计并合成了两种新的合成卡西酮,(1)α-哌啶基苯丙酮(PIPP)和(2)α-哌啶基戊硫酮(PIVT),它们在氮原子上有哌啶环取代基。此后,我们通过小鼠条件性位置偏爱(CPP)和大鼠自身给药(SA)评估这两种化合物是否具有滥用潜力。我们还研究了这些物质在每日注射7天并进行激发后是否能在小鼠中诱导运动敏化。进行qRT-PCR分析以确定它们对纹状体中多巴胺相关基因的影响。PIPP(10和30mg/kg)在小鼠中诱导了CPP,但PIVT没有。然而,两种合成卡西酮都未被大鼠自身给药,也未在小鼠中诱导运动敏化。qRT-PCR分析表明,PIPP而非PIVT降低了纹状体中多巴胺转运体基因的表达。这些数据表明,PIPP而非PIVT具有奖赏效应,这可能归因于其影响多巴胺转运体基因表达的能力。总之,本研究表明PIPP可能具有滥用潜力。提倡对这类卡西酮及相关药物进行仔细监测。