Shekar Aparna, Aguilar Jenny I, Galli Greta, Cozzi Nicholas V, Brandt Simon D, Ruoho Arnold E, Baumann Michael H, Matthies Heinrich J G, Galli Aurelio
Department of Pharmacology, Vanderbilt University, Nashville, TN 37232-8548, United States; Vanderbilt Brain Institute, Vanderbilt University, Nashville, TN 37232-8548, United States; Neuroscience Program in Substance Abuse (N-PISA), Vanderbilt University, Nashville, TN 37232-8548, United States.
University School of Nashville, Nashville, TN 37212, United States.
J Chem Neuroanat. 2017 Oct;83-84:69-74. doi: 10.1016/j.jchemneu.2017.01.004. Epub 2017 Feb 3.
Synthetic cathinones are similar in chemical structure to amphetamines, and their behavioral effects are associated with enhanced dopaminergic signaling. The past ten years of research on the common constituent of bath salts, MDPV (the synthetic cathinone 3,4-methylenedioxypyrovalerone), has aided the understanding of how synthetic cathinones act at the dopamine (DA) transporter (DAT). Several groups have described the ability of MDPV to block the DAT with high-affinity. In this study, we demonstrate for the first time a new mode of action of MDPV, namely its ability to promote DAT-mediated DA efflux. Using single cell amperometric assays, we determined that low concentrations of MDPV (1nM) can cause reverse transport of DA via DAT. Notably, administration of MDPV leads to hyperlocomotion in Drosophila melanogaster. These data describe further how MDPV acts at the DAT, possibly paving the way for novel treatment strategies for individuals who abuse bath salts.
合成卡西酮在化学结构上与安非他明相似,其行为效应与增强的多巴胺能信号传导有关。过去十年对浴盐常见成分3,4-亚甲基二氧吡咯戊酮(MDPV,一种合成卡西酮)的研究,有助于理解合成卡西酮如何作用于多巴胺(DA)转运体(DAT)。多个研究小组已描述了MDPV以高亲和力阻断DAT的能力。在本研究中,我们首次证明了MDPV的一种新作用模式,即其促进DAT介导的DA外流的能力。使用单细胞安培法测定,我们确定低浓度的MDPV(1nM)可通过DAT引起DA的逆向转运。值得注意的是,给予MDPV会导致黑腹果蝇活动亢进。这些数据进一步描述了MDPV如何作用于DAT,可能为滥用浴盐的个体开辟新的治疗策略。