Science Department, Chatham University, Pittsburgh, Pennsylvania (C.S., S.S.B., S.L.B., B.Z., E.R.B.) and Departments of Computational and Systems Biology (M.H.C.) and Cell Biology (A.S.), School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Science Department, Chatham University, Pittsburgh, Pennsylvania (C.S., S.S.B., S.L.B., B.Z., E.R.B.) and Departments of Computational and Systems Biology (M.H.C.) and Cell Biology (A.S.), School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania
J Pharmacol Exp Ther. 2023 Aug;386(2):266-273. doi: 10.1124/jpet.122.001573. Epub 2023 Jun 22.
The alkylamine stimulant 1,3-dimethylamylamine (DMAA) is used nonmedically as an appetite suppressant and exercise performance enhancer despite adverse cardiovascular effects that have limited its legal status. There is scant research describing the mechanism of action of DMAA, making it difficult to gauge risks or therapeutic potential. An important molecular target of structurally related phenethylamines, such as amphetamine, for regulating mood, cognition, movement, and the development of substance use disorder is the dopamine transporter, which limits the range and magnitude of dopamine signaling via reuptake from the extracellular space. The present studies were therefore initiated to characterize the effects of DMAA on dopamine transporter function. Specifically, we tested the hypothesis that DMAA exhibits substrate-like effects on dopamine transporter function and trafficking. In transport assays in human embryonic kidney cells, DMAA inhibited dopamine uptake by the human dopamine transporter in a competitive manner. Docking analysis and molecular dynamics simulations supported these findings, revealing that DMAA binds to the S1 substrate binding site and induces a conformational change from outward-facing open to outward-facing closed states, similar to the known substrates. Further supporting substrate-like effects of DMAA, the drug stimulated dopamine transporter endocytosis in a heterologous expression system via cocaine- and protein kinase A-sensitive mechanisms, mirroring findings with amphetamine. Together, these data indicate that DMAA elicits neurologic effects by binding to and regulating function of the dopamine transporter. Furthermore, pharmacologic distinctions from amphetamine reveal structural determinants for regulating transporter conformation and add mechanistic insight for the regulation of dopamine transporter endocytosis. SIGNIFICANCE STATEMENT: The alkylamine stimulant 1,3-dimethylamylamine (DMAA) is used as an appetite suppressant and athletic performance enhancer and is structurally similar to amphetamine, but there is scant research describing its mechanism of action. Characterizing the effects of DMAA on dopamine transporter function supports evaluation of potential risks and therapeutic potential while also revealing mechanistic details of dynamic transporter-substrate interactions.
烷基胺兴奋剂 1,3-二甲基戊胺(DMAA)被非医学用于抑制食欲和增强运动表现,尽管其具有不利的心血管作用,限制了其合法地位。关于 DMAA 的作用机制的研究很少,因此难以评估其风险或治疗潜力。结构上与苯丙胺等有关的苯乙胺的一个重要分子靶标是多巴胺转运体,它通过从细胞外空间再摄取来限制多巴胺信号的范围和幅度,从而调节情绪、认知、运动和物质使用障碍的发展。因此,进行了本研究来表征 DMAA 对多巴胺转运体功能的影响。具体来说,我们检验了 DMAA 对多巴胺转运体功能和转运表现出类似底物的作用的假设。在人胚肾细胞中的转运测定中,DMAA 以竞争性方式抑制人多巴胺转运体摄取多巴胺。对接分析和分子动力学模拟支持了这些发现,表明 DMAA 结合到 S1 底物结合位点,并诱导从外向开放状态到外向闭合状态的构象变化,类似于已知的底物。进一步支持 DMAA 的类似底物的作用,该药物通过可卡因和蛋白激酶 A 敏感的机制刺激多巴胺转运体的内吞作用,与安非他命的发现一致。这些数据表明,DMAA 通过结合和调节多巴胺转运体的功能来产生神经作用。此外,与安非他命的药理学差异揭示了调节转运体构象的结构决定因素,并为多巴胺转运体内吞作用的调节提供了机制见解。