Laboratory of Neuropharmacology and Behavior, School of Medicine, Faculty of Medical Sciences, University of Santiago de Chile;
Laboratory of Neurobiology, Faculty of Chemistry and Biology, University of Santiago de Chile.
Curr Neuropharmacol. 2013 Sep;11(5):521-34. doi: 10.2174/1570159X11311050007.
Besides stimulants and hallucinogens, whose psychotropic effects are shared by many structurally related molecules exhibiting different efficacies and potencies in humans, the phenylisopropylamine MDMA (3,4-methylenedioxymethamphetamine, XTC, "Ecstasy") is the prototypical representative of a separate class of psychotropic substance, able to elicit the so-called entactogenic syndrome in healthy humans. This reversible altered state of consciousness, usually described as an "open mind state", may have relevant therapeutic applications, both in psychotherapy and as a pharmacological support in many neuropsychiatric disorders with a high rate of treatment failure. Nevertheless, a comprehensive and systematic exploration of the structure-activity relationships associated with entactogenic activity has remained incomplete and controversial, highlighting the possibility that MDMA might represent a pharmacological rarity in the field of psychotropics. As the latter is still an open question, the pharmacological characterization of MDMA analogues remains the logical strategy to attempt the elucidation of the structural requirements needed to elicit typical MDMA-like effects. Intriguingly, almost no experimental evidence supports the existence of actual MDMA analogues that truly resemble the whole pharmacological profile of MDMA, probably due to its complex (and partially not fully understood) mechanism of action that includes a disruption of monoaminergic neurotransmission. The present review presents a brief summary of the pharmacology of MDMA, followed by the evidence accumulated over the years regarding the characterization of classical structurally related MDMA analogues in different models and how this state of the art highlights the need to develop new and better MDMA analogues.
除了兴奋剂和致幻剂,其精神作用被许多具有不同功效和效力的结构相关分子所共享,苯丙胺类 MDMA(3,4-亚甲基二氧基甲基苯丙胺,摇头丸,“快乐丸”)是一种单独类别的精神药物的典型代表,能够在健康人中引起所谓的快感综合征。这种可逆的意识改变状态,通常被描述为“开放的心态状态”,可能具有相关的治疗应用,无论是在心理治疗中,还是作为许多神经精神障碍的药理学支持,这些障碍的治疗失败率很高。然而,与快感相关的活性相关的结构-活性关系的全面和系统探索仍然不完整和有争议,突出表明 MDMA 可能代表精神药物领域的药理学罕见情况。由于后者仍然是一个悬而未决的问题,因此 MDMA 类似物的药理学特征仍然是尝试阐明引发典型 MDMA 样效应所需的结构要求的合理策略。有趣的是,几乎没有实验证据支持真正类似于 MDMA 整个药理学特征的实际 MDMA 类似物的存在,这可能是由于其复杂的(部分未完全理解)作用机制,包括单胺能神经传递的中断。本综述简要总结了 MDMA 的药理学,随后介绍了多年来关于不同模型中经典结构相关 MDMA 类似物的特征描述的积累证据,以及该领域的最新进展如何突出需要开发新的和更好的 MDMA 类似物。