在一项对健康参与者进行的随机双盲交叉试验中,R-MDMA、S-MDMA 和外消旋亚甲二氧基甲基苯丙胺的急性效应。

IF 6.6 1区 医学 Q1 NEUROSCIENCES Neuropsychopharmacology Pub Date : 2024-08-23 DOI:10.1038/s41386-024-01972-6
Isabelle Straumann, Isidora Avedisian, Aaron Klaiber, Nimmy Varghese, Anne Eckert, Deborah Rudin, Dino Luethi, Matthias E Liechti
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引用次数: 0

摘要

外消旋 3,4-亚甲二氧基甲基苯丙胺(MDMA)能迅速提高情绪、共鸣感、信任感和与他人的亲近感,被研究用于辅助心理治疗。临床前研究表明,S-亚甲二氧基甲基苯丙胺释放单胺类物质和催产素的作用比 R-MDMA 更强,而 R-MDMA 对血清素-5-羟色胺-2A 受体的刺激作用更强。S-MDMA 可能具有更强的兴奋剂特性,而 R-MDMA 可能更像迷幻剂。不过,S-和 R-MDMA 的急性效应尚未在对照人体研究中进行过检测。我们采用双盲、随机、安慰剂对照、交叉设计的方法,在 24 名健康参与者中比较了亚甲二氧基甲基苯丙胺(125 毫克)、S-亚甲二氧基甲基苯丙胺(125 毫克)、R-亚甲二氧基甲基苯丙胺(125 毫克和 250 毫克)和安慰剂的急性效应。结果测量包括主观、自主神经和不良反应、药代动力学以及血浆催产素、催乳素和皮质醇浓度。与 R-MDMA(125 毫克和 250 毫克)和亚甲二氧基甲基苯丙胺(125 毫克)相比,S-MDMA(125 毫克)能引起更大的主观效应("刺激"、"药物兴奋"、"快乐"、"开放")和更高的血压升高。出乎意料的是,R-MDMA 并没有比 S-MDMA 产生更多类似迷幻药的效果。S-MDMA 对血浆催乳素的升高作用高于亚甲二氧基甲基苯丙胺,S-MDMA 对血浆皮质醇和催产素的升高作用高于亚甲二氧基甲基苯丙胺和 R-MDMA。服用 S-MDMA 后,其血浆消除半衰期为 4.1 小时。服用 125 毫克和 250 毫克 R-MDMA 后,半衰期分别为 12 小时和 14 小时。服用外消旋亚甲二氧基甲基苯丙胺后,S-MDMA 和 R-MDMA 的半衰期分别为 5.1 小时和 11 小时。与服用 S-MDMA 相比,服用 R-MDMA 后 CYP2D6 形成的 MDMA 代谢物 4-hydroxy-3-methoxymethamphetamine 的浓度较低。药代动力学研究结果与 R-MDMA 介导的 CYP2D6 抑制作用一致。在本研究中,S-MDMA 具有更强的类似兴奋剂的作用,这可能反映出 S-MDMA 的药效更高,而不是 S-MDMA 和 R-MDMA 之间的质量差异。预计 S-MDMA、MDMA 和 R-MDMA 的急性效应分别为 100 毫克、125 毫克和 300 毫克,还需要进一步研究:试验注册:ClinicalTrials.gov identifier:NCT05277636.
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Acute effects of R-MDMA, S-MDMA, and racemic MDMA in a randomized double-blind cross-over trial in healthy participants.

Racemic 3,4-methylenedioxymethamphetamine (MDMA) acutely increases mood, feelings of empathy, trust, and closeness to others and is investigated to assist psychotherapy. Preclinical research indicates that S-MDMA releases monoamines and oxytocin more potently than R-MDMA, whereas R-MDMA more potently stimulates serotonin 5-hydroxytryptamine-2A receptors. S-MDMA may have more stimulant properties, and R-MDMA may be more psychedelic-like. However, acute effects of S- and R-MDMA have not been examined in a controlled human study. We used a double-blind, randomized, placebo-controlled, crossover design to compare acute effects of MDMA (125 mg), S-MDMA (125 mg), R-MDMA (125 mg and 250 mg), and placebo in 24 healthy participants. Outcome measures included subjective, autonomic, and adverse effects, pharmacokinetics, and plasma oxytocin, prolactin, and cortisol concentrations. S-MDMA (125 mg) induced greater subjective effects ("stimulation," "drug high," "happy," "open") and higher increases in blood pressure than R-MDMA (both 125 and 250 mg) and MDMA (125 mg). Unexpectedly, R-MDMA did not produce more psychedelic-like effects than S-MDMA. S-MDMA increased plasma prolactin more than MDMA, and S-MDMA increased plasma cortisol and oxytocin more than MDMA and R-MDMA. The plasma elimination half-life of S-MDMA was 4.1 h after administration. The half-life of R-MDMA was 12 and 14 h after the administration of 125 and 250 mg, respectively. Half-lives for S-MDMA and R-MDMA were 5.1 h and 11 h, respectively, after racemic MDMA administration. Concentrations of the CYP2D6-formed MDMA-metabolite 4-hydroxy-3-methoxymethamphetamine were lower after R-MDMA administration compared with S-MDMA administration. The pharmacokinetic findings are consistent with the R-MDMA-mediated inhibition of CYP2D6. Stronger stimulant-like effects of S-MDMA in the present study may reflect the higher potency of S-MDMA rather than qualitative differences between S-MDMA and R-MDMA. Equivalent acute effects of S-MDMA, MDMA, and R-MDMA can be expected at doses of 100, 125, and 300 mg, respectively, and need to be investigated.Trial registration: ClinicalTrials.gov identifier: NCT05277636.

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来源期刊
Neuropsychopharmacology
Neuropsychopharmacology 医学-精神病学
CiteScore
15.00
自引率
2.60%
发文量
240
审稿时长
2 months
期刊介绍: Neuropsychopharmacology is a reputable international scientific journal that serves as the official publication of the American College of Neuropsychopharmacology (ACNP). The journal's primary focus is on research that enhances our knowledge of the brain and behavior, with a particular emphasis on the molecular, cellular, physiological, and psychological aspects of substances that affect the central nervous system (CNS). It also aims to identify new molecular targets for the development of future drugs. The journal prioritizes original research reports, but it also welcomes mini-reviews and perspectives, which are often solicited by the editorial office. These types of articles provide valuable insights and syntheses of current research trends and future directions in the field of neuroscience and pharmacology.
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