Bonomo Yvonne A, Norman Amanda F, Collins Lisa, Ross Margaret, Dwyer Justin, Perkins Daniel, Sarris Jerome
Department of Addiction Medicine, St Vincent's Hospital Melbourne, Melbourne, VIC, Australia.
Department of Medicine, University of Melbourne, Melbourne, VIC, Australia.
Front Psychiatry. 2025 Aug 15;16:1545915. doi: 10.3389/fpsyt.2025.1545915. eCollection 2025.
Ayahuasca is a psychedelic compound of N, N, Dimethyltryptamine (DMT) and harmala alkaloids used for spiritual and medicinal applications in traditional settings. A range of potential psychotherapeutic mechanisms have been proposed for ayahuasca. These are thought to contribute to improvements in various psychiatric conditions including mood disorders and substance dependence. This open label exploratory study explored safety, tolerability, physical, mental health and psychedelic effects of three Acacia based formulations in 9 healthy volunteers with prior use of Ayahuasca.
Formulations derived from two Acacia species (1mg/kg DMT and 4mg/kg of harmalas) were tested in a cross-over design in 5 adults; a third formulation (ACL-010) was tested in 4 adults at two dosages (1mg/kg DMT and 4mg/kg of harmalas, and then 1.4mg/kg DMT and 5.6mg of harmalas).
All formulations had a good safety profile. No serious adverse events were reported. Physical examination, vital signs, and pathology revealed no clinically significant changes across the course of the study. The subjective experience of all formulations was generally rated similar to Ayahuasca. Four-week follow-up measures of psychological wellbeing and perceptual effects showed little difference between formulations. The strength and quality of the psychedelic experience elicited with ACL-010 was rated as similar or more beneficial than Ayahuasca.
Our results indicate DMT formulations derived from the Acacia species represent a feasible alternative to traditional Ayahuasca for future clinical trials and possibly clinical contexts. The small sample size and open label design limit generalizability of results.
https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=384191&isReview=true, identifier ACTRN12622001315707.
阿亚瓦斯卡是一种由N,N - 二甲基色胺(DMT)和哈尔满生物碱组成的致幻化合物,在传统环境中用于精神和医学用途。人们已经提出了一系列阿亚瓦斯卡潜在的心理治疗机制。这些机制被认为有助于改善包括情绪障碍和物质依赖在内的各种精神疾病。这项开放标签探索性研究探讨了三种基于阿拉伯胶的配方对9名曾使用过阿亚瓦斯卡的健康志愿者的安全性、耐受性、身心健康和致幻效果。
从两种阿拉伯胶树种中提取的配方(1mg/kg DMT和4mg/kg哈尔满)在5名成年人中采用交叉设计进行测试;第三种配方(ACL - 010)在4名成年人中以两种剂量(1mg/kg DMT和4mg/kg哈尔满,然后是1.4mg/kg DMT和5.6mg哈尔满)进行测试。
所有配方都具有良好的安全性。未报告严重不良事件。体格检查、生命体征和病理学检查显示在研究过程中没有临床上显著的变化。所有配方的主观体验总体上被评为与阿亚瓦斯卡相似。四周的心理健康和感知效果随访测量显示配方之间几乎没有差异。ACL - 010引发的致幻体验的强度和质量被评为与阿亚瓦斯卡相似或更有益。
我们的结果表明,源自阿拉伯胶树种的DMT配方代表了传统阿亚瓦斯卡的一种可行替代方案,可用于未来的临床试验以及可能的临床环境。样本量小和开放标签设计限制了结果的普遍性。