Co-administration of midazolam and psilocybin: differential effects on subjective quality versus memory of the psychedelic experience

IF 5.8 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2024-09-12 DOI:10.1038/s41398-024-03059-8
Christopher R. Nicholas, Matthew I. Banks, Richard C. Lennertz, Cody J. Wenthur, Bryan M. Krause, Brady A. Riedner, Richard F. Smith, Paul R. Hutson, Christina J. Sauder, John D. Dunne, Leor Roseman, Charles L. Raison
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Abstract

Aspects of the acute experience induced by the serotonergic psychedelic psilocybin predict symptomatic relief in multiple psychiatric disorders and improved well-being in healthy participants, but whether these therapeutic effects are immediate or are based on memories of the experience is unclear. To examine this, we co-administered psilocybin (25 mg) with the amnestic benzodiazepine midazolam in 8 healthy participants and assayed the subjective quality of, and memory for, the dosing-day experience. We identified a midazolam dose that allowed a conscious psychedelic experience to occur while partially impairing memory for the experience. Furthermore, midazolam dose and memory impairment tended to associate inversely with salience, insight, and well-being induced by psilocybin. These data suggest a role for memory in therapeutically relevant behavioral effects occasioned by psilocybin. Because midazolam blocks memory by blocking cortical neural plasticity, it may also be useful for evaluating the contribution of the pro-neuroplastic properties of psychedelics to their therapeutic activity.

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同时服用咪达唑仑和迷幻剂:对迷幻体验的主观质量和记忆的不同影响
5-羟色胺能迷幻药迷幻素诱导的急性体验预示着多种精神疾病的症状会得到缓解,健康参与者的幸福感也会得到改善,但这些治疗效果是立竿见影还是基于对体验的记忆尚不清楚。为了研究这个问题,我们在 8 名健康参与者中同时服用了西洛滨(25 毫克)和抗失忆的苯二氮卓类药物咪达唑仑,并测定了服药当天体验的主观质量和记忆。我们确定了一种咪达唑仑剂量,这种剂量既能让人产生有意识的迷幻体验,又能部分削弱对体验的记忆。此外,咪达唑仑剂量和记忆损伤往往与迷幻剂诱导的突出性、洞察力和幸福感成反比。这些数据表明,记忆在迷幻药引起的治疗相关行为效应中扮演着重要角色。由于咪达唑仑通过阻断大脑皮层的神经可塑性来阻断记忆,因此也可以用来评估迷幻药的神经可塑性对其治疗活性的贡献。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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