Psilocybin alters brain activity related to sensory and cognitive processing in a time-dependent manner

Marek Nikolic, Pedro Mediano, Tom Froese, David Reydellet, Tomas Palenicek
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Abstract

Psilocybin is a classic psychedelic and a novel treatment for mood disorders. Psilocybin induces dose-dependent transient (4-6 hours) usually pleasant changes in perception, cognition, and emotion by non-selectively agonizing the 5-HT2A receptors and negatively regulating serotonin reuptake, and long-term positive antidepressant effect on mood and well-being. Long-term effects are ascribed to the psychological quality of the acute experience, increase in synaptodensity and temporary (1-week) down-regulation of 5-HT2A receptors. Electroencephalography, a non-invasive neuroimaging tool, can track the acute effects of psilocybin; these include the suppression of alpha activity, decreased global connectivity, and increased brain entropy (i.e. brain signal diversity) in eyes-closed resting-state. However, few studies investigated how these modalities are affected together through the psychedelic experience. The current research aimed to evaluate the psilocybin intoxication temporal EEG profile. 20 healthy individuals (10 women) underwent oral administration of psilocybin (0.26 mg/kg) as part of a placebo-controlled cross-over study, resting-state 5-minute eyes closed EEG was obtained at baseline and 1, 1.5, 3, 6, and 24 hours after psilocybin administration. Absolute power, relative power spectral density (PSD), power envelope global functional connectivity (GFC), Lempel-Ziv complexity (LZ), and a Complexity via State-Space Entropy Rate (CSER) were obtained together with measures of subjective intensity of experience. Absolute power decreased in alpha and beta band, but increased in delta and gamma frequencies. 24h later was observed a broadband decrease. The PSD showed a decrease in alpha occipitally between 1 and 3 hours and a decrease in beta frontally at 3 hours, but power spectra distribution stayed the same 24h later. The GFC showed decrease acutely at 1, 1.5, and 3 hours in the alpha band. LZ and showed an increase at 1 and 1.5 hours. Decomposition of CSER into functional bands shows a decrease in alpha band but increase over higher frequencies. Further, complexity over a source space showed opposing changes in the Default Mode Network (DMN) and visual network between conditions, suggesting a relationship between signal complexity, stimulus integration, and perception of self. In an exploratory attempt, we found that a change in gamma GFC in DMN correlates with oceanic boundlessness. Psychological effects of psilocybin may be wrapped in personal interpretations and history unrelated to underlying neurobiological changes, but changes to perception of self may be bound to perceived loss of boundary based on whole brain synchrony with the DMN in higher frequency bands.
迷幻药以时间依赖的方式改变与感觉和认知处理有关的大脑活动
迷幻药是一种经典的迷幻剂,也是一种治疗情绪障碍的新型药物。迷幻药通过非选择性地激动 5-HT2A 受体和负向调节血清素再摄取,在感知、认知和情绪方面诱发剂量依赖性的短暂变化(4-6 小时),通常是令人愉悦的变化,并对情绪和幸福感产生长期积极的抗抑郁作用。长期效果归因于急性体验的心理素质、突触密度的增加和 5-HT2A 受体的暂时(1 周)下调。脑电图是一种非侵入性神经成像工具,可以追踪迷幻药的急性效应;这些效应包括在闭眼静息状态下阿尔法活动受抑制、全局连接性降低和大脑熵(即大脑信号多样性)增加。然而,很少有研究调查迷幻体验如何同时影响这些模式。目前的研究旨在评估迷幻药中毒的时间脑电图特征。作为安慰剂对照交叉研究的一部分,20 名健康人(10 名女性)口服了迷幻药(0.26 毫克/千克),并在基线和服用迷幻药后 1、1.5、3、6 和 24 小时采集了静息状态 5 分钟闭眼脑电图。在测量主观体验强度的同时,还获得了绝对功率、相对功率谱密度(PSD)、功率包络全局功能连通性(GFC)、Lempel-Ziv 复杂性(LZ)和状态空间熵率复杂性(CSER)。阿尔法和贝塔波段的绝对功率有所下降,但德尔塔和伽马频率有所上升。24 小时后,观察到宽带下降。PSD 显示,在 1 至 3 小时内,阿尔法频段在枕部下降,3 小时后,贝塔频段在前部下降,但 24 小时后,功率谱分布保持不变。GFC在1小时、1.5小时和3小时时显示α波段急剧下降。LZ则在1小时和1.5小时后出现增加。将 CSER 分解为功能波段后发现,α 波段有所下降,但高频率有所上升。此外,在不同条件下,信号源空间的复杂性在默认模式网络(DMN)和视觉网络中显示出相反的变化,这表明信号复杂性、刺激整合和自我感知之间存在关系。在探索性尝试中,我们发现 DMN 中伽马 GFC 的变化与海洋无边界性相关。迷幻药的心理效应可能包含在个人解释和历史中,与潜在的神经生物学变化无关,但自我感知的变化可能与感知到的边界丧失有关,其基础是全脑与 DMN 在较高频段上的同步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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