Fuini Evan, Chang Arnold, Ortiz Richard J, Nasseef Taufiq, Edwards Josh, Latta Marc, Gonzalez Elias, Woodward Taylor J, Axe Bryce, Maheswari Ashwath, Cavallaro Noah, Bradshaw Heather B, Kulkarni Praveen P, Ferris Craig F
Department Pharmaceutical Sciences, Northeastern University, Boston, MA, United States.
Center for Translational Neuroimaging, Northeastern University, Boston, MA, United States.
Front Neurosci. 2025 May 1;19:1554049. doi: 10.3389/fnins.2025.1554049. eCollection 2025.
Psilocybin is a hallucinogen with complex neurobiological and behavioral effects. This is the first study to use MRI to follow functional changes in brain activity in response to different doses of psilocybin in fully awake, drug naive rats. We hypothesized that psilocybin would show a dose-dependent increase in activity in the prefrontal cortex and thalamus, while decreasing hippocampal activity. Female and male rats were given IP injections of vehicle or psilocybin in doses of 0.03 mg/kg, 0.3 mg/kg, and 3.0 mg/kg while fully awake during the imaging session. These levels were validated by measuring psilocybin and its metabolite, psilocin. Changes in BOLD signal were recorded over a 20 min window. Data for resting state functional connectivity were collected approximately 35 min post injection. All data were registered to rat 3D MRI atlas with 169 brain areas providing site-specific changes in global brain activity and changes in functional connectivity. Treatment with psilocybin resulted in a significant dose-dependent increase in positive BOLD signal. The areas most affected by the acute presentation of psilocybin were the somatosensory cortex, basal ganglia and thalamus. Males and females showed different sensitivity to psilocybin dose, with females exhibiting greater activation than males at 0.3 mg/kg, especially in thalamic and basal ganglia regions. There was a significant dose-dependent global increase in functional connectivity, highlighted by hyperconnectivity to the cerebellum. Brain areas hypothesized to be involved in loss of sensory filtering and organization of sensory motor stimuli, such as the cortico-striato-thalamo-cortical circuit and the claustrum, showed increased activation at higher doses of psilocybin. Indeed, the general neuroanatomical circuitry associated with the psychedelic experience was affected but the direction of the BOLD signal and pattern of activity between neural networks was inconsistent with the human literature.
裸盖菇素是一种具有复杂神经生物学和行为效应的致幻剂。这是第一项在完全清醒、未接触过药物的大鼠中,利用磁共振成像(MRI)追踪不同剂量裸盖菇素引起的大脑活动功能变化的研究。我们假设,裸盖菇素会使前额叶皮质和丘脑的活动呈剂量依赖性增加,同时降低海马体的活动。在成像过程中,雌雄大鼠均在完全清醒状态下接受腹腔注射(IP)生理盐水或剂量为0.03毫克/千克、0.3毫克/千克和3.0毫克/千克的裸盖菇素。通过测量裸盖菇素及其代谢产物脱磷酸裸盖菇素对这些剂量进行了验证。在20分钟窗口内记录血氧水平依赖(BOLD)信号的变化。注射后约35分钟收集静息态功能连接的数据。所有数据均被注册到具有169个脑区的大鼠三维MRI图谱中,以提供全脑活动的位点特异性变化和功能连接的变化。裸盖菇素治疗导致正性BOLD信号显著呈剂量依赖性增加。受裸盖菇素急性作用影响最大的区域是体感皮层、基底神经节和丘脑。雄性和雌性对裸盖菇素剂量表现出不同的敏感性,雌性在0.3毫克/千克时比雄性表现出更大的激活,特别是在丘脑和基底神经节区域。功能连接存在显著的剂量依赖性整体增加,并以与小脑过度连接为突出表现。据推测参与感觉过滤丧失和感觉运动刺激组织的脑区,如皮质-纹状体-丘脑-皮质回路和屏状核,在较高剂量的裸盖菇素作用下显示激活增加。事实上与迷幻体验相关的一般神经解剖学回路受到了影响,但BOLD信号方向和神经网络之间的活动模式与人类文献不一致。