Frautschi Paloma C, Singh Ajay P, Stowe Nicholas A, Yu John-Paul J
Department of Radiology (P.C.F., A.P.S., J.-P.J.Y.), University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Graduate Program in Cellular and Molecular Biology (A.P.S., J.-P.J.Y.), University of Wisconsin-Madison, Madison, Wisconsin.
AJNR Am J Neuroradiol. 2024 Feb 15;45(7):833-40. doi: 10.3174/ajnr.A8118.
The neurobiological mechanisms underpinning psychiatric disorders such as treatment-resistant major depression, post-traumatic stress disorder, and substance use disorders, remain unknown. Psychedelic compounds, such as psilocybin, lysergic acid diethylamide, and N,N-dimethyltryptamine, have emerged as potential therapies for these disorders because of their hypothesized ability to induce neuroplastic effects and alter functional networks in the brain. Yet, the mechanisms underpinning the neurobiological treatment response remain obscure. Quantitative neuroimaging is uniquely positioned to provide insight into the neurobiological mechanisms of these emerging therapies and quantify the patient treatment response. This review aims to synthesize our current state-of-the-art understanding of the functional changes occurring in the brain following psilocybin, lysergic acid diethylamide, or N,N-dimethyltryptamine administration in human participants with fMRI and PET. We further aim to disseminate our understanding of psychedelic compounds as they relate to neuroimaging with the goal of improved diagnostics and treatment of neuropsychiatric illness.
诸如难治性重度抑郁症、创伤后应激障碍和物质使用障碍等精神疾病背后的神经生物学机制仍然不明。诸如裸盖菇素、麦角酸二乙胺和N,N-二甲基色胺等致幻化合物,因其具有诱导神经可塑性效应和改变大脑功能网络的假定能力,已成为这些疾病的潜在治疗方法。然而,神经生物学治疗反应背后的机制仍然不清楚。定量神经成像在洞察这些新兴疗法的神经生物学机制以及量化患者治疗反应方面具有独特的优势。本综述旨在综合我们目前对人类受试者在服用裸盖菇素、麦角酸二乙胺或N,N-二甲基色胺后通过功能磁共振成像(fMRI)和正电子发射断层扫描(PET)所观察到的大脑功能变化的最新认识。我们还旨在传播我们对致幻化合物与神经成像之间关系的理解,以期改善神经精神疾病的诊断和治疗。