Husain Muhammad Ishrat, Ledwos Nicole, Fellows Elise, Baer Jenna, Rosenblat Joshua D, Blumberger Daniel M, Mulsant Benoit H, Castle David J
Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
Department of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Front Psychiatry. 2023 Feb 10;13:1076459. doi: 10.3389/fpsyt.2022.1076459. eCollection 2022.
Current treatment options for major depressive disorder (MDD) have limited efficacy and are associated with adverse effects. Recent studies investigating the antidepressant effect of serotonergic psychedelics-also known as classic psychedelics-have promising preliminary results with large effect sizes. In this context, we conducted a review of the putative neurobiological underpinnings of the mechanism of antidepressant action of these drugs.
A narrative review was conducted using PubMed to identify published articles evaluating the antidepressant mechanism of action of serotonergic psychedelics.
Serotonergic psychedelics have serotonin (5HT)2A agonist or partial agonist effects. Their rapid antidepressant effects may be mediated-in part-by their potent 5HT2A agonism, leading to rapid receptor downregulation. In addition, these psychedelics impact brain derived neurotrophic factor and immunomodulatory responses, both of which may play a role in their antidepressant effect. Several neuroimaging and neurophysiology studies evaluating mechanistic change from a network perspective can help us to further understand their mechanism of action. Some, but not all, data suggest that psychedelics may exert their effects, in part, by disrupting the activity of the default mode network, which is involved in both introspection and self-referential thinking and is over-active in MDD.
The mechanisms of action underlying the antidepressant effect of serotonergic psychedelics remains an active area of research. Several competing theories are being evaluated and more research is needed to determine which ones are supported by the most robust evidence.
目前用于治疗重度抑郁症(MDD)的方法疗效有限且伴有不良反应。最近对血清素能致幻剂(也称为经典致幻剂)抗抑郁作用的研究取得了有前景的初步结果,效应量较大。在此背景下,我们对这些药物抗抑郁作用机制的假定神经生物学基础进行了综述。
使用PubMed进行叙述性综述,以确定评估血清素能致幻剂抗抑郁作用机制的已发表文章。
血清素能致幻剂具有血清素(5-羟色胺,5HT)2A激动剂或部分激动剂作用。它们快速的抗抑郁作用可能部分由其强效的5HT2A激动作用介导,导致受体快速下调。此外,这些致幻剂会影响脑源性神经营养因子和免疫调节反应,这两者可能在其抗抑郁作用中发挥作用。一些从网络角度评估机制变化的神经影像学和神经生理学研究有助于我们进一步了解它们的作用机制。部分(而非全部)数据表明,致幻剂可能部分通过破坏默认模式网络的活动发挥作用,该网络参与内省和自我参照思维,在MDD中过度活跃。
血清素能致幻剂抗抑郁作用的潜在机制仍是一个活跃的研究领域。几种相互竞争的理论正在评估中,需要更多研究来确定哪些理论得到了最有力的证据支持。