Wolf Gilly, Singh Sandeep, Blakolmer Karin, Lerer Leonard, Lifschytz Tzuri, Heresco-Levy Uriel, Lotan Amit, Lerer Bernard
Psychedelics Research Group, Biological Psychiatry Laboratory and Hadassah BrainLabs, Hadassah Medical Center-Hebrew University, Jerusalem, Israel.
Back of The Yards Algae Sciences, Chicago, IL, USA.
Mol Psychiatry. 2023 Jan;28(1):44-58. doi: 10.1038/s41380-022-01832-z. Epub 2022 Oct 24.
Schizophrenia is a widespread psychiatric disorder that affects 0.5-1.0% of the world's population and induces significant, long-term disability that exacts high personal and societal cost. Negative symptoms, which respond poorly to available antipsychotic drugs, are the primary cause of this disability. Association of negative symptoms with cortical atrophy and cell loss is widely reported. Psychedelic drugs are undergoing a significant renaissance in psychiatric disorders with efficacy reported in several conditions including depression, in individuals facing terminal cancer, posttraumatic stress disorder, and addiction. There is considerable evidence from preclinical studies and some support from human studies that psychedelics enhance neuroplasticity. In this Perspective, we consider the possibility that psychedelic drugs could have a role in treating cortical atrophy and cell loss in schizophrenia, and ameliorating the negative symptoms associated with these pathological manifestations. The foremost concern in treating schizophrenia patients with psychedelic drugs is induction or exacerbation of psychosis. We consider several strategies that could be implemented to mitigate the danger of psychotogenic effects and allow treatment of schizophrenia patients with psychedelics to be implemented. These include use of non-hallucinogenic derivatives, which are currently the focus of intense study, implementation of sub-psychedelic or microdosing, harnessing of entourage effects in extracts of psychedelic mushrooms, and blocking 5-HT2A receptor-mediated hallucinogenic effects. Preclinical studies that employ appropriate animal models are a prerequisite and clinical studies will need to be carefully designed on the basis of preclinical and translational data. Careful research in this area could significantly impact the treatment of one of the most severe and socially debilitating psychiatric disorders and open an exciting new frontier in psychopharmacology.
精神分裂症是一种广泛存在的精神障碍,影响着全球0.5%-1.0%的人口,并导致严重的长期残疾,给个人和社会带来高昂代价。对现有抗精神病药物反应不佳的阴性症状是导致这种残疾的主要原因。阴性症状与皮质萎缩和细胞丢失之间的关联已被广泛报道。迷幻药物正在精神疾病领域经历重大复兴,在包括抑郁症、晚期癌症患者、创伤后应激障碍和成瘾等多种病症中均有疗效报道。临床前研究有大量证据,人体研究也提供了一些支持,表明迷幻药物可增强神经可塑性。在本观点文章中,我们探讨了迷幻药物在治疗精神分裂症的皮质萎缩和细胞丢失以及改善与这些病理表现相关的阴性症状方面发挥作用的可能性。使用迷幻药物治疗精神分裂症患者时,最主要的担忧是诱发或加重精神病症状。我们考虑了几种可以实施的策略,以减轻致幻效应的风险,从而能够对精神分裂症患者使用迷幻药物进行治疗。这些策略包括使用非致幻衍生物(目前是深入研究的重点)、采用亚致幻剂量或微剂量给药、利用迷幻蘑菇提取物中的协同效应以及阻断5-HT2A受体介导的致幻效应。采用合适动物模型的临床前研究是前提条件,临床研究需要根据临床前和转化数据进行精心设计。在这一领域进行仔细研究可能会对这种最严重且使社会功能受损的精神障碍之一的治疗产生重大影响,并在精神药理学领域开辟一个令人兴奋的新前沿。