Laboratory of Pharmacology and Brain Biostructure, Pharmacology Department, Maj Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Pharmacol Rep. 2023 Dec;75(6):1350-1361. doi: 10.1007/s43440-023-00546-5. Epub 2023 Oct 30.
Psychedelics are compounds acting by serotonin 5-hydroxytryptamine (5-HT) receptor activation and induce several behavioral responses. They are of special interest because of their positive effects on neuropsychiatric disorders (depression and posttraumatic stress disorder). However, several findings revealed that some psychedelic actions are similar to symptoms observed in schizophrenia (psychosis, sensorimotor gating impairments, attention, and working memory deficits) which might limit their clinical applications. Psychedelics activate some neurotransmitters, i.e., serotonergic, and glutamatergic, that are also impaired in schizophrenia. Therefore, the neurobiological background of psychedelics and schizophrenia is partially similar. Another important aspect to discuss is the perspective of using psychedelics in schizophrenia therapy. Postmortem studies showed a loss of synapses in schizophrenia, and the positive effects of psychedelics on neuroplasticity (synaptogenesis, neurogenesis, and neuritogenesis) might be essential in the context of schizophrenia therapy. However, because of psychedelics' psychotic action, the recommended doses of psychedelics in schizophrenia treatment are not established, and subpsychedelic dosing or microdosing are considered. Exploratory studies are needed to determine the tolerability of treatment and appropriate dosing regimen. Another therapeutic option is using non-hallucinogenic psychedelic analogs that also induce neuroplastic outcomes but do not have psychotogenic effects. Further preclinical and clinical studies are needed to recognize the potential effectiveness of 5-HT agonists in schizophrenia therapy.
致幻剂通过激活血清素 5-羟色胺(5-HT)受体而起作用,并引起多种行为反应。它们特别有趣,因为它们对神经精神疾病(抑郁症和创伤后应激障碍)有积极影响。然而,一些发现表明,一些致幻剂的作用类似于精神分裂症中观察到的症状(精神病、感觉运动门控障碍、注意力和工作记忆缺陷),这可能限制了它们的临床应用。致幻剂激活了一些神经递质,即血清素能和谷氨酸能,这些递质在精神分裂症中也受到损害。因此,致幻剂和精神分裂症的神经生物学背景部分相似。另一个需要讨论的重要方面是在精神分裂症治疗中使用致幻剂的前景。尸检研究表明精神分裂症存在突触丧失,而致幻剂对神经可塑性(突触发生、神经发生和神经突生成)的积极影响在精神分裂症治疗中可能至关重要。然而,由于致幻剂的致精神病作用,在精神分裂症治疗中推荐的致幻剂剂量尚未确定,因此考虑使用亚致幻剂量或微剂量。需要进行探索性研究来确定治疗的耐受性和适当的剂量方案。另一种治疗选择是使用非致幻性致幻剂类似物,它们也能诱导神经可塑性,但没有致精神病作用。需要进一步的临床前和临床研究来认识 5-HT 激动剂在精神分裂症治疗中的潜在有效性。