Psychedelics, entactogens and psychoplastogens for depression and related disorders.

IF 6.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Daniel Hoyer
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引用次数: 0

Abstract

Currently, the most actively investigated rapidly acting antidepressants, anxiolytics and/or anti PTSD agents, include psychedelics e.g. psilocybin, LSD, N,N-dimethyltryptamine, ayahuasca; non-hallucinogenic entactogens, e.g. MDMA; psychoplastogens which rapidly promote neuroplasticity, e.g. ibogaine, ketamine and esketamine; and other atypicals e.g. dextromorphan/bupropion, esmethadone. Late-stage clinical trials support psychedelics and/or MDMA-assisted psychotherapy as rapidly acting treatments for major depressive disorder (MDD), treatment-resistant depression (TRD), PTSD or generalised anxiety disorders (GAD). Psilocybin, MDMA and LSD were granted FDA breakthrough status for TRD/MDD, PTSD and GAD, respectively, although FDA recently rejected the new drug application of MDMA in PTSD. Most of these drugs target the 5-HT and monoamine systems. Classical psychedelics act as 5-HT2A receptor agonists, although LSD, DMT and psilocybin target other 5-HT and/or dopamine receptors. Psychedelic-dependent 5-HT2A receptor agonism also has profound anti-(neuro)inflammatory effects. Advanced imaging studies suggest that brain 5-HT levels are reduced in depression. Functional magnetic resonance studies show that neural networks (cortico thalamic, salience, default mode) are profoundly impaired in depression. Such network defects are corrected upon psychedelic/entactogen treatment, offering a unique opportunity to serve as biomarkers for depression, anxiety and PTSD precision medicine trials. Psychedelics and entactogens target common end pathways, namely neuroplasticity/synaptogenesis, either directly via monoamine or glutamate receptors and/or indirectly, via BDNF and mTORC1 pathways. Together, these findings strongly support a biological basis for MDD, GAD, PTSD and related conditions, which can be considered as mixed biochemical, neurological and neuroimmune disorders, and are profoundly modified by psychedelics, entactogens and the newly developed psychoplastogens.

抑郁症及相关疾病的致幻剂、致幻剂和精神致塑剂。
目前,研究最活跃的速效抗抑郁药、抗焦虑药和/或抗创伤后应激障碍药物包括致幻剂,如裸盖菇素、LSD、N、N-二甲基色胺、死藤水;非致幻性致幻剂,如MDMA;迅速促进神经可塑性的精神致塑剂,如伊博格碱、氯胺酮和艾氯胺酮;还有其他非典型药物,如右旋吗啡/安非他酮,艾美沙酮。后期临床试验支持致幻剂和/或mdma辅助心理治疗作为重度抑郁症(MDD)、难治性抑郁症(TRD)、创伤后应激障碍(PTSD)或广泛性焦虑症(GAD)的快速治疗。Psilocybin, MDMA和LSD分别被FDA授予TRD/MDD, PTSD和GAD的突破性地位,尽管FDA最近拒绝了MDMA治疗PTSD的新药申请。这些药物大多针对5-羟色胺和单胺系统。经典致幻剂作为5-HT2A受体激动剂,尽管LSD、DMT和裸盖菇素靶向其他5-HT和/或多巴胺受体。致幻剂依赖的5-HT2A受体激动作用也具有深远的抗(神经)炎症作用。先进的成像研究表明,抑郁症患者的大脑5-羟色胺水平降低。功能性磁共振研究表明,抑郁症患者的神经网络(皮质丘脑、突出性、默认模式)严重受损。这种网络缺陷在迷幻药/恩托因治疗后得到纠正,为抑郁症、焦虑症和创伤后应激障碍精准医学试验提供了独特的生物标志物。致幻剂和致幻剂针对共同的末端通路,即神经可塑性/突触发生,直接通过单胺或谷氨酸受体和/或间接通过BDNF和mTORC1途径。总之,这些发现有力地支持了MDD、GAD、PTSD及其相关疾病的生物学基础,这些疾病可以被认为是生化、神经和神经免疫的混合疾病,并被致幻剂、致幻剂和新开发的精神致幻剂深刻地改变。
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来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
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