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[血清素5-羟色胺受体对血清素能致幻剂抗抑郁作用的贡献]

[Contribution of serotonin 5-HT receptor to antidepressant effect of serotonergic psychedelics].

作者信息

Ibi Daisuke

机构信息

Department of Chemical Pharmacology, Meijo University.

出版信息

Nihon Yakurigaku Zasshi. 2023 May 1;158(3):229-232. doi: 10.1254/fpj.22141. Epub 2023 Mar 29.

Abstract

Major depressive disorder presents a substantial global health burden, and at least 30-40% of patients exhibit treatment resistance to antidepressants. Ketamine, an NMDA receptor antagonist, is used as an anesthetic agent. In 2019, the U.S. Food and Drug Administration (FDA) approved esketamine (the S-enantiomer of ketamine) as a therapeutic agent for treatment-resistant depression; however, this drug has reportedly been associated with serious side effects such as dissociative symptoms, thus limiting its clinical use as an antidepressant. Recently, various clinical studies have reported that psilocybin, the psychoactive substance found in magic mushrooms, has a fast-acting and long-lasting antidepressant effect in patients with major depressive disorder, including those resistant to conventional treatment. Furthermore, psilocybin is a psychoactive drug that is relatively harmless compared to ketamine and other similar substances. Accordingly, the FDA has designated psilocybin as a "breakthrough therapy approach" for the treatment of major depressive disorder. Additionally, serotonergic psychedelics such as psilocybin and lysergic acid diethylamide show some potential in the treatment of depression, anxiety, and addiction. The increased attention the use of psychedelics has attracted as a psychiatric disorder treatment approach is referred to as the "psychedelic renaissance". Pharmacologically, psychedelics cause hallucinations by stimulating cortical serotonin 5-HT receptors (5-HT2A), although whether 5-HT2A is responsible for the manifestation of their therapeutic effects remains unclear. Furthermore, it is unclear whether the hallucinations and "mystical experience" that the patients go through because of 5-HT2A activation by psychedelics is essential for the therapeutic effect of these substances. Future research should elucidate the molecular and neural mechanisms underlying the therapeutic effects of psychedelics. This review summarizes the therapeutic effects of psychedelics on psychiatric disorders such as major depressive disorder in clinical and pre-clinical studies, and discusses the possibility of 5-HT2A as a novel therapeutic target.

摘要

重度抑郁症给全球带来了沉重的健康负担,至少30%-40%的患者对抗抑郁药存在治疗抵抗。氯胺酮是一种N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,用作麻醉剂。2019年,美国食品药品监督管理局(FDA)批准艾氯胺酮(氯胺酮的S-对映体)作为治疗抵抗性抑郁症的治疗药物;然而,据报道该药物会引发诸如解离症状等严重副作用,因此限制了其作为抗抑郁药的临床应用。最近,多项临床研究报告称,裸盖菇中发现的精神活性物质赛洛西宾对重度抑郁症患者,包括对传统治疗有抵抗性的患者,具有快速起效且持久的抗抑郁作用。此外,与氯胺酮和其他类似物质相比,赛洛西宾是一种相对无害的精神活性药物。因此,FDA已将赛洛西宾指定为治疗重度抑郁症的“突破性治疗方法”。此外,诸如赛洛西宾和麦角酸二乙胺等血清素能致幻剂在治疗抑郁症、焦虑症和成瘾方面显示出一定潜力。致幻剂作为一种精神疾病治疗方法所引起的关注度增加被称为“致幻剂复兴”。从药理学角度来看,致幻剂通过刺激皮层血清素5-羟色胺受体(5-HT2A)引发幻觉,尽管5-HT2A是否是其治疗效果表现的原因仍不清楚。此外,尚不清楚患者因致幻剂激活5-HT2A而经历的幻觉和“神秘体验”对于这些物质的治疗效果是否至关重要。未来的研究应阐明致幻剂治疗效果背后潜在的分子和神经机制。本综述总结了致幻剂在临床和临床前研究中对重度抑郁症等精神疾病的治疗效果,并讨论了5-HT2A作为新型治疗靶点的可能性。

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