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氯胺酮治疗抑郁症:临床治疗进展、快速抗抑郁作用机制以及与血清素能致幻剂的对比

Ketamine for Depression: Advances in Clinical Treatment, Rapid Antidepressant Mechanisms of Action, and a Contrast with Serotonergic Psychedelics.

作者信息

Kojic Marina, Saelens Johan, Kadriu Bashkim, Zarate Carlos A, Kraus Christoph

机构信息

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.

出版信息

Curr Top Behav Neurosci. 2022;56:141-167. doi: 10.1007/7854_2022_313.

Abstract

The approval of ketamine for treatment-resistant depression has created a model for a novel class of rapid-acting glutamatergic antidepressants. Recent research into other novel rapid-acting antidepressants - most notably serotonergic psychedelics (SPs) - has also proven promising. Presently, the mechanisms of action of these substances are under investigation to improve these novel treatments, which also exhibit considerable side effects such as dissociation. This chapter lays out the historical development of ketamine as an antidepressant, outlines its efficacy and safety profile, reviews the evidence for ketamine's molecular mechanism of action, and compares it to the proposed mechanism of SPs. The evidence suggests that although ketamine and SPs act on distinct primary targets, both may lead to rapid restoration of synaptic deficits and downstream network reconfiguration. In both classes of drugs, a glutamate surge activates α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) throughput and increases in brain-derived neurotrophic factor (BDNF) levels. Taken together, these novel antidepressant mechanisms may serve as a framework to explain the rapid and sustained antidepressant effects of ketamine and may be crucial for developing new rapid-acting antidepressants with an improved side effect profile.

摘要

氯胺酮获批用于治疗难治性抑郁症,为一类新型速效谷氨酸能抗抑郁药树立了典范。近期对其他新型速效抗抑郁药的研究——最显著的是血清素能致幻剂(SPs)——也已证明颇具前景。目前,正在研究这些物质的作用机制,以改进这些新型治疗方法,这些治疗方法也存在如解离等相当多的副作用。本章阐述了氯胺酮作为抗抑郁药的历史发展,概述了其疗效和安全性概况,回顾了氯胺酮分子作用机制的证据,并将其与SPs的拟议作用机制进行比较。证据表明,尽管氯胺酮和SPs作用于不同的主要靶点,但两者都可能导致突触缺陷的快速恢复和下游网络重构。在这两类药物中,谷氨酸激增会激活α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)通量,并提高脑源性神经营养因子(BDNF)水平。综上所述,这些新型抗抑郁机制可能为解释氯胺酮的快速和持续抗抑郁作用提供一个框架,并且对于开发具有改善副作用的新型速效抗抑郁药可能至关重要。

相似文献

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Mechanisms of ketamine action as an antidepressant.氯胺酮作为抗抑郁药的作用机制。
Mol Psychiatry. 2018 Apr;23(4):801-811. doi: 10.1038/mp.2017.255. Epub 2018 Mar 13.
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本文引用的文献

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Urothelial toxicity of esketamine in the treatment of depression.治疗抑郁症时氯胺酮的尿路上皮细胞毒性。
Psychopharmacology (Berl). 2020 Nov;237(11):3295-3302. doi: 10.1007/s00213-020-05611-y. Epub 2020 Jul 26.

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