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新型抗抑郁治疗药物的研究进展。

New investigational agents for the treatment of major depressive disorder.

机构信息

Department of Neurobiology, Maj Institute of Pharmacology Polish Academy of Sciences, Krakow, Poland.

Department of Psychiatry, Jagiellonian University Medical College, Krakow, Poland.

出版信息

Expert Opin Investig Drugs. 2022 Oct;31(10):1053-1066. doi: 10.1080/13543784.2022.2113376. Epub 2022 Aug 24.

Abstract

INTRODUCTION

Pharmacotherapy of depression is characterized by the delayed onset of action, chronic treatment requirements, and insufficient effectiveness. Ketamine, with its rapid action and long-lasting effects, represents a breakthrough in the modern pharmacotherapy of depression.

AREAS COVERED

The current review summarizes the latest findings on the mechanism of the antidepressant action of ketamine and its enantiomers and metabolites. Furthermore, the antidepressant potential of psychedelics, non-hallucinogenic serotonergic modulators, and metabotropic glutamate receptor ligands was discussed.

EXPERT OPINION

Recent data indicated that to achieve fast and long-acting antidepressant-like effects, compounds must induce durable effects on the architecture and density of dendritic spines in brain regions engaged in mood regulation. Such mechanisms underlie the actions of ketamine and psychedelics. These compounds trigger hallucinations; however, it is thought that these effects might be essential for their antidepressant action. Behavioral studies with serotonergic modulators affecting 5-HT1A (biased agonists), 5-HT4 (agonists), and 5-HT-7 (antagonists) receptors exert rapid antidepressant-like activity, but they seem to be devoid of these effects. Another way to avoid psychomimetic effects and achieve the desired rapid antidepressant-like effects is combined therapy. In this respect, ligands of metabotropic receptors show some potential.

摘要

简介

抗抑郁药物治疗的特点是作用起效慢、需要长期治疗、疗效不足。氯胺酮具有起效快、作用持久的特点,是抗抑郁药物治疗的一大突破。

涵盖领域

本文综述了氯胺酮及其对映异构体和代谢物抗抑郁作用机制的最新研究结果。此外,还讨论了致幻剂、非致幻性 5-羟色胺能调节剂和代谢型谷氨酸受体配体的抗抑郁潜力。

专家意见

最近的数据表明,为了达到快速和长效的抗抑郁样作用,化合物必须对参与情绪调节的脑区中的树突棘的结构和密度产生持久的影响。这些机制是氯胺酮和致幻剂作用的基础。这些化合物会引发幻觉;然而,人们认为这些作用可能对其抗抑郁作用至关重要。影响 5-HT1A(偏激动剂)、5-HT4(激动剂)和 5-HT-7(拮抗剂)受体的 5-羟色胺能调节剂的行为研究具有快速的抗抑郁样活性,但它们似乎缺乏这些作用。另一种避免致幻作用并达到预期快速抗抑郁样作用的方法是联合治疗。在这方面,代谢型谷氨酸受体配体显示出一定的潜力。

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