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基于谷氨酸的新型抗抑郁药物研发。

Glutamate-Based Drug Discovery for Novel Antidepressants.

机构信息

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

出版信息

Expert Opin Drug Discov. 2016 Sep;11(9):873-83. doi: 10.1080/17460441.2016.1213234. Epub 2016 Aug 2.

Abstract

INTRODUCTION

Classic antidepressants that modulate monoaminergic systems are not sufficiently effective and require long systematic application. Recent studies suggest that substances that modulate glutamatergic system may produce an antidepressant effect which is not only faster but also more sustained.

AREAS COVERED

In this paper, the authors summarize the results of studies on antidepressant action of ketamine in patients with severe refractory depression, which have demonstrated high efficacy in a very short time after a single dose. Due to the adverse effects of ketamine that substantially exclude it from the daily use by patients, efforts have been made to find other NMDA receptor antagonists, which could mimic the therapeutic effect of ketamine but without the side effects. Intensive studies to elucidate ketamine's mechanism of antidepressant action have also been conducted. Herein, the results of research showing that metabotropic glutamate (mGlu) receptors could be the target of novel antidepressants are also presented.

EXPERT OPINION

The intensive preclinical and clinical research on NMDA and mGlu receptor ligands, which is currently going on, could contribute to the awaited breakthrough in the field of novel antidepressant drug discovery. This line of research may also lead to a new understanding of the biological basis of depression.

摘要

简介

调节单胺能系统的经典抗抑郁药效果不够显著,需要长期系统应用。最近的研究表明,调节谷氨酸能系统的物质可能产生更快且更持久的抗抑郁作用。

涵盖领域

本文作者总结了氯胺酮在重度难治性抑郁症患者中抗抑郁作用的研究结果,这些研究表明氯胺酮在单次给药后很短的时间内就具有很高的疗效。由于氯胺酮的不良反应使其不能被患者日常使用,因此人们努力寻找其他 NMDA 受体拮抗剂,这些拮抗剂可以模拟氯胺酮的治疗效果,但没有副作用。为了阐明氯胺酮的抗抑郁作用机制,也进行了大量的研究。本文还介绍了研究结果表明代谢型谷氨酸(mGlu)受体可能是新型抗抑郁药的靶点。

专家意见

目前正在进行的 NMDA 和 mGlu 受体配体的深入临床前和临床研究,可能有助于在新型抗抑郁药物发现领域取得预期的突破。这项研究也可能导致对抑郁生物学基础的新理解。

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