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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.

DOI:10.1080/17460441.2016.1213234
PMID:27409299
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。

相似文献

1
Glutamate-Based Drug Discovery for Novel Antidepressants.基于谷氨酸的新型抗抑郁药物研发。
Expert Opin Drug Discov. 2016 Sep;11(9):873-83. doi: 10.1080/17460441.2016.1213234. Epub 2016 Aug 2.
2
Targeting metabotropic glutamate receptors for rapid-acting antidepressant drug discovery.靶向代谢型谷氨酸受体以发现速效抗抑郁药物。
Expert Opin Drug Discov. 2021 Feb;16(2):147-157. doi: 10.1080/17460441.2020.1822814. Epub 2020 Sep 23.
3
Targeting metabotropic glutamate receptors for the treatment of depression and other stress-related disorders.靶向代谢型谷氨酸受体治疗抑郁症和其他与应激相关的障碍。
Neuropharmacology. 2021 Sep 15;196:108687. doi: 10.1016/j.neuropharm.2021.108687. Epub 2021 Jun 25.
4
What is the mechanism of Ketamine's rapid-onset antidepressant effect? A concise overview of the surprisingly large number of possibilities.氯胺酮快速起效的抗抑郁作用机制是什么?对大量惊人可能性的简要概述。
J Clin Pharm Ther. 2017 Apr;42(2):147-154. doi: 10.1111/jcpt.12497. Epub 2017 Jan 22.
5
Targeting glutamate signalling in depression: progress and prospects.靶向抑郁症谷氨酸信号:进展与展望。
Nat Rev Drug Discov. 2017 Jul;16(7):472-486. doi: 10.1038/nrd.2017.16. Epub 2017 Mar 17.
6
NMDA antagonists under investigation for the treatment of major depressive disorder.正在研究用于治疗重度抑郁症的 NMDA 拮抗剂。
Expert Opin Investig Drugs. 2014 Sep;23(9):1181-92. doi: 10.1517/13543784.2014.918951. Epub 2014 May 12.
7
mGlu receptors as potential targets for novel antidepressants.代谢型谷氨酸受体作为新型抗抑郁药的潜在靶点。
Curr Opin Pharmacol. 2018 Feb;38:24-30. doi: 10.1016/j.coph.2018.02.001. Epub 2018 Feb 24.
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Targeting of NMDA receptors in the treatment of major depression.靶向N-甲基-D-天冬氨酸受体治疗重度抑郁症
Curr Pharm Des. 2014;20(32):5151-9. doi: 10.2174/1381612819666140110120435.
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mGlu2/3 receptor as a novel target for rapid acting antidepressants.代谢型谷氨酸受体2/3作为速效抗抑郁药的新靶点。
Adv Pharmacol. 2020;89:289-309. doi: 10.1016/bs.apha.2020.04.001. Epub 2020 May 22.
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mGlu2/3 and mGlu5 receptors: potential targets for novel antidepressants.mGlu2/3 和 mGlu5 受体:新型抗抑郁药的潜在靶点。
Neuropharmacology. 2013 Mar;66:40-52. doi: 10.1016/j.neuropharm.2012.05.022. Epub 2012 May 26.

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4-F-PCP, a Novel PCP Analog Ameliorates the Depressive-Like Behavior of Chronic Social Defeat Stress Mice via NMDA Receptor Antagonism.4-氟-PCP,一种新型PCP类似物,通过拮抗NMDA受体改善慢性社会挫败应激小鼠的抑郁样行为。
Biomol Ther (Seoul). 2023 Mar 1;31(2):227-239. doi: 10.4062/biomolther.2022.159. Epub 2023 Feb 15.
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Ketamine: The final frontier or another depressing end?氯胺酮:是最终的前沿领域还是又一个令人沮丧的结局?
Behav Brain Res. 2020 Apr 6;383:112508. doi: 10.1016/j.bbr.2020.112508. Epub 2020 Feb 1.
4
The Effect of Glutamatergic Modulators on Extracellular Glutamate: How Does this Information Contribute to the Discovery of Novel Antidepressants?谷氨酸能调节剂对细胞外谷氨酸的影响:这些信息如何助力新型抗抑郁药的发现?
Curr Ther Res Clin Exp. 2019 Sep 10;91:25-32. doi: 10.1016/j.curtheres.2019.100566. eCollection 2019.
5
Role of Serotonergic System in the Antidepressant Actions of mGlu2/3 Receptor Antagonists: Similarity to Ketamine.5-羟色胺能系统在 mGlu2/3 受体拮抗剂抗抑郁作用中的作用:与氯胺酮的相似性。
Int J Mol Sci. 2019 Mar 13;20(6):1270. doi: 10.3390/ijms20061270.
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New drugs in psychiatry: focus on new pharmacological targets.精神医学中的新药:聚焦新的药理学靶点。
F1000Res. 2017 Mar 30;6:397. doi: 10.12688/f1000research.10233.1. eCollection 2017.