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Investigational NMDA receptor modulators for depression.

机译:抑郁症的研究性NMDA受体调节剂。

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INTRODUCTION: With regards to depression, the role of N-methyl-D-aspartate receptor (NMDA) was pursued many years ago, mainly in the form of preclinical studies. Since then, there have been several clinical data in the literature indicating the efficacy of NMDA receptor antagonists of either stand-alone or as an adjunct therapy in depression and depression-related diseases. AREAS COVERED: The present review focuses on clinical data of well-known and recently discovered NMDA receptor antagonists/modulators and their mechanisms of action. EXPERT OPINION: Several NMDA receptor modulators have been tested in both human and animal studies to examine their potential antidepressant activity. Most of the compounds that exhibited beneficial properties in the animal tests and models of depression either have never been tested or did not show efficacy in humans. For some of them, such as ketamine, where a consistently reproducible antidepressant effect was found, clinical use is limited by a variety of adverse effects. However, ketamine has become a standard tool for identifying the biological factors associated with rapid antidepressant action and, as such, is a novel target for the development of new therapeutics.
机译:简介:关于抑郁症,N-甲基-D-天门冬氨酸受体(NMDA)的作用已在很多年前进行了研究,主要是以临床前研究的形式进行的。从那以后,文献中已有数项临床数据表明,NMDA受体拮抗剂在抑郁症和与抑郁症有关的疾病中,既可以单独使用,也可以作为辅助疗法使用。覆盖的区域:本综述着重于已知和最近发现的NMDA受体拮抗剂/调节剂的临床数据及其作用机理。专家意见:几种NMDA受体调节剂已经在人和动物研究中进行了测试,以检查其潜在的抗抑郁活性。在动物试验和抑郁症模型中显示出有益特性的大多数化合物都尚未经过测试或未在人体中显示功效。对于其中的一些药物(如氯胺酮),其抗抑郁作用一直可再现,其临床应用受到各种不良反应的限制。然而,氯胺酮已成为鉴定与快速抗抑郁作用有关的生物学因素的标准工具,因此,氯胺酮是开发新疗法的新靶标。

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