Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2010 Sep;122(3):192-210.
doi: 10.1111/j.1600-0447.2009.01529.x. Epub 2010 Jan 25.

An update on the role of glutamate in the pathophysiology of depression

Affiliations
Review

An update on the role of glutamate in the pathophysiology of depression

Nicholas D Mitchell et al. Acta Psychiatr Scand. 2010 Sep.

Abstract

Objective: To review the literature on the involvement of glutamate (Glu), including its interactions with other neurochemical systems, in the pathophysiology of depression.

Method: A MEDLINE search using the terms glutamate, depression and major depressive disorder, was performed.

Results: Alterations in proteins involved in glutamatergic signalling are implicated in variations in behaviour in animal models of depression. Drugs acting at Glu receptors appear to have antidepressant-like effects in these models, and traditional antidepressant pharmacotherapies act on the glutamatergic system. Recent evidence from genetic studies and in vivo spectroscopy also correlate glutamatergic dysfunction with depression. Trials of N-methyl-d-aspartate receptor antagonists in humans have provided mixed results.

Conclusion: A growing body of evidence indicates that the glutamatergic system is involved in the pathophysiology of depression, and may represent a target for intervention.

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources