Evidence map›Paper›PMID 30723288›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

The susceptibility to chronic social defeat stress is related to low hippocampal extrasynaptic NMDA receptor function.

Yiu Chung Tse, Joëlle Lopez, Alexandre Moquin, Shui-Ming Alice Wong, Dusica Maysinger, Tak Pan Wong

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Deficits in integrative NMDA receptors caused by Grin1 disruption can be rescued in adulthood.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  5. Article
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  7. Review
  8. Article
  9. Article
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  11. Article
  12. Animal models of major depression: drawbacks and challenges.Journal of neural transmission (Vienna, Austria : 1996) · 2019
    Review
  13. Negative Memory Engrams in the Hippocampus Enhance the Susceptibility to Chronic Social Defeat Stress.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Yiu Chung TseDouglas Mental Health University Institute, 6875 LaSalle Blvd, Montreal, QC, Canada.
Joëlle LopezDouglas Mental Health University Institute, 6875 LaSalle Blvd, Montreal, QC, Canada.
Alexandre MoquinDepartment of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.
Shui-Ming Alice WongDouglas Mental Health University Institute, 6875 LaSalle Blvd, Montreal, QC, Canada.
Dusica MaysingerDepartment of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.
Tak Pan WongDouglas Mental Health University Institute, 6875 LaSalle Blvd, Montreal, QC, Canada. takpan.wong@mcgill.ca.
Douglas Mental Health University Institute · CAMcGill University · CA

Funding

Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) 137003
6 · The paper itself

Abstract

N-methyl-D-aspartate receptors (NMDARs) have been highly implicated in the pathogenesis and treatment of depression. While NMDARs can be found inside and outside glutamate synapses, it remains unclear if NMDARs at synaptic (sNMDAR) and extrasynaptic locations (exNMDAR) play different roles in the formation of depression-related behaviors. Using chronic social defeat stress (CSDS), an animal model for anxiety- and depression-related behaviors, we found that mice susceptible to CSDS exhibited low hippocampal exNMDAR function. Raising exNMDAR function by enhancing the release of glutamate from astrocytic cystine-glutamate antiporters or targeting extrasynaptic receptors with agonist-coated gold nanoparticles that cannot enter the synaptic cleft prevented social avoidance behavior in stressed mice. Interestingly, ketamine, which is a fast-acting antidepressant, exhibited stronger blockade to sNMDARs than to exNMDARs. These findings suggest that the susceptibility and resilience of mice toward CSDS is related to low and high exNMDAR function in the hippocampus, respectively. Enhancing exNMDAR function could be a novel treatment approach for mood and anxiety disorders.

Indexed as

AnimalsAnxietyCA1 Region, HippocampalDepressionDisease Models, AnimalMaleMice, Inbred C57BLNeuronsReceptors, N-Methyl-D-AspartateSocial BehaviorStress, PsychologicalSynapsesReceptors, N-Methyl-D-Aspartate

Identifiers

PMID30723288
PMCPMC6785155
OpenAlexW2913788158

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.