Evidence map›Paper›PMID 32709968›Full record

ArticleScientific reports2020

Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat.

Megan E Fox, Antonio Figueiredo, Miriam S Menken, Mary Kay Lobo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cue-Dependent Fear Learning Drives Nucleus Accumbens Spine Plasticity.bioRxiv : the preprint server for biology · 2026
    Article
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  13. Molecular, Circuit, and Stress Response Characterization of Ventral Pallidum Npas1-Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  14. Review
  15. Article
  16. Life extension factor klotho regulates behavioral responses to stress via modulation of GluN2B function in the nucleus accumbens.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  17. Article
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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

4 authors at 1 institution in 1 country.

Megan E FoxDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, 20 Penn St, HSFII Building, Rm 265, Baltimore, MD, 21201, USA.
Antonio Figueiredo *Department of Anatomy and Neurobiology, University of Maryland School of Medicine, 20 Penn St, HSFII Building, Rm 265, Baltimore, MD, 21201, USA.
Miriam S Menken *Department of Anatomy and Neurobiology, University of Maryland School of Medicine, 20 Penn St, HSFII Building, Rm 265, Baltimore, MD, 21201, USA.
Mary Kay LoboDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, 20 Penn St, HSFII Building, Rm 265, Baltimore, MD, 21201, USA. mklobo@som.umaryland.edu.
University of Maryland, Baltimore · US

Funding

The neurocircuitry of depression: Molecular and Cell Subtype MechanismsR01MH106500 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI LOBO, MARY KAY · 2015 to 2024
$4.5M
Circuit-specific molecular mechanisms in fentanyl use and relapseK99DA050575 · NIDA · UNIVERSITY OF MARYLAND BALTIMORE · PI FOX, MEGAN ELIZABETH · 2020 to 2021
$352k
molecular mechanisms of dendritic remodeling in depressionF32MH116574 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI FOX, MEGAN ELIZABETH · 2018 to 2020
$188k
NIDA NIH HHS K99 DA050575NIDA NIH HHS K99DA050575NIMH NIH HHS F32 MH116574NIMH NIH HHS F32MH116574NIMH NIH HHS R01 MH106500NIMH NIH HHS R01MH106500
6 · The paper itself

Abstract

Stress alters the structure and function of brain reward circuitry and is an important risk factor for developing depression. In the nucleus accumbens (NAc), structural and physiological plasticity of medium spiny neurons (MSNs) have been linked to increased stress-related and depression-like behaviors. NAc MSNs have opposing roles in driving stress-related behaviors that is dependent on their dopamine receptor expression. After chronic social defeat stress, NAc MSNs exhibit increased dendritic spine density. However, it remains unclear if the dendritic spine plasticity is MSN subtype specific. Here we use viral labeling to characterize dendritic spine morphology specifically in dopamine D2 receptor expressing MSNs (D2-MSNs). After chronic social defeat, D2-MSNs exhibit increased spine density that is correlated with enhanced social avoidance behavior. Together, our data indicate dendritic spine plasticity is MSN subtype specific, improving our understanding of structural plasticity after chronic stress.

Indexed as

Social DefeatAnimalsCell CountDendritic SpinesMaleMiceNucleus AccumbensReceptors, Dopamine D2Stress, PsychologicalTime FactorsReceptors, Dopamine D2

Identifiers

PMID32709968
PMCPMC7381630
OpenAlexW3043865936

What OpenQuestion holds

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LicenceCC BY
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.