Evidence map›Paper›PMID 24623766›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Prefrontal cortical circuit for depression- and anxiety-related behaviors mediated by cholecystokinin: role of ΔFosB.

Vincent Vialou, Rosemary C Bagot, Michael E Cahill, Deveroux Ferguson, Alfred J Robison, David M Dietz, Barbara Fallon, Michelle Mazei-Robison, Stacy M Ku, Eileen Harrigan and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% 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

172 citing papers in PubMed, 1 synthesis or guideline pooled it, 295 citations in OpenAlex.

  1. Pooled it
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  11. nNOS-expressing neurons in the mPFC mediate depression-related behaviors in mice through pPVT-mPFC projections.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
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112 more citing papers are in PubMed but not listed here.

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

15 authors at 5 institutions in 5 countries.

Vincent VialouFishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, Department of Physiology, Michigan State University, Lansing, Michigan 48824, Department of Pharmacology and Toxicology, University of Buffalo, Buffalo, New York 14214, Department of Psychology, University of British Columbia, Vancouver, British Columbia, Canada, Department of Psychiatry, University of Pennsylvania Medical School, Philadelphia, Pennsylvania 19104, and Institut National de la Santé et de la Recherche Médicale, U1130, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8246, and Université Pierre et Marie Curie, UM CR18, Sorbonne Université, Paris, France.
Rosemary C Bagot
Michael E Cahill
Deveroux Ferguson
Alfred J Robison
David M Dietz
Barbara Fallon
Michelle Mazei-Robison
Stacy M Ku
Eileen Harrigan
Catherine A Winstanley
Tej Joshi
Jian Feng
Olivier Berton
Eric J Nestler
Allen Institute for Brain Science · USMichigan State University · USUniversity at Buffalo, State University of New York · USUniversity of British Columbia · CAUniversity of Pennsylvania · US

Funding

REPRESSIVE HISTONE AND DNA METHYLATION IN RODENT DEPRESSION MODELSP50MH096890 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI NESTLER, ERIC J. · 2012 to 2021
$20.2M
Using neuroeconomics to disentangle the transcriptional mechanisms underlying resilience versus susceptibility to stressR01MH051399 · NIMH · YALE UNIVERSITY · PI NESTLER, ERIC J. · 1994 to 2023
$10.2M
Role of HDAC6 in a murine model of affective disorder and antidepressant actionR01MH087581 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BERTON, OLIVIER · 2010 to 2014
$2.1M
Training Program in Mental Health ResearchT32MH096678 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SALTON, STEPHEN R, SHAPIRO, MATTHEW L · 2012 to 2016
$1.1M
Dissecting Lateral Hypothalamic Input to Midbrain Neurons and its Role in Social Defeat StressF31MH108326 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KU, STACY · 2016 to 2017
$72k
NIMH NIH HHS F31 MH108326NIMH NIH HHS P50 MH096890NIMH NIH HHS R01 MH051399NIMH NIH HHS R01 MH087581NIMH NIH HHS T32 MH096678
6 · The paper itself

Abstract

Decreased medial prefrontal cortex (mPFC) neuronal activity is associated with social defeat-induced depression- and anxiety-like behaviors in mice. However, the molecular mechanisms underlying the decreased mPFC activity and its prodepressant role remain unknown. We show here that induction of the transcription factor ΔFosB in mPFC, specifically in the prelimbic (PrL) area, mediates susceptibility to stress. ΔFosB induction in PrL occurred selectively in susceptible mice after chronic social defeat stress, and overexpression of ΔFosB in this region, but not in the nearby infralimbic (IL) area, enhanced stress susceptibility. ΔFosB produced these effects partly through induction of the cholecystokinin (CCK)-B receptor: CCKB blockade in mPFC induces a resilient phenotype, whereas CCK administration into mPFC mimics the anxiogenic- and depressant-like effects of social stress. We previously found that optogenetic stimulation of mPFC neurons in susceptible mice reverses several behavioral abnormalities seen after chronic social defeat stress. Therefore, we hypothesized that optogenetic stimulation of cortical projections would rescue the pathological effects of CCK in mPFC. After CCK infusion in mPFC, we optogenetically stimulated mPFC projections to basolateral amygdala or nucleus accumbens, two subcortical structures involved in mood regulation. Stimulation of corticoamygdala projections blocked the anxiogenic effect of CCK, although no effect was observed on other symptoms of social defeat. Conversely, stimulation of corticoaccumbens projections reversed CCK-induced social avoidance and sucrose preference deficits but not anxiogenic-like effects. Together, these results indicate that social stress-induced behavioral deficits are mediated partly by molecular adaptations in mPFC involving ΔFosB and CCK through cortical projections to distinct subcortical targets.

Indexed as

AnimalsAnti-Anxiety AgentsAnxiety DisordersBrain MappingCholecystokininChronic DiseaseDepressive DisorderIndolesLimbic SystemMaleMeglumineMiceMice, Inbred C57BLNeural PathwaysPrefrontal CortexProto-Oncogene Proteins c-fosAnti-Anxiety AgentsCholecystokininFosb protein, mouseIndolesMegluminePD 134308Proto-Oncogene Proteins c-fosReceptor, Cholecystokinin BaccumbensamygdalaanxietyCCKdepressionmPFC

Identifiers

PMID24623766
PMCPMC3951691
OpenAlexW2003443050

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.