Evidence map›Paper›PMID 31723165›Full record

ArticleScientific reports2019

Social defeat stress-specific increase in c-Fos expression in the extended amygdala in mice: Involvement of dopamine D1 receptor in the medial prefrontal cortex.

Chisato Numa, Hirotaka Nagai, Masayuki Taniguchi, Midori Nagai, Ryota Shinohara, Tomoyuki Furuyashiki

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 70 citations in OpenAlex.

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  14. Sexual differentiation of neural mechanisms of stress sensitivity during puberty.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Review
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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

6 authors at 2 institutions in 2 countries.

Chisato NumaDivision of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.ORCID http://orcid.org/0000-0001-7744-8434
Hirotaka NagaiDivision of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.ORCID http://orcid.org/0000-0003-0983-8670
Masayuki TaniguchiDivision of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Midori NagaiDivision of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.
Ryota ShinoharaDivision of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan.ORCID http://orcid.org/0000-0001-5279-2642
Tomoyuki FuruyashikiDivision of Pharmacology, Graduate School of Medicine, Kobe University, Kobe, 650-0017, Japan. tfuruya@med.kobe-u.ac.jp.
Japan Agency for Medical Research and Development · JPYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We recently reported that dopamine D1 receptor in the medial prefrontal cortex (mPFC) is activated by subthreshold social defeat stress and suppresses the induction of depressive-like behavior in mice. However, which mPFC projection(s) mediates this antidepressant-like effect remains poorly understood. Here we show that social defeat stress specifically increased c-Fos expression, a marker for neuronal activity, in distinct brain regions involved in emotional regulation, relative to novelty-induced exploration. Among these brain areas, D1 knockdown in the mPFC decreased social defeat stress-induced c-Fos expression in the interstitial nucleus of the posterior limb of the anterior commissure (IPAC), a subregion of the extended amygdala. Using retrograde adeno-associated virus vectors and transgenic mice expressing Cre recombinase under the D1 promoter, we also found that D1-expressing deep-layer pyramidal neurons in the mPFC send direct projections to the IPAC. These findings indicate that social defeat stress specifically activates neurons in distinct brain areas, among which the IPAC is regulated by dopamine D1 receptor in the mPFC perhaps through direct projections. Thus, this study provides hints toward identifying neural circuits that underlie antidepressant-like effects of stress-induced dopamine D1 receptor signaling in the mPFC.

Indexed as

Behavior, AnimalSocial BehaviorStress, PsychologicalAmygdalaAnimalsBenzazepinesDopamine AgonistsMaleMiceMice, Inbred C57BLMice, Inbred ICRPrefrontal CortexProto-Oncogene Proteins c-fosReceptors, Dopamine D1BenzazepinesDopamine AgonistsDrd1 protein, mouseProto-Oncogene Proteins c-fosReceptors, Dopamine D1SK&F 81297

Identifiers

PMID31723165
PMCPMC6854085
OpenAlexW2986069316

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.