Evidence map›Paper›PMID 25774879›Full record

ArticlePloS one2015

Hepatocyte nuclear factor 4 alpha is a key factor related to depression and physiological homeostasis in the mouse brain.

Kyosuke Yamanishi, Nobutaka Doe, Miho Sumida, Yuko Watanabe, Momoko Yoshida, Hideyuki Yamamoto, Yunfeng Xu, Wen Li, Hiromichi Yamanishi, Haruki Okamura and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Comparative rhythmic transcriptome profiling of human and mouse striatal subregions.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  3. Molecular Mechanisms of IL18 in Disease.International journal of molecular sciences · 2023
    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

11 authors at 2 institutions in 1 country.

Kyosuke YamanishiDepartment of Neuropsychiatry, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan; Hirakata General Hospital for Developmental Disorders, Hirakata, Osaka, Japan.
Nobutaka DoeLaboratory of Neurogenesis and CNS Repair, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan; Section of Behavioral Science, Kouiken Co., Ltd., Akashi, Hyogo, Japan.
Miho SumidaSection of Behavioral Science, Kouiken Co., Ltd., Akashi, Hyogo, Japan.
Yuko WatanabeHirakata General Hospital for Developmental Disorders, Hirakata, Osaka, Japan.
Momoko YoshidaHirakata General Hospital for Developmental Disorders, Hirakata, Osaka, Japan.
Hideyuki YamamotoLaboratory of Tumor Immunology and Cell Therapy, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Yunfeng XuLaboratory of Tumor Immunology and Cell Therapy, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Wen LiLaboratory of Tumor Immunology and Cell Therapy, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Hiromichi YamanishiHirakata General Hospital for Developmental Disorders, Hirakata, Osaka, Japan.
Haruki OkamuraLaboratory of Tumor Immunology and Cell Therapy, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Hisato MatsunagaDepartment of Neuropsychiatry, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Hyogo Medical University · JPHiraka General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder (MDD) is a common psychiatric disorder that involves marked disabilities in global functioning, anorexia, and severe medical comorbidities. MDD is associated with not only psychological and sociocultural problems, but also pervasive physical dysfunctions such as metabolic, neurobiological and immunological abnormalities. Nevertheless, the mechanisms underlying the interactions between these factors have yet to be determined in detail. The aim of the present study was to identify the molecular mechanisms responsible for the interactions between MDD and dysregulation of physiological homeostasis, including immunological function as well as lipid metabolism, coagulation, and hormonal activity in the brain. We generated depression-like behavior in mice using chronic mild stress (CMS) as a model of depression. We compared the gene expression profiles in the prefrontal cortex (PFC) of CMS and control mice using microarrays. We subsequently categorized genes using two web-based bioinformatics applications: Ingenuity Pathway Analysis and The Database for Annotation, Visualization, and Integrated Discovery. We then confirmed significant group-differences by analyzing mRNA and protein expression levels not only in the PFC, but also in the thalamus and hippocampus. These web tools revealed that hepatocyte nuclear factor 4 alpha (Hnf4a) may exert direct effects on various genes specifically associated with amine synthesis, such as genes involved in serotonin metabolism and related immunological functions. Moreover, these genes may influence lipid metabolism, coagulation, and hormonal activity. We also confirmed the significant effects of Hnf4a on both mRNA and protein expression levels in the brain. These results suggest that Hnf4a may have a critical influence on physiological homeostasis under depressive states, and may be associated with the mechanisms responsible for the interactions between MDD and the dysregulation of physiological homeostasis in humans.

Indexed as

AnimalsCells, CulturedDepressionDisease Models, AnimalGene Expression ProfilingHepatocyte Nuclear Factor 4HippocampusHomeostasisMaleMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisPrefrontal CortexThalamusHepatocyte Nuclear Factor 4Hnf4a protein, mouse

Identifiers

PMID25774879
PMCPMC4361552
OpenAlexW2092716111

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.