Evidence map›Paper›PMID 35928791›Full record

ArticleFrontiers in behavioral neuroscience2022

Mouse Model of Weak Depression Exhibiting Suppressed cAMP Signaling in the Amygdala, Lower Lipid Catabolism in Liver, and Correlated Gut Microbiota.

Kousuke Shimada, Masakatsu Nohara, Akihito Yasuoka, Asuka Kamei, Fumika Shinozaki, Kaori Kondo, Ryo Inoue, Takashi Kondo, Keiko Abe

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The Molecular Gut-Brain Axis in Early Brain Development.International journal of molecular sciences · 2022
    Review
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

9 authors at 4 institutions in 1 country.

Kousuke ShimadaGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Masakatsu NoharaGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Akihito YasuokaGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Asuka KameiGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Fumika ShinozakiGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Kaori KondoGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Ryo InoueLaboratory of Animal Science, Kyoto Prefectural University, Kyoto, Japan.
Takashi KondoGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Keiko AbeGroup for Food Functionality Assessment, Kanagawa Institute of Industrial Science and Technology, Kawasaki, Japan.
Kanagawa Institute of Technology · JPRIKEN Center for Integrative Medical Sciences · JPKyoto Prefectural University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To establish a mouse model of weak depression, we raised 6-week-old C57BL/6N mice in single (SH) or group housing (GH) conditions for 2 weeks. The SH group showed less social interaction with stranger mice, learning disability in behavioral tests, and lower plasma corticosterone levels. The cecal microbiota of the SH group showed significant segregation from the GH group in the principal coordinate analysis (PCoA). Transcriptome analysis of the amygdala and liver detected multiple differentially expressed genes (DEGs). In the amygdala of SH mice, suppression of the cyclic adenine monophosphate (cAMP) signal was predicted and confirmed by the reduced immunoreactivity of phosphorylated cAMP-responsive element-binding protein. In the liver of SH mice, downregulation of beta-oxidation was predicted. Interestingly, the expression levels of over 100 DEGs showed a significant correlation with the occupancy of two bacterial genera,

Indexed as

amygdalacorticosteronecyclic adenosine monophosphate (cAMP)depressionmicrobiotanicotinamide adenine dinucleotide

Identifiers

PMID35928791
PMCPMC9345170
OpenAlexW4280593560

What OpenQuestion holds

Textmetadata
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.