Evidence map›Paper›PMID 40753152›Full record

ArticleTranslational psychiatry2025

Chronic stress in mice: how gut bacteria influence gene activity in key brain neurons.

Wenxia Jiang, Yifan Li, Jie Yang, Xunmin Tan, Ruimin Tian, Guojing Ma, Jing Wu, Jianping Zhang, Yu Huang, Ping Liu and 8 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

18 authors.

Wenxia JiangDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yifan LiDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jie YangDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Xunmin TanDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Ruimin TianDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Guojing MaDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jing WuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jianping ZhangDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID http://orcid.org/0009-0000-2999-2945
Yu HuangDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID http://orcid.org/0000-0003-2493-3879
Ping LiuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Minghao YuanDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Xiaodong SongDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Leyao LuoDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Xingyu ZhouDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID http://orcid.org/0009-0003-1320-5603
Hongzhou ZuoDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Ma-Li WongDepartment of Psychiatry, College of Medicine, SUNY Upstate Medical University, Syracuse, NY, USA.
Julio LicinoDepartment of Psychiatry, Cornell University, Ithaca, NY, USA.
Peng ZhengDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China. pengzheng_cqmu@yeah.net.ORCID http://orcid.org/0000-0002-9864-6832

Funding

China Postdoctoral Science Foundation 2024MD754023
6 · The paper itself

Abstract

Major depressive disorder (MDD) is a serious mental disorder. Increasing evidence suggests that changes of gut microbiota are involved in pathogenesis of depression, yet the underlying mechanisms remains unknown. Here, chronic unpredictable mild stress (CUMS) mice model was constructed to mimic depression. We characterized the microbial composition and function of control, bedding exchange, and CUMS mice through 16S rRNA gene and metagenomic sequencing. Additionally, single-nucleus RNA sequencing (snRNA-seq) was used to compare the transcriptomic changes in the hypothalamus of these three groups. We found that replacing the bedding of CUMS mice with that of control mice could reverse the depressive-like behaviors. The microbial signatures of bedding exchange group trended towards the control group at the genus level. The abundance of g_norank_f_Muribaculaceae significantly increased in the bedding exchange group compared to CUMS group. Meanwhile, we found that the CUMS mice were characterized by cell-specific transcriptomic changes in hypothalamus. Notably, the transcriptomes of excitatory neurons in the hypothalamus were mainly affected, and these changes could be effectively reversed by bedding exchange treatment. The gene modules analysis revealed that the gut microbiota mainly modulated glyoxylate and dicarboxylate metabolism as well as arginine biosynthesis in hypothalamic excitatory neurons. Our findings provide new insights into the pathogenesis of depression.

Indexed as

Gastrointestinal MicrobiomeHypothalamusMajor Depressive DisorderNeuronsStress, PsychologicalAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLRNA, Ribosomal, 16STranscriptomeRNA, Ribosomal, 16S

Identifiers

PMID40753152
PMCPMC12318120

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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.