Evidence map›Paper›PMID 42599179›Full record

ArticleJournal of Zhejiang University. Science. B2026

IL-1β pathway-dependent regulation of glutamate receptor activity by gut microbiota in bipolar depression.

Anying Tang, Yi Chen, Kaijing Ding, Jinyu Zhang, Le Xu, Wenhao Chen, Shaohua Hu, Jianbo Lai

Abstract read
In one paragraph

Article in Journal of Zhejiang University. Science. B, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Anying TangDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Yi ChenDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Kaijing DingAffiliated Mental Health Center & Hangzhou Seventh People's Hospital, Zhejiang University School of Medicine, Hangzhou 310013, China.
Jinyu ZhangDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Le XuDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Wenhao ChenDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Shaohua HuDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China. dorhushaohua@zju.edu.cn.
Jianbo LaiDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China. dorhushaohua@zju.edu.cn, laijianbo@zju.edu.cn.

Funding

the Fundamental Research Funds for the Central Universities 2023ZFJH01-01 and 2024ZFJH01-01the Key R&D Program of Zhejiang Province 2024C03098 and 2025C02109the Major Science and Technology Plan Guidance Project of Xiaoshan District 2023316the National Key Research and Development Program of China 2023YFC2506200 and 2023YFC2506203the National Natural Science Foundation of China 82571735 and 82471542the Research Project of Jinan Microecological Biomedicine Shandong Laboratory JNL-2023001B
6 · The paper itself

Abstract

objectivesNeuroinflammation may disrupt neurotransmitter signaling. This study investigated whether gut microbiota-induced neuroinflammation can regulate glutamate pathways in bipolar disorder (BD).

methodsFecal microbiota transplantation (FMT) was performed to observe behavioral changes in the antibiotic-treated C57BL/6J male mouse model of bipolar depression. Gut microbial structure, circulating, and prefrontal levels of inflammatory factors, microglial activation, and transcription levels of

resultsCompared with the control mice, "BD" mice displayed depression-like behaviors, with a lower diversity of gut bacteria and a decreased abundance of certain species. In addition, "BD" mice showed increased levels of inflammatory factors (e.g., IL-1β) in the serum and prefrontal cortex, microglial activation, and changes in the messenger RNA (mRNA) levels of

conclusionsThe findings suggest that gut microbiota may influence glutamate receptor gene expression via an IL-1β-dependent pathway in a mouse model of BD, potentially contributing to neuroinflammatory mechanisms relevant to this disorder.

Indexed as

Bipolar DisorderGastrointestinal MicrobiomeInterleukin-1betaReceptors, GlutamateAnimalsDisease Models, AnimalFecal Microbiota TransplantationInterleukin 1 Receptor Antagonist ProteinMaleMiceMice, Inbred C57BLMicrogliaReceptors, N-Methyl-D-AspartateSignal TransductionIL1B protein, mouseInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinReceptors, GlutamateReceptors, N-Methyl-D-AspartateBipolar disorderGlutamate receptorGut microbiotaInterleukin-1 (IL-1)Neuroinflammation

Identifiers

PMID42599179
PMCPMC13474199

What Socratic holds

Textmetadata
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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 Socratic graph.