Evidence map›Paper›PMID 25603858›Full record

ArticleThe international journal of neuropsychopharmacology2015

NLRP3 Inflammasome Mediates Chronic Mild Stress-Induced Depression in Mice via Neuroinflammation.

Yi Zhang, Lei Liu, Yun-Zi Liu, Xiao-Liang Shen, Teng-Yun Wu, Ting Zhang, Wei Wang, Yun-Xia Wang, Chun-Lei Jiang

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
144citing papers in PubMed, 3 pooled it
7.2field-weighted citation impact, top 2% 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

144 citing papers in PubMed, 3 syntheses or guidelines pooled it, 309 citations in OpenAlex.

  1. Pooled it
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  3. Where do we stand on fMRI in awake mice?Cerebral cortex (New York, N.Y. : 1991) · 2024
    Pooled it
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84 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Yi ZhangLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Lei LiuLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Yun-Zi LiuLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Xiao-Liang ShenLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Teng-Yun WuLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Ting ZhangLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Wei WangLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Yun-Xia WangLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China.
Chun-Lei JiangLaboratory of Stress Medicine, Faculty of Psychology and Mental Health (Drs Y. Zhang, L. Liu, Y.-Z. Liu, X.-L. Shen, T.-Y. Wu, W. Wang, Y.-X. Wang, and C.-L. Jiang) and Department of Naval Aviation Medicine (Dr T. Zhang), Second Military Medical University, Shanghai, China. cljiang@vip.163.com cloudywang66@163.com.
Second Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence from both clinical and experimental research indicates that the immune-brain interaction plays a pivotal role in the pathophysiology of depression. A multi-protein complex of the innate immune system, the NLRP3 inflammasome regulates cleavage and secretion of proinflammatory cytokine interleukin-1β. The inflammasome detects various pathogen-associated molecule patterns and damage-associated molecule patterns, which then leads to a series of immune-inflammatory reactions.

methodsTo explore the role of inflammasome activation in the underlying biological mechanisms of depression, we established a mouse model of depression with unpredictable chronic mild stress.

resultsMice subjected to chronic mild stress for 4 weeks had significantly higher serum corticosterone levels, serum interleukin-1β levels, and hippocampal active interleukin-1β protein levels. They also displayed depressive-like symptoms, including decreased sucrose preference and increased immobility time. Moreover, the hippocampi of chronic mild stress-exposed mice had significantly higher activity of caspase-1, which accompanied by higher protein levels of NLRP3 and the apoptotic speck-containing protein with a card. Pretreatment with the NLRP3 inflammasome inhibitor VX-765 decreased serum and hippocampal levels of interleukin-1β protein and significantly moderated the depressive-like behaviors induced by chronic mild stress.

conclusionsThese data suggest the NLRP3 inflammasome mediates stress-induced depression via immune activation. Future procedures targeting the NLRP3 inflammasome may have promising effects in the prevention and treatment of depression.

Indexed as

AnimalsAntidepressive AgentsAnti-Inflammatory Agents, Non-SteroidalCarrier ProteinsCaspase 1Chronic DiseaseCorticosteroneDepressive DisorderDietary SucroseDipeptidesDisease Models, AnimalFood PreferencesHippocampusInflammationInterleukin-1betaMaleAntidepressive AgentsAnti-Inflammatory Agents, Non-SteroidalbelnacasanCarrier ProteinsCaspase 1CorticosteroneDietary SucroseDipeptidesIL1B protein, mouseInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousepara-Aminobenzoatesdepressioninflammationinterleukin-1βNLRP3 inflammasomestress

Identifiers

PMID25603858
PMCPMC4571628
OpenAlexW2145910522

What OpenQuestion holds

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LicenceCC BY-NC
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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.