Evidence map›Paper›PMID 31439031›Full record

ArticleMicrobiome2019

Gut microbiota from NLRP3-deficient mice ameliorates depressive-like behaviors by regulating astrocyte dysfunction via circHIPK2.

Yuan Zhang, Rongrong Huang, Mengjing Cheng, Lirui Wang, Jie Chao, Junxu Li, Peng Zheng, Peng Xie, Zhijun Zhang, Honghong Yao

Open access · goldAbstract read
In one paragraph

Article in Microbiome, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed, 3 pooled it
26.0field-weighted citation impact, top 1% 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

134 citing papers in PubMed, 3 syntheses or guidelines pooled it, 257 citations in OpenAlex.

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74 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

10 authors at 5 institutions in 2 countries.

Yuan ZhangDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Rongrong HuangDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Mengjing ChengDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Lirui WangSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China.
Jie ChaoDepartment of Physiology, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Junxu LiDepartment of Pharmacology and Toxicology, University at Buffalo, Buffalo, NY, USA.
Peng ZhengDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Peng XieDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Zhijun ZhangDepartment of Neurology of Affiliated ZhongDa Hospital, Institute of Neuropsychiatry of Southeast University, Nanjing, Jiangsu, China.
Honghong YaoDepartment of Pharmacology, School of Medicine, Southeast University, Nanjing, Jiangsu, China. yaohh@seu.edu.cn.
Southeast University · CNChongqing Medical University · CNChina Pharmaceutical University · CNUniversity at Buffalo, State University of New York · USZhongda Hospital Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammasomes have been found to interact with the gut microbiota, and this effect is associated with depression, but the mechanisms underlying this interaction have not been elucidated in detail.

resultsThe locomotor activity of NLRP3 KO mice was significantly greater than that of their WT littermates, while cohousing and transplantation of the NLRP3 KO gut microbiota avoid the effects of NLRP3 KO on the general locomotor activity at baseline. Meanwhile, transplantation of the NLRP3 KO microbiota alleviated the CUS-induced depressive-like behaviors. The compositions of the gut microbiota in NLRP3 KO mice and WT mice were significantly different in terms of the relative abundance of Firmicutes, Proteobacteria, and Bacteroidetes. Fecal microbiota transplantation (FMT) from NLRP3 KO mice significantly ameliorated the depressive-like behavior induced by chronic unpredictable stress (CUS) in recipient mice. Given the correlation between circular RNA HIPK2 (circHIPK2) and depression and the observation that the level of circHIPK2 expression was significantly increased in CUS-treated mice compared with that in the control group, further experiments were performed. FMT significantly ameliorated astrocyte dysfunction in recipient mice treated with CUS via inhibition of circHIPK2 expression.

conclusionsOur study illustrates the involvement of the gut microbiota-circHIPK2-astrocyte axis in depression, providing translational evidence that transplantation of the gut microbiota from NLRP3 KO mice may serve as a novel therapeutic strategy for depression.

Indexed as

Fecal Microbiota TransplantationGastrointestinal MicrobiomeAnimalsAstrocytesBehavior, AnimalDepressionMaleMiceMice, Inbred C57BLNLR Family, Pyrin Domain-Containing 3 ProteinProtein Serine-Threonine KinasesHipk2 protein, mouseNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseProtein Serine-Threonine KinasesAstrocytecircHIPK2DepressionGut microbiomeNLPR3

Identifiers

PMID31439031
PMCPMC6706943
OpenAlexW2969822493

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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.