Evidence map›Paper›PMID 36909723›Full record

ArticleFrontiers in cellular and infection microbiology2023

Tryptophan metabolism as bridge between gut microbiota and brain in chronic social defeat stress-induced depression mice.

Jing Xie, Wen-Tao Wu, Jian-Jun Chen, Qi Zhong, Dandong Wu, Lingchuan Niu, Sanrong Wang, Yan Zeng, Ying Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. TheFoods (Basel, Switzerland) · 2026
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  15. Frontiers in pharmacology · 2024
    Review
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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.

Jing XieChongqing Emergency Medical Center, Central Hospital of Chongqing University, Chongqing, China.
Wen-Tao WuInstitute of Life Sciences, Chongqing Medical University, Chongqing, China.
Jian-Jun ChenInstitute of Life Sciences, Chongqing Medical University, Chongqing, China.
Qi ZhongInstitute of Life Sciences, Chongqing Medical University, Chongqing, China.
Dandong WuDepartment of Rehabilitation, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Lingchuan NiuDepartment of Rehabilitation, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Sanrong WangDepartment of Rehabilitation, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yan ZengDepartment of Psychology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Ying WangDepartment of Rehabilitation, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Chongqing Medical University · CNDalian Medical University · CNChongqing Emergency Medical Center · CNSecond Affiliated Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Backgrounds: Gut microbiota plays a critical role in the onset and development of depression, but the underlying molecular mechanisms are unclear. This study was conducted to explore the relationships between gut microbiota and host's metabolism in depression. Methods: Chronic social defeat stress (CSDS) model of depression was established using C57BL/6 male mice. Fecal samples were collected from CSDS group and control group to measure gut microbiota and microbial metabolites. Meanwhile, tryptophan metabolism-related metabolites in hippocampus were also analyzed. Results: CSDS successfully induced depressive-like behaviors in CSDS group. The 24 differential bacterial taxa between the two groups were identified, and 14 (60.87%) differential bacterial taxa belonged to phylum Firmicutes. Functional analysis showed that tryptophan metabolism was significantly affected in CSDS mice. Meanwhile, 120 differential microbial metabolites were identified, and two key tryptophan metabolism-related metabolites (tryptophan and 5-hydroxytryptophan (5-HTP)) were significantly decreased in feces of CSDS mice. The correlation analysis found the significant relationships between tryptophan and differential bacterial taxa under Firmicutes, especially genus Conclusions: Our results showed that tryptophan metabolism might have an important role in the crosstalk between gut microbioa and brain in depression, and phylum Firmicutes, especially genus

Indexed as

DepressionGastrointestinal MicrobiomeAnimalsBacteriaBrainMaleMiceMice, Inbred C57BLSocial DefeatStress, PsychologicalTryptophanTryptophandepressionFirmicutesgut microbiotaLactobacillustryptophan

Identifiers

PMID36909723
PMCPMC9999000
OpenAlexW4321787654

What OpenQuestion holds

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LicenceCC BY
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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.