Evidence map›Paper›PMID 39421970›Full record

ArticleAnnals of medicine2024

Limosilactobacillus-related 3-OMDP as a potential therapeutic target for depression.

Qi Zhong, Wentao Wu, Jing Xie, Jiao-Lin Wang, Ke Xu, Yi Ren, Jianjun Chen, Peng Xie

Abstract read
In one paragraph

Article in Annals of medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Impact of gut microbiota on endometriosis: linking physical injury to mental health.Frontiers in cellular and infection microbiology · 2025
    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

8 authors.

Qi ZhongInstitute of Neuroscience, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, China.
Wentao WuInstitute of Neuroscience, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, China.
Jing XieChongqing Emergency Medical Center, Central Hospital of Chongqing University, Chongqing, China.
Jiao-Lin WangInstitute of Neuroscience, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, China.
Ke XuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Yi RenDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jianjun ChenInstitute of Neuroscience, School of Basic Medical Sciences, Chongqing Medical University, Chongqing, China.
Peng XieDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID 0000-0002-0081-6048

Funding

Predicting implementation from organizational readiness to changeI01HX000214 · VA · VA PUGET SOUND HEALTHCARE SYSTEM · PI BLEVINS, DEAN, HELFRICH, CHRISTIAN D · 2011 to 2013
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HSRD VA I01 HX000214
6 · The paper itself

Abstract

objectiveGut microbiota was closely involved in the pathogenesis of depression, but the underlying molecular mechanisms in depression remained unclear. This study was conducted to investigate the relationship between neurotransmitters/inflammatory factors and gut microbiota in depressed mice. MATERIALS AND

methodsA chronic social defeat stress (CSDS) depression model was established. Gut microbial composition was detected in faeces, neurotransmitters were detected in faeces, colon, blood and hippocampus, and inflammatory factors were detected in hippocampus. After a key neurotransmitter was identified, intervention experiment was conducted to explore whether it could improve depressive-like behaviours.

resultsSix differential genera in faeces, 14 differential neurotransmitters in gut-brain axis, and two differential inflammatory factors (interleukin-1 beta (IL-1β) and interleukin-6 (IL-6)) in hippocampus were identified in depressed mice. There were significant correlations among differential genera, differential neurotransmitters and IL-1β/IL-6. Among these differential neurotransmitters, 3-O-Methyldopa (3-OMDP) was found to be consistently decreased in faeces, colon, blood and hippocampus, and 3-OMDP was significantly correlated to Limosilactobacillus and IL-1β. After receiving 3-OMDP, the depressive-like behaviours in depressed mice were improved and the increased IL-1β/IL-6 levels were reversed.

conclusionsThese results indicated that gut microbiota might affect host's inflammation levels in brain through regulating neurotransmitters, eventually leading to the onset of depression. 'Limosilactobacillus-3-OMDP-IL-1β/IL-6' might be a potential pathway in the crosstalk of gut and brain, and 3-OMDP held the promise as a therapeutic target for depression.

Indexed as

DepressionDisease Models, AnimalGastrointestinal MicrobiomeHippocampusAnimalsBehavior, AnimalBrain-Gut AxisFecesInterleukin-1betaInterleukin-6MaleMiceMice, Inbred C57BLNeurotransmitter AgentsStress, PsychologicalIL1B protein, mouseInterleukin-1betaInterleukin-6Neurotransmitter AgentsDepressiongut microbiotainflammatoryneurotransmitters

Identifiers

PMID39421970
PMCPMC11492388

What OpenQuestion holds

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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.