Evidence map›Paper›PMID 38195757›Full record

ArticleCommunications biology2024

Oral D-ribose causes depressive-like behavior by altering glycerophospholipid metabolism via the gut-brain axis.

Ke Xu, Yi Ren, Shuang Zhao, Jinzhou Feng, Qingyuan Wu, Xue Gong, Jianjun Chen, Peng Xie

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.1field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  20. Supplemental effects ofFrontiers in immunology · 2024
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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

8 authors at 4 institutions in 2 countries.

Ke XuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, 400016, Chongqing, China.ORCID 0000-0002-7689-750X
Yi RenDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, 400016, Chongqing, China.
Shuang ZhaoDepartment of Infectious Diseases, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, Institute for Viral Hepatitis, The Second Affiliated Hospital of Chongqing Medical University, 400010, Chongqing, China.
Jinzhou FengDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, 400016, Chongqing, China.
Qingyuan WuNational Health Commission Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, 400016, Chongqing, China.
Xue GongNational Health Commission Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, 400016, Chongqing, China.
Jianjun ChenInstitute of Life Sciences, Chongqing Medical University, 400016, Chongqing, China. chenjianjun@cqmu.edu.cn.ORCID 0000-0002-6439-5123
Peng XieDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, 400016, Chongqing, China. xiepeng@cqmu.edu.cn.ORCID 0000-0002-0081-6048
The Affiliated Yongchuan Hospital of Chongqing Medical University · CNChongqing Medical University · CNChongqing Three Gorges Central Hospital · CNDalian Medical University · CN

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

Our previous work has shown that D-ribose (RIB)-induced depressive-like behaviors in mice. However, the relationship between variations in RIB levels and depression as well as potential RIB participation in depressive disorder is yet unknown. Here, a reanalysis of metabonomics data from depressed patients and depression model rats is performed to clarify whether the increased RIB level is positively correlated with the severity of depression. Moreover, we characterize intestinal epithelial barrier damage, gut microbial composition and function, and microbiota-gut-brain metabolic signatures in RIB-fed mice using colonic histomorphology, 16 S rRNA gene sequencing, and untargeted metabolomics analysis. The results show that RIB caused intestinal epithelial barrier impairment and microbiota-gut-brain axis dysbiosis. These microbial and metabolic modules are consistently enriched in peripheral (fecal, colon wall, and serum) and central (hippocampus) glycerophospholipid metabolism. In addition, three differential genera (Lachnospiraceae_UCG-006, Turicibacter, and Akkermansia) and two types of glycerophospholipids (phosphatidylcholine and phosphatidylethanolamine) have greater contributions to the overall correlations between differential genera and glycerophospholipids. These findings suggest that the disturbances of gut microbiota by RIB may contribute to the onset of depressive-like behaviors via regulating glycerophospholipid metabolism, and providing new insight for understanding the function of microbiota-gut-brain axis in depression.

Indexed as

Brain-Gut AxisGastrointestinal MicrobiomeAnimalsGlycerophospholipidsHumansLipid MetabolismMiceRatsRiboseGlycerophospholipidsRibose

Identifiers

PMID38195757
PMCPMC10776610
OpenAlexW4390746322

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.