Evidence map›Paper›PMID 34026284›Full record

ArticleJournal of advanced research2021

Comprehensive analysis of the lysine acetylome and succinylome in the hippocampus of gut microbiota-dysbiosis mice.

Lanxiang Liu, Haiyang Wang, Xuechen Rao, Ying Yu, Wenxia Li, Peng Zheng, Libo Zhao, Chanjuan Zhou, Juncai Pu, Deyu Yang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of advanced research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 18% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

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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

15 authors at 4 institutions in 1 country.

Lanxiang LiuDepartment of Neurology, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, China.
Haiyang WangCollege of Stomatology and Affiliated Stomatological Hospital of Chongqing Medical University, 401147, China.
Xuechen RaoNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Ying YuNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Wenxia LiNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Peng ZhengNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Libo ZhaoDepartment of Neurology, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, China.
Chanjuan ZhouNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Juncai PuNHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Deyu YangDepartment of Neurology, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, China.
Liang FangDepartment of Neurology, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, China.
Ping JiCollege of Stomatology and Affiliated Stomatological Hospital of Chongqing Medical University, 401147, China.
Jinlin SongCollege of Stomatology and Affiliated Stomatological Hospital of Chongqing Medical University, 401147, China.
Hong WeiDepartment of Laboratory Animal Science, College of Basic Medical Sciences, Third Military Medical University, Chongqing 400038, China.
Peng XieDepartment of Neurology, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, China.
The Affiliated Yongchuan Hospital of Chongqing Medical University · CNStomatological Hospital of Chongqing Medical University · CNChongqing Medical University · CNArmy Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Major depressive disorder is caused by gene-environment interactions, and the host microbiome has been recognized as an important environmental factor. However, the underlying mechanisms of the host-microbiota interactions that lead to depression are complex and remain poorly understood. Objectives: The present study aimed to explore the possible mechanisms underlying gut microbiota dysbiosis-induced depressive-like behaviors. Methods: We used high-performance liquid chromatography-tandem mass spectrometry to analyze alterations in the hippocampal lysine acetylome and succinylome in male mice that had received gut microbiota from fecal samples of either patients with major depressive disorder or healthy controls. This was followed by bioinformatic analyses. Results: A total of 315 acetylation sites on 223 proteins and 624 succinylation sites on 494 proteins were differentially expressed in the gut microbiota-dysbiosis mice. The significantly acetylated proteins were primarily associated with carbon metabolism disruption and gene transcription suppression, while the synaptic vesicle cycle and protein translation were the most significantly altered functions for succinylated proteins. Additionally, our findings suggest that gut microbiota dysbiosis disturbs mitochondria-mediated biological processes and the MAPK signaling pathway through crosstalk between acetylation and succinylation on relevant proteins. Conclusions: This is the first study to demonstrate modifications in acetylation and succinylation in gut microbiota-dysbiosis mice. Our findings provide new avenues for exploring the pathogenesis of gut microbiota dysbiosis-related depression, and highlight potential targets for depression treatment.

Indexed as

Gastrointestinal MicrobiomeAcetylationAnimalsChromatography, High Pressure LiquidDepressionDysbiosisFecal Microbiota TransplantationGene-Environment InteractionHippocampusHumansLysineMajor Depressive DisorderMaleMiceProtein Processing, Post-TranslationalProteomeLysineProteomeSuccinic AcidAcetylationDepressionGut microbiotaHippocampusPosttranslational modificationsSuccinylation

Identifiers

PMID34026284
PMCPMC8132208
OpenAlexW3113068769

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.