Evidence map›Paper›PMID 40346552›Full record

ArticleBMC musculoskeletal disorders2025

LC-MS/MS based metabolomics reveals the mechanism of skeletal muscle regeneration.

Lei Yi, Kaiming Wang, Sui Liufu, Wenwu Chen, Bohe Chen, Xiaolin Liu, Caihong Liu, Jingwen Liu, Xin Xu, Haiming Ma

Abstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

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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

10 authors.

Lei YiCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Kaiming Wang *College of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Sui LiufuCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Wenwu ChenCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Bohe ChenCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Xiaolin LiuCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Caihong LiuCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Jingwen LiuCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Xin XuCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China.
Haiming MaCollege of Animal Science and Technology, Hunan Agricultural University, Changsha, PR, 410128, China. mahaiming2000@163.com.

Funding

Biological Breeding-National Science and Technology Major Project No.2023ZD04046Hunan Provincial Department of Education Scientific Research Project 23B1097Major Science and Technology Special Plan of Yunnan Province 202202AE090032Postgraduate Scientific Research Innovation Project of Hunan Agriculture University 2023XC006Postgraduate Scientific Research Innovation Project of Hunan Province CX20230713Research and Application of Key Technologies for High-Efficiency Breeding of Tibetan Pigs XZ202501ZY0143Research and Application of Superior Germplasm Resources and Key Technologies for Efficient Breeding of Tibetan Pigs SNQYKJXT-01The program of talent of science & technology and platforms of Yunnan Province 202305AF150211
6 · The paper itself

Abstract

backgroundSkeletal muscle possesses a robust regenerative capacity and can effectively repair itself following injury. However, research on the metabolic changes during skeletal muscle regeneration in large animals remains relatively limited. Therefore, in this study, we used pigs as a model and applied non-targeted LC-MS/MS metabolomic technology to reveal the metabolic changes during skeletal muscle regeneration, and conducted an in-depth exploration of important signaling pathways, which can provide a reference for further research on the mechanisms promoting skeletal muscle regeneration.

methodsIn this study, we used 18 piglets aged 35 days and weighing 7.10 ± 0.90 kg to construct a skeletal muscle regeneration model. These piglets were randomly divided into three treatment groups (n = 6) and injected with cardiotoxins (CTX) in the right longissimus dorsi muscle. They were euthanized on the 1st, 4th, and 16th days post-injection to collect right longissimus dorsi muscle samples as the treatment group. Additionally, the left longissimus dorsi muscle of piglets on the 4th day post-injection was selected as the control group. Phenotypic changes in skeletal muscle regeneration were determined through H&E staining, immunofluorescence, and Western Blot analysis, and LC-MS/MS untargeted metabolomics technology was utilized to explore the differential expressed metabolites (DEMs) involved in skeletal muscle regeneration.

resultsPhenotyping results showed that the regeneration model showed 3 stages of inflammation, regeneration and remodeling, which indicated successful model construction. Non-targeted LC-MS/MS metabolomics analysis showed significant differences in the structure of metabolites in these 3 stages. (1) In the inflammatory stage, a total of 198 DEMs were identified, which were mainly enriched in the pathways regulating the inflammatory response. (2) in the repair stage, 264 DEMs were identified, which were mainly enriched in pathways that inhibit inflammatory response and promote protein synthesis. (3) During the remodeling stage, 102 DEMs were identified, which were mainly enriched in the pathways that inhibit protein depletion and promote protein deposition. Temporal expression analysis revealed metabolites consistent with changes in the skeletal muscle regeneration process and found that these metabolite functions were mainly enriched in inhibiting inflammatory responses, alleviating myofibrillar lysis, and promoting muscle growth. Among them, (R)-Lipoic acid, 8-Hydroxyguanosine, and Uridine 5'-monophosphate maybe key metabolites associated with skeletal muscle regeneration.

conclusionThe skeletal muscle regeneration mechanism was systematically explored, and the metabolite time series analysis during skeletal muscle regeneration revealed some key metabolites that reflect the degree of skeletal muscle damage.

Indexed as

MetabolomicsMuscle, SkeletalRegenerationAnimalsChromatography, LiquidLiquid Chromatography-Mass SpectrometrySignal TransductionSwineTandem Mass SpectrometryLC-MS/MSMetabolomicsSkeletal muscle regeneration

Identifiers

PMID40346552
PMCPMC12065226

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.