Evidence map›Paper›PMID 41673803›Full record

ArticleBMC microbiology2026

Multi-omics analysis of the gut-liver axis revealed the effects of different exercise interventions in NAFLD mice.

Chao-Rui Hu, Chuan-Fei Zeng, Huan Li, Mingliang Wei, Shi-Qian Liu, Lian-Yun Li, Yong Xiao, Min Wu, Ming-Kai Chen

Abstract read
In one paragraph

Article in BMC microbiology, 2026. 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

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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Chao-Rui Hu *Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Chuan-Fei Zeng *Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Huan Li *Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Mingliang WeiFrontier Science Center for Immunology and Metabolism, Hubei Key Laboratory of Cell Homeostasis, Hubei Key Laboratory of Developmentally Originated Disease, College of Life Sciences, Taikang Center for Life and Medical Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Shi-Qian LiuDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Lian-Yun LiFrontier Science Center for Immunology and Metabolism, Hubei Key Laboratory of Cell Homeostasis, Hubei Key Laboratory of Developmentally Originated Disease, College of Life Sciences, Taikang Center for Life and Medical Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Yong XiaoDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Min WuFrontier Science Center for Immunology and Metabolism, Hubei Key Laboratory of Cell Homeostasis, Hubei Key Laboratory of Developmentally Originated Disease, College of Life Sciences, Taikang Center for Life and Medical Sciences, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China.
Ming-Kai ChenDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, Hubei, 430072, China. kaimingchen@163.com.

Funding

National Key Research and Development Program of China 2023YFA0913400National Key Research and Development Program of China 2023YFC2507405
6 · The paper itself

Abstract

backgroundGrowing evidence indicates that gut microbiota may play a potential role in NAFLD. Exercise was recognized as an effective intervention for NAFLD, but the effects of these exercise modalities on gut microbiota in NAFLD remain unclear.

resultsC57BL/6J mice were divided into a normal diet control group (NC) and a high-fat diet (HFD) group. After 8 weeks on the HFD, the mice were further divided into three groups: HFD, HFD + AE (HAE), and HFD + RE (HRE), and treated for 12 weeks. Body weight and liver weight of the mice were measured, and samples (blood, liver, colon, and feces) were collected for serum and liver biochemical analysis. RT-PCR was performed to analyze genes related to intestinal barrier function, along with 16 S rRNA gene sequencing and RNA-seq analysis. AE and RE effectively mitigated HFD-induced increases in body weight and liver weight in mice. Serum and liver lipid levels, as well as liver enzyme levels, were significantly reduced following AE and RE interventions. Additionally, HFD-induced gut microbiota dysbiosis was reversed by AE and RE interventions. These interventions increased the abundance of the beneficial bacterium Odoribacter while eliminating the harmful bacteria Mycoplasma and Lachnoclostridiumgan. Specifically, AE increased the abundance of beneficial Candidatus_Sacleftimonas and reduced harmful Enterococcus and Dubosiella, while RE enhanced beneficial Christensenellaceae_R-7_group and reduced harmful Streptococcus and Lactococcus, thus modifying intestinal metabolism. Transcriptomic analysis revealed that liver improvement through AE and RE was associated with lipid metabolism and inflammatory genes, which exhibited consistent changes with the gut microbiota.

conclusionAE and RE could effectively prevent HFD-induced NAFLD and might serve as a reference for understanding the contribution of the gut microbiota due to their effects on altering liver lipid metabolism and maintaining gut microbiota homeostasis. Meanwhile, we suggest that combining AE and RE may result in more significant improvements.

Indexed as

Gastrointestinal MicrobiomeLiverNon-alcoholic Fatty Liver DiseasePhysical Conditioning, AnimalAnimalsBacteriaBody WeightDiet, High-FatDisease Models, AnimalDysbiosisFecesLipid MetabolismMaleMiceMice, Inbred C57BLMultiomicsRNA, Ribosomal, 16SAerobic exerciseGut microbiotaNonalcoholic fatty liver diseaseResistance exercise

Identifiers

PMID41673803
PMCPMC12998337

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.