Evidence map›Paper›PMID 40411313›Full record

ArticleJournal of gastroenterology and hepatology2025

Ileal FXR Knockdown Ameliorates MASLD Progression in Rats via Modulating Bile Acid Metabolism Mediated by Gut Microbiota.

Junjun Wang, Jiaqi Gao, Qingqing Zhang, Jingyi Lu, Yufei Yang, Xiaobo Cai, Hui Dong, Lungen Lu

Abstract read
In one paragraph

Article in Journal of gastroenterology and hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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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.

Junjun WangDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.
Jiaqi GaoDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.
Qingqing ZhangDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.
Jingyi LuDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.
Yufei YangDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.
Xiaobo CaiDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0000-0002-2450-6167
Hui DongDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.
Lungen LuDepartment of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0000-0003-4280-6662

Funding

National Natural Science Foundation of China 82170620Shanghai Municipal Hospital Development Center SHDC2022CRT011
6 · The paper itself

Abstract

BACKGROUND AND

aimMetabolic dysfunction associated steatotic liver disease (MASLD) is the predominant cause of chronic liver disease, with dysregulation of bile acid (BA) metabolism and intestinal microbiota being intricately associated with MASLD progression. In this study, we investigated the role of ileal FXR in MASLD progression and BA metabolism in portal blood.

methodsSprague-Dawley rats were fed a typical western diet for 20 weeks, followed by local perfusion of AAV2-shNr1h4 to downregulate Nr1h4 expression in ileum tissue. To investigate the effect of ileal FXR on BA reabsorption and gut microbiota, portal blood and cecal fecal samples were collected from MASLD rats injected with AAV2-Ctrl or AAV2-shNr1h4 for metabolomics targeting BAs and 16S rRNA sequencing analysis.

resultsOur results showed that hepatic steatosis and inflammation were alleviated, whereas the reabsorption of secondary BAs and unconjugated BAs into the portal blood was enhanced when ileal FXR was knocked down. Furthermore, knockdown of ileal FXR resulted in a significant alteration in composition of the cecal microbiota, characterized by an increasing abundance of microbes involved in secondary BA production, including Escherichia, Adlercreutzia, Eubacterium, and Clostridium.

conclusionThese findings suggest that downregulation of ileal FXR ameliorates the progression of MASLD in rats by modulating BA metabolism mediated by the gut microbiota, indicating that ileal FXR might be a potential therapeutic target for the treatment of MASLD.

Indexed as

Bile Acids and SaltsFatty LiverGastrointestinal MicrobiomeGene Knockdown TechniquesIleumReceptors, Cytoplasmic and NuclearAnimalsDisease Models, AnimalDisease ProgressionDown-RegulationMaleRatsRats, Sprague-DawleyReceptor, Farnesoid X-ActivatedBile Acids and SaltsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and Nuclearbile acid metabolismFXRgut microbiotaileumMASLD

Identifiers

PMID40411313
PMCPMC12315790

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.