Evidence map›Paper›PMID 41194697›Full record

ArticleAnnals of medicine2025

ACT001 alleviates MASLD through gut microbiota-bile acid-FXR axis in mice.

Bin Niu, Jing Liu, Hui Zhou, Weike Chu, Xue Wu, Yibing Zhou, Ze Chen, Yonggang Liu, Yuqiang Mi, Ping Li

Abstract read
In one paragraph

Article in Annals of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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.

Bin NiuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Jing LiuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.ORCID 0009-0002-7077-4784
Hui ZhouClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Weike ChuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Xue WuClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Yibing ZhouClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Ze ChenClinical School of the Second People's Hospital, Tianjin Medical University, Tianjin, China.
Yonggang LiuDepartment of Pathology, Tianjin Second People's Hospital, Tianjin, China.
Yuqiang MiDepartment of Hepatology, Tianjin Second People's Hospital, Tianjin, China.
Ping LiDepartment of Hepatology, Tianjin Second People's Hospital, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveACT001 is a novel sesquiterpene lactone derivative with noteworthy antineoplastic and anti-inflammatory properties. This study aimed to investigate the efficacy of ACT001 against metabolic dysfunction associated steatotic liver disease (MASLD) pathogenesis in two established murine models, and to elucidate its regulatory role in the gut microbiota-bile acid-FXR axis. MATERIALS AND

methodsA high-fat diet (HFD) and a methionine-choline-deficient (MCD) diet induced two MASLD models in C57BL/6J mice. Histological analysis was performed, biochemical indices were measured, and the expression of tight junctions and farnesoid X receptor (FXR)-related pathways was detected. Gut microbiota was assessed by 16S rDNA sequencing, while bile acids (BAs) in fecal samples were analyzed using UPLC/MS-MS.

resultsACT001 decreased liver injury, alleviated hepatic lipid accumulation, and restored intestinal barrier integrity. Furthermore, 16S rDNA illustrated that ACT001 could partially rebalance intestinal dysbacteriosis and upregulate the relative abundance of various bacteria, especially

conclusionACT001 exerted a multifactorial therapeutic effect on MASLD, potentially linked to the regulation of the gut microbiota-BAs-FXR axis. Thus, it has the potential to be an effective treatment for MASLD.

Indexed as

Bile Acids and SaltsFatty LiverGastrointestinal MicrobiomeLactonesNon-alcoholic Fatty Liver DiseaseReceptors, Cytoplasmic and NuclearSesquiterpenesAnimalsDiet, High-FatDisease Models, AnimalLiverMaleMiceMice, Inbred C57BLReceptor, Farnesoid X-ActivatedBile Acids and SaltsLactonesReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearSesquiterpenesACT001bile acidfarnesoid X receptorgut microbiotaMASLD

Identifiers

PMID41194697
PMCPMC12599161

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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 OpenQuestion graph.