Evidence map›Paper›PMID 41276549›Full record

ArticleScientific reports2025

IL-22 attenuates MAFLD progression by modulating oxidative stress and ferroptosis.

Suxia Li, Yaxi Zhang, Peipei Li, Xuan Xue, Lijuan Huo

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Suxia LiShanxi Medical University, Taiyuan, 03000, Shanxi, China.
Yaxi ZhangShanxi Medical University, Taiyuan, 03000, Shanxi, China.
Peipei LiShanxi Medical University, Taiyuan, 03000, Shanxi, China.
Xuan XueShanxi Medical University, Taiyuan, 03000, Shanxi, China.
Lijuan HuoDepartment of Gastroenterology, First Hospital of Shanxi Medical University, Taiyuan, 030000, Shanxi, China. mymail5296@163.com.

Funding

National Major Science and Technology Projects of China 2013ZX10002004
6 · The paper itself

Abstract

Metabolic-associated fatty liver disease (MAFLD) is a common liver disease in clinical practice and currently has limited standardized medications or treatments. The study aimed to evaluate the therapeutic effects of interleukin-22 (IL-22) on metabolic dysfunction-associated steatohepatitis (MASH) and fibrosis, and to explore its underlying molecular mechanisms. Male C57BL/6J mice were fed a choline-deficient, L-amino acid-defined, high-fat diet (CDAHFD) for 12 weeks and treated with different doses of IL-22 intraperitoneally. IL-22 treatment significantly reduced hepatic lipid accumulation, suppressed hepatic stellate cell (HSC) activation, and prevented liver fibrosis. It also attenuated oxidative stress, evidenced by elevated SOD levels and reduced ROS, MDA levels. Meanwhile, changes in mitochondria morphology, along with alterations in GSH and Fe

Indexed as

Fatty LiverFerroptosisInterleukinsOxidative StressAnimalsDiet, High-FatDisease Models, AnimalDisease ProgressionHepatic Stellate CellsInterleukin-22Lipid MetabolismLiverLiver CirrhosisMaleMiceMice, Inbred C57BLInterleukin-22InterleukinsNF-E2-Related Factor 2Reactive Oxygen SpeciesAML-12 cells.FerroptosisIL-22InflammationMetabolic-associated fatty liver diseaseOxidative stress

Identifiers

PMID41276549
PMCPMC12749523

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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.