Evidence map›Paper›PMID 41692775›Full record

ArticleScientific reports2026

Ferrostatin 1 exerts multifaceted hepatic protection against alcoholic liver injury by inhibiting ferroptosis.

Linna Yu, Haihan Zhang, Yun Wang, Linting Xun, Xueru Zhao, Yu Liu, Anxing Zhang, Zhengji Song

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Ferroptosis in liver biology and diseases.Hepatology communications · 2026
    Review
  2. Article
  3. 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

8 authors.

Linna YuDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China.
Haihan ZhangDepartment of Radiology, Second Affiliated Hospital of Yunnan University of Traditional Chinese Medicine, Kunming, China.
Yun WangDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China.
Linting XunDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China.
Xueru ZhaoDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China.
Yu LiuDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China.
Anxing ZhangDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China.
Zhengji SongDepartment of Gastroenterology, The First People's Hospital of Yunnan Province, Kunming, China. song4715@163.com.

Funding

Yunnan Fundamental Research Projects 202301AU070167Yunnan Provincial Clinical Medicine Center for Digestive System Diseases 2024YNLCYXZX0111
6 · The paper itself

Abstract

While ferroptosis is implicated in alcoholic liver disease, its precise mechanisms of action are not fully defined. This study aims to investigate the protective role of the ferroptosis inhibitor Ferrostatin-1 (Fer-1) against alcoholic liver injury, exploring its underlying mechanisms. Using mice models of acute and chronic ethanol exposure, we assessed the effects of Fer-1. We evaluated liver function, histopathological damage, and key molecular markers related to ferroptosis, metabolism, and inflammation. Fer-1 significantly improved liver function and alleviated tissue damage, including lipid accumulation and fibrosis. It enhanced antioxidant capacity and reduced iron overload, oxidative stress, and lipid peroxidation. Furthermore, Fer-1 improved dysregulated iron and lipid metabolism and attenuated inflammation. Notably, these protective effects appear to be independent of the Nrf2/HO-1 pathway, autophagy, and NLRP3 inflammasome. Fer-1 exerts multi-faceted protection against alcoholic liver injury by specifically inhibiting ferroptosis. It blocks the vicious cycle of alcohol-induced metabolic imbalances, oxidative stress, and inflammation, offering new potential strategies for treating alcoholic liver disease.

Indexed as

CyclohexylaminesFerroptosisLiver Diseases, AlcoholicPhenylenediaminesAnimalsDisease Models, AnimalEthanolInflammasomesIronLipid MetabolismLipid PeroxidationLiverMaleMiceMice, Inbred C57BLNF-E2-Related Factor 2CyclohexylaminesEthanolferrostatin-1InflammasomesIronNF-E2-Related Factor 2NLR Family, Pyrin Domain-Containing 3 ProteinPhenylenediaminesAlcoholic liver injuryFerroptosisFerrostatin-1Inflammatory responseIron metabolismOxidative stress

Identifiers

PMID41692775
PMCPMC12996462

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.