Evidence map›Paper›PMID 39887668›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

α-Lipoic Acid Ameliorates Arsenic-Induced Lipid Disorders by Promoting Peroxisomal β-Oxidation and Reducing Lipophagy in Chicken Hepatocyte.

Yangfei Zhao, Mingyue Guo, Ting Pei, Chenqi Shang, Yirong Chen, Liying Zhao, Yiguang Lu, Chen Liang, Jundong Wang, Jianhai Zhang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Compound Abrus cantoniensis Extract Alleviates AFBAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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.

Yangfei ZhaoCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Mingyue GuoCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Ting PeiCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Chenqi ShangCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Yirong ChenCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Liying ZhaoCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Yiguang LuCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Chen LiangCollege of Animal Science, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Jundong WangCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.
Jianhai ZhangCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi, 030801, China.ORCID https://orcid.org/0000-0001-6005-8376

Funding

Earmarked Fund for Modern Agro-industry Technology Research SystemFundamental Research Program of Shanxi Province 20210302124063Fundamental Research Program of Shanxi Province 202403021211193National Key Research and Development Program of China 2023YFD1801100National Natural Science Foundation of China 32072934Research Project Supported by Shanxi Scholarship Council of China 2022-101Top Youth Talent Plan of Shanxi Province 2019
6 · The paper itself

Abstract

Liver disease poses a significant threat to global public health, with arsenic (As) recognized as a major environmental toxin contributing to liver injury. However, the specific mechanisms and the protective effects of α-lipoic acid (LA) remain unclear. Therefore, this study employs network toxicology and network pharmacology to comprehensively analyze the hepatotoxic mechanism of As and the hepatoprotective mechanism of LA, and further verifies the mechanisms of peroxisomal β-oxidation and lipophagy in the process. The network analysis results show that As induces liver damage mainly through autophagy, apoptosis, lipid metabolism, and oxidative stress, whereas LA exerts its hepatoprotective properties mainly by regulating lipid metabolism. Further verifications find that As inhibits SIRT1 expression, activates the P53 and Notch pathways, damages mitochondria, inhibits peroxisomal β-oxidation, increases lipid accumulation, and enhances lipophagy in the liver, while LA intervention alleviates As-induced lipid accumulation and enhances lipophagy by targeting SIRT1, ameliorating mitochondrial damage, enhancing peroxisomal β-oxidation, thereby alleviating As-induced liver damage. This study further clarifies the mechanism of As hepatotoxicity and provides a theoretical basis for LA as a potential hepatoprotective agent.

Indexed as

ArsenicAutophagyHepatocytesLipid MetabolismPeroxisomesThioctic AcidAnimalsChickensLiverOxidation-ReductionOxidative StressArsenicThioctic Acidalpha‐lipoic acidarsenichepatotoxicitylipophagyperoxisomal β‐oxidation

Identifiers

PMID39887668
PMCPMC11923885

What Socratic holds

Textmetadata
LicenceCC BY
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.