Evidence map›Paper›PMID 40918406›Full record

ArticleMediators of inflammation2025

Electroacupuncture Attenuates Hepatic Ischemia-Reperfusion Injury by Modulating the Esr1/TAK1-JNK/p38 Signaling Pathway in Rats.

Xiaofang Fan, Wei Guo, Xiaodan Yang, Hao Zhang, Bruno Fink, Lingyu Hu, Xiaoguang Wang

Abstract read
In one paragraph

Article in Mediators of inflammation, 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

7 authors.

Xiaofang FanFaculty of Graduate Studies, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang, China.ORCID https://orcid.org/0009-0000-4238-0652
Wei GuoFaculty of Graduate Studies, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang, China.ORCID https://orcid.org/0009-0001-9855-7952
Xiaodan YangDepartment of Surgery, The Second Affiliated Hospital of Jiaxing University, Jiaxing 314000, Zhejiang, China.ORCID https://orcid.org/0009-0001-3144-9199
Hao ZhangRhine-Nahr-Palatinate Heart and Vascular Center, Salinenstraße 35a, Bad Kreuznach 55543, Germany.ORCID https://orcid.org/0009-0003-7962-0957
Bruno FinkNoxygen Science Transfer and Diagnostics GmbH., Lindenmatte 42, Elzach 79215, Germany.ORCID https://orcid.org/0000-0003-1504-5132
Lingyu HuDepartment of Surgery, The Second Affiliated Hospital of Jiaxing University, Jiaxing 314000, Zhejiang, China.ORCID https://orcid.org/0000-0002-5698-7700
Xiaoguang WangFaculty of Graduate Studies, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang, China.ORCID https://orcid.org/0000-0002-3919-7109

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Electroacupuncture (EA) has demonstrated protective effects against hepatic ischemia-reperfusion injury (HIRI) in rat models. This study aimed to explore the underlying molecular mechanisms by which EA exerts its protective effects against HIRI. Gene expression microarray data from the Gene Expression Omnibus (GEO) database were analyzed to identify genes associated with HIRI, followed by differential expression analysis. Our results revealed that EA treatment significantly reduced serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, as well as myeloperoxidase (MPO) activity in liver tissues. Histological analysis indicated decreased necrotic areas and apoptosis in EA-treated liver tissues. Molecular assessments demonstrated that EA downregulated Esr1 expression and inhibited the activation of the TAK1-JNK/p38 signaling pathway, thereby reducing hepatocyte apoptosis and inflammatory responses. These findings suggest that EA serves as a potent therapeutic approach to alleviate HIRI by targeting the Esr1/TAK1-JNK/p38 signaling pathway.

Indexed as

ElectroacupunctureEstrogen Receptor alphaLiverMAP Kinase Kinase Kinasesp38 Mitogen-Activated Protein KinasesReperfusion InjuryAlanine TransaminaseAnimalsApoptosisAspartate AminotransferasesMaleMAP Kinase Kinase Kinase 7MAP Kinase Signaling SystemRatsRats, Sprague-DawleySignal TransductionAlanine TransaminaseAspartate AminotransferasesEstrogen Receptor alphaMAP Kinase Kinase Kinase 7MAP Kinase Kinase Kinasesp38 Mitogen-Activated Protein KinaseselectroacupunctureEsr1 genehepatic ischemia-reperfusion injuryhepatocyte apoptosisinflammation modulationTAK1–JNK/p38 signaling pathway

Identifiers

PMID40918406
PMCPMC12413952

What Socratic holds

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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.