Evidence map›Paper›PMID 41809881›Full record

ArticleWorld journal of gastroenterology2026

Xing-Pi-Qing-Gan decoction alleviates alcoholic liver disease by down-regulating

Na-Fei Huang, Ping Ling, Yu-Jie Xu, Xiao-Feng Feng, Yi Zheng, Tao Sun

Abstract read
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Article in World journal of gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Na-Fei HuangThe Second School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang Province, China.
Ping LingThe Second School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang Province, China.
Yu-Jie XuHangzhou School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang Province, China.
Xiao-Feng FengThe Second School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, Zhejiang Province, China.
Yi ZhengDepartment of Clinical Nutrition, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou 310005, Zhejiang Province, China.
Tao SunDepartment of Hepatology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou 310005, Zhejiang Province, China. 20171075@zcmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlcoholic liver disease (ALD) is driven by oxidative stress, lipid metabolism, inflammation, and apoptosis. Current therapies lack efficacy in targeting multi-pathway mechanisms. Xing-Pi-Qing-Gan decoction (XPQG) is an improved traditional Chinese medicine designed to alleviate ALD, but its molecular mechanism remains unknown.

aimTo illustrate the therapeutic targets and molecular pathways of XPQG for the treatment of ALD by integrating chemical profiling, network pharmacology, transcriptomics, and experimental verification

methodsThe components of XPQG were analyzed using ultra-high performance liquid chromatography quadrupole-time-of-flight mass spectrometry. Then, the protective effect of XPQG on ethanol-induced liver injury, especially its regulatory effect on

resultsIn ethanol-treated HepG2 cells, XPQG dose-dependently reduced the formation of lipid droplets, inhibited the expression of tumor necrosis factor-α, interleukin-6, interleukin-1β, and alleviated oxidative stress. In mice, XPQG (15.2 g/kg) lowered the liver/body weight ratio, alanine aminotransferase, aspartate aminotransferase, γ-glutamyl transferase; H&E and Oil Red O demonstrated a reduction in steatosis. Network pharmacology and RNA-seq converged on MAPK signaling, suggesting

conclusionIn summary, the results of the study suggest that XPQG is effective in improving ethanol-induced acute liver injury (ALD). Its mechanism involves the suppression of

Indexed as

Drugs, Chinese HerbalLiver Diseases, AlcoholicTranscription Factor CHOPAnimalsAntioxidantsDisease Models, AnimalDown-RegulationEthanolHeme Oxygenase-1Hep G2 CellsHumansLiverMaleMembrane ProteinsMiceMice, Inbred C57BLAntioxidantsDrugs, Chinese HerbalEthanolHeme Oxygenase-1Hmox1 protein, mouseMembrane ProteinsNFE2L2 protein, humanNF-E2-Related Factor 2Transcription Factor CHOPAlcoholic liver diseaseDDIT3Nrf2/HO-1Oxidative stressXing-Pi-Qing-Gan decoction

Identifiers

PMID41809881
PMCPMC12968574

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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.