Evidence map›Paper›PMID 41968707›Full record

ArticleEndocrine, metabolic & immune disorders drug targets2026

Stigmasterol, the Active Ingredient in Huanglian Decoction, Inhibits the MAOA-NF-κB-MLCK Pathway to Improve the Inflammation in Rats With Reflux Esophagitis.

Huan Wang, Lin Li, Jian Han, Yan Li, Jun Yang, Wangzhong Qiu, Liuhua Yao

Abstract read
In one paragraph

Article in Endocrine, metabolic & immune disorders drug targets, 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

7 authors.

Huan WangDepartment of Spleen and Stomach Diseases, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.ORCID 0000-0003-4908-8624
Lin LiDepartment of Laboratory, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.ORCID 0009-0006-7218-3506
Jian HanDepartment of Spleen and Stomach Diseases, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.ORCID 0009-0007-3974-580X
Yan LiDepartment of Spleen and Stomach Diseases, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.
Jun YangDepartment of Spleen and Stomach Diseases, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.ORCID 0009-0003-6651-7328
Wangzhong QiuDepartment of Spleen and Stomach Diseases, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.ORCID 0009-0000-9706-7807
Liuhua YaoDepartment of Spleen and Stomach Diseases, Yueyang Hospital of Traditional Chinese Medicine, Yueyang, China.ORCID 0009-0004-1156-743X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTraditional Chinese medicine (TCM) shows significant potential in treating reflux oesophagitis (RE).

methodsWe employed network pharmacology, metabolomics, and molecular docking to analyze the active ingredients and interaction targets of HD and RE. An

resultsNetwork pharmacology has identified monoamine oxidase A (MAOA) as a core target of HD in the treatment of RE. Metabolomic analysis revealed Stigmasterol to be the active component of HD. Functional studies demonstrated that HD and Stigmasterol enhanced cell viability in acid-exposed conditions, mitigated inflammation, and increased the expression of occludin, claudin- 1, and ZO-1, while simultaneously reducing levels of p-p65, MLCK, and MAOA. Molecular docking revealed that stigmasterol binds to MAOA. Notably, the protective effect of Stigmasterol on Het-1A was negated by the overexpression of MAOA. Furthermore, DISCUSSION: This study elucidates the role and mechanism of HD in RE. However, further clinical trials are needed to assess its applicability in clinical practice.

conclusionStigmasterol, the active ingredient in HD, inhibits the NF-κB-MLCK pathway via MAOA, thereby reducing RE-related cellular inflammation. This research offers novel insights for RE treatment.

Indexed as

Drugs, Chinese HerbalEsophagitis, PepticMonoamine OxidaseNF-kappa BStigmasterolAnimalsAnti-Inflammatory AgentsCell LineHumansInflammation MediatorsMaleMolecular Docking SimulationRatsRats, Sprague-DawleySignal TransductionAnti-Inflammatory AgentsDrugs, Chinese HerbalhuanglianInflammation MediatorsMonoamine OxidaseNF-kappa BStigmasterolHuanglian decoctionMAOANF-κB-MLCK pathwayReflux Esophagitis

Identifiers

PMID41968707
PMCPMC13591449

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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.