Evidence map›Paper›PMID 42439331›Full record

ArticleEndocrine, metabolic & immune disorders drug targets2026

Mechanistic Study of Yibi Decoction in Treating Rheumatoid Arthritis

Chuanhong Huang, Shangtong Chen, Yueping Chen, Tian Xia

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

4 authors.

Chuanhong HuangGraduate Department, Guangxi University of Chinese Medicine, Nanning, Guangxi, 530000 China.ORCID 0009-0005-6729-6285
Shangtong ChenGraduate Department, Guangxi University of Chinese Medicine, Nanning, Guangxi, 530000 China.
Yueping ChenDepartment of Orthopedics and Hand Surgery, Ruikang Hospital affiliated to Guangxi University of Chinese Medicine, Nanning, Guangxi, 530011 China.
Tian XiaCollege of Orthopedics and Traumatology, Guangxi University of Chinese Medicine, Nanning, Guangxi, 530000 China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

objectiveTo investigate the therapeutic effects of Yibi Decoction (YBD) in rheumatoid arthritis (RA) and to elucidate the underlying mechanisms, with a particular focus on the JAK/STAT signaling pathway.

methodsNetwork pharmacology analysis was employed to predict the bioactive compounds and potential therapeutic targets of Yibi Decoction. A collagen-induced arthritis (CIA) rat model was established to validate the predicted effects

resultsNetwork pharmacology analysis identified 128 bioactive components in YBD, among which quercetin and luteolin were predicted to be key active compounds. In CIA rats, YBD treatment significantly downregulated the expression of IL-6, IL-17, IL-23, JAK2, and STAT3 in ankle joint tissues (P < 0.05), and markedly reduced serum levels of anti-cyclic citrullinated peptide (anti-CCP) antibodies and rheumatoid factor (P < 0.05). In parallel, the arthritis index was significantly decreased, and histopathological examination revealed substantial attenuation of synovial hyperplasia and cartilage destruction. DISCUSSION: These findings suggest that YBD exerts anti-rheumatoid arthritis effects through a multi-component, multi-target regulatory mechanism involving inhibition of the JAK/STAT signaling pathway. Quercetin and luteolin may contribute to these effects by suppressing pro-inflammatory cytokine production and ameliorating joint pathological changes.

conclusionYBD ameliorates rheumatoid arthritis by suppressing the JAK/STAT signaling pathway and associated inflammatory responses, thereby providing a mechanistic basis for its potential therapeutic application in rheumatoid arthritis.

Indexed as

Antirheumatic AgentsArthritis, ExperimentalArthritis, RheumatoidDrugs, Chinese HerbalJanus Kinase 2STAT3 Transcription FactorAnimalsMaleNetwork PharmacologyRatsRats, Sprague-DawleySignal TransductionAntirheumatic AgentsDrugs, Chinese HerbalJak2 protein, ratJanus Kinase 2Stat3 protein, ratSTAT3 Transcription FactorDecoctionIL17/IL23 axisimmunemediated diseasesJAK2/STAT3 signalingnetwork pharmacologyrheumatoid arthritistripterygium wilfordii

Identifiers

PMID42439331
PMCPMC13635966

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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.