Evidence map›Paper›PMID 42801243›Full record

ArticleJournal of inflammation research2026

Astragaloside IV Modulates the Immune Response in Rheumatoid Arthritis and is Associated with Inhibition of the NAV2-Wnt/β-Catenin Signaling Cascade.

Yao Ma, Qianyu Guo, Meie Liang, Zhen Li, Liyun Zhang

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Article in Journal of inflammation research, 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

5 authors.

Yao MaThe Third Clinical College, Shanxi University of Chinese Medicine, Jinzhong, 030619, People's Republic of China.
Qianyu GuoDepartment of Rheumatology and Immunology, Shanxi Medical University Third Hospital, Shanxi Bethune Hospital (Shanxi Academy of Medical Sciences), Tongji Shanxi Hospital, Taiyuan, 030032, People's Republic of China.
Meie LiangDepartment of Rheumatology and Immunology, Shanxi Medical University Third Hospital, Shanxi Bethune Hospital (Shanxi Academy of Medical Sciences), Tongji Shanxi Hospital, Taiyuan, 030032, People's Republic of China.ORCID 0009-0002-4724-5390
Zhen LiCollege of Basic Medical Sciences, Shanxi University of Chinese Medicine, Jinzhong, 030619, People's Republic of China.
Liyun ZhangThe Third Clinical College, Shanxi University of Chinese Medicine, Jinzhong, 030619, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by progressive joint destruction and systemic inflammation, with limited long-term efficacy and clinically important adverse effects of current treatments. Astragaloside IV (ASIV), the core active saponin component isolated from Objective: This study aimed to investigate whether ASIV alleviates RA by modulating the Methods: A collagen-induced arthritis (CIA) model was established in female Wistar rats. The animals were randomly divided into four groups (n=6 per group initially, final n=3 per group based on modeling success criteria): healthy controls (NOR group), CIA model (CIA group), methotrexate-treated (MTX group, positive control, 0.9 mg/kg/week), and ASIV-treated (ASIV group, 50 mg/kg/day). Following a 4-week intervention period initiated on day 14 post-primary immunization, we evaluated arthritis severity (arthritis scores, vs volume), bone microstructure (micro-CT), histopathological features (H&E, Safranin O, Masson, TRAP staining), and serum levels of inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-17A, IL-10, IL-13, detected by enzyme-linked immunosorbent assay (ELISA)) via abdominal aorta blood collection. Messenger RNA and protein expression levels of NAV2, Wnt3a, and β-catenin in the spleen and joint tissues were quantified using quantitative real-time polymerase chain reaction (qRT-PCR), Western blot, and immunohistochemistry (IHC). All data were analyzed using GraphPad Prism 8.3.0. Normality and homogeneity of variances were verified before analysis; one-way ANOVA followed by Tukey's post-hoc test was applied for multiple group comparisons, and independent Results: Compared with the NOR group, rats in the CIA model group exhibited significant joint swelling, elevated arthritis scores, severe bone microstructure destruction, and disordered serum cytokine profiles, with increased pro-inflammatory factors (TNF-α, IL-1β, IL-6, IL-17A) and decreased anti-inflammatory factors (IL-10, IL-13) ( Conclusion: ASIV attenuated CIA-associated inflammatory and structural changes and was associated with reduced

Indexed as

asztragaloside IVcollagen-induced arthritisimmunoregulationNAV2-Wnt/β-catenin signaling pathwayrheumatoid arthritis

Identifiers

PMID42801243
PMCPMC13615836

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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.