Evidence map›Paper›PMID 39907970›Full record

ArticleClinical rheumatology2025

Protective effects of Catalpol to attenuate TNF- α and collagen-induced inflammation in vitro HFLS-RA cells and in vivo mice models for the treatment of rheumatoid arthritis.

Bin Wu, Qinyan Dong, Qin Zhang, Fangqin Jin, Jiangping Weng

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

5 authors.

Bin WuDepartment of Orthopaedics, The Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, China.
Qinyan DongDepartment of Orthopaedics, The Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, China.
Qin ZhangDepartment of Orthopaedics, The Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, China.
Fangqin JinDepartment of Orthopaedics, The Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, China.
Jiangping WengDepartment of Orthopaedics, The Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, Zhejiang, China. wjp19810211@sina.com.ORCID http://orcid.org/0009-0006-6306-3000

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background/rationaleRheumatoid Arthritis (RA) is a prolonged autoimmune condition marked by persistent inflammation, causing joint damage and bone erosion. Catalpol (CAT), an iridoid glycoside, offers anti-inflammatory benefits, warranting its study in RA models.

objectiveTo investigate the anti-inflammatory effects of CAT in RA by evaluating its impact on cellular and animal RA models.

methodsIn vitro biological actions of CAT were investigated by the methods of cell viability, proliferation, migration, invasion, apoptosis, ROS generation, double luciferase reporter assay for NF-κB-p65 activity, Nitrite release detection, and RT-qPCR for gene expression in Tumor Necrosis Factor-alpha (TNF-α)-induced Human Fibroblast-Like Synoviocytes from RA patients (HFLS-RA) (cellular RA model). Arthritis severity, joint cellular structure, gene expression, inflammatory factors, and joint inflammation studies were investigated in mice with collagen-induced arthritis (CIA) (animal RA model). KEY

resultsCAT treatment groups showed significant improvements (P < 0.001) in cell viability, migration, invasion, and apoptosis compared to the TNF-α-induced group. ROS generation and the activity of NF-κB-p65 were significantly reduced (P < 0.001). Nitrite release was decreased (P < 0.01, P < 0.001) in CAT-treatment groups. Pro-inflammatory and bone-metabolizing cytokine gene expression was markedly downregulated (P < 0.05, P < 0.001) in the cellular RA model. CIA mice treated with CAT exhibited significantly reduced arthritis severity, paw edema, and arthritis index (P < 0.05, P < 0.01). Joint pathology scores showed improvement (P < 0.001) in CAT-treatment groups. In the animal RA model, bone-metabolizing and inflammatory cytokine gene expression was significantly reduced in CAT-treatment groups (P < 0.01, P < 0.001).

conclusionCAT effectively reduces RA's inflammation and bone metabolism issues, suggesting its potential as a therapeutic agent for RA treatments. Key Points • Plant-derived Catalpol compound is an effective choice for rheumatoid arthritis treatment due to its anti-inflammatory potential. • CAT's effects were tested on TNF-α-induced HFLS-RA cells and in CIA mice, assessing cell viability, apoptosis, ROS generation, arthritis severity, inflammatory factors, and joint inflammation studies. • The administration of CAT could greatly enhance cell health and reduce inflammation markers and arthritis symptoms. • Observed significant reduction of RA inflammation and bone issues, confirming CAT as a therapeutic agent in RA treatment.

Indexed as

Anti-Inflammatory AgentsArthritis, ExperimentalArthritis, RheumatoidIridoid GlucosidesSynoviocytesTumor Necrosis Factor-alphaAnimalsApoptosisCell MovementCell ProliferationCell SurvivalDisease Models, AnimalHumansInflammationMaleMiceAnti-Inflammatory AgentscatalpolIridoid GlucosidesReactive Oxygen SpeciesTumor Necrosis Factor-alphaCatalpolCollagen-induced arthritisNF-κB signaling pathwayRheumatoid arthritisSynovial inflammation

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.