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Cited by 30Gout, Hyperuricemia, Uric AcidInflammasome and immune disordersNatural Compounds in Disease Treatment

The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.

Pharmacological basis for use of madecassoside in gouty arthritis: anti-inflammatory, anti-hyperuricemic, and NLRP3 inhibition

Lu, Xiaohui, Zeng, Runming, Lin, Jing, Hu, Jun, Rong, Zhijie, Xu, Weicai, Liu, Zewa, Zeng, Wanting·2019·Immunopharmacology and Immunotoxicology

Abstract

Objectives: Gouty arthritis is caused by the deposition of monosodium urate (MSU) crystals in joints, which is associated with the rise of serum urate content. This study aims to investigate the therapeutic effect of Madecassoside on gouty arthritis and hyperuricemia. Methods: DBA/1 mice were intradermally injected with MSU to stimulate joint inflammation or intraperitoneally injected with MSU to trigger peritonitis. Moreover, ICR mice were exposed to potassium oxonate to stimulate hyperuricemia. Results: Madecassoside repressed MSU-triggered pad swelling, joint 99mTc uptake, and joint inflammation in DBA/1 mice with gouty arthritis. Neutrophil infiltration and IL-1β & IL-6 & MCP-1 secretion was also alleviated in lavage fluids from DBA/1 mice with peritonitis due to Madecassoside treatment. Furthermore, Madecassoside decreased MSU-induced neutrophil cytosolic factor 1, caspase-1 and NLRP3 expression in mice with peritoneal inflammation. In hyperuricemic mice, Madecassoside improved renal dysfunction. Serum uric acid, BUN, and creatinine were down-regulated by Madecassoside. Conclusion: These findings indicate that Madecassoside has potential to ameliorate inflammation in both acute gouty arthritis model and peritonitis model, probably via regulating IL-1β and NLRP3 expression. Practical point: Madecassoside also exhibited a urate-lowering effect and a renal protective effect in hyperuricemic mice.

Overview

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Crossref · 10.1080/08923973.2019.1590721

Cites

45 of 45 references verified0 citation errors · 0 not checkable

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Citations

Cites

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Research works printed but not linked: 3

  1. Crittenden DB, Pillinger MH. The year in gout - 2010–2011. Bull Nyu Hosp Jt Dis. 2011;69:257–263.
  2. Joosten LA, Netea MG, Fantuzzi G, et al. Inflammatory arthritis in caspase 1 gene-deficient mice: contribution of proteinase 3 to caspase 1-independent. Rheum Arthr. 2009;60:3651–3662.
  3. Hilmi BA, Asmahan MI, Rosman A. Use of newly available febuxostat in a case of chronic tophaceous gout contraindicated to allopurinol and probenecid. Med J Malaysia. 2012;67:125–126.

Cited by

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Metadata

Authors
Lu, X., Zeng, R., Lin, J., Hu, J., Rong, Z., Xu, W., Liu, Z., & Zeng, W.
Affiliations
  • First Affiliated Hospital of Shantou University Medical College (CN)
  • Department of Orthopedic Surgery, The First Affiliate Hospital of Shantou University Medical College
  • University College London (GB)
Corresponding author
Lu, Xiaohui
Venue
Immunopharmacology and Immunotoxicology
Published
2019-03-04
Volume
41
Issue
2
Pages
277-284
ISSN
  • 0892-3973 (ISSN-L)
  • 1532-2513
OpenAlex
W2945752146
Cited by
30
References
45
Citations by year
2026: 3 · 2025: 4 · 2024: 6 · 2023: 5 · 2022: 2 · 2021: 6 · 2020: 3 · 2019: 1
FWCI
2.31
Type
journal article
Language
en
Open access
closed
Licence
doi.org/10.1080/policies-text-data-mining (tdm)
Locations
  • Immunopharmacology and Immunotoxicology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Nephrology › Gout, Hyperuricemia, Uric Acid
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
  • Health Sciences › Medicine › Complementary and alternative medicine › Natural Compounds in Disease Treatment
Keywords
madecassoside, gout, hyperuricemia, monosodium urate crystals, NLRP3 inflammasome, IL-1β, interleukin-6, MCP-1, neutrophil infiltration, peritonitis, potassium oxonate, renal protection, anti-inflammatory activity, caspase-1
MeSH terms
NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Anti-Inflammatory Agents, omega-Chloroacetophenone, Inflammation, Male, Mice, Inbred ICR, Neutrophils, Peritonitis, Triterpenes, Uric Acid, Arthritis, Gouty, Cytokines, Neutrophil Infiltration, Hyperuricemia

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CoChat. (2026). Citation check: Pharmacological basis for use of madecassoside in gouty arthritis: anti-inflammatory, anti-hyperuricemic, and NLRP3 inhibition. https://app.cochat.ai/papers/10.1080/08923973.2019.1590721
The paper
Lu, X., Zeng, R., Lin, J., Hu, J., Rong, Z., Xu, W., Liu, Z., & Zeng, W. (2019). Pharmacological basis for use of madecassoside in gouty arthritis: anti-inflammatory, anti-hyperuricemic, and NLRP3 inhibition. Immunopharmacology and Immunotoxicology. https://doi.org/10.1080/08923973.2019.1590721

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.