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Journal of veterinary pharmacology and therapeutics2007; 30(6); 523-533; doi: 10.1111/j.1365-2885.2007.00905.x

Differential anti-inflammatory and chondroprotective effects of simulated digests of indomethacin and an herbal composite (Mobility) in a cartilage explant model of articular inflammation.

Abstract: Herbs are an increasingly popular treatment option for horses with cartilage inflammation, despite a relative paucity of research demonstrating efficacy. The research objective was to evaluate the differential anti-inflammatory and chondroprotective efficacy of a simulated digest of indomethacin and a commercially available herbal product in a cartilage model of osteoarthritis. Cartilage explant was integrated with simulated digestion of indomethacin and the herbal product in order to account, at least in part, for the actions of major digestive enzymes and pH. The resulting digests were ultrafiltrated (50 kDa), to account for absorption from the GI tract and movement into the cartilage matrix. We hypothesized that (i) a simulated digest of indomethacin would block interleukin 1 beta-(IL-1) dependent formation of prostaglandin E2 (PGE2) and nitric oxide (NO) without protecting cartilage against IL-1-induced glycosaminoglycan (GAG) release, and (ii) the herbal product would reduce PGE2 and NO in IL-1-stimulated explants, and inhibit release of GAG, in IL-1-stimulated explants. Results showed that indomethacin is an effective anti-inflammatory, evidenced by strong inhibition of IL-1-induced PGE2 and NO from cartilage explants. However, indomethacin provided no protection against IL-1-induced GAG release. Simulated digest of the herbal extract significantly inhibited IL-1-induced NO production and GAG release, while having a slight increase in PGE2. These data provide evidence for the anti-inflammatory effect of indomethacin on IL-1-stimulated cartilage explants, and the herbal product Mobility may be a useful adjunct in arthritis because of its chondroprotective properties in IL-1-stimulated cartilage.
Publication Date: 2007-11-10 PubMed ID: 17991220DOI: 10.1111/j.1365-2885.2007.00905.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article studies the effectiveness of a standard non-steroidal anti-inflammatory drug, indomethacin, and a herbal product named Mobility in treating inflammation in horse cartilage. The study shows that while indomethacin was efficient in reducing inflammation, the herbal product was more effective in protecting the cartilage from damage caused by inflammation.

Objective of the Research

  • The primary aim of this research was to compare the anti-inflammatory and chondroprotective (cartilage-protective) effects of an artificial digestion of indomethacin (NSAID drug) and a prevalent herbal product. The cartilage model of osteoarthritis was used for this experiment.

Methodology

  • A cartilage explant was used as the inflammation model and was integrated with simulated digestion of indomethacin and the herbal product.
  • The simulated digestion was designed in a way to mimic the functions of primary digestive enzymes and pH levels, to provide a realistic scenario about how these substances work within the body.
  • The digested mixtures were then ultrafiltrated to replicate the absorption process that would have naturally taken place in the gastrointestinal tract and the movement into the cartilage matrix.

Hypotheses and Results

  • The researchers hypothesized that indomethacin would block the formation of pro-inflammatory mediators, PGE2 and NO, but it would not provide protection against the IL-1-induced release of GAG, a molecule associated with cartilage degradation.
  • It was also hypothesized that the herbal product would reduce levels of PGE2 and NO while inhibiting the release of GAG in an inflamed cartilage model.
  • The results showed that indomethacin did, in fact, block the production of PGE2 and NO but did not prevent GAG release. This indicates while indomethacin can reduce inflammation, it does not prevent cartilage degradation.
  • On the other hand, the herbal product reduced NO production and GAG release but increased PGE2 slightly. This indicates that although the herbal product may not control inflammation as effectively as indomethacin, it does a better job at preserving cartilage in inflammatory conditions.

Implications

  • The study concludes that indomethacin has an anti-inflammatory effect on cartilage explants stimulated by IL-1. Nevertheless, the herbal product Mobility has shown evidence of chondroprotective properties in the same model and therefore may serve as a beneficial addition in arthritis treatment due to its ability to protect against cartilage degradation.

Cite This Article

APA
Pearson W, Orth MW, Lindinger MI. (2007). Differential anti-inflammatory and chondroprotective effects of simulated digests of indomethacin and an herbal composite (Mobility) in a cartilage explant model of articular inflammation. J Vet Pharmacol Ther, 30(6), 523-533. https://doi.org/10.1111/j.1365-2885.2007.00905.x

Publication

ISSN: 0140-7783
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 30
Issue: 6
Pages: 523-533

Researcher Affiliations

Pearson, W
  • CanTox Health Sciences International, Mississauga, ON, Canada. wpearson@cantox.com
Orth, M W
    Lindinger, M I

      MeSH Terms

      • Animals
      • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
      • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
      • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
      • Cartilage, Articular / drug effects
      • Cartilage, Articular / metabolism
      • Dinoprostone / biosynthesis
      • Dose-Response Relationship, Drug
      • Drug Therapy, Combination
      • Horse Diseases / drug therapy
      • Horse Diseases / metabolism
      • Horse Diseases / pathology
      • Horses
      • Indomethacin / administration & dosage
      • Indomethacin / pharmacology
      • Indomethacin / therapeutic use
      • Interleukin-1 / biosynthesis
      • Models, Biological
      • Nitric Oxide / biosynthesis
      • Osteoarthritis / drug therapy
      • Osteoarthritis / veterinary
      • Phytotherapy
      • Plant Bark
      • Plant Preparations / administration & dosage
      • Plant Preparations / pharmacology
      • Plant Preparations / therapeutic use
      • Protective Agents / administration & dosage
      • Protective Agents / pharmacology
      • Protective Agents / therapeutic use
      • Salix
      • Swine

      Citations

      This article has been cited 2 times.
      1. Pearson W, Kott LS. A biological extract of turmeric (Curcuma longa) modulates response of cartilage explants to lipopolysaccharide. BMC Complement Altern Med 2019 Sep 11;19(1):252.
        doi: 10.1186/s12906-019-2660-zpubmed: 31506082google scholar: lookup
      2. Pearson W, Fletcher RS, Kott LS, Hurtig MB. Protection against LPS-induced cartilage inflammation and degradation provided by a biological extract of Mentha spicata. BMC Complement Altern Med 2010 May 11;10:19.
        doi: 10.1186/1472-6882-10-19pubmed: 20459798google scholar: lookup