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Comparison of the effect of polysulfated glycosaminoglycan, corticosteroids, and sodium hyaluronate in the potentiation of a subinfective dose of Staphylococcus aureus in the midcarpal joint of horses.

Abstract: Four groups of 8 horses each had 1 midcarpal joint injected with 33 colony-forming units (CFU) of viable Staphylococcus aureus plus: 1 ml of saline solution (group 1, control), 250 mg of polysulfated glycosaminoglycan (PSGAG, group 2), 100 mg of methylprednisolone acetate (group 3), or 20 mg of sodium hyaulronate (group 4). Horses were euthanatized, and samples were obtained on the basis of clinical signs of septic arthritis that were nonresponsive to phenylbutazone administration. One group-1 horse, all 8 group-2 horses, 3 group-3 horses, and 4 group-4 horses were culture-positive for S aureus and had clinical signs, results of synovial fluid analysis, and histopathologic findings that were consistent with sepsis. The addition of 250 mg of PSGAG increased the development of sepsis significantly (P = 0.001), compared with results in control horses. Differences in the development of sepsis between horses injected with methylprednisolone acetate or sodium hyaluronate and control horses were not significant.
Publication Date: 1989-12-01 PubMed ID: 2610426
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research paper primarily investigates the impact of polysulfated glycosaminoglycan (PSGAG), corticosteroids, and sodium hyaluronate on staphylococcus aureus-induced arthritis in horses. The study found that the administration of PSGAG notably increased the occurrence of sepsis, while the effects of corticosteroids and sodium hyaluronate were insignificant.

Research Procedure

  • The experiment included four groups of horses, each having eight members. Every horse had one midcarpal joint injected with a known dosage of Staphylococcus aureus bacteria, along with other experimental substances.
  • The horses in the control group (group 1) had the bacteria plus a saline solution. Group 2 received polysulfated glycosaminoglycan (PSGAG), group 3 was dosed with methylprednisolone acetate (a corticosteroid), and group 4 had sodium hyaluronate added.

Results and Observations

  • The progress of horses was monitored by looking for symptoms of septic arthritis that didn’t respond to phenylbutazone treatment. At this stage, the horses were euthanized and samples were taken for further analysis.
  • Observations indicated that one horse from the control group, all horses from the PSGAG group, three from the corticosteroid group, and four from the sodium hyaluronate group showed positive culture for Staphylococcus aureus. Moreover, they exhibited clinical signs, synovial fluid analysis, and histopathologic findings that were suggestive of sepsis.
  • Notably, the group that received PSGAG had a significant increase in the development of sepsis compared to the control group (P = 0.001).
  • Contrarily, the change in the development of sepsis in horses treated with methylprednisolone acetate or sodium hyaluronate was not statistically significant when compared to the control horses. These substances did not appear to influence the persistence or worsening of the Staphylococcus aureus infection.

Conclusion

  • The study, therefore, concludes that polysulfated glycosaminoglycan, when combined with a Staphylococcus aureus infection, can significantly increase the risk of sepsis in horses. Hence, the use of PSGAG in horses, particularly those at risk of Staphylococcus aureus infection, should be reassessed and regulated.
  • Although this study did not find significant effects of corticosteroids and sodium hyaluronate on the infection, further research is needed to confirm these observations and fully understand their relationship with Staphylococcus aureus-induced sepsis in horses.

Cite This Article

APA
Gustafson SB, McIlwraith CW, Jones RL. (1989). Comparison of the effect of polysulfated glycosaminoglycan, corticosteroids, and sodium hyaluronate in the potentiation of a subinfective dose of Staphylococcus aureus in the midcarpal joint of horses. Am J Vet Res, 50(12), 2014-2017.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 50
Issue: 12
Pages: 2014-2017

Researcher Affiliations

Gustafson, S B
  • Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins 80523.
McIlwraith, C W
    Jones, R L

      MeSH Terms

      • Adrenal Cortex Hormones / administration & dosage
      • Adrenal Cortex Hormones / pharmacology
      • Animals
      • Carpus, Animal / microbiology
      • Forelimb / microbiology
      • Glycosaminoglycans / administration & dosage
      • Glycosaminoglycans / pharmacology
      • Horse Diseases / microbiology
      • Horses / microbiology
      • Hyaluronic Acid / administration & dosage
      • Hyaluronic Acid / pharmacology
      • Injections, Intra-Articular
      • Joint Diseases / microbiology
      • Joint Diseases / veterinary
      • Staphylococcal Infections / microbiology
      • Staphylococcal Infections / veterinary
      • Staphylococcus aureus / pathogenicity
      • Virulence

      Citations

      This article has been cited 4 times.
      1. White GW. Polysulfated glycosaminoglycan as a treatment for osteoarthritis in veterinary medicine: Summary of the pharmacological, laboratory, and clinical data. Open Vet J 2025 Sep;15(9):4007-4023.
        doi: 10.5455/OVJ.2025.v15.i9.6pubmed: 41200294google scholar: lookup
      2. Krause DM, Pezzanite LM, Griffenhagen GM, Hendrickson DA. Comparison of equine synovial sepsis rate following intrasynovial injection in ambulatory versus hospital settings. Equine Vet J 2022 May;54(3):523-530.
        doi: 10.1111/evj.13485pubmed: 34115426google scholar: lookup
      3. Pezzanite L, Chow L, Piquini G, Griffenhagen G, Ramirez D, Dow S, Goodrich L. Use of in vitro assays to identify antibiotics that are cytotoxic to normal equine chondrocytes and synovial cells. Equine Vet J 2021 May;53(3):579-589.
        doi: 10.1111/evj.13314pubmed: 32544273google scholar: lookup
      4. Zhou ZH, Rajabi M, Chen T, Karnaukhova E, Kozlowski S. Oversulfated chondroitin sulfate inhibits the complement classical pathway by potentiating C1 inhibitor. PLoS One 2012;7(10):e47296.
        doi: 10.1371/journal.pone.0047296pubmed: 23077587google scholar: lookup