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Equine veterinary journal1987; 19(1); 15-18; doi: 10.1111/j.2042-3306.1987.tb02569.x

Pathogenesis of degenerative joint disease.

Abstract: Proteoglycan degradation is central to the development of degenerative joint disease. Proteoglycans may be degraded by lysosomal enzymes from chondrocytes, synoviocytes or leucocytes. Collagen and matrix degradation occurs either by direct damage or due to degrading enzymes released into synovial fluid. Once the pathological sequence has begun it continues in a cyclic manner unless arrested by the ability of chondrocytes to synthesise sufficient matrix components. Treatment should ideally be directed to this end.
Publication Date: 1987-01-01 PubMed ID: 3319576DOI: 10.1111/j.2042-3306.1987.tb02569.xGoogle Scholar: Lookup
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Summary

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The research article summarizes that the process of proteoglycan degradation is fundamental to the development of degenerative joint disease, with both direct damage and degrading enzymes contributing to collagen and matrix breakdown. If unaddressed, this pathological sequence can continue repetitively, necessitating chondrocyte’s synthesis of enough matrix components to halt the process. Best treatments, therefore, are those focused on this outcome.

Role of Proteoglycan in Degenerative Joint Disease

  • The study proposes that proteoglycan degradation is a key part of developing degenerative joint disease. Proteoglycans are vital components of the cartilage matrix that help provide it with its unique load-bearing and elastic properties. Their degradation can result in the breakdown of the cartilage, leading to joint pain and dysfunction.
  • The enzymes required for this degradation can come from chondrocytes (cells that produce and maintain the cartilage matrix), synoviocytes (cells that line the synovial joint cavities and produce synovial fluid), or leucocytes (white blood cells that respond to inflammation and infection).

Collagen and Matrix Degradation

  • Alongside proteoglycan degradation, the research highlights that collagen and matrix degradation also contributes to degenerative joint disease. These can occur due to direct damage (like a physical injury) or as a result of degrading enzymes being released into the synovial fluid.
  • The synovial fluid functions as a lubricant in joint cavities and is rich in proteins and enzymes. Any imbalance in this composition, such as elevated levels of destructive enzymes, can contribute to joint degeneration.

The Cyclic Sequence of Degeneration

  • Once triggered, the pathological sequence of joint degeneration can continue in a recurring cycle. This cycle can only be broken if chondrocytes can produce sufficient matrix components to repair the damaged cartilage and restore normal joint function.

Effective Treatment Strategy

  • According to the study, an ideal treatment should be targeted towards enhancing the chondrocytes’ ability to synthesize enough matrix components, maintaining the structural integrity of the joints and postponing or preventing the progression of degenerative joint disease.

Cite This Article

APA
Clyne MJ. (1987). Pathogenesis of degenerative joint disease. Equine Vet J, 19(1), 15-18. https://doi.org/10.1111/j.2042-3306.1987.tb02569.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 19
Issue: 1
Pages: 15-18

Researcher Affiliations

Clyne, M J

    MeSH Terms

    • Animals
    • Cartilage, Articular / pathology
    • Horse Diseases / etiology
    • Horses
    • Osteoarthritis / etiology
    • Osteoarthritis / veterinary
    • Proteoglycans / metabolism

    References

    This article includes 21 references

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