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Veterinary journal (London, England : 1997)2003; 166(1); 52-57; doi: 10.1016/s1090-0233(02)00305-2

Articular chondrocyte apoptosis in equine osteoarthritis.

Abstract: Osteoarthritis (OA) is the most common joint disease in horses. Chondrocyte apoptosis has been implicated as a major pathological OA change in humans and experimental animals but no studies have been performed on equine OA. Articular cartilage was collected from three normal and five OA horses. Histopathological changes were scored by a modified Mankin grading system. A terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay was performed to identify chondrocyte apoptosis. Nitric oxide (NO) production from chondrocytes was indirectly evaluated by immunohistochemistry with polyclonal antibody to nitrotyrosine. The histopathological score and percentage of chondrocyte apoptosis from the OA cartilages were significantly higher than from normal cartilages. There was a significant correlation between histopathological grade and the percentage of chondrocyte apoptosis. OA cartilages exhibited stronger immunoreactivity to nitrotyrosine than normal cartilage. Topographical distributions of chondrocyte apoptosis, cartilage matrix degeneration, and NO production overlapped in equine OA cartilages, suggesting that these pathological phenomena are closely interrelated.
Publication Date: 2003-06-06 PubMed ID: 12788017DOI: 10.1016/s1090-0233(02)00305-2Google Scholar: Lookup
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  • Journal Article

Summary

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This study analyses the presence of chondrocyte cell death (apoptosis) in horses affected by osteoarthritis, the most common joint disease in these animals. The research findings indicate a significant correlation between the severity of the disease and the percentage of cell death.

Understanding the Study

  • The research focuses on osteoarthritis (OA), a common joint disease in horses, and the role of chondrocyte apoptosis (cell death) in this disease. Previous studies in humans and other animals suggest this type of cell death might be a crucial factor in OA progression; however, this had not been researched in horses before.
  • The study involved collecting and comparing cartilage from three healthy horses and five horses with OA. The degree of disease (histopathological changes) in the collected samples was evaluated using a modified Mankin grading system, a well-established scale for assessing the severity of OA.
  • Chondrocyte apoptosis was identified using a labeling assay known as TUNEL. This technique makes it possible to visualize and quantify the percentage of cell death in tissue samples. Additionally, the production of nitric oxide (NO) was indirectly evaluated by using immunohistochemistry, a method to detect specific proteins in cells of a tissue section, with an antibody to nitrotyrosine.

Key Findings

  • The study found that cartilages from horses with OA had a significantly higher histopathological score and a greater percentage of chondrocyte apoptosis than samples from normal horses, suggesting a correlation between the progression of the disease and cell death.
  • The level of immunoreactivity to nitrotyrosine was stronger in cartilages from OA horses, which suggests elevated NO production in these samples. This is important because excessive NO, a signaling molecule involved in many pathological processes, can lead to tissue damage and is associated with inflammatory diseases such as OA.
  • The researchers also found that the spatial distribution, or the topographical locations, of chondrocyte apoptosis, cartilage matrix degeneration, and NO production overlapped in the OA cartilages. This observation implies that these pathological processes are interconnected and might play a significant role in the progression of OA in horses.

Cite This Article

APA
Kim DY, Taylor HW, Moore RM, Paulsen DB, Cho DY. (2003). Articular chondrocyte apoptosis in equine osteoarthritis. Vet J, 166(1), 52-57. https://doi.org/10.1016/s1090-0233(02)00305-2

Publication

ISSN: 1090-0233
NlmUniqueID: 9706281
Country: England
Language: English
Volume: 166
Issue: 1
Pages: 52-57

Researcher Affiliations

Kim, D Y
  • Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.
Taylor, H W
    Moore, R M
      Paulsen, D B
        Cho, D-Y

          MeSH Terms

          • Animals
          • Apoptosis / physiology
          • Cartilage, Articular / metabolism
          • Cartilage, Articular / pathology
          • Chondrocytes / metabolism
          • Chondrocytes / pathology
          • Horse Diseases / metabolism
          • Horse Diseases / pathology
          • Horses
          • Immunohistochemistry / veterinary
          • In Situ Nick-End Labeling / veterinary
          • Nitric Oxide / biosynthesis
          • Osteoarthritis / metabolism
          • Osteoarthritis / pathology
          • Osteoarthritis / veterinary
          • Tyrosine / analogs & derivatives
          • Tyrosine / metabolism

          Citations

          This article has been cited 10 times.
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