Back to Reference Library
veterinary
anatomy
nutrition
farriery
2003
Expert Opinion

Articular chondrocyte apoptosis in equine osteoarthritis.

Authors: Kim D Y, Taylor H W, Moore R M, Paulsen D B, Cho D-Y

Journal: Veterinary journal (London, England : 1997)

Summary

# Editorial Summary Programmed cell death of chondrocytes has been recognised as a driving mechanism in human and experimentally-induced osteoarthritis, yet this phenomenon had never been characterised in naturally occurring equine OA until this 2003 investigation. Kim and colleagues examined articular cartilage from three healthy horses and five with established OA, using the modified Mankin scoring system to grade histopathological damage alongside TUNEL assays to quantify chondrocyte apoptosis, and immunohistochemistry to measure nitric oxide (NO) production as a marker of inflammatory activity. The researchers found significantly elevated apoptosis rates and histopathological scores in OA cartilage compared to normal tissue, with a strong positive correlation between structural damage grade and the percentage of apoptotic chondrocytes; moreover, nitric oxide production was markedly increased in diseased cartilage and showed topographical overlap with both apoptotic activity and matrix degradation. These results suggest that chondrocyte death is not merely a consequence of established OA but rather an integral part of a coordinated pathological cascade involving inflammatory mediators, indicating that therapeutic strategies targeting cell death pathways and nitric oxide signalling could represent valuable disease-modifying approaches during the progressive phases of joint disease in horses.

Read the full abstract on PubMed

Practical Takeaways

  • Chondrocyte apoptosis is a key mechanism in equine OA pathology, supporting therapeutic strategies that target cell death pathways and nitric oxide production
  • The correlation between histological changes and apoptosis suggests monitoring apoptotic markers could help assess OA severity and progression in clinical cases
  • Understanding the interrelationship between NO production and chondrocyte death opens potential therapeutic targets for early intervention in equine joint disease

Key Findings

  • Chondrocyte apoptosis percentage was significantly higher in OA cartilage compared to normal cartilage
  • Strong positive correlation found between histopathological grade and percentage of chondrocyte apoptosis
  • OA cartilages showed stronger nitrotyrosine immunoreactivity indicating increased nitric oxide production compared to normal cartilage
  • Topographical distributions of chondrocyte apoptosis, matrix degeneration, and nitric oxide production overlapped, indicating these pathological phenomena are closely interrelated

Conditions Studied

osteoarthritis

Related References

Relationship between synovial fluid levels of glycosaminoglycans, hydroxyproline and general MMP activity and the presence and severity of articular cartilage change on the proximal articular surface of P1.

van den Boom R, van der Harst M R, Brommer H, Brama P A J, Barneveld A, van Weeren P R, DeGroot J(2005)Equine veterinary journal

Comparison of the Effects of Interleukin-1 on Equine Articular Cartilage Explants and Cocultures of Osteochondral and Synovial Explants.

Byron Christopher R, Trahan Richard A(2017)Frontiers in veterinary science

Spontaneous production of nitric oxide (NO), prostaglandin (PGE2) and neutral metalloproteinases (NMPs) in media of explant cultures of equine synovial membrane and articular cartilage from normal and osteoarthritic joints.

von Rechenberg B, McIlwraith C W, Akens M K, Frisbie D D, Leutenegger C, Auer J A(2000)Equine veterinary journal

Gene therapy approaches for equine osteoarthritis.

Thampi Parvathy, Samulski R Jude, Grieger Joshua C, Phillips Jennifer N, McIlwraith C Wayne, Goodrich Laurie R(2022)Frontiers in veterinary science

An experimentally induced osteoarthritis model in horses performed on both metacarpophalangeal and metatarsophalangeal joints: Technical, clinical, imaging, biochemical, macroscopic and microscopic characterization.

Bertoni Lélia, Jacquet-Guibon Sandrine, Branly Thomas, Legendre Florence, Desancé Mélanie, Mespoulhes Céline, Melin Martine, Hartmann Daniel-Jean, Schmutz Amandine, Denoix Jean-Marie, Galéra Philippe, Demoor Magali, Audigié Fabrice(2020)PloS one