Comparison of proteoglycan and collagen in articular cartilage of horses with naturally developing osteochondrosis and healing osteochondral fragments of experimentally induced fractures.
Abstract: To compare articular cartilage from horses with naturally developing osteochondrosis (OC) with normal articular cartilage and healing cartilage obtained from horses with experimentally induced osteochondral fractures. Methods: 109 specimens of articular cartilage from 78 horses. Methods: Morphologic characteristics, proteoglycan (PG), and type II collagen were analyzed in articular cartilage of OC specimens (group 1), matched healing cartilage obtained 40 days after experimentally induced osteochondral fractures (group 2), and matched normal cartilage from the same sites (group 3). Results: 79 specimens of OC cartilage were obtained from horses. Ex vivo PG synthesis was significantly greater in the femoral cartilage, compared with synthesis in the tibial cartilage, and significantly greater for groups 1 and 2, compared with group 3. For groups 1 and 2, femoral fragments had significantly greater PG content, compared with PG content in tibial fragments. Keratan sulfate content was significantly less in group 3, compared with groups 1 and 2. Cartilage from the OC specimens had loss of structural architecture. The OC tissue bed stained positive for chondroitin sulfate and type II collagen, but the fracture bed did not. Conclusions: Our analyses could not distinguish articular cartilage from horses with OC and a healing fracture. Both resembled an anabolic, reparative process. Immunohistochemical analysis suggested a chondromyxoid tissue in the OC bed that was morphologically similar to fibrous tissue but phenotypically resembled hyaline cartilage. Thus, tissue in the OC bed may be degenerative cartilage, whereas tissue in the fracture bed may be reparative fibrous callus.
Publication Date: 2005-12-13 PubMed ID: 16334944DOI: 10.2460/ajvr.2005.66.1881Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research study investigates the distinct biological composition of articular cartilage in horses suffering from a natural condition called osteochondrosis (OC) compared to normal and healing cartilage from experimentally induced fractures. The research finds that the characteristics of OC and healing fracture cartilage are similar, suggesting similar biological repair methods are happening in both.
Research Methodology
- The research compared articular cartilage from 78 horses and divided the specimens into three groups. Group one consisted of OC specimens, group two involved healing cartilage obtained 40 days after experimentally induced fractures, and group three comprised normal articular cartilage from the same sites.
- Each group’s Morphologic characteristics, proteoglycan (PG), and type II collagen were thoroughly assessed. Proteoglycan and type II collagen are essential components of cartilage, playing a crucial role in maintaining its structure and function.
Key Findings
- The findings showed that the horses’ ex vivo PG synthesis was significantly greater in femoral cartilage compared to tibial cartilage. Notably, this synthesis was markedly higher in groups 1 and 2 than in group 3.
- The research noted a significant loss of structural architecture in cartilage from OC specimens. The OC tissue bed tested positive for chondroitin sulfate and type II collagen; however, these components were not present in the fracture bed.
- The keratan sulfate content significantly less in group 3 compared to groups 1 and 2. Keratan sulfate is another critical component of cartilage, contributing to its flexibility and resistance to compression.
Conclusion
- Following their comprehensive analyses, the researchers concluded that OC cartilage and healing fracture cartilage share significant similarities. This conclusion suggests that the cartilage’s biological repair processes might be similar in both states.
- The results also suggest the tissue in an OC bed might be a degenerative cartilage, whereas in the fracture bed, it could represent a reparative fibrous callus. This analysis is based on the tissue’s morphological resemblance and biochemical characteristics to these components.
Cite This Article
APA
Bertone AL, Bramlage LR, McIlwraith CW, Malemud CJ.
(2005).
Comparison of proteoglycan and collagen in articular cartilage of horses with naturally developing osteochondrosis and healing osteochondral fragments of experimentally induced fractures.
Am J Vet Res, 66(11), 1881-1890.
https://doi.org/10.2460/ajvr.2005.66.1881 Publication
Researcher Affiliations
- Comparative Orthopedic Research Laboratories, Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus 43210, USA.
MeSH Terms
- Animals
- Cartilage, Articular / diagnostic imaging
- Cartilage, Articular / metabolism
- Cartilage, Articular / pathology
- Cartilage, Articular / surgery
- Collagen Type II / metabolism
- Female
- Femur / pathology
- Fracture Healing / physiology
- Horse Diseases / diagnostic imaging
- Horse Diseases / metabolism
- Horse Diseases / pathology
- Horses
- Immunohistochemistry / veterinary
- In Vitro Techniques
- Male
- Osteochondritis / diagnostic imaging
- Osteochondritis / metabolism
- Osteochondritis / pathology
- Osteochondritis / veterinary
- Proteoglycans / metabolism
- Radiography
- Tibia / pathology
Citations
This article has been cited 3 times.- Mendoza L, Piquemal D, Lejeune JP, Vander Heyden L, Noguier F, Bruno R, Sandersen C, Serteyn D. Age-dependent expression of osteochondrosis-related genes in equine leukocytes. Vet Rec Open 2015;2(1):e000058.
- Corbin LJ, Blott SC, Swinburne JE, Sibbons C, Fox-Clipsham LY, Helwegen M, Parkin TD, Newton JR, Bramlage LR, McIlwraith CW, Bishop SC, Woolliams JA, Vaudin M. A genome-wide association study of osteochondritis dissecans in the Thoroughbred. Mamm Genome 2012 Apr;23(3-4):294-303.
- Jasiński T, Turek B, Kaczorowski M, Brehm W, Skierbiszewska K, Domino M. Equine temporomandibular joint diseases: A systematic review. Equine Vet J 2025 Nov;57(6):1427-1445.
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