Analyze Diet
Equine veterinary journal2007; 40(1); 30-39; doi: 10.2746/042516407X239836

Epiphyseal cartilage canal blood supply to the tarsus of foals and relationship to osteochondrosis.

Abstract: Pathological changes in the blood supply to growth cartilage have been implicated in the pathogenesis of osteochondrosis (OC) in horses, but have not been reported using vascular perfusion techniques. Objective: To describe the developmental pattern of cartilage canal vessels in the distal tibial epiphysis and talar growth cartilage of foals. Methods: Nine foals bred from parents with OC were sacrificed between the ages of 0 and 7 weeks to undergo a barium perfusion procedure. The distal end of the tibia and the entire talus were cleared in methyl salicylate and perfused vessels studied in the intact bones. Slabs with a thickness of 4-5 mm from 3 predilection sites for OC were examined in the stereomicroscope and with light microscopy. Results: Cartilage canals were present for a limited period of growth. Perfused vessels initially entered canals from the perichondrium. Vessels in the proximal portion of canals retained their perichondrial arterial source throughout. With time, the ossification front advanced to incorporate the mid-portion of canals; and anastomoses formed between canal vessels and subchondral vessels. A shift occurred and vessels in the distal terminus of canals came to use subchondral vessels as their arterial source. Twelve histological lesions were found in 7 foals. All contained necrotic vessels surrounded by necrotic growth cartilage and 3 caused macroscopically visible delay in endochondral ossification. Lesions were located where vessels traversed the ossification front to enter the distal terminus of canals. Conclusions: Cartilage canal vessels are particularly susceptible to failure at the point where they cross the ossification front, with consequences for the viability of those chondrocytes that depend on them. Conclusions: A better understanding of how lesions of OC arise may improve the ability to identify, monitor, prevent and treat this disorder. Involvement of cartilage canals in the pathogenesis of equine tarsal OC plausibly explains several clinical features of this disease.
Publication Date: 2007-12-18 PubMed ID: 18083657DOI: 10.2746/042516407X239836Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • 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.

Researchers examined the blood supply to the growth cartilage in foals to understand its development and its relation to osteochondrosis, a bone disorder. It was found that the blood vessels are susceptible to failure at certain points, which could potentially lead to lesions of osteochondrosis.

Study Objective and Methods

  • The study aimed to discern the developmental pattern of cartilage canal vessels in foals’ distal tibial epiphysis and talar growth cartilage, particularly with relation to osteochondrosis (OC), a disease attributed to changes in the blood supply to growth cartilage.
  • The researchers used a sample of nine foals aged between 0 and 7 weeks, explicitly bred from parents with osteochondrosis (OC). The young horses were euthanized to allow for a barium perfusion procedure.
  • The distal end of the tibia and the entire talus were cleared with methyl salicylate. This allowed the researchers to investigate the perfused vessels in the intact bones.
  • Slabs about 4-5mm thick from three favored sites of OC were examined under a stereomicroscope and light microscopy for further analysis.

Results and Explanation

  • It was found that cartilage canals are present for a limited growth period, with perfused vessels initially entering canals from the perichondrium.
  • With time, an ossification front advanced to incorporate the mid-portion of canals and anastomoses (the connection between two blood vessels) formed between canal vessels and subchondral vessels.
  • Ultimately, a shift occurred wherein the vessels in the distal end of the canals started to use subchondral vessels as their arterial source.
  • The researchers found twelve histological lesions in seven of the nine foals. These lesions all contained necrotic (dead tissue) vessels surrounded by necrotic growth cartilage, and three of these lesions resulted in a visible delay in endochondral ossification.
  • These potentially disease-causing lesions were located where vessels crossed the ossification front to enter the distal terminus of canals.

Conclusions

  • Based on these findings, the study concluded that the vessels supplying the cartilage canals are particularly vulnerable at the point where they cross the ossification front. This susceptibility impacts chondrocyte (cartilage cell) viability that depends on them.
  • The researchers suggest that a better understanding of the formation of OC lesions might enhance the ability to identify, monitor, prevent, and treat OC. The involvement of cartilage canals in the development of equine tarsal OC can potentially explain several clinical characteristics of this disease.

Cite This Article

APA
Olstad K, Ytrehus B, Ekman S, Carlson CS, Dolvik NI. (2007). Epiphyseal cartilage canal blood supply to the tarsus of foals and relationship to osteochondrosis. Equine Vet J, 40(1), 30-39. https://doi.org/10.2746/042516407X239836

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 40
Issue: 1
Pages: 30-39

Researcher Affiliations

Olstad, K
  • The Norwegian School of Veterinary Science, Department of Companion Animal Clinical Sciences, Section for Equine Medicine and Surgery, Oslo, Norway.
Ytrehus, B
    Ekman, S
      Carlson, C S
        Dolvik, N I

          MeSH Terms

          • Aging
          • Animals
          • Animals, Newborn
          • Cartilage, Articular / blood supply
          • Cartilage, Articular / pathology
          • Female
          • Growth Plate / blood supply
          • Growth Plate / pathology
          • Horse Diseases / pathology
          • Horse Diseases / physiopathology
          • Horse Diseases / prevention & control
          • Horses
          • Male
          • Osteochondritis / pathology
          • Osteochondritis / physiopathology
          • Osteochondritis / prevention & control
          • Osteochondritis / veterinary
          • Prevalence
          • Regional Blood Flow
          • Reperfusion / veterinary
          • Tarsus, Animal / blood supply
          • Tarsus, Animal / pathology
          • Tibia / blood supply
          • Tibia / pathology
          • Treatment Outcome

          Citations

          This article has been cited 31 times.
          1. Van Cauter R, Serteyn D, Lejeune JP, Rousset A, Caudron I. Evaluation of the appearance of osteochondrosis lesions by two radiographic examinations in sport horses aged from 12 to 36 months. PLoS One 2023;18(5):e0286213.
            doi: 10.1371/journal.pone.0286213pubmed: 37220101google scholar: lookup
          2. Fjordbakk CT, Marques-Smith P. The equine patellar ligaments and the infrapatellar fat pad - a microanatomical study. BMC Vet Res 2023 Jan 23;19(1):20.
            doi: 10.1186/s12917-023-03579-3pubmed: 36691004google scholar: lookup
          3. Lemirre T, Santschi E, Girard C, Fogarty U, Chapuis L, Richard H, Beauchamp G, Laverty S. Maturation of the equine medial femoral condyle osteochondral unit. Osteoarthr Cartil Open 2020 Mar;2(1):100029.
            doi: 10.1016/j.ocarto.2020.100029pubmed: 36474556google scholar: lookup
          4. Olstad K, Gangsei LE, Kongsro J. A method for labelling lesions for machine learning and some new observations on osteochondrosis in computed tomographic scans of four pig joints. BMC Vet Res 2022 Aug 31;18(1):328.
            doi: 10.1186/s12917-022-03426-xpubmed: 36045350google scholar: lookup
          5. Olstad K, Aasmundstad T, Kongsro J, Grindflek E. Osteochondrosis and other lesions in all intervertebral, articular process and rib joints from occiput to sacrum in pigs with poor back conformation, and relationship to juvenile kyphosis. BMC Vet Res 2022 Jan 18;18(1):44.
            doi: 10.1186/s12917-021-03091-6pubmed: 35042517google scholar: lookup
          6. Chau MM, Klimstra MA, Wise KL, Ellermann JM, Tóth F, Carlson CS, Nelson BJ, Tompkins MA. Osteochondritis Dissecans: Current Understanding of Epidemiology, Etiology, Management, and Outcomes. J Bone Joint Surg Am 2021 Jun 16;103(12):1132-1151.
            doi: 10.2106/JBJS.20.01399pubmed: 34109940google scholar: lookup
          7. Rothschild BM, Wayne Lambert H. Distinguishing between congenital phenomena and traumatic experiences: Osteochondrosis versus osteochondritis. J Orthop 2021 Jan-Feb;23:185-190.
            doi: 10.1016/j.jor.2021.01.006pubmed: 33551611google scholar: lookup
          8. Olstad K, Wormstrand B, Kongsro J, Grindflek E. Computed tomographic development of physeal osteochondrosis in pigs. BMC Vet Res 2019 Dec 17;15(1):454.
            doi: 10.1186/s12917-019-2163-7pubmed: 31847840google scholar: lookup
          9. Tóth F, Johnson CP, Mills B, Nissi MJ, Nykänen O, Ellermann J, Ludwig KD, Tompkins M, Carlson CS. Evaluation of the Suitability of Miniature Pigs as an Animal Model of Juvenile Osteochondritis Dissecans. J Orthop Res 2019 Oct;37(10):2130-2137.
            doi: 10.1002/jor.24353pubmed: 31115932google scholar: lookup
          10. Hendrickson EHS, Lykkjen S, Dolvik NI, Olstad K. Prevalence of osteochondral lesions in the fetlock and hock joints of Standardbred horses that survived bacterial infection before 6 months of age. BMC Vet Res 2018 Dec 10;14(1):390.
            doi: 10.1186/s12917-018-1726-3pubmed: 30526583google scholar: lookup
          11. Semevolos SA, Duesterdieck-Zellmer KF, Larson M, Kinsley MA. Expression of pro-apoptotic markers is increased along the osteochondral junction in naturally occurring osteochondrosis. Bone Rep 2018 Dec;9:19-26.
            doi: 10.1016/j.bonr.2018.06.003pubmed: 29998174google scholar: lookup
          12. Hellings IR, Dolvik NI, Ekman S, Olstad K. Cartilage canals in the distal intermediate ridge of the tibia of fetuses and foals are surrounded by different types of collagen. J Anat 2017 Oct;231(4):615-625.
            doi: 10.1111/joa.12650pubmed: 28620929google scholar: lookup
          13. Sevane N, Dunner S, Boado A, Cañon J. Polymorphisms in ten candidate genes are associated with conformational and locomotive traits in Spanish Purebred horses. J Appl Genet 2017 Aug;58(3):355-361.
            doi: 10.1007/s13353-016-0385-ypubmed: 27917442google scholar: lookup
          14. van der Zaag EJ, Weerts EA, van den Belt AJ, Back W. Clinicopathological findings in horses with a bi- or tripartite navicular bone. BMC Vet Res 2016 Apr 9;12:74.
            doi: 10.1186/s12917-016-0698-4pubmed: 27061802google scholar: lookup
          15. Bertholle CP, Meijer E, Back W, Stegeman A, van Weeren PR, van Nes A. A longitudinal study on the performance of in vivo methods to determine the osteochondrotic status of young pigs. BMC Vet Res 2016 Mar 24;12:62.
            doi: 10.1186/s12917-016-0682-zpubmed: 27012925google scholar: lookup
          16. McCoy AM, Beeson SK, Splan RK, Lykkjen S, Ralston SL, Mickelson JR, McCue ME. Identification and validation of risk loci for osteochondrosis in standardbreds. BMC Genomics 2016 Jan 12;17:41.
            doi: 10.1186/s12864-016-2385-zpubmed: 26753841google scholar: lookup
          17. Hellings IR, Ekman S, Hultenby K, Dolvik NI, Olstad K. Discontinuities in the endothelium of epiphyseal cartilage canals and relevance to joint disease in foals. J Anat 2016 Jan;228(1):162-75.
            doi: 10.1111/joa.12391pubmed: 26471892google scholar: lookup
          18. Tóth F, Nissi MJ, Ellermann JM, Wang L, Shea KG, Polousky J, Carlson CS. Novel Application of Magnetic Resonance Imaging Demonstrates Characteristic Differences in Vasculature at Predilection Sites of Osteochondritis Dissecans. Am J Sports Med 2015 Oct;43(10):2522-7.
            doi: 10.1177/0363546515596410pubmed: 26286878google scholar: lookup
          19. Olstad K, Hendrickson EH, Ekman S, Carlson CS, Dolvik NI. Local Morphological Response of the Distal Femoral Articular-Epiphyseal Cartilage Complex of Young Foals to Surgical Stab Incision and Potential Relevance to Cartilage Injury and Repair in Children. Cartilage 2013 Jul;4(3):239-48.
            doi: 10.1177/1947603513480024pubmed: 26069670google scholar: lookup
          20. Zanon G, DI Vico G, Marullo M. Osteochondritis dissecans of the talus. Joints 2014 Jul-Sep;2(3):115-23.
            doi: 10.11138/jts/2014.2.3.115pubmed: 25606554google scholar: lookup
          21. Olstad K, Kongsro J, Grindflek E, Dolvik NI. Consequences of the natural course of articular osteochondrosis in pigs for the suitability of computed tomography as a screening tool. BMC Vet Res 2014 Sep 9;10:212.
            doi: 10.1186/s12917-014-0212-9pubmed: 25199991google scholar: lookup
          22. McCoy AM, Toth F, Dolvik NI, Ekman S, Ellermann J, Olstad K, Ytrehus B, Carlson CS. Articular osteochondrosis: a comparison of naturally-occurring human and animal disease. Osteoarthritis Cartilage 2013 Nov;21(11):1638-47.
            doi: 10.1016/j.joca.2013.08.011pubmed: 23954774google scholar: lookup
          23. Tóth F, Nissi MJ, Zhang J, Benson M, Schmitter S, Ellermann JM, Carlson CS. Histological confirmation and biological significance of cartilage canals demonstrated using high field MRI in swine at predilection sites of osteochondrosis. J Orthop Res 2013 Dec;31(12):2006-12.
            doi: 10.1002/jor.22449pubmed: 23939946google scholar: lookup
          24. Armstrong AR, Buko EO, Johnson CP, Tóth F. Longitudinal In Vivo 3T MRI of Naturally Occurring Early Osteochondrosis Lesions in the Piglet Humeral Epiphyseal Cartilage and Growth Plate. J Orthop Res 2025 Nov;43(11):1934-1941.
            doi: 10.1002/jor.70044pubmed: 40783804google scholar: lookup
          25. Martinez-Saez L, Marín-García PJ, Llobat ML. Osteochondrosis in horses: An overview of genetic and other factors. Equine Vet J 2026 Jan;58(1):6-19.
            doi: 10.1111/evj.14518pubmed: 40302410google scholar: lookup
          26. Olstad K. Science-in-brief: Recent advances in failure of the blood supply to growth cartilage, osteochondrosis and developmental orthopaedic disease. Equine Vet J 2025 Sep;57(5):1161-1166.
            doi: 10.1111/evj.14486pubmed: 39924168google scholar: lookup
          27. Hoey S, Fogarty U, McAllister H, Puggioni A, Cloak B, Richard H, Skelly C, Laverty S. Ultrasonographic assessment of equine metacarpal cartilage thickness is more accurate than computed tomographic arthrography. Vet Radiol Ultrasound 2025 Jan;66(1):e13444.
            doi: 10.1111/vru.13444pubmed: 39367616google scholar: lookup
          28. Tóth F, Buko EO, Armstrong AR, Johnson CP. Relationship between the extent of vascular injury and the evolution of surgically induced osteochondrosis lesions in a piglet model. PLoS One 2024;19(8):e0308641.
            doi: 10.1371/journal.pone.0308641pubmed: 39116161google scholar: lookup
          29. Olstad K, Bugge MD, Ytrehus B, Kallerud AS. Closure of the neuro-central synchondrosis and other physes in foal cervical spines. Equine Vet J 2025 Jan;57(1):217-231.
            doi: 10.1111/evj.14093pubmed: 38594893google scholar: lookup
          30. Tóth F, Nissi MJ, Armstrong AR, Buko EO, Johnson CP. Epiphyseal cartilage vascular architecture at the distal humeral osteochondritis dissecans predilection site in juvenile pigs. J Orthop Res 2024 Apr;42(4):737-744.
            doi: 10.1002/jor.25732pubmed: 37971288google scholar: lookup
          31. Olstad K, Ekman S, Björnsdóttir S, Fjordbakk CT, Hansson K, Sigurdsson SF, Ley CJ. Osteochondrosis in the central and third tarsal bones of young horses. Vet Pathol 2024 Jan;61(1):74-87.
            doi: 10.1177/03009858231185108pubmed: 37431760google scholar: lookup