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Differences in extracellular matrix proteins between Friesian horses with aortic rupture, unaffected Friesians and Warmblood horses.

Abstract: Unlike in Warmblood horses, aortic rupture is quite common in Friesian horses, in which a hereditary trait is suspected. The aortic connective tissue in affected Friesians shows histological changes such as medial necrosis, elastic fibre fragmentation, mucoid material accumulation and fibrosis with aberrant collagen morphology. However, ultrastructural examination of the collagen fibres of the mid-thoracic aorta has been inconclusive in further elucidating the pathogenesis of the disease. Objective: To assess several extracellular matrix (ECM) components biochemically in order to explore a possible underlying breed-related systemic ECM defect in Friesians with aortic rupture. Methods: Cadaver study. Methods: Tissues from affected Friesians (n = 18), unaffected Friesians (n = 10) and Warmblood horses (n = 30) were compared. Samples were taken from the thoracic aorta at the level of the rupture site, from two locations caudal to the rupture and from the deep digital flexor tendon. Total collagen content, post-translational modifications of collagen formation including lysine hydroxylation, and hydroxylysylpyridinoline (HP), lysylpyridinoline (LP) and pyrrole cross-links were analysed. Additionally, elastin cross-links, glycosaminoglycan content and matrix metalloproteinase (MMP) activity were assessed. Results: Significantly increased MMP activity and increased LP and HP cross-linking, lysine hydroxylation and elastin cross-linking were found at the site of rupture in affected Friesians. These changes may reflect processes involved in healing and aneurysm formation. Unaffected Friesians had less lysine hydroxylation and pyrrole cross-linking within the tendons compared with Warmblood horses. No differences in the matrix of the aorta were found between normal Warmbloods and Friesian horses. Conclusions: Small sample size. Conclusions: The differences in collagen parameters in tendon tissue may reflect differences in connective tissue metabolism between Friesians and Warmblood horses.
Publication Date: PubMed ID: 27859600
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Summary

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This research aims to understand the biochemistry of aortic rupture in Friesian horses, an issue not commonly found in Warmblood horses. It suspects a genetic, breed-related systemic defect in Friesians’ extracellular matrix (ECM), which could potentially cause this condition.

Methodology

  • The researchers conducted a cadaver study with tissues from 18 affected Friesian horses, 10 unaffected Friesians, and 30 Warmblood horses.
  • They compared samples taken from the thoracic aorta at the rupture site, two locations caudal to the rupture, and from the deep digital flexor tendon.
  • The analysis focused on the total collagen content, lysine hydroxylation, and cross-links of hydroxylysylpyridinoline (HP), lysylpyridinoline (LP), and pyrrole. Additionally, they evaluated elastin cross-links, glycosaminoglycan content, and matrix metalloproteinase (MMP) activity.

Findings

  • Significant increases in MMP activity, LP and HP cross-linking, lysine hydroxylation, and elastin cross-linking were observed at the site of rupture in affected Friesians. These might be indicative of the healing processes and aneurysm formation.
  • Compared to Warmblood horses, unaffected Friesians had lower lysine hydroxylation and pyrrole cross-linking in the tendons.
  • The matrix of the aorta demonstrated no differences between normal Warmblood horses and Friesian horses.

Conclusions

  • Due to the small sample size of the study, extrapolation of the result should be done cautiously.
  • The differences observed in collagen parameters within tendon tissue might be due to the difference in connective tissue metabolism between Friesians and Warmblood horses.
  • The prevalent aortic rupture in Friesian horses could be linked to an inherent breed-related systemic defect, as suspected originally. Further research is warranted to confirm these findings and understand the underlying biochemistry in depth.

Cite This Article

APA
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Citations

This article has been cited 5 times.
  1. Giessen EJM, Stas EKL, Grinwis GCM, Veraa S. Imaging Findings of Congenital Distal Interphalangeal Joint Dysplasia in a 3-Month-Old Friesian Foal. Vet Radiol Ultrasound 2025 Sep;66(5):e70076.
    doi: 10.1111/vru.70076pubmed: 40831150google scholar: lookup
  2. Toor IS, Rückerl D, Mair I, Ainsworth R, Meloni M, Spiroski AM, Benezech C, Felton JM, Thomson A, Caporali A, Keeble T, Tang KH, Rossi AG, Newby DE, Allen JE, Gray GA. Eosinophil Deficiency Promotes Aberrant Repair and Adverse Remodeling Following Acute Myocardial Infarction. JACC Basic Transl Sci 2020 Jul;5(7):665-681.
    doi: 10.1016/j.jacbts.2020.05.005pubmed: 32760855google scholar: lookup
  3. Casola C, Pot SA, Lavaud A, Voelter K. Corneal cross-linking as a treatment for corneal dystrophy with secondary bacterial infection in a Friesian horse. Clin Case Rep 2020 Apr;8(4):709-715.
    doi: 10.1002/ccr3.2725pubmed: 32274042google scholar: lookup
  4. Vera L, De Clercq D, Van Steenkiste G, Decloedt A, Chiers K, van Loon G. Differences in ultrasound-derived arterial wall stiffness parameters and noninvasive blood pressure between Friesian horses and Warmblood horses. J Vet Intern Med 2020 Mar;34(2):893-901.
    doi: 10.1111/jvim.15705pubmed: 32032455google scholar: lookup
  5. Saey V, Tang J, Ducatelle R, Croubels S, De Baere S, Schauvliege S, van Loon G, Chiers K. Elevated urinary excretion of free pyridinoline in Friesian horses suggests a breed-specific increase in collagen degradation. BMC Vet Res 2018 Apr 25;14(1):139.
    doi: 10.1186/s12917-018-1454-8pubmed: 29699546google scholar: lookup