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Journal of veterinary dentistry2006; 23(3); 143-147; doi: 10.1177/089875640602300303

Collagen fiber architecture of the periodontal ligament in equine cheek teeth.

Abstract: The objective of this study was to examine the spatial arrangement of the fiber apparatus of the equine periodontium which is supposed to meet two contrary requirements: (1) to attach the tooth firmly and elastically to the alveolar bone; and, to be appropriately remodeled and reconstructed in order to facilitate the prolonged eruption of the tooth. Specimens of periodontal ligament were obtained from the buccal and lingual/palatal aspects of the first molars from the maxilla and mandible of 12 horses. The animals were assigned to three age groups. Histological sections were prepared from three specific horizontal levels of the periodontal ligament and examined with conventional and polarized-light microscopy. At the gingival level, collagen fascicles (diameter > 200 microm) were densely packed. Their spatial alignment was the same in all age groups. The architecture of the collagen fiber apparatus differed at the middle and apical levels in the three age groups. There was a clear distinction between fibers, bundles, and fascicles. Bundling of collagen fibers, density of the fiber arrangement, and collagen fascicles with an alveolo-cemental orientation increased with age. The collagen fiber apparatus of the equine periodontal ligament is highly adaptive, responding continuously to the dynamic changes in the periodontal environment. Site-specific arrangements and age-dependent structural variations are assumed to maintain tooth support as the reserve crown gradually decreases in length with progressive dental attrition. Most of the age-dependent changes to the periodontal ligament in teeth examined in this study occurred at the apical level. The apical region of young teeth had no periodontal attachment, while the roots of older teeth were firmly attached to the alveolus. When evaluating periodontal ligament development, the individual tooth's 'dental age' should be considered rather than the animal's age to account for individual tooth eruption times.
Publication Date: 2006-10-07 PubMed ID: 17022193DOI: 10.1177/089875640602300303Google Scholar: Lookup
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  • Journal Article

Summary

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This study investigates the architecture of collagen fibers in the periodontal ligament of equine cheek teeth, relating it to the animal’s age and position of the tooth. The focus is on how these fibers adapt to the continuous changes in the periodontal environment, enabling the prolonged eruption of teeth and attaching them to the alveolar bone.

Objective and Methodology

  • The research aimed to explore the arrangement of the fiber apparatus in horses’ periodontium, which has dual roles: allowing the tooth to firmly yet flexibly attach to the alveolar bone, and accommodating the tooth’s prolonged eruption.
  • To achieve this, scientists collected specimens of periodontal ligament from different parts of the first molars from the maxilla and mandible of 12 horses, categorizing them into three age groups.
  • They prepared histological sections from three specific horizontal levels of the periodontal ligament and analyzed them with conventional and polarized-light microscopy. These levels included the gingival level, middle level, and apical level.

Findings

  • The gingival level exhibited densely packed collagen fascicles with the same spatial alignment across all age groups.
  • The fiber apparatus’ architecture varied at the middle and apical levels among the three age groups. Differences included a clear distinction between fibers, bundles, and fascicles, all of which increased in terms of bundling, density arrangement and orientation with age.
  • Researchers discovered that the collagen fiber apparatus of the equine periodontal ligament is highly adaptive, constantly responding to dynamic changes in the periodontal environment.
  • The variations in site-specific arrangements and age-dependent structural transformations likely help maintain tooth support as the reserve crown’s length gradually decreases due to dental attrition.

Implications and Conclusions

  • The study observed that most of the age-dependent changes to the periodontal ligament occur at the apical level. Younger teeth had no periodontal attachment at this level, while the roots of older teeth were firmly attached to the alveolus.
  • When investigating periodontal ligament development, the researchers suggested considering the tooth’s ‘dental age’ over the animal’s physical age. This factor adjusts for individual tooth eruption times, yielding a more precise age assessment.

Cite This Article

APA
Staszyk C, Wulff W, Jacob HG, Gasse H. (2006). Collagen fiber architecture of the periodontal ligament in equine cheek teeth. J Vet Dent, 23(3), 143-147. https://doi.org/10.1177/089875640602300303

Publication

ISSN: 0898-7564
NlmUniqueID: 9426426
Country: United States
Language: English
Volume: 23
Issue: 3
Pages: 143-147

Researcher Affiliations

Staszyk, Carsten
  • Institute of Anatomy, University of Veterinary Medicine Hannover, Germany. Carsten.Staszyk@tiho-hannover.de
Wulff, Wiebke
    Jacob, Hans-Georg
      Gasse, Hagen

        MeSH Terms

        • Age Factors
        • Animals
        • Cadaver
        • Collagen / ultrastructure
        • Elastic Tissue / anatomy & histology
        • Elastic Tissue / ultrastructure
        • Female
        • Horses / anatomy & histology
        • Male
        • Periodontal Ligament / anatomy & histology
        • Periodontal Ligament / ultrastructure
        • Tooth Root

        Citations

        This article has been cited 7 times.
        1. Sterkenburgh T, Schulz-Kornas E, Nowak M, Staszyk C. A Computerized Simulation of the Occlusal Surface in Equine Cheek Teeth: A Simplified Model.. Front Vet Sci 2021;8:789133.
          doi: 10.3389/fvets.2021.789133pubmed: 35047585google scholar: lookup
        2. Kau S, Failing K, Staszyk C. Computed Tomography (CT)-Assisted 3D Cephalometry in Horses: Interincisal Angulation of Clinical Crowns.. Front Vet Sci 2020;7:434.
          doi: 10.3389/fvets.2020.00434pubmed: 32851019google scholar: lookup
        3. Wang C, Zhou X, Chen Y, Zhang J, Chen W, Svensson P, Wang K. Somatosensory profiling of patients with plaque-induced gingivitis: a case-control study.. Clin Oral Investig 2020 Feb;24(2):875-882.
          doi: 10.1007/s00784-019-02963-4pubmed: 31222434google scholar: lookup
        4. Schrock P, Lüpke M, Seifert H, Staszyk C. Three-dimensional anatomy of equine incisors: tooth length, enamel cover and age related changes.. BMC Vet Res 2013 Dec 9;9:249.
          doi: 10.1186/1746-6148-9-249pubmed: 24321365google scholar: lookup
        5. Cordes V, Lüpke M, Gardemin M, Seifert H, Staszyk C. Periodontal biomechanics: finite element simulations of closing stroke and power stroke in equine cheek teeth.. BMC Vet Res 2012 Jul 11;8:60.
          doi: 10.1186/1746-6148-8-60pubmed: 22607543google scholar: lookup
        6. Mensing N, Gasse H, Hambruch N, Haeger JD, Pfarrer C, Staszyk C. Isolation and characterization of multipotent mesenchymal stromal cells from the gingiva and the periodontal ligament of the horse.. BMC Vet Res 2011 Aug 2;7:42.
          doi: 10.1186/1746-6148-7-42pubmed: 21810270google scholar: lookup
        7. Lake SP, Miller KS, Elliott DM, Soslowsky LJ. Effect of fiber distribution and realignment on the nonlinear and inhomogeneous mechanical properties of human supraspinatus tendon under longitudinal tensile loading.. J Orthop Res 2009 Dec;27(12):1596-602.
          doi: 10.1002/jor.20938pubmed: 19544524google scholar: lookup