Literature DB >> 17022193

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

Carsten Staszyk1, Wiebke Wulff, Hans-Georg Jacob, Hagen Gasse.   

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.

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Year:  2006        PMID: 17022193     DOI: 10.1177/089875640602300303

Source DB:  PubMed          Journal:  J Vet Dent        ISSN: 0898-7564            Impact factor:   0.857


  6 in total

1.  Somatosensory profiling of patients with plaque-induced gingivitis: a case-control study.

Authors:  Chen Wang; Xin Zhou; Yaming Chen; Jinglu Zhang; Wu Chen; Peter Svensson; Kelun Wang
Journal:  Clin Oral Investig       Date:  2019-06-20       Impact factor: 3.573

2.  Effect of fiber distribution and realignment on the nonlinear and inhomogeneous mechanical properties of human supraspinatus tendon under longitudinal tensile loading.

Authors:  Spencer P Lake; Kristin S Miller; Dawn M Elliott; Louis J Soslowsky
Journal:  J Orthop Res       Date:  2009-12       Impact factor: 3.494

3.  Periodontal biomechanics: finite element simulations of closing stroke and power stroke in equine cheek teeth.

Authors:  Vanessa Cordes; Matthias Lüpke; Moritz Gardemin; Hermann Seifert; Carsten Staszyk
Journal:  BMC Vet Res       Date:  2012-07-11       Impact factor: 2.741

4.  Isolation and characterization of multipotent mesenchymal stromal cells from the gingiva and the periodontal ligament of the horse.

Authors:  Niels Mensing; Hagen Gasse; Nina Hambruch; Jan-Dirk Haeger; Christiane Pfarrer; Carsten Staszyk
Journal:  BMC Vet Res       Date:  2011-08-02       Impact factor: 2.741

5.  Three-dimensional anatomy of equine incisors: tooth length, enamel cover and age related changes.

Authors:  Patricia Schrock; Matthias Lüpke; Hermann Seifert; Carsten Staszyk
Journal:  BMC Vet Res       Date:  2013-12-09       Impact factor: 2.741

6.  A Computerized Simulation of the Occlusal Surface in Equine Cheek Teeth: A Simplified Model.

Authors:  Tomas Sterkenburgh; Ellen Schulz-Kornas; Michael Nowak; Carsten Staszyk
Journal:  Front Vet Sci       Date:  2022-01-03
  6 in total

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