open access

Vol 81, No 4 (2022)
Original article
Submitted: 2021-08-07
Accepted: 2021-08-26
Published online: 2021-10-07
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Periodontal ligament regulatory role in experimental diabetic rat model of periodontium remodelling

A. Petrović1, M. Trandafilović2, G. Drevenšek3, A. Plut4, M. Drevenšek45
·
Pubmed: 34642931
·
Folia Morphol 2022;81(4):1031-1041.
Affiliations
  1. Department of Histology and Embryology, Faculty of Medicine, University of Niš, Serbia
  2. Department of Anatomy, Faculty of Medicine, University of Niš, Serbia
  3. Institute of Pharmacology and Experimental Toxicology, Faculty of Medicine, University of Ljubljana, Slovenia
  4. Department of Orthodontics, University Medical Centre Ljubljana, Ljubljana, Slovenia
  5. Department of Orthodontics, Faculty of Medicine, University of Ljubljana, Slovenia

open access

Vol 81, No 4 (2022)
ORIGINAL ARTICLES
Submitted: 2021-08-07
Accepted: 2021-08-26
Published online: 2021-10-07

Abstract

Background: Diabetes, among multiple systemic harmful health issues, also may deteriorate normal regenerative and reparative functions of periodontium. The aim of this research was to study the role of periodontal ligament in tissue remodelling under the orthodontic appliance stimulation in two rat experimental models (healthy Wistar rats and Goto-Kakizaki, rodent model of non-obese type 2 diabetes).
Materials and methods: Four groups of rats were defined: Wistar (WI; n = 8) and Goto-Kakizaki (GK; n = 8) control groups without orthodontic appliances, and Wistar (n = 16) and Goto-Kakizaki (n = 16) appliance groups with orthodontic appliances. After 42 days, rats were sacrificed and histopathology descriptive analysis about periodontal ligament and adjacent structures was performed as well as cellularity of periodontal ligament and Kappa curvature of tooth roots were measured.
Results: Goto-Kakizaki control rats showed statistically significantly higher cellularity in comparison with Wistar control rats (p < 0.001). Both applied groups (WI 44.63 ± 6.68; GK 79.58 ± 10.06) also showed statistically significantly higher cellularity (p < 0.001) in comparison with control groups (WI 34.48 ± 6.92; GK 45.31 ± 11.18). Applied groups (WI 0.197 ± 0.2; GK 0.126 ± 0.083) had statistically significant higher values of Kappa curvature in comparison with control groups (WI 0.023 ± 0.011; GK 0.037 ± 0.011) (WI appliance vs. WI control: p < 0.001; GK appliance vs. GK control: p < 0.05). Agitated periodontal ligament caused different degrees of cementoclasia and additionally dentinoclasia, altering the natural root curvature.
Conclusions: Although not significantly different (WI and GK appliance groups) according to degree of molar roots odontoclasia, higher cellularity of agitated GK periodontal ligament could be influencing factor for, as previously reported, elevated osteoclast mobilization and possible prolonged periodontium reconstitution.

Abstract

Background: Diabetes, among multiple systemic harmful health issues, also may deteriorate normal regenerative and reparative functions of periodontium. The aim of this research was to study the role of periodontal ligament in tissue remodelling under the orthodontic appliance stimulation in two rat experimental models (healthy Wistar rats and Goto-Kakizaki, rodent model of non-obese type 2 diabetes).
Materials and methods: Four groups of rats were defined: Wistar (WI; n = 8) and Goto-Kakizaki (GK; n = 8) control groups without orthodontic appliances, and Wistar (n = 16) and Goto-Kakizaki (n = 16) appliance groups with orthodontic appliances. After 42 days, rats were sacrificed and histopathology descriptive analysis about periodontal ligament and adjacent structures was performed as well as cellularity of periodontal ligament and Kappa curvature of tooth roots were measured.
Results: Goto-Kakizaki control rats showed statistically significantly higher cellularity in comparison with Wistar control rats (p < 0.001). Both applied groups (WI 44.63 ± 6.68; GK 79.58 ± 10.06) also showed statistically significantly higher cellularity (p < 0.001) in comparison with control groups (WI 34.48 ± 6.92; GK 45.31 ± 11.18). Applied groups (WI 0.197 ± 0.2; GK 0.126 ± 0.083) had statistically significant higher values of Kappa curvature in comparison with control groups (WI 0.023 ± 0.011; GK 0.037 ± 0.011) (WI appliance vs. WI control: p < 0.001; GK appliance vs. GK control: p < 0.05). Agitated periodontal ligament caused different degrees of cementoclasia and additionally dentinoclasia, altering the natural root curvature.
Conclusions: Although not significantly different (WI and GK appliance groups) according to degree of molar roots odontoclasia, higher cellularity of agitated GK periodontal ligament could be influencing factor for, as previously reported, elevated osteoclast mobilization and possible prolonged periodontium reconstitution.

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Keywords

periodontal ligament, fibroblast, orthodontic appliance, tooth root, remodelling, periodontium

About this article
Title

Periodontal ligament regulatory role in experimental diabetic rat model of periodontium remodelling

Journal

Folia Morphologica

Issue

Vol 81, No 4 (2022)

Article type

Original article

Pages

1031-1041

Published online

2021-10-07

Page views

4202

Article views/downloads

797

DOI

10.5603/FM.a2021.0101

Pubmed

34642931

Bibliographic record

Folia Morphol 2022;81(4):1031-1041.

Keywords

periodontal ligament
fibroblast
orthodontic appliance
tooth root
remodelling
periodontium

Authors

A. Petrović
M. Trandafilović
G. Drevenšek
A. Plut
M. Drevenšek

References (29)
  1. Al-Qawasmi RA, Hartsfield JK, Everett ET, et al. Genetic predisposition to external apical root resorption. Am J Orthod Dentofacial Orthop. 2003; 123(3): 242–252.
  2. Arita K, Hotokezaka H, Hashimoto M, et al. Effects of diabetes on tooth movement and root resorption after orthodontic force application in rats. Orthod Craniofac Res. 2016; 19(2): 83–92.
  3. Baur PS, Barratt GF, Brown GM, et al. Ultrastructural evidence for the presence of "fibroclasts" and "myofibroclasts" in wound healing tissues. J Trauma. 1979; 19(10): 744–756.
  4. Beertsen W, McCulloch CA, Sodek J. The periodontal ligament: a unique, multifunctional connective tissue. Periodontol 2000. 1997; 13: 20–40.
  5. Chen B, Wu W, Sun W, et al. RANKL expression in periodontal disease: where does RANKL come from? Biomed Res Int. 2014; 2014: 731039.
  6. Cho MI, Garant PR. Mirror symmetry of newly divided rat periodontal ligament fibroblasts in situ and its relationship to cell migration. J Periodontal Res. 1985; 20(2): 185–200.
  7. Davidovitch Z. Tooth movement. Crit Rev Oral Biol Med. 1991; 2(4): 411–450.
  8. Esterre P, Dedet JP, Guerret S, et al. Matrix remodelling and fibroblast phenotype in early lesions of human cutaneous leishmaniasis. Pathol Res Pract. 1991; 187(8): 924–930.
  9. Everts V, van der Zee E, Creemers L, et al. Phagocytosis and intracellular digestion of collagen, its role in turnover and remodelling. Histochem J. 1996; 28(4): 229–245.
  10. Garant PR, Cho MI. Cytoplasmic polarization of periodontal ligament fibroblasts. Implications for cell migration and collagen secretion. J Periodontal Res. 1979; 14(2): 95–106.
  11. GuilhermeAJV. Histological evaluation of the periodontal ligament of Wistar rats under the effect of acute hipotireoidism inducted by metimazol (tapazol®).Dostoral Thesis,Faculdade de Ciências Médicas da Universidade Estadual de Campinas, Brasil 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/313461.
  12. Harris E, Kineret S, Tolley E. A heritable component for external apical root resorption in patients treated orthodontically. Am J Orthod Dentofacial Orthop. 1997; 111(3): 301–309.
  13. Henneman S, Von den Hoff JW, Maltha JC. Mechanobiology of tooth movement. Eur J Orthod. 2008; 30(3): 299–306.
  14. Howard PS, Kucich U, Taliwal R, et al. Mechanical forces alter extracellular matrix synthesis by human periodontal ligament fibroblasts. J Periodontal Res. 1998; 33(8): 500–508.
  15. Krishnan V, Davidovitch Z. Cellular, molecular, and tissue-level reactions to orthodontic force. Am J Orthod Dentofacial Orthop. 2006; 129(4): 469.e1–469.32.
  16. Newman W. Possible etiologic factors in external root resorption. Am J Orthod. 1975; 67(5): 522–539.
  17. Pilon J, Kuijpers-Jagtman A, Maltha J. Magnitude of orthodontic forces and rate of bodily tooth movement. An experimental study. Am J Orthod Dentofacial Orthop. 1996; 110(1): 16–23.
  18. Plut A, Sprogar Š, Drevenšek G, et al. Bone remodeling during orthodontic tooth movement in rats with type 2 diabetes. Am J Orthod Dentofacial Orthop. 2015; 148(6): 1017–1025.
  19. Rippin JW. Collagen turnover in the periodontal ligament under normal and altered functional forces. I. Young rat molars. J Periodontal Res. 1976; 11(2): 101–107.
  20. Rippin JW. Collagen turnover in the periodontal ligament under normal and altered functional forces. II. Adult rat molars. J Periodontal Res. 1978; 13(2): 149–154.
  21. Sokos D, Everts V, de Vries TJ. Role of periodontal ligament fibroblasts in osteoclastogenesis: a review. J Periodontal Res. 2015; 50(2): 152–159.
  22. Sprogar S, Vaupotic T, Cör A, et al. The endothelin system mediates bone modeling in the late stage of orthodontic tooth movement in rats. Bone. 2008; 43(4): 740–747.
  23. Svoboda EL, Shiga A, Deporter DA. A stereologic analysis of collagen phagocytosis by fibroblasts in three soft connective tissues with differing rates of collagen turnover. Anat Rec. 1981; 199(4): 473–480.
  24. Ten Cate AR, Deporter DA, Freeman E. The role of fibroblasts in the remodeling of periodontal ligament during physiologic tooth movement. Am J Orthod. 1976; 69(2): 155–168.
  25. Villarino ME, Lewicki M, Ubios AM. Bone response to orthodontic forces in diabetic Wistar rats. Am J Orthod Dentofacial Orthop. 2011; 139(4 Suppl): S76–S82.
  26. Von den Hoff JW. Effects of mechanical tension on matrix degradation by human periodontal ligament cells cultured in collagen gels. J Periodontal Res. 2003; 38(5): 449–457.
  27. Weltman B, Vig KWL, Fields HW, et al. Root resorption associated with orthodontic tooth movement: a systematic review. Am J Orthod Dentofacial Orthop. 2010; 137(4): 462–76; discussion 12A.
  28. Yang CY. Effect RANKL Produced by Periodontal Ligament Cells on Orthodontic Tooth Movement. Doctoral Thesis, University of Pennsylvania, USA 2016. https://repository.upenn.edu/dental_theses/.
  29. Zheng J, Chen S, Albiero ML, et al. Diabetes activates periodontal ligament fibroblasts via NF-κB in vivo. J Dent Res. 2018; 97(5): 580–588.

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