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Regenerative capacity of augmented bone in rat calvarial guided bone augmentation model

  • Kubota, Tatsuya (Division of Applied Oral Sciences, Nihon University Graduate School of Dentistry) ;
  • Hasuike, Akira (Department of Periodontology, Nihon University School of Dentistry) ;
  • Ozawa, Yasumasa (Division of Applied Oral Sciences, Nihon University Graduate School of Dentistry) ;
  • Yamamoto, Takanobu (Division of Applied Oral Sciences, Nihon University Graduate School of Dentistry) ;
  • Tsunori, Katsuyoshi (Department of Periodontology, Nihon University School of Dentistry) ;
  • Yamada, Yutaka (Private Practice) ;
  • Sato, Shuichi (Department of Periodontology, Nihon University School of Dentistry)
  • Received : 2016.12.26
  • Accepted : 2017.02.12
  • Published : 2017.04.30

Abstract

Purpose: Guided bone regeneration (GBR) is the most widely used technique to regenerate and augment bones. Even though augmented bones (ABs) have been examined histologically in many studies, few studies have been conducted to examine the biological potential of these bones and the healing dynamics following their use. Moreover, whether the bone obtained from the GBR procedure possesses the same functions as the existing autogenous bone is uncertain. In particular, little attention has been paid to the regenerative ability of GBR bone. Therefore, the present study histologically evaluated the regenerative capacity of AB in the occlusive space of a rat guided bone augmentation (GBA) model. Methods: The calvaria of 30 rats were exposed, and plastic caps were placed on the right of the calvaria in 10 of the 30 rats. After a 12-week healing phase, critical-sized calvarial bone defects (diameter: 5.0 mm) were trephined into the dorsal parietal bone on the left of the calvaria. Bone particles were harvested from the AB or the cortical bone (CB) using a bone scraper and transplanted into the critical defects. Results: The newly generated bone at the defects' edge was evaluated using micro-computed tomography (micro-CT) and histological sections. In the micro-CT analysis, the radiopacity in both the augmented and the CB groups remained high throughout the observational period. In the histological analysis, the closure rate of the CB was significantly higher than in the AB group. The numbers of cells positive for runt-related transcription factor 2 (Runx2) and tartrate-resistant acid phosphatase (TRAP) in the AB group were larger than in the CB group. Conclusions: The regenerative capacity of AB in the occlusive space of the rat GBA model was confirmed. Within the limitations of this study, the regenerative ability of the AB particulate transplant was inferior to that of the CB particulate transplant.

Keywords

References

  1. Simion M, Trisi P, Piattelli A. Vertical ridge augmentation using a membrane technique associated with osseointegrated implants. Int J Periodontics Restorative Dent 1994;14:496-511.
  2. Simion M, Jovanovic SA, Trisi P, Scarano A, Piattelli A. Vertical ridge augmentation around dental implants using a membrane technique and autogenous bone or allografts in humans. Int J Periodontics Restorative Dent 1998;18:8-23.
  3. Tinti C, Parma-Benfenati S, Polizzi G. Vertical ridge augmentation: what is the limit? Int J Periodontics Restorative Dent 1996;16:220-9.
  4. Schmid J, Hammerle CH, Stich H, Lang NP. Supraplant, a novel implant system based on the principle of guided bone generation. A preliminary study in the rabbit. Clin Oral Implants Res 1991;2:199-202. https://doi.org/10.1034/j.1600-0501.1991.020407.x
  5. Linde A, Thoren C, Dahlin C, Sandberg E. Creation of new bone by an osteopromotive membrane technique: an experimental study in rats. J Oral Maxillofac Surg 1993;51:892-7. https://doi.org/10.1016/S0278-2391(10)80111-9
  6. Jovanovic SA, Schenk RK, Orsini M, Kenney EB. Supracrestal bone formation around dental implants: an experimental dog study. Int J Oral Maxillofac Implants 1995;10:23-31.
  7. Nyman S, Lindhe J, Karring T, Rylander H. New attachment following surgical treatment of human periodontal disease. J Clin Periodontol 1982;9:290-6. https://doi.org/10.1111/j.1600-051X.1982.tb02095.x
  8. Nyman S, Gottlow J, Karring T, Lindhe J. The regenerative potential of the periodontal ligament. An experimental study in the monkey. J Clin Periodontol 1982;9:257-65. https://doi.org/10.1111/j.1600-051X.1982.tb02065.x
  9. Yamada Y, Nanba K, Ito K. Effects of occlusiveness of a titanium cap on bone generation beyond the skeletal envelope in the rabbit calvarium. Clin Oral Implants Res 2003;14:455-63. https://doi.org/10.1034/j.1600-0501.2003.00832.x
  10. Yamada Y, Sato S, Yagi H, Ujiie H, Ezawa S, Ito K. Correlation in the densities of augmented and existing bone in guided bone augmentation. Clin Oral Implants Res 2012;23:837-45. https://doi.org/10.1111/j.1600-0501.2011.02204.x
  11. Schenk RK, Buser D, Hardwick WR, Dahlin C. Healing pattern of bone regeneration in membrane-protected defects: a histologic study in the canine mandible. Int J Oral Maxillofac Implants 1994;9:13-29.
  12. Kochi G, Sato S, Ebihara H, Hirano J, Arai Y, Ito K. A comparative study of microfocus CT and histomorphometry in the evaluation of bone augmentation in rat calvarium. J Oral Sci 2010;52:203-11. https://doi.org/10.2334/josnusd.52.203
  13. Oginuma T, Sato S, Udagawa A, Saito Y, Arai Y, Ito K. Autogenous bone with or without hydroxyapatite bone substitute augmentation in rat calvarium within a plastic cap. Oral Surg Oral Med Oral Pathol Oral Radiol 2012;114:S107-13. https://doi.org/10.1016/j.oooo.2011.08.004
  14. Shino H, Hasuike A, Arai Y, Honda M, Isokawa K, Sato S. Melatonin enhances vertical bone augmentation in rat calvaria secluded spaces. Med Oral Patol Oral Cir Bucal 2016;21:e122-6.
  15. Wen B, Li Z, Nie R, Liu C, Zhang P, Miron RJ, et al. Influence of biphasic calcium phosphate surfaces coated with Enamel Matrix Derivative on vertical bone growth in an extra-oral rabbit model. Clin Oral Implants Res 2016;27:1297-304. https://doi.org/10.1111/clr.12740
  16. Hosoya A, Ninomiya T, Hiraga T, Zhao C, Yoshiba K, Yoshiba N, et al. Alveolar bone regeneration of subcutaneously transplanted rat molar. Bone 2008;42:350-7. https://doi.org/10.1016/j.bone.2007.09.054
  17. Gruber R, Baron M, Busenlechner D, Kandler B, Fuerst G, Watzek G. Proliferation and osteogenic differentiation of cells from cortical bone cylinders, bone particles from mill, and drilling dust. J Oral Maxillofac Surg 2005;63:238-43. https://doi.org/10.1016/j.joms.2004.04.030
  18. Urban IA, Lozada JL, Jovanovic SA, Nagursky H, Nagy K. Vertical ridge augmentation with titanium-reinforced, dense-PTFE membranes and a combination of particulated autogenous bone and anorganic bovine bone-derived mineral: a prospective case series in 19 patients. Int J Oral Maxillofac Implants 2014;29:185-93. https://doi.org/10.11607/jomi.3346
  19. Urban IA, Nagursky H, Lozada JL. Horizontal ridge augmentation with a resorbable membrane and particulated autogenous bone with or without anorganic bovine bone-derived mineral: a prospective case series in 22 patients. Int J Oral Maxillofac Implants 2011;26:404-14.

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