Histomorphometric evaluation of bone regeneration using autogenous bone and beta-tricalcium phosphate in diabetic rabbits

  • Milka Živadinović Clinic of Oral Surgery, Faculty of Dental Medicine, University of Belgrade, Belgrade, Serbia
  • Miroslav Andrić Clinic of Oral Surgery, Faculty of Dental Medicine, University of Belgrade, Belgrade, Serbia
  • Verica Milošević Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Belgrade, Serbia
  • Milica Manojlović-Stojanoski Department of Cytology, Institute for Biological Research “Siniša Stanković”, University of Belgrade, Belgrade, Serbia
  • Branislav Prokić Department for Surgery, Orthopedic and Ophthalmology, Faculty of Veterinary Medicine, University of Belgrade, Belgrade, Serbia
  • Bogomir Prokić Department for Surgery, Orthopedic and Ophthalmology, Faculty of Veterinary Medicine, University of Belgrade, Belgrade, Serbia
  • Aleksandar Dimić Department of Otorhinolaryngology, Military Medical Academy, Belgrade, Serbia
  • Dejan Ćalasan Clinic of Oral Surgery, Faculty of Dental Medicine, University of Belgrade, Belgrade, Serbia
  • Božidar M Brković Clinic of Oral Surgery, Faculty of Dental Medicine, University of Belgrade, Belgrade, Serbia
Keywords: rabbitis, diabetes mellitus, bone regeneration, transplantation, autologous, beta-tricalcium phosphate,

Abstract


Background/Aim. The mechanism of impaired bone healing in diabetes mellitus includes different tissue and cellular level activities due to micro- and macrovascular changes. As a chronic metabolic disease with vascular complications, diabetes affects a process of bone regeneration as well. The therapeutic approach in bone regeneration is based on the use of osteoinductive autogenous grafts as well as osteoconductive synthetic material, like a β-tricalcium phosphate. The aim of the study was to determine the quality and quantity of new bone formation after the use of autogenous bone and β-tricalcium phosphate in the model of calvarial critical-sized defect in rabbits with induced diabetes mellitus type I. Methods. The study included eight 4-month-old Chincilla rabbits with alloxan-induced diabetes mellitus type I. In all animals, there were surgically created two calvarial bilateral defects (diameter 12 mm), which were grafted with autogenous bone and β-tricalcium phosphate (n = 4) or served as unfilled controls (n = 4). After 4 weeks of healing, animals were sacrificed and calvarial bone blocks were taken for histologic and histomorphometric analysis. Beside descriptive histologic evaluation, the percentage of new bone formation, connective tissue and residual graft were calculated. All parameters were statistically evaluated by Friedman Test and post hock Wilcoxon Singed Ranks Test with a significance of p < 0.05. Results. Histology revealed active new bone formation peripherally with centrally located connective tissue, newly formed woven bone and well incorporated residual grafts in all treated defects. Control samples showed no bone bridging of defects. There was a significantly more new bone in autogeonous graft (53%) compared with β-tricalcium phosphate (30%), (p < 0.030) and control (7%), (p < 0.000) groups. A significant difference was also recorded between β-tricalcium phosphate and control groups (p < 0.008). Conclusion. In the present study on the rabbit grafting model with induced diabetes mellitus type I, the effective bone regeneration of critical bone defects was obtained using autogenous bone graft.

References

Erdogan Ö, Charudilaka S, Tatli U, Damlar I. A review on alveo-lar bone augmentation and dental implant success in diabetic patients. J Oral Surg 2010; 3(4): 115–19.

He H, Liu R, Desta T, Leone C, Gerstenfeld LC, Graves DT. Dia-betes causes decreased osteoclastogenesis, reduced bone for-mation, and enhanced apoptosis of osteoblastic cells in bacte-ria stimulated bone loss. Endocrinology 2004; 145(1): 447−52.

Nevins ML, Karimbux NY, Weber HP, Giannobile WV, Fiorellini JP. Wound healing around endosseous implants in experi-mental diabetes. Int J Oral Maxillofac Implants 1998; 13(5): 620−9.

Kotsovilis S, Karoussis IK, Fourmousis I. A comprehensive and critical review of dental implant placement in diabetic animals and patients. Clin Oral Impl Res 2006; 17(5): 587–99.

Lu H, Kraut D, Gerstenfeld LC, Graves DT. Diabetes interferes with the bone formation by affecting the expression of tran-scription factors that regulate osteoblast differentiation. Endo-crinology 2003; 144(1): 346–52.

Krakauer JC, Mckenna MJ, Buderer NF, Rao DS, Whitehouse FW, Michael Parfitt AM. Bone loss and bone turnover in diabetes. Diabetes 1995; 44(7): 775−82.

Falanga V. Wound healing and its impairment in the diabetic foot. Lancet 2005; 366(9498): 1736–43.

Maruyama K, Asai J, Ii M, Thorne T, Losordo DW, D'Amore PA. Decreased macrophage number and activation lead to reduced lymphatic vessel formation and contribute to impaired diabetic would healing. Am J Pathol 2007; 170(4): 1178–89.

Schmitz JP, Hollinger JO. The critical size defect as an experi-mental model for craniomandibulofacial nonunions. Clin Or-thop Relat Res 1986; (205): 299−308.

Mardas N, Derekz X, Donos N, Dard M. Experimental morel for bone regeneration in oral and cranio-maxillofacial-surgery. J Invest Surg 2014; 27(1): 32−49.

Giannoudis PV, Dinopoulos H, Tsiridis E. Bone substitutes: an update. Injury 2005; 36 Suppl 3: S20−7.

Bidic SM, Calvert JW, Marra K, Kumta P, Campbell P, Mitchell R, et al. Rabbit calvarial wound healing by means of seeded Caprotite® scaffolds. J Dent Res 2003; 82(2): 131−5.

Murai M, Sato S, Fukase Y, Yamada Y, Komiyama K, Ito K. Ef-fects of different sizes of β-tricalcium phosphate particles on bone augmentation within a titanium cap in rabbit calvarium. Dent Mater J 2006; 25(1): 87−96.

Vieira EM, Ueno CS, Valva VN, Goulart MG, Nogueira Tde O, Gomes M. Bone regeneration in cranioplasty and clinical com-plications in rabbits with alloxan-induced diabetes. Braz Oral Res 2008; 22(2): 184−91.

Gomes MF, Destro MF, Banzi EC, Vieira EM, Morosolli AR, Gou-lart MG. Optical density of bone repair after implantation of homogenous demineralized dentin matrix in diabetic rabbits. Braz Oral Res 2008; 22(3): 275-80.

Esteves JC, Aranega AM, Borrasca AG, Fattah CM, Garcia-Junior IR. Repair process of surgical defects filled with autogenous bone grafts in tibiae of diabetic rats. J Appl Oral Sci 2008; 16(5): 316−20.

Mariano R, Messora M, de Morais A, Nagata M, Furlaneto F, Avelino C et al. Bone healing in critical-size defects treated with platelet-rich plasma: a histologic and histometric study in the calvaria of diabetic rat. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2010; 109(1): 72−8.

Cooper G, Mooney M, Gosain A, Campbell P, Losee J, Huard J. Testing the critical size in calvarial bone defects: revisiting the concept of a critical-size defect. Plast Reconstr Surg 2010; 125(6): 1685–92.

Zerbo IR, Zijderveld SA, de Boer A, Bronckers AL, de Lange G, ten Bruggenkate CM, et al. Histomorphometry of human sinus floor augmentation using a porous beta-tricalcium phosphate: a prospective study. Clin Oral Implants Res 2004; 15(6): 724−32.

Brkovic B, Prasad H, Rohrer M, Konandreas G, Agrogiannis G, An-tunovic D, et al. Beta-tricalcium phosphate/type I collagen cones with or without a barrier membrane in human extraction socket healing: clinical, histologic, histomorphometric and immunohistochemical evaluation. Clin Oral Investig 2012; 16(2): 581−90.

Park JW, Kim JM, Lee HJ, Jeong SH, Suh JY, Hanawa T. Bone healing with oxytocin-loaded microporous β TCP bone substitute in ectopic bone formation model and critical-sized osseous defect in rat. J Clin Periodontol 2014, 41(2): 181−90.

Pripatnanont P, Nuntanaranont T, Vongvatcharanon S, Lim-lertmongkol S. Osteoconductive Effects of 3 Heat-Treated Hy-droxyapatites in Rabbit Calvarial Defects. J Oral Maxillofac Surg 2007; 65(12): 2418−24.

Humber CC, Sandor GK, Davis JM, Peel SA, Brkovic B, Kim YD, et al. Bone healing with an in situ-formed bioresorbable poly-ethylene glycol hydrogel membrane in rabbit calvarial defects. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2010, 109(3): 372−84.

Retzepi M, Lewis MP, Donos N. Effect of diabetes and metabolic control on de novo bone formation following guided bone regeneration. Clin Oral Impl Res 2010; 21(1): 71–9.

Claro FA, Lima JR, Salgado MA, Gomes MF. Porous Polyeth-ylene for tissue engineering applications in diabetic rats treated with calcitonin: histomorphometric analysis. Int J Oral Maxil-lofac Implants 2005; 20(2): 211−9.

Calvo-Guirado JL, Ramirez-Fernandez MP, Delgado-Ruiz RA, Mate-Sanchez JE, Velasquez P, de Aza PN. Influence of Biphasic β TCP with and without the use of collagen membrane on bone healing of surgically critical sized defects. A radiological, histo-logical and histomorphometric study. Clin Oral Impl Res 2014, 25(11): 1228−38.

Published
2017/03/14
Section
Original Paper