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1.
Angle Orthod ; 93(4): 476-481, 2023 07 01.
Article in English | MEDLINE | ID: mdl-36928563

ABSTRACT

OBJECTIVES: To evaluate the effect of systemic administration of omega-3 fatty acids on orthodontic tooth movement (OTM) with histological analysis. MATERIALS AND METHODS: OTM was induced in 20 adult albino New Zealand rabbits, divided into omega-3 and control groups, with nickel-titanium coil springs for 21 days. Omega-3 or saline was given every day via oral gavage during the experimental period. Animals were sacrificed for histomorphometric analysis of alveolar bone remodeling after 21 days of OTM. RESULTS: A significant difference in OTM amount was found in the third week of OTM with means of 1.445 ± 0.13 and 1.72 ± 0.15 for the experimental and control groups, respectively. Histomorphometric analysis showed a significant reduction in the area of active bone-resorptive lacunae and a significant increase in osteoblastic activity in the omega-3 group after 3 weeks. CONCLUSIONS: Strong evidence of the osteoclastic inhibitory effect of systemic omega-3 was found, which reduced the percentage and amount of OTM.


Subject(s)
Bone Resorption , Fatty Acids, Omega-3 , Animals , Rabbits , Rats , Bone Remodeling , Bone Resorption/pathology , Fatty Acids, Omega-3/pharmacology , Osteoclasts/pathology , Rats, Wistar , Tooth Movement Techniques
2.
J Oral Maxillofac Surg ; 73(12): 2257-72, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26215489

ABSTRACT

PURPOSE: The aim of the present study was to evaluate the effect of a porous silica-calcium phosphate composite (SCPC50) loaded with and without recombinant human bone morphogenetic protein-2 (rhBMP-2) on alveolar ridge augmentation in saddle-type defects. MATERIALS AND METHODS: Micro-granules of SCPC50 resorbable bioactive ceramic were coated with rhBMP-2 10 mg and then implanted into a saddle-type defect (12 × 7 mm) in a dog mandible and covered with a collagen membrane. Control groups included defects grafted with SCPC50 granules without rhBMP-2 and un-grafted defects. Bone healing was evaluated at 8 and 16 weeks using histologic and histomorphometric techniques. The increase in bone height and total defect fill were assessed for each specimen using the ImageJ 1.46 program. The release kinetics of rhBMP-2 was determined in vitro. The height of the bone in the grafted defects and the total defect fill were statistically analyzed. RESULTS: SCPC50 enhanced alveolar ridge augmentation as indicated by the increased vertical bone height, bone surface area, and bone volume after 16 weeks. SCPC50-rhBMP-2 provided a sustained release profile of a low effective dose (BMP-2 4.6 ± 1.34 pg/mL per hour) during the 1- to 21-day period. The slow rate of release of rhBMP-2 from SCPC50 accelerated synchronized complete bone regeneration and graft material resorption in 8 weeks. Successful rapid reconstruction of the alveolar ridge by SCPC50 and SCPC50-rhBMP-2 occurred without any adverse excessive bone formation, inflammation, or fluid-filled voids. CONCLUSIONS: Results of this study suggest that SCPC50 is an effective graft material to preserve the alveolar ridge after tooth extraction. Coating SCPC50-rhBMP-2 further accelerated bone regeneration and a considerable increase in vertical bone height. These findings make SCPC50 the primary choice as a carrier for rhBMP-2. SCPC50-rhBMP-2 can serve as an alternative to autologous bone grafting.


Subject(s)
Alveolar Ridge Augmentation/methods , Bone Morphogenetic Protein 2/therapeutic use , Calcium Phosphates/therapeutic use , Ceramics/therapeutic use , Silicates/therapeutic use , Alveolar Ridge Augmentation/instrumentation , Animals , Bone Development/drug effects , Bone Morphogenetic Protein 2/administration & dosage , Dogs , Drug Implants/administration & dosage , Mandible/surgery , Recombinant Proteins/administration & dosage , Recombinant Proteins/therapeutic use
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