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Recombinant osteoprotegerin effects during orthodontic movement in a rat model.
Fernández-González, Felipe J; Cañigral, Aránzazu; López-Caballo, José L; Brizuela, Aritza; Cobo, Teresa; de Carlos, Félix; Suazo, Iván; Pérez-González, Yurena; Vega, Jose A.
Affiliation
  • Fernández-González FJ; *Department of Orthodontics and Dentofacial Orthopedics, University of Oviedo, Oviedo, Spain, fjvazquezvega@gmail.com.
  • Cañigral A; *Department of Orthodontics and Dentofacial Orthopedics, University of Oviedo, Oviedo, Spain.
  • López-Caballo JL; *Department of Orthodontics and Dentofacial Orthopedics, University of Oviedo, Oviedo, Spain.
  • Brizuela A; **Department of Oral Implantology, School of Medicine and Dentistry, University of the Basque Country, Leioa, Spain.
  • Cobo T; *Department of Orthodontics and Dentofacial Orthopedics, University of Oviedo, Oviedo, Spain.
  • de Carlos F; *Department of Orthodontics and Dentofacial Orthopedics, University of Oviedo, Oviedo, Spain.
  • Suazo I; ***Director de Postgrado e investigacion, Universidad Autónoma de Chile, Chile.
  • Pérez-González Y; ****Specialist in Implantology at the University of Salamanca, Spain.
  • Vega JA; *****Department of Morphology and Cell Biology, Facultad de Medicina, University of Oviedo, Oviedo, Spain and ******Facultad Ciencias de la Salud, Universidad Autónoma de Chile, Chile.
Eur J Orthod ; 38(4): 379-85, 2016 Aug.
Article in En | MEDLINE | ID: mdl-26293288
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Anchorage is one of the most challenging sides in orthodontics. The use of biological modulators that inhibit osteoclasts could be a solution to address these problems and provide new adjunctive approaches. The aim of this study was to assess the effectiveness of recombinant osteoprotegerin fusion protein (OPG-Fc) in orthodontic anchorage. MATERIALS AND

METHODS:

Two groups of male Sprague-Dawley rats were utilized. The animals in the experimental group received twice-weekly injections with high dose of OPG-Fc (5.0mg/kg) in mesial and distal mucosa of the first molars, and those in the control group received no drugs. Right first maxillary molars were mesialized using a calibrated nickel-titanium spring connected to an anterior mini-screw. Tooth movement was measured by two blinded observers using scanned and magnified stone casts. Receptor activator of nuclear factor κB (RANK), run-related transcription factor 2 (Runx2), type I collagen, vimentin, matrix metalloproteinases 2 and 9, S100 protein and the putative mechanoproteins acid-sensing ion channel (ASIC2) and transient receptor potential vainilloid 4 (TRPV4) were evaluated using immunohistochemistry.

RESULTS:

OPG-Fc group showed an important decreased in mesial molar movement with only 52%, 31%, and 22% of the total mesial molar movement compared with control group at Days 7, 14, and 21, respectively (P < 0.001). RANK ligand and Runx2 positive cells were severely reduced after OPG-Fc treatment. Periodontal ligament architecture, cell arrangement, and immunohistochemical patter for vimentin, type I collagen and the mechanoproteins TRPV4 and ASIC2 were altered by tooth movement and all these parameters altered by the applied treatment.

CONCLUSIONS:

OPG-Fc effectively inhibits osteoclastogenesis resulting in improved bone quantity and orthodontic anchorage. Based on present results, OPG-Fc could have clinical utility in preventing undesired tooth movements.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Tooth Mobility / Tooth Movement Techniques / Osteoprotegerin Type of study: Prognostic_studies Language: En Journal: Eur J Orthod Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Tooth Mobility / Tooth Movement Techniques / Osteoprotegerin Type of study: Prognostic_studies Language: En Journal: Eur J Orthod Year: 2016 Type: Article