A pharmacodynamic investigation into the efficacy of osteoprotegerin during aseptic inflammation

Aust Orthod J. 2012 Nov;28(2):219-24.

Abstract

Background: Osteoprotegerin (OPG), as an osteoclast antagonist, limits mineralised tissue resorption under physiological conditions. Previous work investigating OPG in a rat periodontal ligament (PDL) ankylosis model found no inhibitory effect on osteoclasts when OPG was administered at a dosage of 2.5mg/kg.

Aims: The object of this study was to determine whether dosages higher than 2.5 mg/kg of OPG were required to limit osteoclastic activity in an aseptic inflammatory model in rats.

Materials and methods: Dry ice was applied for 15 minutes to the upper right first molar crown of eighteen, 8-week-old, male Sprague-Dawley rats. Three groups of 3 were injected with OPG at dosages of 2.5, 5.0 and 7.5 mg/kg of body weight immediately following the thermal insult. After 7 days, the rats were sacrificed and each maxilla processed for histological examination and stained for osteoclastic activity using tartrate-resistant acid phosphatase (TRAP). Osteoclast population numbers were estimated via light microscopy and results were analysed using a comparative mixed model statistical analysis.

Results: Results showed OPG inhibited osteoclastic activity in a dose-dependent manner. From 2.5 mg/kg to 7.5 mg/kg, osteoclast populations were linearly reduced by 39.78% (p < 0.05). OPG did not appear to affect the inflammatory process and had varied efficacy in different regions of individual teeth.

Conclusion: Although osteoclastic activity reduced, it was not completely eliminated, perhaps because dosages were still inadequate, or additional factors might influence OPG and osteoclast activation in the aseptic inflammatory model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Phosphatase / analysis
  • Animals
  • Biomarkers / analysis
  • Cell Count
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Dry Ice / adverse effects
  • Freezing / adverse effects
  • Inflammation / pathology
  • Isoenzymes / analysis
  • Male
  • Maxilla / pathology
  • Molar / injuries
  • Necrosis
  • Odontoblasts / drug effects
  • Odontoblasts / pathology
  • Osteoclasts / drug effects*
  • Osteoclasts / pathology
  • Osteoprotegerin / administration & dosage
  • Osteoprotegerin / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Root Resorption / pathology
  • Tartrate-Resistant Acid Phosphatase
  • Tooth Crown / injuries

Substances

  • Biomarkers
  • Dry Ice
  • Isoenzymes
  • Osteoprotegerin
  • Tnfrsf11b protein, rat
  • Acid Phosphatase
  • Tartrate-Resistant Acid Phosphatase