Published in

American Academy of Implant Dentistry, Journal of Oral Implantology, 2(41), p. e24-e29

DOI: 10.1563/aaid-joi-d-13-00074

Links

Tools

Export citation

Search in Google Scholar

Vascular Alterations in the Sprague-Dawley Rat Mandible During Intravenous Bisphosphonate Therapy

This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Full text: Unavailable

Red circle
Preprint: archiving forbidden
Red circle
Postprint: archiving forbidden
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Abstract Long-term use of intravenous bisphosphonates, such as zoledronic acid (zoledronate), has been linked to bisphosphonate-related osteonecrosis of the jaw (BRONJ). Invasive dental surgery seems to trigger the bone necrosis in most cases. Purpose: To determine the effects of zoledronic acid on the vascular structure of the rat mandible. Methods and Materials: Extracted of the mandibular first molar in rats that received two IV injections of zoledronate (20 µg/kg), 4 weeks apart. Zoledronate-treated rats (n=18) were then compared to a control group of untreated rats (n=18). At the 4th, 8th, and 12th week after molar extraction, eight rat mandibles from each group were perfused with 35% radiopaque triphenylbismuth in methyl methacrylate via carotid artery perfusion. Mandibles were harvested and examined by micro-CT to assess the spatial and dimensional changes of the vasculature as a result of zoledronate treatment. Results: The micro-CT analysis showed that zoledronic acid-treated rats had blood vessels that were thicker, less connected, and less ordered than control rats that were not exposed to zoledronic acid. Conclusions: This study demonstrated that treatment with zoledronic acid in rats is associated with vascular changes in alveolar bone. Further studies are underway to explore whether these vascular changes contribute to the pathogenesis of BRONJ.