Friday, March 23, 2012: 2 p.m. - 3:15 p.m.
Presentation Type: Poster Session
Y. KAMIYA1, M. XU
1, A. UTREJA
2, C. PILBEAM
3, S. LEE
4, H.L. AGUILA
5, J. CHEN
1, and S. WADHWA
1,
1Collage of Dental Medicine-Division of Orthodontics, Columbia University, New York, NY,
2Department of Craniofacial Sciences, University of Connecticut Health Center, Farmington, CT,
3Musculoskeletal INSTITUTE, University of Connecticut Health Center, Farmington, CT,
4Center on Aging, University of Connecticut Health Center, Farmington, CT,
5Department of Immunology, University of Connecticut Health Center, Farmington, CT
Objective: Intermittent PTH treatment is a common therapy for the treatment of osteoporosis and unlike other osteoporosis therapies is able to cause an anabolic response in the periosteum. The temporomandibular joint is composed of the mandibular condyle, the articular portion of the temporal bone and a disc that are covered by fibrocartilage. Unlike other joints, the cartilage of the mandibular condyle is derived from periosteum. Therefore, the goal of this study was to examine if similar to bone, intermittent PTH therapy is anabolic in the temporomandibular joint (TMJ).
Method: Intermittent PTH (80μg/kg) or vehicle was injected to young mice (6-7 weeks old male C57BL/6) once a day for fourteen days. Gene expression of chondrocyte maturation markers, proliferation, condylar cartilage thickness and micro-CT analysis was evaluated in the mandibular condyle from both treatment groups.
Result: In young growing mice, intermittent PTH therapy caused a significant increase in the mandibular condylar cartilage thickness and VEGF expression compared to vehicle treated controls. Further PTH treatment caused a significant decrease in OPG expression. And in the subchondral bone, PTH treatment caused a significant decrease in bone volume compared to vehicle treated group.
Conclusion: Intermittent PTH treatment (80μg/kg/day) caused increased condylar cartilage thickness but a decrease in mandibular condylar bone density in young growing mice.
This abstract is based on research that was funded entirely or partially by an outside source: R01DE020097
Keywords: Oral biology, TMJ and masticatory muscles and Temporomandibular joint