Conclusion
Oral topical administration of JTE013 alleviated periodontal inflammatory bone loss induced by ligature placement in mice.
Methods
C57BL/6 mice were placed with silk ligatures at the left maxillary second molar to induce experimental periodontitis. Mice were treated with JTE013 or control vehicle (dimethyl sulfoxide, DMSO) oral topically on the ligatures once daily. After 15 days of treatment, RNA was extracted from the lingual mucosal tissues to quantify IL-1β, IL-6, and TNF mRNA levels in the tissues. Alveolar bone loss was determined by micro-computed tomography. Sagittal periodontal tissue sections were cut and stained by hematoxylin and eosin (H&E) for general histology, or stained by tartrate-resistant acid phosphatase (TRAP) for osteoclasts.
Results
Treatment with JTE013 attenuated ligature-induced alveolar bone loss compared with DMSO treatment. Treatment with JTE013 reduced IL-1β, IL-6, and TNF mRNA levels in murine gingival mucosal tissues, inhibited leukocyte infiltration in the periodontal tissues, and decreased the number of osteoclasts in the periodontal tissues compared with controls.