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Resveratrol enhances bone formation by modulating inflammation in the mouse periodontitis model

Authors :
Jae-Kwang Jung
Yam Prasad Aryal
Sang-Hyun Kim
Chang-Hyeon An
Ji-Youn Kim
Tae-Hoon Lee
Wern-Joo Sohn
Jae-Young Kim
Hitoshi Yamamoto
Nirpesh Adhikari
Jung-Hong Ha
So-Young Choi
Jo-Young Suh
Seo-Young An
Youngkyun Lee
Source :
Journal of periodontal researchREFERENCES. 56(4)
Publication Year :
2021

Abstract

Objective To evaluate the effect of resveratrol on periodontal bone regeneration after local delivery and to determine its effect on inflammatory mediators. Background Resveratrol is considered an anti-inflammatory polyphenolic stilbene involved in the modulation of inflammation. Materials and methods Periodontitis was induced in mouse molars using a 5-day ligature model followed by the left second molar extraction and 50 µM resveratrol treatment for 1 and 2 weeks. We then examined specimens treated for 1 week histologically and with immunostaining. Microfocus-computed tomography (micro-CT) was used to examine the bone volume formation. Results After 1 week of treatment, proinflammatory cytokine levels (TNF-alpha and IL6), cells exhibiting neutrophil and macrophage marker (MPO), cell proliferation marker (Ki67), and preosteoblastic marker (RUNX2) reactivity decreased in the resveratrol-treated specimens compared to the control group. In contrast, we observed a higher number of CD31-, F4/80-, and osteocalcin- (OCN-) positive cells in the resveratrol-treated specimens. After 2 weeks, micro-CT confirmed an increased bone mass in the region of the extraction socket in the resveratrol-treated group. Conclusion After 1 week, the resveratrol-treated specimens revealed evidence of inflammation modulation compared to the control group. These data suggest that resveratrol not only affects inflammation control but also is useful for treating periodontitis-related tissue defects and bone regeneration.

Details

ISSN :
16000765
Volume :
56
Issue :
4
Database :
OpenAIRE
Journal :
Journal of periodontal researchREFERENCES
Accession number :
edsair.doi.dedup.....bc7dda81daf0399a58d34c5a1fed46ab