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Yunnan Baiyao Might Mitigate Periodontitis Bone Destruction by Inhibiting Autophagy and Promoting Osteoblast Differentiation in vivo, ex vivo and in vitro

离体 自噬 体内 成骨细胞 体外 化学 牙周炎 生物 药理学 细胞生物学 医学 内科学 生物化学 生物技术 细胞凋亡
作者
Wang Liu,Yanjie Li,Yuanyuan An,Ruoyu Zhao,Chenxi Wei,Xiaobin Ren,Hongbing He
出处
期刊:Journal of Inflammation Research [Dove Medical Press]
卷期号:Volume 17: 2271-2284 被引量:1
标识
DOI:10.2147/jir.s454694
摘要

Background and Objective: Periodontitis is an inflammatory disease that eventually destroys tooth-supporting tissue.Yunnan Baiyao (YNBY), a traditional Chinese medicine compound with haemostatic and anti-inflammatory properties has shown therapeutic potential in several diseases.Our previous study revealed that YNBY suppressed osteoclast differentiation in periodontitis.The purpose of this study is to investigate the influences of YNBY on osteoblasts and explore its potential mechanisms.Materials and Methods: A rat periodontitis model was established by ligation of maxillary second molars.After the end of modelling, histopathological observation by hematoxylin-eosin (HE) staining and Masson trichrome staining, detection of bone resorption by Micro-CT scanning, detection of osteoclasts by tartrate-resistant acid phosphatase (TRAP) staining, expression of osteocalcin (OCN) and microtubule-associated protein 1 light chain 3 (LC3) by immunohistochemistry. Lipopolysaccharides was used to irritate MC3T3-E1 osteoblastic cells and ex vivo calvarial organ as an in vitro model of inflammation.CCK-8 assay was performed to examine the toxicity of YNBY to MC3T3-E1 osteoblastic cells.Osteogenesis was assessed with alizarin red staining, immunofluorescence staining, Western blot and immunohistochemical staining.Transmission electron microscopy, fluorescent double staining, Western blot and immunohistochemical staining were employed to detect autophagy.Results: Histological and micro-CT analyses revealed that YNBY gavage reduced bone loss caused by experimental periodontitis and upregulated osteogenic proteins in vivo.YNBY attenuated the production of autophagy-related proteins in periodontitis rats.Additionally, YNBY promoted osteogenesis by inhibiting inflammation-induced autophagy in vitro.Furthermore, YNBY suppressed LPS-mediated bone resorption and promoted the production of osteoblast-related proteins in inflamed calvarial tissues ex vivo. Conclusion:This study demonstrated, through in vivo, in vitro and ex vivo experiments, that YNBY promoted osteoblast differentiation by suppressing autophagy, which markedly alleviated bone destruction caused by periodontitis.
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