期刊
ARCHIVES OF ORAL BIOLOGY
卷 120, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.archoralbio.2020.104944
关键词
Cynaroside; Lipopolysaccharide; Periodontal ligament cells; Inflammation; Periodontitis
资金
- Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (IPET) through the Agri-Bio Industry Technology Development Program - Ministry of Agriculture, Food and Rural Affairs (MAFRA) [317003-4]
Objective: To investigate whether cynaroside protects human periodontal ligament (hPDL) cells from lipopolysaccharide (LPS)-induced damage and inflammation and to analyze the underlying mechanism. Methods: LPS was used to stimulate hPDL and RAW264.7 cells. MTT assay was used to detect cell viability, and protein expression levels were measured via western blot analysis. Nitrite oxide and prostaglandin E-2 were used to quantify the inflammatory response. Alizarin Red S staining was used to detect mineralized nodules. Results: Cynaroside inhibited the expression of iNOS, COX-2, TNF-alpha, and IL-6 in LPS-stimulated hPDL and RAW264.7 cells without cytotoxicity. Furthermore, cynaroside significantly suppressed LPS-induced protein expression of matrix metalloproteinase 3. Additionally, cynaroside prevented LPS-induced NF-kappa B p65 subunit translocation to the nucleus by inhibiting the phosphorylation and degradation of I kappa B-alpha. Moreover, cynaroside could restore the mineralization ability of hPDL cells reduced by LPS. Conclusion: Cynaroside protected hPDL cells from LPS-induced damage and inflammation via inhibition of NF-kappa B activation. These results suggest that cynaroside may be a potential therapeutic agent for the alleviation of periodontitis.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据