Inhibitory Effect of Myricetin on Matrix Metalloproteinase Expression and Activity in Periodontal Inflammation.
10.11620/IJOB.2016.41.4.163
- Author:
Seon Yle KO
1
Author Information
1. Department of Oral biochemistry and Institute of Dental Science, Dankook University, Republic of Korea. seonyleko@dankook.ac.kr
- Publication Type:Original Article
- Keywords:
myricetin;
matrix metalloproteinase;
PDLF;
osteoclastogenesis
- MeSH:
Chronic Periodontitis;
Fibroblasts;
Inflammation*;
Interleukin-6;
Osteoclasts;
Peptide Hydrolases;
Periodontal Ligament;
Phosphorylation;
Plants, Medicinal;
Signal Transduction;
Tea
- From:International Journal of Oral Biology
2016;41(4):163-173
- CountryRepublic of Korea
- Language:English
-
Abstract:
Flavonoid myricetin, usually found in tea and medicinal plants, has antioxidant and anti-inflammatory effects. Our objectives in this study were to verify the effects of myricetin on periodontal ligament fibroblasts (PDLFs) under inflammatory conditions and to observe its effects on osteoclast generation and on cytokine expression in RAW264.7 cells. To determine the effects of myricetin on PDLFs, we examined the expression and activity of proteolytic enzymes, including MMP-1, MMP-2, and MMP-8, which all play an important role in chronic periodontitis. We observed the effects of myricetin on intracellular signal transduction to verify the molecular mechanism involved. By measuring the formation of TRAP–positive multinucleated cells and the expression and activity of MMP-8, we were able to assess the effects of myricetin on osteoclast generation. In addition, by measuring the secretion of IL-6 and NO, we could evaluate the effects of myricetin on inflammatory mediators. We found that Myricetin had no effect on the viability of the PDLFs in the presence of inflammation, but it did decrease both the expression of MMP-1 and MMP-8 and the enzyme activity of MMP-2 and MMP-8 in these fibroblasts. Myricetin also decreased the lipopolysaccharide-stimulated phosphorylation of JNK, p38 signaling, IKKB, AKT, and p65RelA in the PDLFs. In the RAW264.7 cells, myricetin inhibited both the expression and the activity of MMP-8. Furthermore, Myricetin not only suppressed the generation of LPS-stimulated osteoclasts, but it also slightly inhibited LPS-stimulated degradation of IkB and decreased the release of LPS-induced IL-6 and NO. These findings suggest that myricetin alleviates the tissue-destructive processes that occur during periodontal inflammation.
