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6-Shogaol Inhibits Advanced Glycation End-Products-Induced IL-6 and ICAM-1 Expression by Regulating Oxidative Responses in Human Gingival Fibroblasts.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2019 Oct 15; Vol. 24 (20). Date of Electronic Publication: 2019 Oct 15. - Publication Year :
- 2019
-
Abstract
- Advanced glycation end-products (AGEs) cause diabetes mellitus (DM) complications and accumulate more highly in periodontal tissues of patients with periodontitis and DM. AGEs aggravate periodontitis with DM by increasing the expression of inflammation-related factors in periodontal tissues. 6-Shogaol, a major compound in ginger, has anti-inflammatory and anti-oxidative activities. However, the influence of shogaol on DM-associated periodontitis is not well known. In this study, the effects of 6-shogaol on AGEs-induced oxidative and anti-oxidative responses, and IL-6 and ICAM-1 expression in human gingival fibroblasts (HGFs) were investigated. When HGFs were cultured with 6-shogaol and AGEs, the activities of reactive oxygen species (ROS) and antioxidant enzymes (heme oxygenase-1 [HO-1] and NAD(P)H quinone dehydrogenase 1 [NQO1]), and IL-6 and ICAM-1 expressions were investigated. RAGE expression and phosphorylation of MAPKs and NF-κB were examined by western blotting. 6-Shogaol significantly inhibited AGEs-induced ROS activity, and increased HO-1 and NQO1 levels compared with the AGEs-treated cells. The AGEs-stimulated expression levels of receptor of AGE (RAGE), IL-6 and ICAM-1 and the phosphorylation of p38, ERK and p65 were attenuated by 6-shogaol. These results suggested that 6-shogaol inhibits AGEs-induced inflammatory responses by regulating oxidative and anti-oxidative activities and may have protective effects on periodontitis with DM.<br />Competing Interests: All authors have no conflicts of interest related to this study.
- Subjects :
- Cell Line
Gingiva cytology
Glycation End Products, Advanced metabolism
Heme Oxygenase-1 genetics
Heme Oxygenase-1 metabolism
Humans
Intercellular Adhesion Molecule-1 metabolism
Interleukin-6 metabolism
Mitogen-Activated Protein Kinases metabolism
NAD(P)H Dehydrogenase (Quinone) genetics
NAD(P)H Dehydrogenase (Quinone) metabolism
Reactive Oxygen Species metabolism
Signal Transduction drug effects
Catechols pharmacology
Fibroblasts drug effects
Fibroblasts metabolism
Gene Expression Regulation drug effects
Glycation End Products, Advanced genetics
Intercellular Adhesion Molecule-1 genetics
Interleukin-6 genetics
Oxidative Stress drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 24
- Issue :
- 20
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 31619000
- Full Text :
- https://doi.org/10.3390/molecules24203705