共 19 条
Nobiletin Decreases Inflammatory Mediator Expression in Tumor Necrosis Factor-Stimulated Human Periodontal Ligament Cells
被引:8
作者:

Hosokawa, Yoshitaka
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Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Conservat Dent, Tokushima, Japan Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Conservat Dent, Tokushima, Japan

Hosokawa, Ikuko
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Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Conservat Dent, Tokushima, Japan Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Conservat Dent, Tokushima, Japan

Ozaki, Kazumi
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机构:
Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Oral Hlth Care Promot, Tokushima, Japan Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Conservat Dent, Tokushima, Japan
机构:
[1] Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Conservat Dent, Tokushima, Japan
[2] Tokushima Univ, Grad Sch, Inst Biomed Sci, Dept Oral Hlth Care Promot, Tokushima, Japan
关键词:
CYTOKINES;
D O I:
10.1155/2021/5535844
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Nobiletin, a biologically active substance in the skin of citrus fruits, has been reported to be an effective anti-inflammatory, anticancer, and antimicrobial agent. In this study, we aimed to examine the anti-inflammatory effects of nobiletin on tumor necrosis factor- (TNF-) stimulated human periodontal ligament cells (HPDLCs). Our results demonstrated that nobiletin treatment could decrease the expressions of inflammatory cytokines (C-X-C motif chemokine ligand (CXCL)10, C-C motif chemokine ligand (CCL)2, and interleukin- (IL-) 8), matrix metalloproteinases (MMPs) (MMP1 and MMP3), and prostaglandin-endoperoxide synthase 2 (PTGS2) in TNF-stimulated HPDLCs. Moreover, we revealed that nobiletin could inhibit the activation of nuclear factor- (NF-) kappa B and protein kinase B (AKT1) pathways in TNF-stimulated HPDLCs. Furthermore, nobiletin treatment enhanced nuclear factor, erythroid 2 like 2 (NFE2L2) and heme oxygenase 1 (HMOX1) expressions in TNF-stimulated HPDLCs. In conclusion, these findings suggest that nobiletin can inhibit inflammatory responses in TNF-stimulated HPDLCs by inhibiting NF-kappa B and AKT1 activations and upregulating the NFE2L2 and HMOX1 expression.
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