Green tea catechins inhibit Porphyromonas gulae LPS-induced inflammatory responses in human gingival epithelial cells.


Journal

Journal of oral biosciences
ISSN: 1880-3865
Titre abrégé: J Oral Biosci
Pays: Netherlands
ID NLM: 101226721

Informations de publication

Date de publication:
09 2022
Historique:
received: 06 05 2022
revised: 24 05 2022
accepted: 25 05 2022
pubmed: 7 6 2022
medline: 28 9 2022
entrez: 6 6 2022
Statut: ppublish

Résumé

To determine the anti-inflammatory effects of green tea catechins in immortalized human gingival epithelial cells (Ca9-22) stimulated with Porphyromonas gulae lipopolysaccharide (LPS). Ca9-22 cells were incubated with P. gulae LPS (10 μg/ml) with or without green tea catechins, epigallocatechin-3-gallate (EGCg), epigallocatechin (EGC), epicatechin-3-gallate (ECG), and epicatechin (EC) (each at 50 μM), for 6 or 24 h. Real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay were used to determine the induction of cyclooxygenase 2 (COX2), tumor necrosis factor alpha (TNF-ɑ), interleukin 6 (IL-6), and IL-8. Furthermore, the expression of toll-like receptors (TLRs) 2 and 4 was examined using real-time PCR and western blotting analysis, and phosphorylation of the p38 and ERK1/2 was examined using western blotting analysis. At the mRNA and protein levels, EGCg, EGC, ECG, and EC were found to significantly inhibit COX2, TNF-ɑ, IL-6, and IL-8. Furthermore, the levels of ERK1/2 and p38 phosphorylation induced by P. gulae LPS were decreased following the addition of each of the catechins, as well as TLR2 and 4 mRNA and protein. These findings indicate that green tea catechins are potent inhibitors of inflammatory responses induced by P. gulae LPS, and may also be useful for prevention and/or attenuation of periodontitis.

Identifiants

pubmed: 35660639
pii: S1349-0079(22)00091-3
doi: 10.1016/j.job.2022.05.006
pii:
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Interleukin-6 0
Interleukin-8 0
Lipopolysaccharides 0
RNA, Messenger 0
Tea 0
Toll-Like Receptor 2 0
Tumor Necrosis Factor-alpha 0
Catechin 8R1V1STN48
Cyclooxygenase 2 EC 1.14.99.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

352-358

Informations de copyright

Copyright © 2022 Japanese Association for Oral Biology. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest There are no conflicts of interest to declare.

Auteurs

Sho Yoshida (S)

Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Hiroaki Inaba (H)

Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan. Electronic address: hinaba@okayama-u.ac.jp.

Ryota Nomura (R)

Department of Pediatric Dentistry, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan; Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, Osaka, Japan.

Kazuhiko Nakano (K)

Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, Osaka, Japan.

Michiyo Matsumoto-Nakano (M)

Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

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Classifications MeSH