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  1. 学術雑誌掲載論文
  2. ISRN pharmacology
  1. 成果物登録者(学内著者)一覧
  2. A
  3. 荒 敏昭
  1. 成果物登録者(学内著者)一覧
  2. K
  3. 喜多村 洋幸
  1. 成果物登録者(学内著者)一覧
  2. U
  3. 浦野 浩子

Preventive Effects of a Kampo Medicine, Kakkonto, on Inflammatory Responses via the Suppression of Extracellular Signal-Regulated Kinase Phosphorylation in Lipopolysaccharide-Treated Human Gingival Fibroblasts

https://mdu.repo.nii.ac.jp/records/2669
https://mdu.repo.nii.ac.jp/records/2669
8c38a973-a032-4dcc-8d2a-cdce222d85cb
名前 / ファイル ライセンス アクション
2016-ja-010.pdf 本文 (894.1 kB)
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Item type 松本歯学/学術雑誌論文 / Journal Article(1)
公開日 2017-05-18
タイトル
タイトル Preventive Effects of a Kampo Medicine, Kakkonto, on Inflammatory Responses via the Suppression of Extracellular Signal-Regulated Kinase Phosphorylation in Lipopolysaccharide-Treated Human Gingival Fibroblasts
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Kitamura, Hiroyuki

× Kitamura, Hiroyuki

Kitamura, Hiroyuki

Urano, Hiroko

× Urano, Hiroko

Urano, Hiroko

Ara, Toshiaki

× Ara, Toshiaki

Ara, Toshiaki

抄録
内容記述タイプ Abstract
内容記述 Periodontal disease is accompanied by inflammation of the gingiva and destruction of periodontal tissues, leading to alveolar bone loss in severe clinical cases. The chemical mediator prostaglandin E2 (PGE2) and cytokines such as interleukin- (IL-)6 and IL-8 have been known to play important roles in inflammatory responses and tissue degradation. In the present study, we investigated the effects of a kampo medicine, kakkonto (TJ-1), on the production of prostaglandin E2 (PGE2), IL-6, and IL-8 by human gingival fibroblasts (HGFs) treated with lipopolysaccharide (LPS) from Porphyromonas gingivalis. Kakkonto concentration dependently suppressed LPS-induced PGE2 production but did not alter basal PGE2 levels. In contrast, kakkonto significantly increased LPSinduced IL-6 and IL-8 production. Kakkonto decreased cyclooxygenase- (COX-)1 activity to approximately 70% at 1mg/mL but did not affect COX-2 activity. Kakkonto did not affect cytoplasmic phospholipase A2 (cPLA2), annexin1, or LPS-induced COX-2 expression. Kakkonto suppressed LPS-induced extracellular signal-regulated kinase (ERK) phosphorylation, which is known to lead to ERK activation and cPLA2 phosphorylation. These results suggest that kakkonto decreased PGE2 production by inhibition of ERK phosphorylation which leads to inhibition of cPLA2 phosphorylation and its activation. Therefore, kakkonto may be useful to improve gingival inflammation in periodontal disease.
書誌情報 en : ISRN pharmacology

巻 2014, 号 Article ID 784019, 発行日 2014-02-18
出版者
出版者 Hindawi Publishing Corporation
ISSN
収録物識別子タイプ ISSN
収録物識別子 2090-5173
PubMed番号
関連タイプ isIdenticalTo
識別子タイプ PMID
関連識別子 info:pmid/24693448
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.1155/2014/784019
関連名称 info:doi/10.1155/2014/784019
権利
権利情報 Copyright © 2014 Hiroyuki Kitamura et al. This is an open access article distributed under the Creative Commons Attribution License(Attribution 3.0 Unported (CC BY 3.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
情報源
関連名称 雑誌掲載論文(電子版)
関連サイト
識別子タイプ URI
関連識別子 https://www.hindawi.com/journals/isrn/2014/784019/
関連名称 Hindawi Limited
関連サイト
識別子タイプ URI
関連識別子 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945151/
関連名称 PubMed Central® (PMC)
フォーマット
内容記述タイプ Other
内容記述 application/pdf
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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