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Preventive Effect of Daiokanzoto (TJ-84) on 5-Fluorouracil-Induced Human Gingival Cell Death through the Inhibition of Reactive Oxygen Species Production

https://tokushima-u.repo.nii.ac.jp/records/2000104
https://tokushima-u.repo.nii.ac.jp/records/2000104
11c72e96-0b88-40e7-b7df-7eabdccbe71b
名前 / ファイル ライセンス アクション
pone_9_11_e112689.pdf pone_9_11_e112689.pdf (1.5 MB)
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Item type 文献 / Documents(1)
公開日 2024-09-25
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
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
出版社版DOI
関連識別子 https://doi.org/10.1371/journal.pone.0112689
関連名称 10.1371/journal.pone.0112689
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル Preventive Effect of Daiokanzoto (TJ-84) on 5-Fluorouracil-Induced Human Gingival Cell Death through the Inhibition of Reactive Oxygen Species Production
タイトル別表記
その他のタイトル TJ-84 Reduces 5-FU-Induced Cell Death in the Gingiva
著者 吉田, 賀弥

× 吉田, 賀弥

WEKO 1211
徳島大学 教育研究者総覧 73175/profile-ja.html
e-Rad_Researcher 60363157

ja 吉田, 賀弥
ISNI

ja-Kana ヨシダ, カヤ

en Yoshida, Kaya

Search repository
吉岡, 昌美

× 吉岡, 昌美

WEKO 1719
e-Rad_Researcher 90243708

ja 吉岡, 昌美
ISNI

ja-Kana ヨシオカ, マサミ

en Yoshioka, Masami

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岡村, 裕彦

× 岡村, 裕彦

WEKO 1256
e-Rad_Researcher 20380024

ja 岡村, 裕彦
ISNI

ja-Kana オカムラ, ヒロヒコ

en Okamura, Hirohiko

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Moriyama, Satomi

× Moriyama, Satomi

en Moriyama, Satomi

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川添, 和義

× 川添, 和義

WEKO 1124
e-Rad_Researcher 00248296

ja 川添, 和義
ISNI

ja-Kana カワゾエ, カズヨシ

en Kawazoe, Kazuyoshi

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Grenier, Daniel

× Grenier, Daniel

en Grenier, Daniel

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日野出, 大輔

× 日野出, 大輔

WEKO 1666
徳島大学 教育研究者総覧 60333/profile-ja.html
e-Rad_Researcher 70189801

ja 日野出, 大輔
ISNI

ja-Kana ヒノデ, ダイスケ

en Hinode, Daisuke

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抄録
内容記述 Daiokanzoto (TJ-84) is a traditional Japanese herbal medicine (Kampo formulation). While many Kampo formulations have been reported to regulate inflammation and immune responses in oral mucosa, there is no evidence to show that TJ-84 has beneficial effects on oral mucositis, a disease resulting from increased cell death induced by chemotherapeutic agents such as 5-fluorouracil (5-FU). In order to develop effective new therapeutic strategies for treating oral mucositis, we investigated (i) the mechanisms by which 5-FU induces the death of human gingival cells and (ii) the effects of TJ-84 on biological events induced by 5-FU. 5-FU-induced lactate dehydrogenase (LDH) release and pore formation in gingival cells (Sa3 cell line) resulted in cell death. Incubating the cells with 5-FU increased the expression of nucleotide-binding domain and leucine-rich repeat containing PYD-3 (NLRP3) and caspase-1. The cleavage of caspase-1 was observed in 5-FU-treated cells, which was followed by an increased secretion of interleukin (IL)-1β. The inhibition of the NLRP3 pathway slightly decreased the effects of 5-FU on cell viability and LDH release, suggesting that NLRP3 may be in part involved in 5-FU-induced cell death. TJ-84 decreased 5-FU-induced LDH release and cell death and also significantly inhibited the depolarization of mitochondria and the up-regulation of 5-FU-induced reactive oxygen species (ROS) and nitric oxide (NO) production. The transcriptional factor, nuclear factor-κB (NF-κB) was not involved in the 5-FU-induced cell death in Sa3 cells. In conclusion, we provide evidence suggesting that the increase of ROS production in mitochondria, rather than NLRP3 activation, was considered to be associated with the cell death induced by 5-FU. The results also suggested that TJ-84 may attenuate 5-FU-induced cell death through the inhibition of mitochondrial ROS production.
書誌情報 en : PLOS ONE

巻 9, 号 11, p. e112689, 発行日 2014-11-12
収録物ID
収録物識別子タイプ EISSN
収録物識別子 19326203
出版者
出版者 PLOS
権利情報
権利情報 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
EID
識別子 286472
言語
言語 eng
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