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  1. 055 医学部附属病院
  2. 0551 学術論文

Cannabidiol induces expression of human cytochrome P450 1A1 that is possibly mediated through aryl hydrocarbon receptor signaling in HepG2 cells

http://hdl.handle.net/10091/00020868
http://hdl.handle.net/10091/00020868
499cb87a-1489-4581-97f6-ebffe5787c00
名前 / ファイル ライセンス アクション
Manuscript Manuscript (LifeSci 2015 Yamaori).pdf (454.0 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-09-18
タイトル
タイトル Cannabidiol induces expression of human cytochrome P450 1A1 that is possibly mediated through aryl hydrocarbon receptor signaling in HepG2 cells
言語
言語 eng
DOI
関連識別子 https://doi.org/10.1016/j.lfs.2015.07.007
関連名称 10.1016/j.lfs.2015.07.007
キーワード
主題 Marijuana, Cannabidiol, CYP1A1, Induction, AhR, Protein tyrosine kinase
資源タイプ
資源 http://purl.org/coar/resource_type/c_6501
タイプ journal article
著者 Yamaori, Satoshi

× Yamaori, Satoshi

en Yamaori, Satoshi

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Kinugasa, Yuka

× Kinugasa, Yuka

en Kinugasa, Yuka

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Jiang, Rongrong

× Jiang, Rongrong

en Jiang, Rongrong

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Takeda, Shuso

× Takeda, Shuso

en Takeda, Shuso

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Yamamoto, Ikuo

× Yamamoto, Ikuo

en Yamamoto, Ikuo

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Watanabe, Kazuhito

× Watanabe, Kazuhito

en Watanabe, Kazuhito

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信州大学研究者総覧へのリンク
氏名 Yamaori, Satoshi
URL https://soar-rd.shinshu-u.ac.jp/profile/ja.jefNgUkh.html
出版者
出版者 PERGAMON-ELSEVIER SCIENCE LTD
引用
内容記述 LIFE SCIENCES.136:87-93(2015)
書誌情報 LIFE SCIENCES

巻 136, p. 87-93, 発行日 2015-09-01
抄録
内容記述 Aims<br/>We herein investigated the inducibility of cytochrome P450 1A1 (CYP1A1) by Δ9-tetrahydrocannabinol, cannabidiol (CBD), and cannabinol, three major phytocannabinoids, using human hepatoma HepG2 cells.<br/>Main methods<br/>The expression of CYP1A1 and the aryl hydrocarbon receptor (AhR) was measured by a quantitative real-time polymerase chain reaction and/or Western blotting.<br/>Key findings<br/>Δ9-Tetrahydrocannabinol and CBD concentration-dependently induced the expression of CYP1A1 mRNA, whereas cannabinol showed little or no induction. Among the phytocannabinoids tested, CBD was the most potent inducer of CYP1A1 expression. The induction of CYP1A1 expression by CBD was significantly attenuated by the knockdown of AhR expression with AhR small interfering RNAs. The role of protein tyrosine kinases (PTKs) in the CBD-mediated induction of CYP1A1 was then examined using herbimycin A, a PTK inhibitor. The upregulation of CYP1A1 by CBD was significantly suppressed by herbimycin A as was the induction by omeprazole but not 3-methylcholanthrene. The inducibility of CYP1A1 by CBD-related compounds was examined to clarify the structural requirements for CBD-mediated CYP1A1 induction. Olivetol, which corresponds to the pentylresorcinol moiety of CBD, significantly induced the expression of CYP1A1, whereas d-limonene, CBD-2′-monomethyl ether, and CBD-2′,6′-dimethyl ether did not.<br/>Significance<br/>These results showed that CBD may have induced human CYP1A1 expression through the activation of PTK-dependent AhR signaling, in which two phenolic hydroxyl groups in the pentylresorcinol moiety of CBD may play structurally important roles.
資源タイプ(コンテンツの種類)
ISSN
収録物識別子タイプ PISSN
収録物識別子 0024-3205
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA00717011
PubMed
識別子タイプ PMID
関連識別子 https://www.ncbi.nlm.nih.gov/pubmed/26187180
関連名称 26187180
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
WoS
URL http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=ShinshuUniv&SrcApp=ShinshuUniv&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000361035500013
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