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Citrus nobiletin suppresses inducible nitric oxide synthase gene expression in interleukin-1β-treated hepatocytes.

Identifieur interne : 001394 ( Ncbi/Merge ); précédent : 001393; suivant : 001395

Citrus nobiletin suppresses inducible nitric oxide synthase gene expression in interleukin-1β-treated hepatocytes.

Auteurs : Emi Yoshigai [Japon] ; Toru Machida ; Tetsuya Okuyama ; Masatoshi Mori ; Hiromitsu Murase ; Ryota Yamanishi ; Tadayoshi Okumura ; Yukinobu Ikeya ; Hoyoku Nishino ; Mikio Nishizawa

Source :

RBID : pubmed:23958298

English descriptors

Abstract

Nobiletin is a polymethoxylated flavone that is abundant in the peels of citrus fruits, such as Citrus unshiu (Satsuma mandarin) and Citrus sinensis. The dried peels of C. unshiu (chinpi) have been included in several formulae of Japanese Kampo medicines. Nobiletin may suppress the induction of inducible nitric oxide synthase (iNOS), which synthesizes the inflammatory mediator nitric oxide (NO) in hepatocytes.

DOI: 10.1016/j.bbrc.2013.08.029
PubMed: 23958298

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pubmed:23958298

Le document en format XML

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<name sortKey="Yoshigai, Emi" sort="Yoshigai, Emi" uniqKey="Yoshigai E" first="Emi" last="Yoshigai">Emi Yoshigai</name>
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<nlm:affiliation>Department of Biomedical Sciences, College of Life Sciences, Kusatsu, Shiga, Japan; Ritsumeikan Global Innovation Research Organization (R-GIRO), Kusatsu, Shiga, Japan.</nlm:affiliation>
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<name sortKey="Murase, Hiromitsu" sort="Murase, Hiromitsu" uniqKey="Murase H" first="Hiromitsu" last="Murase">Hiromitsu Murase</name>
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<name sortKey="Yamanishi, Ryota" sort="Yamanishi, Ryota" uniqKey="Yamanishi R" first="Ryota" last="Yamanishi">Ryota Yamanishi</name>
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<nlm:affiliation>Department of Biomedical Sciences, College of Life Sciences, Kusatsu, Shiga, Japan; Ritsumeikan Global Innovation Research Organization (R-GIRO), Kusatsu, Shiga, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
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<name sortKey="Machida, Toru" sort="Machida, Toru" uniqKey="Machida T" first="Toru" last="Machida">Toru Machida</name>
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<name sortKey="Okuyama, Tetsuya" sort="Okuyama, Tetsuya" uniqKey="Okuyama T" first="Tetsuya" last="Okuyama">Tetsuya Okuyama</name>
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<name sortKey="Mori, Masatoshi" sort="Mori, Masatoshi" uniqKey="Mori M" first="Masatoshi" last="Mori">Masatoshi Mori</name>
</author>
<author>
<name sortKey="Murase, Hiromitsu" sort="Murase, Hiromitsu" uniqKey="Murase H" first="Hiromitsu" last="Murase">Hiromitsu Murase</name>
</author>
<author>
<name sortKey="Yamanishi, Ryota" sort="Yamanishi, Ryota" uniqKey="Yamanishi R" first="Ryota" last="Yamanishi">Ryota Yamanishi</name>
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<author>
<name sortKey="Okumura, Tadayoshi" sort="Okumura, Tadayoshi" uniqKey="Okumura T" first="Tadayoshi" last="Okumura">Tadayoshi Okumura</name>
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<author>
<name sortKey="Ikeya, Yukinobu" sort="Ikeya, Yukinobu" uniqKey="Ikeya Y" first="Yukinobu" last="Ikeya">Yukinobu Ikeya</name>
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<name sortKey="Nishino, Hoyoku" sort="Nishino, Hoyoku" uniqKey="Nishino H" first="Hoyoku" last="Nishino">Hoyoku Nishino</name>
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<name sortKey="Nishizawa, Mikio" sort="Nishizawa, Mikio" uniqKey="Nishizawa M" first="Mikio" last="Nishizawa">Mikio Nishizawa</name>
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<title level="j">Biochemical and biophysical research communications</title>
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<term>Animals</term>
<term>Anti-Inflammatory Agents (pharmacology)</term>
<term>Cells, Cultured</term>
<term>Chromatography, High Pressure Liquid</term>
<term>Citrus (chemistry)</term>
<term>Dose-Response Relationship, Drug</term>
<term>Flavones (pharmacology)</term>
<term>Gene Expression Regulation, Enzymologic</term>
<term>Hepatocytes (drug effects)</term>
<term>Hepatocytes (metabolism)</term>
<term>Interleukin-1beta (pharmacology)</term>
<term>L-Lactate Dehydrogenase (metabolism)</term>
<term>NF-kappa B (metabolism)</term>
<term>Nitric Oxide (metabolism)</term>
<term>Nitric Oxide Synthase Type II (genetics)</term>
<term>Nitric Oxide Synthase Type II (metabolism)</term>
<term>Rats</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Nitric Oxide Synthase Type II</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>L-Lactate Dehydrogenase</term>
<term>NF-kappa B</term>
<term>Nitric Oxide</term>
<term>Nitric Oxide Synthase Type II</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Anti-Inflammatory Agents</term>
<term>Flavones</term>
<term>Interleukin-1beta</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Citrus</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Hepatocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Hepatocytes</term>
</keywords>
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<term>Animals</term>
<term>Cells, Cultured</term>
<term>Chromatography, High Pressure Liquid</term>
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<front>
<div type="abstract" xml:lang="en">Nobiletin is a polymethoxylated flavone that is abundant in the peels of citrus fruits, such as Citrus unshiu (Satsuma mandarin) and Citrus sinensis. The dried peels of C. unshiu (chinpi) have been included in several formulae of Japanese Kampo medicines. Nobiletin may suppress the induction of inducible nitric oxide synthase (iNOS), which synthesizes the inflammatory mediator nitric oxide (NO) in hepatocytes.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">23958298</PMID>
<DateCreated>
<Year>2013</Year>
<Month>9</Month>
<Day>16</Day>
</DateCreated>
<DateCompleted>
<Year>2013</Year>
<Month>11</Month>
<Day>12</Day>
</DateCompleted>
<DateRevised>
<Year>2015</Year>
<Month>11</Month>
<Day>19</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1090-2104</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>439</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2013</Year>
<Month>Sep</Month>
<Day>13</Day>
</PubDate>
</JournalIssue>
<Title>Biochemical and biophysical research communications</Title>
<ISOAbbreviation>Biochem. Biophys. Res. Commun.</ISOAbbreviation>
</Journal>
<ArticleTitle>Citrus nobiletin suppresses inducible nitric oxide synthase gene expression in interleukin-1β-treated hepatocytes.</ArticleTitle>
<Pagination>
<MedlinePgn>54-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.bbrc.2013.08.029</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0006-291X(13)01355-7</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Nobiletin is a polymethoxylated flavone that is abundant in the peels of citrus fruits, such as Citrus unshiu (Satsuma mandarin) and Citrus sinensis. The dried peels of C. unshiu (chinpi) have been included in several formulae of Japanese Kampo medicines. Nobiletin may suppress the induction of inducible nitric oxide synthase (iNOS), which synthesizes the inflammatory mediator nitric oxide (NO) in hepatocytes.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">A C. unshiu peel (CUP) extract was prepared. Primary cultured rat hepatocytes were treated with the CUP extract or nobiletin in the presence of interleukin 1β (IL-1β), which induces iNOS expression. NO production and iNOS gene expression were analyzed.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">High-performance liquid chromatography analyses revealed that the nobiletin content in the CUP extract was 0.14%. Nobiletin dose-dependently reduced the NO levels and decreased iNOS expression at the protein, mRNA and antisense transcript levels. Flavone, which does not contain any methoxy groups, also suppressed iNOS induction. Nobiletin reduced the transcriptional activity of iNOS promoter-luciferase constructs and the DNA-binding activity of nuclear factor κB (NF-κB) in the nuclei.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The suppression of iNOS induction by nobiletin suggests that nobiletin may be responsible for the anti-inflammatory effects of citrus peels and have a therapeutic potential for liver diseases.</AbstractText>
<CopyrightInformation>Copyright © 2013 Elsevier Inc. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Yoshigai</LastName>
<ForeName>Emi</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Department of Biomedical Sciences, College of Life Sciences, Kusatsu, Shiga, Japan; Ritsumeikan Global Innovation Research Organization (R-GIRO), Kusatsu, Shiga, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Machida</LastName>
<ForeName>Toru</ForeName>
<Initials>T</Initials>
</Author>
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<LastName>Okuyama</LastName>
<ForeName>Tetsuya</ForeName>
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<Day>16</Day>
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<Country>United States</Country>
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<NameOfSubstance UI="D047309">Flavones</NameOfSubstance>
</Chemical>
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<NameOfSubstance UI="D053583">Interleukin-1beta</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D016328">NF-kappa B</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>31C4KY9ESH</RegistryNumber>
<NameOfSubstance UI="D009569">Nitric Oxide</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>D65ILJ7WLY</RegistryNumber>
<NameOfSubstance UI="C008661">nobiletin</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.1.1.27</RegistryNumber>
<NameOfSubstance UI="D007770">L-Lactate Dehydrogenase</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.14.13.39</RegistryNumber>
<NameOfSubstance UI="D052247">Nitric Oxide Synthase Type II</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.14.13.39</RegistryNumber>
<NameOfSubstance UI="C496318">Nos2 protein, rat</NameOfSubstance>
</Chemical>
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<CitationSubset>IM</CitationSubset>
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</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
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<Keyword MajorTopicYN="N">Inflammation</Keyword>
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<Keyword MajorTopicYN="N">Plant polyphenol</Keyword>
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<name sortKey="Nishizawa, Mikio" sort="Nishizawa, Mikio" uniqKey="Nishizawa M" first="Mikio" last="Nishizawa">Mikio Nishizawa</name>
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