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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd"[]>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Science and Education Publishing</PublisherName>
      <JournalTitle>Journal of Food and Nutrition Research</JournalTitle>
      <Issn>2333-1240</Issn>
      <Volume>2</Volume>
      <Issue>7</Issue>
      <PubDate PubStatus="epublish">
        <Year>2014</Year>
        <Month>07</Month>
        <Day>24</Day>
      </PubDate>
    </Journal>
    <ArticleTitle>Green Tea Polyphenol Epigallocatechin-3-O-Gallate Attenuates Lipopolysaccharide-induced Nitric Oxide Production in RAW264.7 Cells</ArticleTitle>
    <FirstPage>425</FirstPage>
    <LastPage>428</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Seung-Jae</FirstName>
        <LastName>Lee</LastName>
      </Author>
      <Author>
        <FirstName>Hyun Woo</FirstName>
        <LastName>Kang</LastName>
      </Author>
      <Author>
        <FirstName>Seung Yuan</FirstName>
        <LastName>Lee</LastName>
      </Author>
      <Author>
        <FirstName>Sun Jin</FirstName>
        <LastName>Hur</LastName>
        <Affiliation>Department of Animal Science and Technology, Chung-Ang University, Anseong, Korea</Affiliation>
      </Author>
    </AuthorList>
    <ArticleIdList>
      <ArticleId IdType="pii">JFNR20142716</ArticleId>
      <ArticleId IdType="doi">10.12691/jfnr-2-7-16</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2014</Year>
        <Month>07</Month>
        <Day>08</Day>
      </PubDate>
      <PubDate PubStatus="revised">
        <Year>2014</Year>
        <Month>07</Month>
        <Day>18</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2014</Year>
        <Month>07</Month>
        <Day>24</Day>
      </PubDate>
    </History>
    <Abstract>Epigallocatechin-3-O-gallate (EGCG), the major polyphenol found in green tea, has been shown to downregulate inflammatory responses in macrophages; however, the underlying mechanism has not been understood. Overproduction of nitric oxide (NO) by inducible nitric oxide synthase (iNOS) is known to be closely correlated with the pathology of a variety of diseases and inflammations. In this study, we investigated the inhibitory effect of EGCG on NO production and its molecular mechanism in lipopolysaccharide (LPS)-stimulated macrophage RAW264.7 cells. Besides a decrease in NO secretion, protein levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) also decreased in LPS-stimulated RAW264.7 macrophage cells treated with EGCG. These results suggest that EGCG possesses a potent anti-inflammatory activity.</Abstract>
  </Article>
</ArticleSet>