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  <front>

    <journal-meta>

      <journal-title>International Journal of Pharmacology</journal-title>

      <issn pub-type="ppub">1811-7775</issn>

      <issn pub-type="epub">1812-5700</issn>

      <publisher>

        <publisher-name>Asian Network for Scientific Information</publisher-name>

      </publisher>

    </journal-meta>


    <article-meta>

      <article-id pub-id-type="doi">10.3923/ijp.2018.83.92</article-id>


      <title-group>

        <article-title><![CDATA[Inhibitory Effects of Sulforaphane on Polyphosphate-mediated Septic Responses]]></article-title>

      </title-group>


      <contrib-group>

        <contrib contrib-type="author" xlink:type="simple">


          <name name-style="western">

            <surname>Jeong</surname>

            <given-names>Seongdo</given-names>

          </name>


          <name name-style="western">

            <surname>Ku</surname>

            <given-names>Sae-Kwang</given-names>

          </name>


          <name name-style="western">

            <surname>Bae</surname>

            <given-names>Jong-Sup</given-names>

          </name>


        </contrib>

      </contrib-group>


      <pub-date pub-type="collection">


        <month>1</month>




        <year>2018</year>

      </pub-date>


      <volume>14</volume>

      <issue>1</issue>


      <abstract><![CDATA[<p><b>Background and Objective</b>: Sulforaphane (SFN), a natural isothiocyanate present in cruciferous vegetables, such as broccoli and cabbage, is effective in preventing carcinogenesis, diabetes and inflammatory responses. Human endothelial cell-derived polyphosphate (PolyP) is a proinflammatory mediator. This study was undertaken to investigate whether SFN can modulate PolyP-mediated inflammatory responses in Human Umbilical Vein Endothelial Cells (HUVECs) and mice. <b>Materials and Methods:</b> The anti-inflammatory activities of SFN were determined by measuring the permeability, leukocyte adhesion and migration and activation of proinflammatory proteins in PolyP-activated HUVECs and mice. In addition was determined the beneficial effects of SFN on survival rate in PolyP-injected mice. Statistical relevance was determined by one-way analysis of variance (ANOVA) and Tukey&#146;s post-test. <b>Results</b>: Data showed that SFN inhibits PolyP-mediated barrier disruption, cell adhesion molecule expression and leukocyte to HUVEC adhesion/migration. Notably, PolyP-induced NF-&#954;B activation and TNF-&#945; and IL-6 production were inhibited by SFN in HUVECs. These anti-inflammatory functions of SFN were confirmed in PolyP injected mice. <b>Conclusion</b>: Based on the anti-inflammatory effects of SFN in PolyP-mediated septic response, SFN could be considered a potential agent for the treatment of sepsis and other diseases in which PolyP is viewed as a therapeutic target.</p>]]></abstract>


    </article-meta>

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