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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.2018.68.75</article-id>


      <title-group>

        <article-title><![CDATA[Pharmacokinetics Study of Seven Lignans in Alzheimer&#146;s Rats]]></article-title>

      </title-group>


      <contrib-group>

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


          <name name-style="western">

            <surname>Xiao-tong</surname>

            <given-names>Wang</given-names>

          </name>


          <name name-style="western">

            <surname>Fan</surname>

            <given-names>He</given-names>

          </name>


          <name name-style="western">

            <surname>Xiao-ling</surname>

            <given-names>Sun</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> <I>Schisandra chinensis </I> (<I>S. chinensis</I>) (Turcz., Bail.), is Chinese traditional herbal medicine and the schisandra lignans are the major constituents of <I>S. chinensis</I> responsible for the nephroprotective effect. However, there was no study done on pharmacokinetics of schisandra lignans in Alzheimer&#146;s disease (AD) rat plasma after oral <I>Schisandra chinensis</I> extract (SCE). The aim of this study was to investigate the pharmacokinetic profiles of 7 lignans after oral administration of SCE and compared the difference of the pharmacokinetics profiles between normal and Alzheimer&#146;s disease rats. <b>Materials and Methods:</b> The plasma concentrations of 7 lignans were determined by using a simple and rapid high-performance liquid chromatography. All the rats were divided randomly into two groups (Alzheimer&#146;s and normal groups). Each group received oral administration of 0.1 g kg<SUP>&#150;1</SUP> SCE. The relevant pharmacokinetic parameters were calculated by using the computer program DAS 2.0. <b>Results:</b> The results showed that 7 lignans of <I>Schisandra chinensis</I> could be detected in rat plasma after oral administration of SCE to rats. Gomisin D and schisantherin A had shown better absorption than other lignans. Oral administration of SCE, AD rats showed better absorption than normal rats. <b>Conclusion:</b> It can be concluded that the pharmacokinetics properties of 7 lignans differed between Alzheimer&#146;s rats and normal rats, including AUC<SUB>(0-t)</SUB> and C<SUB>max</SUB> (p&lt;0.05).</p>]]></abstract>


    </article-meta>

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