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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Avicenna J Med Biotech</journal-id>
      <journal-id journal-id-type="publisher-id">arij002</journal-id>
      <journal-title-group>
        <journal-title>Avicenna Journal of Medical Biotechnology</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2008-2835</issn>
      <issn pub-type="epub">2008-4625</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">ajmb60535</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Is Formulary of Maranta Arundinacea Clarias Gariepinus (F-MaCg) a Potential Immunostimulant?</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Zulkifli</surname><given-names>Zulkifli</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Darmawi</surname><given-names>Darmawi</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Usman</surname><given-names>Said</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Fitri Jamil </surname><given-names>Kurnia</given-names></name></contrib></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>15</volume>
      <issue>2</issue>
      <fpage>91</fpage>
      <lpage>99</lpage>
      <history>
        <date date-type="received">
          <day>20</day>
          <month>9</month>
          <year>2022</year>
        </date>
        <date date-type="accepted">
          <day>30</day>
          <month>11</month>
          <year>2022</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background: E&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;xternal factors have the potential to act as immunostimulants in order to influence the body&amp;#39;s protection from many foreign antigens. We intended to investigate the ethanol extract Formulary of F-MaCg effect as an immunostimulant.&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&amp;nbsp;A purely experimental with a completely randomized design was used on twenty-four white male rats. They were divided into four groups:1) G0 [given aquades (5 &lt;em&gt;ml&lt;/em&gt;)]; 2) G1 [given F-MaCg-75 &lt;em&gt;mg/gr&lt;/em&gt; BW (Body Weight)]; 3) G2 (F-MaCg -150 &lt;em&gt;mg/gr&lt;/em&gt; plus Hepatitis B vaccine at the beginning and the end of treatment); and 4) G3 (F-MaCg -300 &lt;em&gt;mg/gr&lt;/em&gt; BW plus hepatitis B vaccine at the end of treatment). The rat&amp;#39;s spleen lymphocyte blast transformation was evaluated on the 15th and 37th days. Lymphocytes were examined using microtetrazolium assays. Optical Density (OD) was measured using an ELISA reader [493 &lt;em&gt;n&lt;span style=&quot;background-color:white&quot;&gt;&amp;mu;&lt;/span&gt;&lt;/em&gt; (nanomicro)]. Observation of lymphocyte viability by a counting chamber using a light microscope and trypan blue 1 % before being cultured with Phytohaemoaglutinin.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&amp;nbsp;Lymphocyte cell viability in the hepatitis B vaccine-induced group on the 15th day showed the highest average value in the G2 (1,484/&lt;em&gt;mcl&lt;/em&gt; of blood); on the 37th day, it was in G3 (1,578/&lt;em&gt;mcl&lt;/em&gt; of blood). The proliferative activity of spleen lymphocytes indicated by the difference in the OD values of the four treatment groups was 0.467, 0.913, 1.619, and 1.473 &lt;em&gt;n&lt;span style=&quot;background-color:white&quot;&gt;&amp;mu;&lt;/span&gt;&lt;/em&gt;, respectively. Histological observations of the spleen showed differences at all given formulary dose concentrations.&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;F-MaCg could be an immunostimulant because of its ability to trigger a cellular immune response.&lt;/span&gt;&lt;/p&gt;

      </p>
      </abstract>
    </article-meta>
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