

<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "journalpublishing3.dtd">
<article xmlns:xlink="https://www.w3.org/1999/xlink">
  <front>
    <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">ajmb60554</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>Activity of Citrus aurantium and Lavandula angustifolia in Alzheimer’s Disease  Symptoms in Male Wistar Rats</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Arasteh</surname><given-names>Amir</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Karimpour</surname><given-names>Morteza</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Fallah</surname><given-names>Faezeh</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Kiani</surname><given-names>Sara</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Kakavan</surname><given-names>Maedeh</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>4</issue>
      <fpage>223</fpage>
      <lpage>231</lpage>
      <history>
        <date date-type="received">
          <day>12</day>
          <month>3</month>
          <year>2023</year>
        </date>
        <date date-type="accepted">
          <day>22</day>
          <month>7</month>
          <year>2023</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; Alzheimer&amp;#39;s Disease (AD) is one of the most prevalent chronic neurodegenerative disorders. The present study aims&amp;nbsp;to better understand the mechanism by which&lt;em&gt; Citrus aurantium&lt;/em&gt; (&lt;em&gt;C. aurantium)&lt;/em&gt; and &lt;em&gt;Lavandula angustifolia&lt;/em&gt; (&lt;em&gt;L. angustifolia)&lt;/em&gt; hydro&amp;ndash;alcoholic extracts were used to treat AD and anti&amp;shy;&amp;ndash;oxidant issues in a laboratory model. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&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; 15 male Wistar rats, weighing 250&amp;plusmn;20 &lt;em&gt;gr&lt;/em&gt;, aged 6&amp;ndash;8 weeks, were used. Amyloids in the brain were found and identified using the shuttle box and Congo red test. ELISA testing for norepinephrine and serotonin, Superoxide Dismutase (SOD), Malondialdehyde (MDA), and Real&amp;ndash;time PCR for expression of the &lt;em&gt;APP&lt;/em&gt; and &lt;em&gt;GLT1&lt;/em&gt; genes were done. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&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; The shuttle box test demonstrated that AD produces behavioral harm, since it significantly reduces passive avoidance learning. The Congo red test revealed that the AD models had much more amyloid beta in their brain tissue than the control. Norepinephrine levels were also decreased by using both extracts in test group. Treatment with both extracts led to a substantial rise in SOD activity and fall in MDA concentration. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:12pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The gene expression data indicated that the relative expression of the &lt;em&gt;APP&lt;/em&gt; and &lt;em&gt;GLT1&lt;/em&gt; genes was shown to be lower in the groups treated with both extracts. &lt;em&gt;C. aurantium&lt;/em&gt; and &lt;em&gt;L. angustifolia&lt;/em&gt; may therefore offer a multi&amp;ndash;target treatment strategy for AD, which calls for more research in this area. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

      </p>
      </abstract>
    </article-meta>
  </front>
    
</article>
