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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of Pharmacy and Health Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPHR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2321-3647</issn>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPHR210007</article-id>
      <title-group>
        <article-title>Experimental Evaluation of Anticonvulsant Activity of Hydrocotyle Asiatica linn (Centella asiatica) in Albino Mice</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Uppala</surname>
            <given-names>Praveen Kumar</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>B</surname>
            <given-names>Murali Krishna</given-names>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
      </contrib-group>
      <aff id="aff1">Assistant Professor, KVK College of Pharmacy, Affiliated to JNTUH, Hyderabad.</aff>
      <aff id="aff2">Assistant Professor, Bhaskara College of Pharmacy, Affiliated to Andhra University, Visakhapatnam.</aff>
      <pub-date pub-type="epub" iso-8601-date="2014-10-01">
        <month>10</month>
        <day>01</day>
        <year>2014</year>
      </pub-date>
      <volume>2</volume>
      <issue>10</issue>
      <abstract>
        <p>To evaluate the antiepileptic activity of Hydrocotyle asiatica linn (aqueous extract) in preventing maximal electroshock (MES) and pentylenetetrazole (PTZ) induced convulsions. To compare its efficacy with standard drugs- phenytoin for MES method and sodium valproate for PTZ method. 48 male albino mice weighing 18-30g are selected and divided into 2 groups of 24 mice each – one group for MES and other group for PTZ method. In MES method, seizures were induced via ear clip electrodes with a current of 50 mA for 0.2 seconds. Each mouse is pretreated with drugs (p.o.) one hour before MES test. The different groups include – Group C1 administered distilled water (0.25ml), Group S1 administered phenytoin (50 mg/kg), Group T1 administered aqueous extract of Hydrocotyle asiatica linn (100 mg/kg) and Group T2 administered aqueous extract of Hydrocotyle asiatica linn (300mg/kg). In PTZ method, seizures were induced by giving PTZ 80 mg/kg s.c. Each mouse is pretreated with drugs one hour before giving PTZ. The different groups include – Group C2 administered distilled water (0.25ml p.o.), Group S2 administered sodium valproate (300mg/kg i.p.), Group T3 administered aqueous extract of Hydrocotyle asiatica linn (100 mg/kg) and Group T4 administered aqueous extract of Hydrocotyle asiatica linn (300mg/kg). The aqueous extract of Hydrocotyle asiatica at a dose of 300mg/kg has shown statistically significant anticonvulsant activity against both MES and PTZ convulsions and its anticonvulsant activity is similar to that of standard sodium valproate (300mg/kg).</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Hydrocotyle</kwd>
        <kwd>asiatica</kwd>
        <kwd>Maximal</kwd>
        <kwd>electroshock</kwd>
        <kwd>seizures</kwd>
        <kwd>Pentylene tetrazole</kwd>
        <kwd>Sodium valproate</kwd>
      </kwd-group>
    </article-meta>
  </front>
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