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    <timestamp>1568869906</timestamp>
    <depositor>
      <depositor_name>Editor</depositor_name>
      <email_address>editor.jddt@gmail.com</email_address>
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    <registrant>UJPR</registrant>
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    <journal>
      <journal_metadata>
        <full_title>Universal Journal of Pharmaceutical Research</full_title>
        <abbrev_title>Univ J Pharm Res</abbrev_title>
        <issn media_type="electronic">2456-8058</issn>
      </journal_metadata>
      <journal_issue>
        <publication_date media_type="online">
          <month>04</month>
          <day>06</day>
          <year>2018</year>
        </publication_date>
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        <titles>
          <title>MYOCARDIAL POTENCY OF AQUEOUS EXTRACT OF HARUNGANA MADAGASCARIENSIS STEM BARK AGAINST ISOPROTERENOL-INDUCED MYOCARDIAL DAMAGE IN RATS</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <given_name>Esther Ngo Lemba</given_name>
            <surname>Tom</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Florette Diane</given_name>
            <surname>Nankia</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Nyemb</given_name>
            <surname>Nyunaï</surname>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>The present study was undertaken to evaluate the effects of Harungana madagascariensis on electrocardiographical, biochemical and histopathological changes in isoproterenol (ISO)-induced myocardial infarction in rats. Male Wistar albino rats were randomly divided and treated with the aqueous extract of Harungana madagascariensis stem bark (AEHM, 200 and 400 mg/kg per os), or normal saline or vitamin E for 7 days with concomitant administration of ISO (85 mg/kg, subcutaneously) on 8th and 9th days, at 24 h interval. The ISO injections to the rats caused cardiac dysfunction evidenced by a marked (P&lt;0.01) elevation in ST-segment, a reduction in R wave amplitude (P&lt;0.01), decrease in endogenous antioxidant reduced glutathione (GSH), increase in malondialdehyde (MDA), a lipid peroxidation marker, increase of cardiac marker enzymes lactate dehydrogenase (LDH), aspartate amino transferase (AST) and alanine amino transferase (ALT). All these changes in cardiac function as well as GSH, MDA and the enzymes (LDH, AST and ALT) were ameliorated when the rats were pretreated with AEHM. Additionally, the protective effects were strengthened by improved histopathological changes, which specifies the protection of cardiomyocytes from the deleterious effects of ISO. This study demonstrates the cardioprotective effect of Harungana madagascariensis on isoproterenolinducedmyocardial infarction in rats. The mechanism might be associated with the enhancement of antioxidant defense, reduction of lipid peroxydation and it is confirmed by amending electrocardiographic pattern, improvement of cardiac markers and less histopathological damages following ISO-induced myocardial infarction. It could provide experimental evidence to support the use of Harungana madagascariensis used in traditional medicine to treat cardiovascular disorders.&#13;
Google Scholar</jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>04</month>
          <day>06</day>
          <year>2018</year>
        </publication_date>
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          <doi>10.22270/ujpr.v3i1.R4</doi>
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