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  <front>

    <journal-meta>

      <journal-title>Journal of Biological Sciences</journal-title>

      <issn pub-type="ppub">1727-3048</issn>

      <issn pub-type="epub">1812-5719</issn>

      <publisher>

        <publisher-name>Asian Network for Scientific Information</publisher-name>

      </publisher>

    </journal-meta>


    <article-meta>

      <article-id pub-id-type="doi">10.3923/jbs.2022.34.41</article-id>


      <title-group>

        <article-title><![CDATA[<i>Cajanus cajan</i></b><b> (L) Mill Sp. Leaf Extract Exacerbates Acute Renal Injury Induced by Acetaminophen in Albino Rats]]></article-title>

      </title-group>


      <contrib-group>

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


          <name name-style="western">

            <surname>Chinonyelum Azubuike</surname>

            <given-names>Nkiruka</given-names>

          </name>


          <name name-style="western">

            <surname>N. Okwuosa</surname>

            <given-names>Chukwugozie</given-names>

          </name>


          <name name-style="western">

            <surname>V. Eze</surname>

            <given-names>Chukwuebuka</given-names>

          </name>


          <name name-style="western">

            <surname>Imo</surname>

            <given-names>Chinedu</given-names>

          </name>


        </contrib>

      </contrib-group>


      <pub-date pub-type="collection">


        <month>1</month>




        <year>2022</year>

      </pub-date>


      <volume>22</volume>

      <issue>1</issue>


      <abstract><![CDATA[<p><b>Background and Objective:</b>  <i>Cajanus cajan</i> is traditionally used for the treatment of various ailments due to its antioxidant properties. The present study investigated the effect <i>C. cajan</i> crude aqueous leaf extract (<i>CCLE </i>) in rats with acetaminophen (APAP)-induced acute renal injury. <b>Materials and Methods:</b>  Preliminary acute toxicity testing of the extract was conducted to determine the oral median lethal dose (LD<sub>50</sub>). Twenty rats were divided into five experimental groups labelled (A-E) of 4 rats per cage. Group A served as the normal control group and was given only water and feed. Rats in groups C, D and E received 100 mg kg<sup>&#150;</sup><sup>1</sup> b.wt., of ascorbic acid, 200 and 500 mg kg<sup>&#150;</sup><sup>1</sup> of <i>CCLE</i>, respectively once daily for 7 days via oral route using an oral cannula. Thirty min after the daily treatments, 600 mg kg<sup>&#150;</sup><sup>1</sup> b.wt., of acetaminophen (APAP) was administered orally to rats in groups B-E. At the end of the treatments, blood samples were collected from the animals via retro-orbital puncture for the estimation of serum urea, creatinine and uric acid levels. The rats were sacrificed under anaesthesia and the kidneys were excised for histopathological analysis. <b>Results:</b>  Acute toxicity testing showed that <i>CCLE</i> has an oral LD<sub>50</sub> of 8000 mg kg<sup>&#150;</sup><sup>1</sup> b.wt. Serum biochemistry showed a statistically significant increase (p&gt;0.05) in creatinine and uric acid levels in all treatment groups when compared to normal control. Histopathological findings revealed the observable renal injury, with <i>CCLE-</i>treated groups showing more severe histomorphological alterations when compared to the APAP (negative) control. <b>Conclusion:</b>  Data obtained suggest that acute toxicity was not observed with <i>C. cajan </i>administration up to 8 g kg<sup>&#150;</sup><sup>1</sup>, however, its co-administration with a high dose of acetaminophen does not protect the kidneys but rather aggravates the acute renal injury.</p>]]></abstract>


    </article-meta>

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