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<records>
  <record>
    <language>eng</language>
    <publisher>Science and Education Publishing</publisher>
    <journalTitle>American Journal of Food and Nutrition</journalTitle>
    <eissn>2374-1163</eissn>
    <publicationDate>2026-05-26</publicationDate>
    <volume>14</volume>
    <issue>3</issue>
    <startPage>82</startPage>
    <endPage>97</endPage>
    <doi>10.12691/ajfn-14-3-1</doi>
    <publisherRecordId>AJFN20261431</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Potential Protective Effects of Poinciana (Delonix regia) Flower Extracts Against Benzo[a]pyrene Induced-hepatotoxicity in Rats</title>
    <authors>
      <author>
        <name>Yousif A. Elhassaneen</name>
        <email>yousif12@hotmail.com</email>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Seham A. Kheder</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Hagar E. Soliman</name>
        <affiliationId>1</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Nutrition and Food Science, Faculty of Home Economics, Menoufia University, Shebin El-Kom, Egypt</affiliationName>
    </affiliationsList>
    <abstract language="eng">During the research, the goal was to test the hepatoprotective ability of a Delonix regia flower ethanol extract (DRFE) on benzo[a]pyrene (B[a]P)-induced hepatic toxicity in rats. Thirty rats in this paper consisted of a normal control group and a hepatotoxic group, which was subjected to DRFE at doses of 200, 400, or 600 mg/kg over the 28 days. B[a]P treatment resulted in significant reductions in body weight (-35.16%), feed intake (-37.48%), feed efficiency ratio (-27.36%), and liver weight (- 24.61%), and an increase in serum liver enzyme (AST, +187%,  ALT, +164%, ALP, +88.6%), total bilirubin (+208.9%) and direct bilirubin (+234.2%), and the reduction in total protein (-25.3%). There was a violation of the balance of glutathione (GSH, -65.76%, GSSG, +31.08%, GSH/GSSG +73.88%), and an increase in the number of ROS (+241.79%) and MDA (+70.87%). The dose-dependent treatment of DRFE restored nutritional and hepatic parameters, the highest dose (600 mg/kg) improving body weight (+47.46%), liver weight (+24.20%), AST (?53.2%), ALT (?44.5%), ALP (?38.6%), total bilirubin (?51.1%), direct bilirubin (?47.8%), total protein (+20.52%), albumin (+32.78%), GSH (+109.97%). Such protective activities are attributed to the DRFE flavonoids, phenolic acids, tannins, sterols, and triterpenoids that have antioxidant, anti-inflammatory and membrane-stabilizing properties, repairing liver functioning, redox, and protein production. In general, DRFE had a good hepatoprotective effect against the B[a]P-induced toxicity with increasing doses which also indicates that it has a high potential in the use as a natural and plant-based agent in reducing the liver damage caused by environmental or dietary hepatotoxins.</abstract>
    <fullTextUrl format="pdf">https://pubs.sciepub.com/ajfn/14/3/1/ajfn-14-3-1.pdf</fullTextUrl>
    <keywords language="eng">
      <keyword>Liver enzyme</keyword>
      <keyword>bilirubin</keyword>
      <keyword>glutathione</keyword>
      <keyword>cytochrome P450</keyword>
      <keyword>lipid peroxidation</keyword>
      <keyword>malondialdehyde</keyword>
    </keywords>
  </record>
</records>