﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Hamadan University of Medical Sciences</PublisherName>
      <JournalTitle>Avicenna Journal of Medical Biochemistry</JournalTitle>
      <Issn>2345-4113</Issn>
      <Volume>13</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2025</Year>
        <Month>10</Month>
        <DAY>31</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Protective Effects of Vernonia amygdalina Extract Against 1-Nitropyrene-Induced Hepatopulmonary Oxidative Injury in Rats</ArticleTitle>
    <FirstPage>27</FirstPage>
    <LastPage>35</LastPage>
    <ELocationID EIdType="doi">10.34172/ajmb.2630</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Omorede</FirstName>
        <LastName>Ikponmwosa-Eweka</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-7654-5635</Identifier>
      </Author>
      <Author>
        <FirstName>Ikenna C.</FirstName>
        <LastName>Maduako</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-1001-4866</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/ajmb.2630</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>08</Month>
        <Day>02</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>09</Month>
        <Day>21</Day>
      </PubDate>
    </History>
    <Abstract>Background: 1-Nitropyrene (1-NP), an environmental pollutant derived from nitro-polycyclic aromatic hydrocarbons, poses serious environmental hazards. Vernonia amygdalina (VA), commonly known as bitter leaf, is widely used in folk medicine due to its pharmacological properties. Objectives: This study investigated the pharmacological role of VA in 1-NP-induced hepatopulmonary oxido-inflammatory stress responses in a murine model. Methods: Experimental animals were randomly divided into five groups of seven rats each and orally treated with 1-NP (250 mg/kg) alone or in combination with VA (50 mg/kg and 100 mg/kg) for 7 consecutive days. Then, glutathione, reactive oxygen and nitrogen species, nitric oxide (NO), and lipid peroxidation levels were biochemically assessed alongside the activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase-4 (GPX4), glutathione-S-transferase (GST), and myeloperoxidase (MPO). Eventually, the enzyme-linked immunosorbent assay was utilized to evaluate regulated upon activation, normal T cell expressed and secreted (RANTES), tumor necrosis factor-alpha (TNF-α), and interleukin-1 beta (IL-1β). Results: VA administration markedly ameliorated 1-NP-induced oxido-inflammatory hepatopulmonary damage by upregulating enzymatic and non-enzymatic antioxidants while diminishing proinflammatory proteins as observed by the reduced levels of RANTES, TNF-α, IL-1β, NO, and MPO activities. Conclusion: Overall, VA prevented 1-NP-induced hepatopulmonary damage by enhancing antioxidant enzymes and inhibiting proinflammatory markers, thereby protecting the organs.  </Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">1-Nitropyrene</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Vernonia amygdalina</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Hepatopulmonary</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">RANTES</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">GPX4</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>