﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Shahrekord University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Herbmed Pharmacology</JournalTitle>
      <Issn>2345-5004</Issn>
      <Volume>8</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2019</Year>
        <Month>01</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Protective and anti-inflammatory effects of silymarin on paraquat-induced nephrotoxicity in rats</ArticleTitle>
    <FirstPage>28</FirstPage>
    <LastPage>34</LastPage>
    <ELocationID EIdType="doi">10.15171/jhp.2019.05</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>Sharifi-Rigi</LastName>
      </Author>
      <Author>
        <FirstName>Esfandiar</FirstName>
        <LastName>Heidarian</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-4701-144X</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/jhp.2019.05</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>04</Month>
        <Day>19</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Paraquat is a quaternary nitrogen herbicide which induces kidney toxicity due to producing oxidative stress. We have investigated the potential protective effects of silymarin on paraquat-induced renal toxicity. Methods: Twenty-four male rats were divided into three groups, group 1, control group; group 2, rats that received paraquat only (25 mg/kg b.w./day, po); animals in group 3, was treated with paraquat (25 mg/kg b.w./day, po) and silymarin (50 mg/kg b.w./day, po). Then, the serum and tissue parameters of the oxidative stress and renal histopathological changes were examined. Results: In group 2 which received paraquat only, a remarkable increase (P&lt;0.05) was observed in serum creatinine, urea, malondialdehyde (MDA), protein carbonyl, and tumor necrosis factor alpha (TNF-α). Also, there was a significant decrease in renal superoxide dismutase, catalase (CAT), ferric reducing ability of plasma (FRAP) and vitamin C in the second group. Oral administration of silymarin significantly decreased serum urea, creatinine, protein carbonyl, MDA, and TNF-α as well as renal histopathological changes. Conclusion: The present study suggests that silymarin has anti-inflammatory and nephroprotective effects against nephrotoxicity caused by paraquat.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Silymarin</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Paraquat</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Kidney injury</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Oxidative stress</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">TNF-α</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>