﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Advanced Pharmaceutical Bulletin</JournalTitle>
      <Issn>2228-5881</Issn>
      <Volume>12</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2022</Year>
        <Month>01</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Protective Role of trans-Chalcone against the Progression from Simple Steatosis to Non-alcoholic Steatohepatitis: Regulation of miR-122, 21, 34a, and 451</ArticleTitle>
    <FirstPage>200</FirstPage>
    <LastPage>205</LastPage>
    <ELocationID EIdType="doi">10.34172/apb.2022.022</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Elham</FirstName>
        <LastName>Karimi-Sales</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-1644-5058</Identifier>
      </Author>
      <Author>
        <FirstName>Sajad</FirstName>
        <LastName>Jeddi</LastName>
      </Author>
      <Author>
        <FirstName>Abbas</FirstName>
        <LastName>Ebrahimi-Kalan</LastName>
      </Author>
      <Author>
        <FirstName>Mohammad Reza</FirstName>
        <LastName>Alipour</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-6484-4267</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/apb.2022.022</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2020</Year>
        <Month>05</Month>
        <Day>14</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>01</Month>
        <Day>29</Day>
      </PubDate>
    </History>
    <Abstract>Purpose: Non-alcoholic steatohepatitis (NASH) is an inflammatory disorder and an aggressiveform of fatty liver disease. Certain microRNAs, including miR-122, 21, 34a, and 451, areinvolved in the transition from steatosis to NASH. This study examined how trans-chalcone (thecore of chalcone derivatives) affects non-alcoholic fatty liver disease (NAFLD) progression byregulating miRNAs.Methods: Male rats were divided into three groups (n = 7/group) as follows: control, rats weregavaged with 10% tween 80 (for two weeks); NASH, rats were gavaged with a high-fat liquiddiet (HFD; for six weeks) and 10% tween 80 (for two weeks); NASH + Chal, rats were gavagedwith the HFD (for six weeks) and trans-chalcone (for two weeks). Hepatic expression levels ofmiR-122, 21, 34a, and 451 were determined.Results: trans-Chalcone reversed histological abnormalities, reduced liver injury markers,and attenuated insulin resistance in HFD-fed rats. In the liver, HFD-induced NASH increasedthe expression level of miR-34a and decreased expression levels of miR-122, 21, and 451.However, trans-chalcone inhibited HFD-induced changes in expression levels of these miRNAs.Conclusion: trans-Chalcone could inhibit the transition from steatosis to NASH through themodulation of miR-122, 21, 34a, and 451 expression levels in the liver.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Non-alcoholic steatohepatitis</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">trans-chalcone</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">miRNAs</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Liver</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Rat</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>