﻿<?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>15</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2026</Year>
        <Month>01</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Investigation of cardioprotective effects of Leea rubra Blume leaves on isoproterenol-induced left ventricular hypertrophy in mice</ArticleTitle>
    <FirstPage>27</FirstPage>
    <LastPage>35</LastPage>
    <ELocationID EIdType="doi">10.34172/jhp.2026.53125</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Md. Abdur Nur</FirstName>
        <LastName>Tushar</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0008-7697-4051</Identifier>
      </Author>
      <Author>
        <FirstName>Md. Mamunur</FirstName>
        <LastName>Rashid</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0001-6816-4752</Identifier>
      </Author>
      <Author>
        <FirstName>Farhad</FirstName>
        <LastName>Hossain</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-1333-474X</Identifier>
      </Author>
      <Author>
        <FirstName>Kazi Mazharul</FirstName>
        <LastName>Islam</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0000-9831-6342</Identifier>
      </Author>
      <Author>
        <FirstName>Md. Ariful</FirstName>
        <LastName>Islam</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-2796-4224</Identifier>
      </Author>
      <Author>
        <FirstName>Farjana</FirstName>
        <LastName>Sharmin</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0003-7629-2898</Identifier>
      </Author>
      <Author>
        <FirstName>Purnima Rani</FirstName>
        <LastName>Das</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0006-2080-6417</Identifier>
      </Author>
      <Author>
        <FirstName>Mohammad A.</FirstName>
        <LastName>Rashid</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-1464-7115</Identifier>
      </Author>
      <Author>
        <FirstName>AHM Khurshid</FirstName>
        <LastName>Alam</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-2690-6559</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jhp.2026.53125</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>05</Month>
        <Day>01</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>08</Month>
        <Day>22</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Cardiac hypertrophy is a risk factor for many cardiovascular diseases (CVDs). Species of the genus Leea have traditional cardioprotective uses, but their direct effects on the heart remain unreported. This study evaluated the cardioprotective activities of a crude methanolic extract (CME) of L. rubra leaves (LRL) in isoproterenol-induced cardiac hypertrophic mice (IIHM) using atorvastatin as a reference treatment. Methods: IIHM (induced with isoproterenol, 5 mg/kg, 7 days, intraperitoneally) were treated with CME of LRL (40 mg/kg or 80 mg/kg, 28 days, orally) and compared with a standard treatment group (atorvastatin, 20 mg/kg, 28 days, orally) and a negative control group (IIHM, placebo). The cardioprotective and hepatoprotective effects of the extract were evaluated by analysing the changes in blood biochemical parameters, including lipid profile (total cholesterol [TC], triglyceride [TG], high-density lipoprotein [HDL], and low-density lipoprotein [LDL]), cardiac troponin I (CTnI), serum glutamic pyruvic transaminase (SGPT), and serum glutamic oxaloacetic transaminase (SGOT). Analysis was conducted using various commercial test kits. The left ventricular weight and body weight (LVW/BW) ratio was also recorded. Results: LRL significantly improved the lipid profile by lowering TC, TG, and LDL while increasing HDL levels (P&lt;0.0001). Significant cardioprotective (reduced serum CTnI level and LVW/BW ratio (P&lt;0.0001)) and hepatoprotective (reduced serum SGPT and SGOT levels (P&lt;0.0001)) activities were observed in IIHM compared with the negative control group. Conclusion: The present study found antihyperlipidemic, cardioprotective, and hepatoprotective activity after LRL treatment in IIHM. Further investigation is required to identify the compounds and molecular mechanisms responsible for these effects.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Leea rubra</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Cardioprotective activity</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Antihyperlipidemic activity</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Ventricular hypertrophy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Hepatoprotective activity</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>