﻿<?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>13</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2024</Year>
        <Month>01</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Magnolia kobus DC leaf ethanol extract alleviated lipopolysaccharide-induced acute lung inflammation by suppressing NF-κB and Nrf2 signaling</ArticleTitle>
    <FirstPage>90</FirstPage>
    <LastPage>100</LastPage>
    <ELocationID EIdType="doi">10.34172/jhp.2024.48116</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Yeyoung</FirstName>
        <LastName>Kim</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-6597-3602</Identifier>
      </Author>
      <Author>
        <FirstName>Soyoung</FirstName>
        <LastName>Lee</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-9949-6477</Identifier>
      </Author>
      <Author>
        <FirstName>Young-Ae</FirstName>
        <LastName>Choi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-6359-5492</Identifier>
      </Author>
      <Author>
        <FirstName>Jae-Min</FirstName>
        <LastName>Chung</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-2942-6641</Identifier>
      </Author>
      <Author>
        <FirstName>Eun-Nam</FirstName>
        <LastName>Kim</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-7473-1453</Identifier>
      </Author>
      <Author>
        <FirstName>Byungheon</FirstName>
        <LastName>Lee</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4561-1027</Identifier>
      </Author>
      <Author>
        <FirstName>Sang-Yong</FirstName>
        <LastName>Kim</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-1819-5913</Identifier>
      </Author>
      <Author>
        <FirstName>Gil-Saeng</FirstName>
        <LastName>Jeong</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-1882-0256</Identifier>
      </Author>
      <Author>
        <FirstName>Sang-Hyun</FirstName>
        <LastName>Kim</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-6160-7354</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jhp.2024.48116</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2023</Year>
        <Month>05</Month>
        <Day>26</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Magnolia kobus DC has been used as herbal medicine to treat coughs and is known to exert biological effects such as anti-inflammatory, antioxidant, and antibacterial properties. We aimed to define the pharmacological effects of M. kobus leaf ethanol extract (MLEE) on acute lung inflammation and explore the underlying mechanisms of action. Methods: For in vitro investigations, RAW 264.7 cells were pretreated with MLEE (1, 10, and 100 μg/mL) and stimulated with lipopolysaccharide (LPS). For in vivo investigations, BALB/c mice were intratracheally administered with LPS for 24 hours after injection of MLEE (0.3, 3, and 30 mg/kg). Hematoxylin and eosin staining was used for histopathology analysis of lung tissue. The phytochemical constituents of MLEE were analyzed using high-performance liquid chromatography. Results: In RAW 264.7 cells, MLEE reduced the activation of the inflammatory mediators (inducible nitric oxide synthase and cyclooxygenase-2) and the nuclear translocation of nuclear factor (NF)-κB and nuclear factor erythroid-2-related factor 2 (Nrf2). The intraperitoneal injection of MLEE (30 mg/kg) attenuated interstitial edema and immune cell infiltration in LPS-induced acute lung inflammation. MLEE also inhibited the activation of cyclooxygenase-2, NF-κB, and Nrf2 in the lung tissue. Conclusion: Taken together, MLEE exerted an anti-inflammatory effect by inhibiting inflammatory and oxidative mediators on acute lung inflammation suggesting that it might be used as a natural drug for treating acute lung inflammatory diseases.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Lung diseases</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Macrophages</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Oxidative stress</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Therapeutics</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Herbal medicine</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>