﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Society of Diabetic Nephropathy Prevention</PublisherName>
      <JournalTitle>Journal of Nephropathology</JournalTitle>
      <Issn>2251-8363</Issn>
      <Volume>13</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2024</Year>
        <Month>08</Month>
        <DAY>10</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Anti-oxidative and anti-inflammatory activity of Achatina fulica mucus in streptozocin-nicotinamide-induced diabetic kidney disease: an animal model study</ArticleTitle>
    <FirstPage>e21465</FirstPage>
    <LastPage>e21465</LastPage>
    <ELocationID EIdType="doi">10.34172/jnp.2023.21465</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Wachid</FirstName>
        <LastName>Putranto</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-3145-4948</Identifier>
      </Author>
      <Author>
        <FirstName>Gigih</FirstName>
        <LastName>Fitriawan</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-9575-9217</Identifier>
      </Author>
      <Author>
        <FirstName>Ratih Tri Kusuma</FirstName>
        <LastName>Dewi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-2408-8783</Identifier>
      </Author>
      <Author>
        <FirstName>Aryo</FirstName>
        <LastName>Suseno</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-9962-5104</Identifier>
      </Author>
      <Author>
        <FirstName>Arief</FirstName>
        <LastName>Nurudhin</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4662-0638</Identifier>
      </Author>
      <Author>
        <FirstName>Yulyani</FirstName>
        <LastName>Werdiningsih</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-4116-5851</Identifier>
      </Author>
      <Author>
        <FirstName>Santy Ayu Puspita</FirstName>
        <LastName>Perdhana</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-5231-2346</Identifier>
      </Author>
      <Author>
        <FirstName>Nurhasan Agung</FirstName>
        <LastName>Prabowo</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-2016-5649</Identifier>
      </Author>
      <Author>
        <FirstName>Yeremia Suryo</FirstName>
        <LastName>Pratama</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-0093-0729</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jnp.2023.21465</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2023</Year>
        <Month>04</Month>
        <Day>16</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2023</Year>
        <Month>07</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Diabetic kidney disease (DKD) progression resulted in increased intrarenal oxidative stress and increased inflammatory resulting in further renal fibrosis. Achatina fulica mucus was regarded to exerts anti-oxidative and anti-inflammatory effect. Objectives: This study aims to observe the effect of administration of A. fulica mucus on oxidative stress and inflammation biomarkers in DKD-induced rats. Methods and Materials: In this study, we used 32 males white Wistar rats divided into four groups; a control, and other three different groups induced with 45 mg/kg streptozocin (STZ) and 110 mg/kg nicotinamide (NA) intra-peritoneally. Achatina fulica mucus was administered orally in the last groups; 3.5 mL/d (S1), and 7 mL/d (S2). Post-test measurement of inflammatory and oxidative biomarker was used to determine the outcome. Results: The study resulted in reduction of malondialdehyde (MDA), transforming growth factor-β (TGF-β), tumor necrosis factor-α (TNF-α), high sensitivity C-reactive protein (hs-CRP), vascular endothelial growth factor (VEGF), and interleukin-1β (IL-1β) in A. fulica mucus administration in our STZ-NA induced rats, with higher dose of the mucus further reduce the inflammatory and oxidative stress biomarkers. Conclusion: Current study showed the potential of A. fulica mucus usage in future management of inflammation and oxidative stress in diabetes and DKD.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Diabetes</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Diabetic nephropathy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Inflammation</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Oxidative stress</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>