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    <identifier>10.57760/sciencedb.03275</identifier>
    <datestamp>2022-11-24T17:07:19Z</datestamp>
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  <dc:date>2022-11-24</dc:date>
  <dc:title>GLP-1RAs regulate lipid metabolism and induce autophagy through AMPK/SIRT1 pathway to improve NAFLD</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.03275</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Human hepatoma HepG2 cells and HL-7702 cells were obtained from the Procell Life Science &amp;amp;Technology Co. Ltd (Wuhan, China) and were grown in Dulbecco&amp;rsquo;s modified Eagle&amp;rsquo;s medium (DMEM) supplemented with 10% fetal bovine serum (FBS) in a 37&amp;deg;C incubator with 5% CO2. To induce hepatic steatosis, cells were treated with 1&amp;thinsp;mM palmitic acid and oleic acid mixture (FFA, Sigma-Aldrich, USA) for 24 hours, For the LRG experiments, cells were incubated for an additional 24 hours in varying LRG concentrations (25, 50, 100 nM) while equal amounts of fatty acid-free bovine serum albumin (BSA) were added to the control cells. To evaluate autophagy, cells were treated with LRG (100 nM) plus chloroquine (CQ, 20 &amp;micro;M, Sigma-Aldrich, USA) or rapamycin (RAPA, 1 &amp;micro;M, Sigma-Aldrich, USA) In addition, steatotic HepG2 cells were exposed to compound C (CC,10 &amp;micro;M, Selleck Chemicals, USA) in the presence of LRG (100 nM) for 24 hours.</dc:description>
  <dc:subject>NAFLD; GLP-1RAs; autophagy</dc:subject>
  <dc:creator>Qiang Zhang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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