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    <identifier>10.57760/sciencedb.17423</identifier>
    <datestamp>2024-11-28T10:16:47Z</datestamp>
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  <dc:date>2024-11-28</dc:date>
  <dc:title>Figure CSE</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.17423</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Fig. 1. Oral administration of Craibiodendron stellatum (Pierre) WW Sm. extract (CSE) alleviated lipopolysaccharide (LPS)-induced lung hyperplasia, macrophage infiltration, and fibrosis in lung tissues and total cells, and inflammatory cytokine production in the bronchoalveolar lavage fluid (BALF) of C57BL/6 mice.Fig. 2. CSE inhibited LPS-induced inflammatory cytokine, iNOS, and COX-2 expression in mice with acute lung injury.Fig. 3. CSE suppressed the LPS-induced NO and inflammatory cytokine production and iNOS and COX-2 expression in RAW 264.7 cells. (A) Nitrite production in RAW 264.7 cells were measured via the Griess assay.&amp;nbsp;Fig. 4. Effect of CSE on LPS-induced NF-&amp;kappa;B and MAPK signaling pathways in RAW 264.7 cells.Fig. 5. CSE reduced LPS-induced ROS production and regulated antioxidation via the Nrf2/Keap1 signaling pathway.Graphical abstract that explain the anstract.</dc:description>
  <dc:subject>Acute lung injury; Craibiodendron stellatum; Lipopolysaccharide; Antiinflammation capacity; Antioxidant capacity; Alveolar macrophage</dc:subject>
  <dc:creator>Gu Da Hye</dc:creator>
  <dc:creator>Kim Min Jeong</dc:creator>
  <dc:creator>Fauziah Ardina Nur</dc:creator>
  <dc:creator>Jung Sung Keun</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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