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    <identifier>10.57760/sciencedb.j00217.04222</identifier>
    <datestamp>2024-11-05T09:22:28Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2024-11-05</dc:date>
  <dc:title>Exploring the mechanism of Jiawei Simiao Powder on monosodium urate crystal-induced RAW264.7 cell inflammation via miR-146a regulation of the TLR4/NF-&amp;kappa;B signaling pathway</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00217.04222</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective: To investigate the mechanism by which Jiawei Simiao San regulates the Toll like receptor 4 (TLR4)/nuclear transcription factor - &amp;kappa; B (NF - &amp;kappa; B) signaling pathway through microRNA-146a (miR-146a) and alleviates the inflammatory response induced by MSU crystals in RAW264.7 cells. Method: RAW264.7 cells were induced with MSU crystals to establish a gouty arthritis model, which was divided into a control group, a model group, a modified Simiao powder group, and a colchicine group. The CCK-8 method was used to detect the activity of each group of cells, ELISA was used to detect the levels of interleukin-1 (IL), IL-6, and tumor necrosis factor (TNF) - &amp;alpha;, RT-PCR was used to detect the mRNA expression of miR-146a and TLR4, myeloid differentiation factor 88 (MyD88), TNF receptor associated factor 6 (TRAF6), and NF - &amp;kappa; B p65, and Western blot was used to detect the protein expression of TLR4, MyD88, TRAF6, and p-NF - &amp;kappa; B p65. The correlation between miR-146a and TLR4, MyD88, TRAF6, NF - &amp;kappa; B p65, and p-NF - &amp;kappa; B p65 was analyzed. As a result, compared with the control group, the expression of miR-16a in the model group cells was significantly reduced (P&amp;lt;0.05), while the mRNA and protein expression of TLR4, MyD88, TRAF6, p-NF - &amp;kappa; B p65 protein expression, and the expression levels of IL-1, IL-6, and TNF - &amp;alpha; were significantly increased (P&amp;lt;0.05); Compared with the model group, the expression of miR-16a in the Jiawei Simiao San group and the colchicine group was significantly increased (P&amp;lt;0.05), while the mRNA and protein expression of TLR4, MyD88, TRAF6, and p-NF - &amp;kappa; B were significantly decreased (P&amp;lt;0.05), and the contents of IL-1, IL-6, and TNF - &amp;alpha; were significantly decreased (P&amp;lt;0.05). The correlation analysis results indicate that miR-146a is negatively correlated with TLR4, MyD88, TRAF6 mRNA and protein expression, as well as p-NF - &amp;kappa; B p65 protein expression (P&amp;lt;0.05). Conclusion: Jiawei Simiao San can alleviate MSU induced gout inflammation by upregulating miR-146a, inhibiting the activation of TLR4/NF - &amp;kappa; B signaling pathway, and reducing the expression of inflammatory factors.&amp;nbsp;</dc:description>
  <dc:subject>Jiawei Simiao Powder; gouty arthritis; monosodium urate crystals; miR-146a; TLR4/NF-κB signaling pathway</dc:subject>
  <dc:creator>Huayan.LI</dc:creator>
  <dc:creator>Peipei.SU</dc:creator>
  <dc:creator>Xin.WANG</dc:creator>
  <dc:creator>Yuanyuan.NIU</dc:creator>
  <dc:creator>Zhenheng.CHEN</dc:creator>
  <dc:creator>Qianhui.SUN</dc:creator>
  <dc:creator>Mingrui.DU</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>
</oai_dc:dc>

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