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        <identifier>oai:figshare.com:article/33771769</identifier>
        <datestamp>2026-09-15T05:35:16Z</datestamp>
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          <dc:title>Table 1_Sleep fragmentation frequency is associated with distinct immune, microbial, and barrier-related profiles in DSS-induced colitis in mice.docx</dc:title>
          <dc:creator>Ming-Shih Tu (24912574)</dc:creator>
          <dc:creator>Ting-An Fan (24912577)</dc:creator>
          <dc:creator>Yueh-Hsiang Huang (5419274)</dc:creator>
          <dc:creator>Ren-Chin Wu (167828)</dc:creator>
          <dc:creator>Chia-Jung Kuo (1525771)</dc:creator>
          <dc:creator>Ning-Hung Chen (291356)</dc:creator>
          <dc:creator>Li-Pang Chuang (447777)</dc:creator>
          <dc:creator>Shih-Wei Lin (447775)</dc:creator>
          <dc:creator>Yen-Lung Chen (447776)</dc:creator>
          <dc:creator>Huang-Yu Yang (166482)</dc:creator>
          <dc:creator>Geng-Hao Liu (5419289)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>epithelial barrier</dc:subject>
          <dc:subject>gut microbiota</dc:subject>
          <dc:subject>microbiota-derived metabolites</dc:subject>
          <dc:subject>short-chain fatty acids</dc:subject>
          <dc:subject>sleep fragmentation</dc:subject>
          <dc:subject>ulcerative colitis</dc:subject>
          <dc:description>Background&lt;p&gt;Sleep fragmentation is common in inflammatory bowel disease, but whether different fragmentation frequencies are associated with distinct biological responses during colitis remains unclear. This study examined endpoint-specific responses to low- and high-frequency sleep fragmentation in DSS-induced colitis in mice.&lt;/p&gt;Methods&lt;p&gt;Male C57BL/6 mice were assigned to Control, DSS, DSS with low-frequency sleep fragmentation (DSS+LSF), DSS with high-frequency sleep fragmentation (DSS+HSF), or high-frequency sleep fragmentation alone (HSF). Colitis was induced with 2% DSS for 7 days. Sleep fragmentation was applied for 12 h/day during the light phase at 60 sweeps/h for LSF or 240 sweeps/h for HSF. Clinical indices, histology, epithelial barrier-associated proteins, inflammatory and stress-related markers, colonic CD4&lt;sup&gt;+&lt;/sup&gt; T-cell subsets, fecal microbiota composition, and fecal SCFAs were assessed.&lt;/p&gt;Results&lt;p&gt;Clinical and macroscopic indices varied across experimental groups, but corrected comparisons among DSS-treated groups were not significant. Plasma corticosterone was increased in both DSS+LSF and DSS+HSF, whereas MPO was higher in DSS+LSF than in DSS+HSF. Colonic Th2 proportions were higher in DSS+HSF than in DSS and DSS+LSF. Other histological, barrier-associated, inflammatory, and metabolic findings were primarily descriptive.&lt;/p&gt;Conclusions&lt;p&gt;Low- and high-frequency sleep fragmentation were associated with distinct, endpoint-specific response profiles during DSS-induced colitis rather than a simple linear increase in disease severity. These findings support frequency-associated, domain-specific responses and warrant further longitudinal and mechanistic investigation.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T05:35:16Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fimmu.2026.1885856.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Sleep_fragmentation_frequency_is_associated_with_distinct_immune_microbial_and_barrier-related_profiles_in_DSS-induced_colitis_in_mice_docx/33771769</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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