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              <text>&lt;a href="http://doi.org/10.1007/s00011-016-1005-3" target="_blank" rel="noreferrer noopener"&gt;http://doi.org/10.1007/s00011-016-1005-3&lt;/a&gt;</text>
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              <text>187–196</text>
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              <text>2</text>
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              <text>66</text>
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                <text>Demethyleneberberine alleviates inflammatory bowel disease in mice through regulating NF-kappaB signaling and T-helper cell homeostasis.</text>
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                <text>Inflammation research : official journal of the European Histamine Research Society ... [et al.]</text>
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                <text>2017</text>
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                <text>2017-02</text>
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                <text>Animals; Anti-Inflammatory Agents/*pharmacology/therapeutic use; Berberine/*analogs &amp; derivatives/pharmacology/therapeutic use; Colitis; Colon/drug effects/immunology/pathology; Cytokines/immunology; Dextran Sulfate; DMB; Female; Helper-Inducer/*drug effects/immunology; Homeostasis/drug effects; Immunoglobulin G/blood; Inbred C57BL; Inflammatory Bowel Diseases/blood/chemically induced/drug therapy/*immunology; Mice; NF-kappa B/*antagonists &amp; inhibitors/immunology; NF-kappaB; RAW 264.7 Cells; Reactive Oxygen Species/metabolism; Signal Transduction/drug effects; Spleen/cytology; T-Lymphocytes; Th cell</text>
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                <text>Chen Yingying; Li Rui-Yan; Shi Mei-Jing; Zhao Ya-Xing; Yan Yan; Xu Xin-Xin; Zhang Miao; Zhao Xiao-Tong; Zhang Yu-Bin</text>
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                <text>OBJECTIVE: The activation of NF-kappaB signaling and unbalance of T-helper (Th) cells have been reported to play a key role in the pathogenesis of colitis. Cortex Phellodendri Chinensis (CPC) is commonly used to treat inflammation and diarrhea. Demethyleneberberine (DMB), a component of CPC, was reported to treat alcoholic liver disease as a novel natural mitochondria-targeted antioxidant in our previous study. In this study, we investigated whether DMB could protect against dextran sulfate sodium (DSS)-induced inflammatory colitis in mice by regulation of NF-kappaB pathway and Th cells homeostatis. METHODS: Inflammatory colitis mice were induced by 3% DSS, and DMB were orally administered on the doses of 150 and 300 mg/kg. In vitro, DMB (10, 20, 40 muM) and N-acetyl cysteine (NAC, 5 mM) were co-cultured with RAW264.7 for 2 h prior to lipopolysaccharide (LPS) stimulation, and splenocytes from the mice were cultured ex vivo for 48 h for immune response test. RESULTS: In vivo, DMB significantly alleviated the weight loss and diminished myeloperoxidase (MPO) activity, while significantly reduced the production of pro-inflammatory cytokines, such as interleukin (IL)-6 and tumor necrosis factor-alpha (TNF-alpha), and inhibited the activation of</text>
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                <text>&lt;a href="http://doi.org/10.1007/s00011-016-1005-3" target="_blank" rel="noreferrer noopener"&gt;10.1007/s00011-016-1005-3&lt;/a&gt;</text>
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                <text>Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).</text>
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        <name>Chen Yingying</name>
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        <name>Li Rui-Yan</name>
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        <name>Shi Mei-Jing</name>
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        <name>Yan Yan</name>
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        <name>Zhang Miao</name>
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        <name>Zhang Yu-Bin</name>
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        <name>Zhao Xiao-Tong</name>
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        <name>Zhao Ya-Xing</name>
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