LL202 protects against dextran sulfate sodium-induced experimental colitis in mice by inhibiting MAPK/AP-1 signaling.
第一作者:
Yuan,Gao
第一单位:
State Key Laboratory of Natural Medicines, Jiangsu Key Laboratory of Carcinogenesis and Intervention, Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China.
作者:
主题词
主动转运, 细胞核(Active Transport, Cell Nucleus);动物(Animals);结肠炎(Colitis);细胞因子类(Cytokines);硫酸葡聚糖(Dextran Sulfate);女(雌)性(Female);类黄酮物质(Flavonoids);基因表达调控(Gene Expression Regulation);人类(Humans);炎症(Inflammation);白细胞介素1β(Interleukin-1beta);白细胞介素6(Interleukin-6);脂多糖类(Lipopolysaccharides);MAP激酶信号系统(MAP Kinase Signaling System);小鼠(Mice);小鼠, 近交C57BL(Mice, Inbred C57BL);新生血管化, 病理性(Neovascularization, Pathologic);一氧化氮合酶Ⅱ型(Nitric Oxide Synthase Type II);过氧化物酶(Peroxidase);RNA, 信使(RNA, Messenger);信号传导(Signal Transduction);转录因子AP-1(Transcription Factor AP-1);肿瘤坏死因子α(Tumor Necrosis Factor-alpha)
DOI
10.18632/oncotarget.11742
PMID
27590510
发布时间
2018-11-13
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Oncotarget
63981-63994页
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