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Emodin suppresses LPS-induced proinflammatory responses and nuclear factor-B activation by disruption of lipid rafts and TLR-4 recruitment in endothelial cells
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作者 guoquan meng Yiyao LIU +1 位作者 Youguang Luo Hong Yang 《医用生物力学》 EI CAS CSCD 2009年第S1期122-122,共1页
Emodin[1,3,8-Trihydroxy-6-methylanthraquinone]has been reported to exhibit vascular anti-inflammatory properties.However,the relevant anti-inflammatory mechanisms are not well understood.The present study was design t... Emodin[1,3,8-Trihydroxy-6-methylanthraquinone]has been reported to exhibit vascular anti-inflammatory properties.However,the relevant anti-inflammatory mechanisms are not well understood.The present study was design to explore the molecular target(s)of emodin in modifying lipopolysaccharide(LPS)-associated signal transduction pathway in human umbilical vein endothelial cells(HUVECs).Cultured HUVECs were pre-incubated with 1 to 50μg/ml emodin for 30 min,LPS-induced proinflammatory cytokines(IL-1,IL-6)and chemokines(IL-8,MCP-1)expression were inhibited dose-dependently,which agreed well with the NF-B activation and IB degradation detected by immunocytochemistry and western blotting,respectively. 展开更多
关键词 TLR Emodin suppresses LPS-induced proinflammatory responses and nuclear factor-B activation by disruption of lipid rafts and TLR-4 recruitment in endothelial cells HUVECs
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