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作 者:洪辉华[1] 赵玮[1] 朱渊红[1] 蔡宛如[2]
机构地区:[1]浙江中医药大学附属第一医院,杭州310006 [2]浙江中医药大学附属第二医院,杭州310005
出 处:《中华中医药杂志》2016年第4期1394-1397,共4页China Journal of Traditional Chinese Medicine and Pharmacy
基 金:国家自然科学基金项目(No.81273678);浙江省自然科学基金项目(No.LQ12H29003)~~
摘 要:目的:观察芪冬活血饮药物血清对脂多糖致炎RAW264.7巨噬细胞TLR4/NF-κB炎性信号通路的影响,探讨其调控炎性反应的机制。方法:将巨噬细胞分为空白对照组、LPS组、空白血清组、空白血清加LPS组、药物血清组、药物血清加LPS组6组。细胞培养24h后,加入血清培养0.5h,然后加入LPS培养12h,测定细胞上清液细胞因子及TLR4、NF-κBp65蛋白及m NRA表达。结果:LPS刺激后TNF-α、IL-1β、IL-10水平升高,芪冬活血饮药物血清可降低TNF-α、IL-1β水平,升高IL-10水平,与空白血清加LPS组比较差异均有统计学意义(P<0.01)。LPS刺激后各组NF-κBp65、TLR4蛋白及m RNA表达增加,芪冬活血饮药物血清可减少NF-κBp65、TLR4蛋白及m RNA表达(P<0.05)。结论:芪冬活血饮药物血清可减轻LPS诱导的巨噬细胞炎性反应,其机制与抑制TLR4/NF-κBp65炎性信号通路及下游炎性因子有关。Objective: To observe the effect of Qidong Huoxue Decoction(QD)-serum on TLR4/NF-kappa B inflammation signaling pathway in RAW264.7 cells, and explore its mechanism. Methods: RAW264.7 cells were divided into six groups: control group, LPS group, blank serum group, blank serum plus LPS group, drug serum group, drug serum plus LPS group. After culturing for 24 h, cells were added the QD-serum for 0.5h, then adding LPS for 12 h. The cytokines and the protein and m RNA expression of TLR4 and NF-κBp65 in cell supernatant were detected. Results: The levels of TNF-α, IL-1β, IL-10 were increased in the LPS stimulated groups. The QD-serum group reduced the levels of IL-1β and TNF-α, and increased the level of IL-10. There were statistical differences among the QD-serum group and blank serum plus PLS group(P〈0.01). The protein and m RNA expression of NF-κBp65 and TLR4 in LPS stimulated groups increased, while QD-serum reduced the expression. Conclusion: QD-serum could relieve the inflammatory responses of macrophages stimulated by LPS, which might be related to the inhibition of TLR4/NF-κBp65 signaling pathway and downstream inflammatory factors.
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