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机构地区:[1]山西省人民医院,030012
出 处:《山西医药杂志》2006年第9期777-779,共3页Shanxi Medical Journal
摘 要:目的观察参附注射液对内毒素介导的人脐静脉细胞Toll样受体4/NF-κB途径及细胞间黏附分子、E-选择素表达的影响。方法健康产妇分娩后的新鲜婴儿脐带,应用胶原酶消化,收集内皮细胞进行培养。实验分为对照组、内毒素组、内毒素+参附组。对照组:M199培养基中不加任何物质。内毒素组:M199培养基中加入脂多糖1 mg/L。内毒素+参附组:预先加入参附注射液10 mL/L,30 min后加入脂多糖1 mg/L。干预1h收集细胞,提取核蛋白测定NF-κB活性,干预12 h后收集细胞检测Toll样受体4、细胞间黏附分子1、E-选择素表达水平。结果内毒素组的Toll样受体4、细胞间黏附分子1、E-选择素表达水平、NF-κB活性均显著高于对照组,内毒素+参附组的Toll样受体4、细胞间黏附分子1、E-选择素表达水平、NF-κB活性均明显低于内毒素组。结论参附注射液可以通过抑制NF-κB活化,减弱Toll样受体4/NF-κB途径,抑制了脂多糖介导的黏附分子表达,从而减轻机体的炎症反应。Objective To investigate the effects of Shenfu injection on lipopolyccharide (LPS)-induced "Toll like receptor-nuclear factor kappa B (TLR4/NF-κB) signal and intercellular adhesion molecule-1 ( ICAM-1 ), E-selection in human umbilical vein endothelial cells(HUVECs). Methods HUVECs obtained from collagenase-digested umbilical veins were cultured and divided into 3 group: ①control group: cuhured in M199 medium without any intervention. ② LPS group: cultured in M199 medium with LPS( 1 mg/L.). ③LPS+ Shenfu group: pretreated with Shenfu injection for 30min before LPS incubation. HUVECs were stimulated for 1 h, and NF-κB P65 activation were examined. HUVECs were stimulated for 12 h and then collected, TLR4, ICAM-1, and E-selection were examined. Results NF-κB P65 activity, TI.R4, ICAM- 1, E-selection mRNA and protein expression were higher in I.PS group than in control group. NF-κB P65 activity,TLR4, ICAM-1 and E-selection mRNA and protein expression were lower in LPS+ Shenfu group than in LPS group. Conclusion Shenfu injection play a role in inhibiting adhesion molecule up-regulation and inflammatory reaction by inhibiting NF-κB activation, and subsequently suppression TLR4ANF-κB signal.
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