文章摘要
何 敏,杨 菁,蒲铃铃,刘 桦,尹小菲.小檗碱通过抑制经典的NLRP3炎症小体活化通路来下调LPS诱导的HUVEC炎症反应*[J].,2019,19(1):38-42
小檗碱通过抑制经典的NLRP3炎症小体活化通路来下调LPS诱导的HUVEC炎症反应*
Berberine Reduces Inflammation induced by Lipopolysaccharide through Suppressing Classical NLRP3 Inflammasome Activiation Pathwayin HUVEC*
投稿时间:2018-03-06  修订日期:2018-03-28
DOI:10.13241/j.cnki.pmb.2019.01.008
中文关键词: 小檗碱  脂多糖  HUVEC  NLRP3炎症小体
英文关键词: Berberine  Lipopolysaccharide  HUVEC  NLRP3 inflammasome
基金项目:四川省大学生创新创业训练计划项目(201413705036)
作者单位E-mail
何 敏 成都医学院生物科学与技术学院 四川 成都 610500 798644028@qq.com 
杨 菁 成都医学院生物科学与技术学院 四川 成都 610501  
蒲铃铃 成都医学院生物科学与技术学院 四川 成都 610502  
刘 桦 成都医学院生物科学与技术学院 四川 成都 610503  
尹小菲 成都医学院生物科学与技术学院 四川 成都 610504  
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中文摘要:
      摘要 目的:探讨小檗碱(Berberine, Ber)对脂多糖(Lipopolysaccharide, LPS)诱导的人脐静脉血管内皮细胞(Human Umbilical Vein Endothelial Cells, HUVEC)炎症反应的抑制作用及相关机制。方法:MTT法检测不同浓度的Ber对HUVEC存活率的影响。以0.05 μg/mL LPS刺激HUVEC建立炎症反应模型,并分别给予1.25、2.5、5μM Ber干预,Elisa检测Ber对炎症因子TNF-α、IL-1β分泌的影响,免疫印迹法检测Ber对NLRP3炎症小体信号通路中NLRP3、MyD88、IL-1β、TLR4、ASC和Caspase-1蛋白表达的影响。结果:不同浓度的Ber对HUVEC增殖均具有抑制作用,且基本呈现浓度梯度,IC50值接近5 μM;与LPS组相比,不同浓度Ber(1.25、2.5、5 μM)均可以显著下调HUVEC中TNF-α、IL-1β炎症因子的分泌(P<0.005及P<0.01),并可以显著抑制细胞中NLRP3、MyD88、IL-1β、TLR4、ASC和Caspase-1蛋白的表达(P<0.05),其抑制作用基本呈剂量关系,以5 μM Ber的抑制效果最佳。结论:Ber可以通过抑制经典的NLRP3炎症小体活化通路来下调LPS诱导的HUVEC炎症反应。
英文摘要:
       ABSTRACT Objective: To investigate the inhibition and related molecular mechanisms of berberine on inflammation induced by LPS in HUVEC. Methods: The viability of different concentrations of berberine on HUVEC cells were determined by MTT. An inflammatory model of HUVEC was induced by 0.05 μg/mL LPS, then 1.25, 2.5, 5 μM berberine were used for intervention. The expressions of TNF-α, IL-1β in cell supernatants were evaluated by ELISA. The expressions of NLRP3, MyD88, IL-1β, TLR4, ASC and Caspase-1 proteins associating with Classical NLRP3 signaling pathway were evaluated by Western blot. Results: The proliferation of HUVEC were restrained by different concentrations of berberine, and there existed a concentration gradient . The IC50 value of berberine on HUVEC was close to 5μM. Compared with LPS group, different concentrations of berberine could significantly reduce the secretions of TNF-α, IL-1β and the expressions of NLRP3, MyD88, IL-1α, TLR4, ASC and Caspase-1 proteins in HUVEC. The inhibition had a dose dependent manner, and 5 μM berberine showed the greatest effect. Conclusion: Berberine could reduce inflammation induced by LPS in HUVEC through suppressing Classical NLRP3 inflammasome activiation pathway.
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