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作 者:王毅飞[1] 伊娜 吴琳英[1] 黄晓淳[1] 梁思虹
机构地区:[1]广州医科大学附属第一医院内分泌科,510120 [2]广州市中医院内分泌科,510130
出 处:《实用医学杂志》2016年第15期2434-2437,共4页The Journal of Practical Medicine
基 金:广东省科技计划项目(编号:2013B021800195);广州医科大学附属第一医院立项课题(编号:201210-gyfyy)
摘 要:目的:探讨米非司酮(RU486)对前脂肪细胞分化及核因子κB(NF-κB)激活的作用。方法:形态观察3T3-L1细胞分化过程,不同RU486浓度的药物(0.1~10 mmol/L)处理细胞48 h,于分化的第9天油红O染色测定甘油三酯相对含量,实时荧光定量PCR法检测PPARγ2、C/EBPa、脂蛋白脂酶(LPL)和脂肪酸合成酶(FAS)的m RNA表达。免疫印迹检测IкBα蛋白水平,免疫荧光观察NF-κB蛋白核移位。结果:甘油三酯相对含量随药物浓度的增加而降低,与对照组比,从0.5μmol/L RU486处理开始甘油三酯相对含量显著性降低(P〈0.05或P〈0.01)。与对照组比,5μmol/L RU486组的PPARγ2、C/EBPa、LPL和FAS m RNA表达均显著性降低(P〈0.01),IκBα蛋白含量降低(P〈0.01),NF-κB由细胞浆到细胞核的核移位。结论:RU486可下调IκBα蛋白水平,激活NF-κB核移位,下调PPARγ2、C/EBPa、LPL和FAS的m RNA表达,抑制前脂肪细胞分化。Objective To investigate the roles of RU486 inhibiting 3T3-L1 pre-adipocytes differentiation and regulating NF-κB activation. Methods Cells were treated with RU486 with concentrations of 0.1 ~ 10μmol / L for 48 h, then the relative contents of triglyceride were analyzed by Oil-Red O staining assay on 9thday during adipogenesis. The m RNA expressions of PPARγ2,C / EBPa, LPL and FAS were further measured by Realtime PCR. IκBα protein level was detected by Western bolt and nuclear translocation of NF-κB was observed by immunofluorescence assay. Results The relative contents of triglyceride decreased with the increasing of RU486 concentration. Compared with the control, the relative contents of triglyceride in RU486-treatment groups from0.5 μmol / L were significantly decreased(P〈0.05 or P〈0.01). Compared with the control, PPARγ2, C /EBPa, LPL and FAS m RNA expression and IκBα protein level were significantly decreased(P〈0.01) and NF-κB nuclear translocated from cytoplasm to nucleus in Group 5 mmol / L RU486. Conclusions RU486 could down regulate IκBα protein level, activate NF-κB nuclear translocation, then down regulate PPARγ2, C / EBPa,LPL and FAS m RNA expression and inhibit adipocytes differentiation.
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