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高燕翔,张勇,刘裕,张乾勇,糜漫天.SREBP-1c在白藜芦醇预防大鼠非酒精性脂肪肝发生中的作用[J].陆军军医大学学报(原第三军医大学学报),2015,37(17):1704-1708.
Gao Yanxiang,Zhang Yong,Liu Yu,Zhang Qianyong,Mi Mantian.SREBP-1c is involved in preventive effect of resveratrol on pathogenesis of nonalcoholic fatty liver disease in rats[J].J Amry Med Univ (J Third Mil Med Univ),2015,37(17):1704-1708.
高燕翔,张勇,刘裕,张乾勇,糜漫天.SREBP-1c在白藜芦醇预防大鼠非酒精性脂肪肝发生中的作用[J].陆军军医大学学报(原第三军医大学学报),2015,37(17):1704-1708. DOI:
Gao Yanxiang,Zhang Yong,Liu Yu,Zhang Qianyong,Mi Mantian.SREBP-1c is involved in preventive effect of resveratrol on pathogenesis of nonalcoholic fatty liver disease in rats[J].J Amry Med Univ (J Third Mil Med Univ),2015,37(17):1704-1708. DOI:
目的 探讨固醇调节元件结合蛋白-1c(SREBP-1c)在白藜芦醇(resveratrol,RSV)预防大鼠通过高脂膳食形成非酒精性脂肪肝(nonalcoholic fatty liver disease,NAFLD)过程中的作用。 方法 40只8周龄雄性SD大鼠按随机数字表法分为4组:对照组(基础饲料,Con组)、高脂膳食组(基础饲料+猪油,HF组),高脂膳食+50 mg/kg RSV组(每天50 mg/kg RSV,HFR50组)和高脂膳食+100 mg/kg RSV组(每天100 mg/kg RSV,HFR100组)。干预8周,每周称量动物体质量和食物消耗量,干预后检测血清和肝脏中脂质含量,肝脏组织HE染色观察脂肪变性情况,Western blot检测pAMPK、SIRT1、SREBP-1c、FAS的蛋白表达以及实时定量PCR分析SREBP-1c和FAS mRNA表达,染色质免疫共沉淀法分析FAS启动子序列SRE与SREBP-1c的结合程度。 结果 白藜芦醇在不影响日常能量摄入的情况下能减少高脂喂养大鼠的体质量(P0.05);白藜芦醇显著降低高脂喂养大鼠血清和肝脏中TG含量(P0.05);高脂喂养诱导大鼠肝脂肪变性,导致大鼠的肝内SIRT1和pAMPK蛋白表达降低(P0.05)、SREBP-1c和FAS mRNA及蛋白表达升高(P0.05)、FAS启动子SRE与SREBP-1c的结合程度增加(P0.05),而白藜芦醇的干预能显著抑制上述效应(P0.05)。 结论 白藜芦醇通过上调高脂喂养大鼠肝内pAMPK与SIRT1蛋白表达和下调SREBP-1c表达与转录活性,预防NAFLD的发生。
Objective To investigate the role of sterol regulatory element binding protein-1c (SREBP-1c) in preventive effect of resveratrol (RSV) on the occurrence of nonalcoholic fatty liver disease (NAFLD) in rats treated with high-fat diet. Methods Forty eight-week-old male SD rats were randomly divided into 4 groups: control group treated with normal diet
high-fat diet group treated with normal diet and lard
high-fat diet+50 mg/kg RSV group
and high-fat diet+100 mg/kg RSV group. During 8-week intervention
the body mass and food consumption were weighed weekly for each rat. After the intervention
the concentrations of total cholesterol (TC) and triglyceride (TG) in the serum and liver were measured. The hepatic steatosis was observed by histological staining with hematoxylin and eosin. The protein levels of pAMPK
SIRT1
SREBP-1c and FAS were determined by Western blotting
and the mRNA levels of SREBP-1c and FAS were measured by quantitative real-time PCR. Meanwhile
the binding degree of FAS promoter sequence SRE and SREBP-1c was analyzed by chromatin immunoprecipitation (ChIP) assay. Results RSV reduced the body mass of the high-fat fed rats(P0.05)
but their daily energy intake had no obvious change. RSV significantly lowered TG levels in the serum and liver of the high-fat fed rats(P0.05). High-fat diet induced hepatic steatosis
and resulted in low protein expression of pAMPK and SIRT1 in the liver of the rats (P0.05)
high mRNA and protein expression of SREBP-1c and FAS (P0.05)
and high binding degree of SRE and SREBP-1c(P0.05)
while RSV significantly inhibited these effects (P0.05). Conclusion RSV can prevent the occurrence of NAFLD in the high-fat fed rats through up-regulating pAMPK and SIRT1 and down-regulating SREBP-1c and transcriptional activity.
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