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消脂汤对FFA诱导NASH细胞模型的影响及其相关机制.

作  者: ;

机构地区: 广州中医药大学

出  处: 《中国实验方剂学杂志》 2017年第23期109-115,共7页

摘  要: 目的:探讨消脂汤对游离脂肪酸(FFA)诱导的非酒精性脂肪性肝炎(NASH)细胞模型的作用及机制。方法:用0.5μmol·L-1FFA诱导Hep G2细胞建立NASH细胞模型,用消脂汤及非诺贝特干预NASH细胞模型;油红O染色观察细胞内脂滴含量;酶联免疫吸附试验(ELISA)检测细胞上清液中肿瘤坏死因子-α(TNF-α),白细胞介素-6(IL-6)含量;蛋白免疫印迹法(Western blot)检测核转录因子-κB(NF-κB)p65,IκB激酶(IKKβ),IκB磷酸化激酶[Phospho-IKKα/β(Ser176/180)],胰岛素受体底物1磷酸化蛋白[Phospho-IRS-1(Ser^307)],胰岛素受体底物-1(IRS-1)蛋白表达。结果:FFA刺激24 h后,模型组内脂滴含量,细胞上清液中TNF-α,IL-6含量高于正常组(P〈0.01),IKKβ,p-IKKα/β(Ser176/180),p-IRS-1(Ser^307),NF-κB(核蛋白)表达明显增加(P〈0.01),IRS-1蛋白表达减少(P〈0.05),各给药组p-IKKα/β(Ser176/180),p-IRS-1(Ser^307),NF-κB p65(核蛋白)表达减少(P〈0.01),尤其是消脂汤高浓度组较非诺贝特p-IKKα/β(Ser176/180),p-IRS-1(Ser^307)蛋白表达显著减少(P〈0.01),各给药组IRS-1蛋白表达明显增加(P〈0.05)。结论:消脂汤可改善FFA诱导的NASH细胞模型中脂质沉积及炎症反应,其机制可能与抑制细胞内IKKα/β,IRS-1 Ser^307的磷酸化及IKKβ,NF-κB p65(核蛋白)表达有关。 Objective: To investigate the effect and mechanism of Xiaozhi decoction on free fatty acids (FFA) -induced non-alcoholic steatohepatitis (NASH) cell model. Method: The NASH model in HepG2 cells was induced by 0.5 μmol·L^-1 FFA. The NASH cell models were established by different concentrations of Xiaozhi decoction and fenofibrate. Oil red O staining was used to observe the content of lipid droplets. Cell supernatant (nuclear faetor-κ-gene binding) NF-κB p65, IkappaB kinase beta (IKKβ), Phospho-IκB kinase alpha/beta [ Phospho-IKKα/β ( Ser176/180)], Phospho-insulin receptor substrate [ Phospho-IRS-1 ( Ser307) ] and insulin receptor substrate-1 (IRS-1) protein were detected by Western blot. Result: The contents of tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) in the supernatant fluid of the model group were significantly higher than those in control group (P 〈 0.01 ). Meanwhile, the expression of IRS-1 was reduced (P 〈 0.05 ), while the levels of IKKβ, p-IKKα/β (Ser176/180) and IRS-1 (Ser307) phosphorylation and nuclear translocation of NF-κB p65 protein were increased in the model group (P 〈 0.01 ). The expressions of IKKα/β ( Ser176/180) and IRS-1 ( Ser307 ) phosphorylation and nuclear translocation of NF-κB p65 protein in each dose group were decreased (P 〈 0.01 ) , especially in high-dose Xiaozhi decoction. The protein expression of IRS-1 was significantly increased (P 〈 0.05) in control group. Conclusion: Xiaozhi decoction can improve lipid deposition and inflammatory reaction in NASH cell model induced by FFA. The mechanism may be related to the inhibition of intracellular IKKα/β (Ser176/180) and IRS-1 (Ser307) phosphorylation and IKKβ, NF-κB nuclear protein expression.

关 键 词: 非酒精性脂肪性肝炎 HEP G2细胞模型 消脂汤 游离脂肪酸 核转录因子-κB IκB抑制蛋白激酶α/β 胰岛素受体底物-1

分 类 号: [R285.5]

领  域: []

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