异甘草酸镁对纤维化大鼠肝脏TGF-β 1及Smad蛋白表达的影响  被引量:11

Effects of magnesium isoglycyrrhizinate on hepatic TGF-β 1 and Smad protein expression in rats with experimental hepatic fibrosis

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作  者:彭忠田[1,2] 李佳[1] 王培[1] 李红梅[2] 刘书香[2] 

机构地区:[1]南华大学附属第一医院感染科,湖南衡阳421001 [2]南华大学附属第一医院肝病研究中心,湖南衡阳421001

出  处:《现代生物医学进展》2011年第2期240-242,共3页Progress in Modern Biomedicine

摘  要:目的:观察异甘草酸镁对四氯化碳诱导的肝纤维化大鼠肝脏组织TGF-β1及Smad蛋白表达的影响,以期揭示其抗纤维化的机制。方法:利用腹腔注射四氯化碳(CCl4)建立大鼠肝纤维化模型,然后应用不同剂量的异甘草酸镁和INF-γ处理,于实验第16周末检测大鼠血清透明质酸(HA)、层粘连蛋白(LN)、III型前胶原(PC-III)、IV型胶原(C-IV)的水平,采用RT-PCR法检测TGF-β1,Smad3,Smad7mRNA的表达。结果:与模型组比较,异甘草酸镁各剂量组血清HA,LN,PC-III,C-IV水平显著下降(P<0.05),肝脏TGF-β1、smad3的表达明显降低(P<0.05),smad7则有所上升。结论:异甘草酸镁可以改善肝纤维化大鼠肝组织纤维化程度,其作用机理与抑制TGF-β1、Smad3mRNA的表达,上调Smad7mRNA的表达有密切关系。Objective:To discuss the probable effects of Magnesium Isoglycyrrhizinate on rats of experimental hepatic fibrosis and its potential molecular mechanisms.Methods:Healthy male SD rats were randomly divided into different groups:normal control,model of hepatic fibrosis,INF-γ-treated and Magnesium Isoglycyrrhizinate-treated groups.Hepatic fibrosis in healthy male SD rats was induced by intraperitoneal injection of Tetrachloride.The serum concentration of Hyaluronic acid(HA),Laminin(LN),Procolagen Type III(PCIII) and Collagen Type IV(C-IV) were assayed with Radioimmunoassay.The mRNA levels of TGFβ1,Smad 3,and Smad 7 in rat's liver tissue were detected with RT-PCR.Results:Compared with model group,the level of serum HA,LN,PC-III,C-IV in Magnesium Isoglycyrrhizinate groups were significantly decreased(P〈0.05),the pathological fibrosis scores were also decreased obviously(P〈0.05),and the expression of TGF-β1,Smad3 mRNA in rat's liver tissue were decreased significantly(P〈0.05),but Smad7 mRNA was increased.Conclusion:The mechanisms of Magnesium Isoglycyrrhizinate on protecting against tetrachloride——induced liver fibrosis in SD rats may be reduced the expression of TGF-β1,Smad3 mRNA,and increase the expression of Smad7 mRNA at the same time.

关 键 词:肝纤维化 异甘草酸镁 大鼠 RT-PCR 

分 类 号:Q953[生物学—动物学] R575.2[医药卫生—消化系统]

 

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