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Evolution of Hepatic Steatosis to Fibrosis and Adenoma Formation in Liver-Specific Growth Hormone Receptor Knockout Mice

机译:肝特异性生长激素受体基因敲除小鼠肝脂肪变性向纤维化和腺瘤形成的演变。

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摘要

>Background: Non-alcoholic fatty liver disease (NAFLD) is one of the most common forms of chronic liver diseases closely associated with obesity and insulin resistance; deficient growth hormone (GH) action in liver has been implicated as a mechanism. Here, we investigated the evolution of NAFLD in aged mice with liver-specific GHR deletion.>Methods: We examined glucose tolerance, insulin responsiveness, and lipid profiles in aged male mice (44–50 weeks) with GHRLD. We performed proteomics analysis, pathway-based Superarray assay, as well as quantitative RT-PCR to gain molecular insight into the mechanism(s) of GHR-deficiency-mediated NAFLD. In addition, we examined the pathological changes of livers of aged GHRLD male mice.>Results: The biochemical profile was consistent with that of the metabolic syndrome: abnormal glucose tolerance, impaired insulin secretion, and hyperlipidemia. RT-qPCR analysis of key markers of inflammation revealed a three- to fivefold increase in TNFα and CCL3, confirming the presence of inflammation. Expression of fibrotic markers (e.g., Col1A2 and Col3A1) was significantly increased, together with a two- to threefold increase in TGFβ transcripts. Proteomics analyses showed a marked decrease of Mup1 and Selenbp2. In addition, pathway-analysis showed that the expression of cell cycle and growth relevant genes (i.e., Ccnd1, Socs2, Socs3, and Egfr) were markedly affected in GHRLD liver. Microscopic analyses (H&E) of GHRLD livers revealed the presence of hepatic adenomas of different stages of malignancy.>Conclusion: Abrogation of GH signaling in male liver leads to metabolic syndrome, hepatic steatosis, increased inflammation and fibrosis, and development of hepatic tumor. Since obesity, a common precursor of NAFLD, is a state of deficient GH secretion and action, the GHRLD model could be used to unravel the contribution of compromised hepatic GH signaling in these pathological processes, and help to identify potential targets for intervention.
机译:>背景:非酒精性脂肪性肝病(NAFLD)是与肥胖症和胰岛素抵抗密切相关的最常见的慢性肝病形式之一;肝脏中缺乏生长激素(GH)作用已被认为是一种机制。在这里,我们调查了具有肝特异性GHR缺失的老年小鼠中NAFLD的演变。>方法:我们检查了GHRLD的老年雄性小鼠(44-50周)的糖耐量,胰岛素反应性和脂质分布。我们进行了蛋白质组学分析,基于途径的Superarray分析以及定量RT-PCR,从而获得了对GHR缺陷介导的NAFLD机制的分子认识。此外,我们还检查了老年GHRLD雄性小鼠肝脏的病理学变化。>结果:生化特征与代谢综合征的特征相符:糖耐量异常,胰岛素分泌受损和高脂血症。炎症关键标志物的RT-qPCR分析显示,TNFα和CCL3增加了三到五倍,从而证实了炎症的存在。纤维化标记物(例如Col1A2和Col3A1)的表达显着增加,而TGFβ转录物则增加了2到3倍。蛋白质组学分析显示Mup1和Selenbp2明显减少。另外,通路分析表明,GHLRD肝脏中细胞周期和生长相关基因(即Ccnd1,Socs2,Socs3和Egfr)的表达受到显着影响。 GHRLD肝脏的显微镜分析(H&E)显示了恶性程度不同的肝腺瘤的存在。>结论:雄性肝中GH信号的减弱会导致代谢综合征,肝脂肪变性,炎症和纤维化增加,以及肝肿瘤的发展。由于肥胖是NAFLD的常见前体,是GH分泌和作用不足的状态,因此GHRLD模型可用于阐明这些病理过程中受损的GH肝信号的贡献,并有助于确定潜在的干预目标。

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