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载脂蛋白E缺陷小鼠食用西方饮食7周会诱发代谢综合征以及伴有肝纤维化的非酒精性脂肪性肝炎。

Seven weeks of Western diet in apolipoprotein-E-deficient mice induce metabolic syndrome and non-alcoholic steatohepatitis with liver fibrosis.

作者信息

Schierwagen Robert, Maybüchen Lara, Zimmer Sebastian, Hittatiya Kanishka, Bäck Christer, Klein Sabine, Uschner Frank E, Reul Winfried, Boor Peter, Nickenig Georg, Strassburg Christian P, Trautwein Christian, Plat Jogchum, Lütjohann Dieter, Sauerbruch Tilman, Tacke Frank, Trebicka Jonel

机构信息

Department of Internal Medicine I, University of Bonn, Germany.

Department of Internal Medicine II, University of Bonn, Germany.

出版信息

Sci Rep. 2015 Aug 11;5:12931. doi: 10.1038/srep12931.

Abstract

Non-alcoholic steatohepatitis (NASH) is characterised by hepatic steatosis, inflammation and fibrosis, which might progress to cirrhosis. Human NASH is associated with metabolic syndrome (MS). Currently, rodent NASH models either lack significant fibrosis or MS. ApoE(-/-) mice are a MS model used in cardiovascular research. The aim of this work was to establish and characterise a novel mouse NASH model with significant fibrosis and MS. ApoE(-/-) and wild-type mice (wt) were fed either a western-diet (WD), methionine-choline-deficient-diet (MCD) or normal chow. Liver histology, RT-PCR, hepatic hydroxyproline content, triglycerides and cholesterol levels, and fasting glucose levels assessed hepatic steatosis, inflammation and fibrosis. Further, portal pressure was measured invasively, and kidney pathology was assessed by histology. ApoE(-/-) mice receiving WD showed abnormal glucose tolerance, hepatomegaly, weight gain and full spectrum of NASH including hepatic steatosis, fibrosis and inflammation, with no sign of renal damage. MCD-animals showed less severe liver fibrosis, but detectable renal pathological changes, besides weight loss and unchanged glucose tolerance. This study describes a murine NASH model with distinct hepatic steatosis, inflammation and fibrosis, without renal pathology. ApoE(-/-) mice receiving WD represent a novel and fast model with all characteristic features of NASH and MS well suitable for NASH research.

摘要

非酒精性脂肪性肝炎(NASH)的特征是肝脂肪变性、炎症和纤维化,可能进展为肝硬化。人类NASH与代谢综合征(MS)相关。目前,啮齿动物NASH模型要么缺乏显著的纤维化,要么缺乏MS。载脂蛋白E基因敲除(ApoE(-/-))小鼠是用于心血管研究的MS模型。这项工作的目的是建立并表征一种具有显著纤维化和MS的新型小鼠NASH模型。给ApoE(-/-)小鼠和野生型(wt)小鼠喂食西式饮食(WD)、蛋氨酸-胆碱缺乏饮食(MCD)或正常饲料。通过肝脏组织学、逆转录聚合酶链反应(RT-PCR)、肝脏羟脯氨酸含量、甘油三酯和胆固醇水平以及空腹血糖水平评估肝脂肪变性、炎症和纤维化。此外,通过侵入性测量门静脉压力,并通过组织学评估肾脏病理。接受WD的ApoE(-/-)小鼠表现出异常的糖耐量、肝肿大、体重增加以及包括肝脂肪变性、纤维化和炎症在内的NASH全貌,且无肾损伤迹象。MCD喂养的动物肝脏纤维化较轻,但除体重减轻和糖耐量未改变外,可检测到肾脏病理变化。本研究描述了一种具有明显肝脂肪变性、炎症和纤维化且无肾脏病理的小鼠NASH模型。接受WD的ApoE(-/-)小鼠代表了一种新型快速模型,具有NASH和MS的所有特征,非常适合NASH研究。

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