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通过高脂肪饮食和四环素联合应用于病态肥胖小鼠建立非酒精性脂肪性肝炎模型。

Development of nonalcoholic steatohepatitis model through combination of high-fat diet and tetracycline with morbid obesity in mice.

机构信息

Tsukuba Research Institute, Banyu Pharmaceutical Co. Ltd., Tsukuba, Japan.

出版信息

Hepatol Res. 2006 Feb;34(2):92-8. doi: 10.1016/j.hepres.2005.12.001. Epub 2006 Jan 19.

Abstract

Nonalcoholic steatohepatitis (NASH) is a chronic liver disease closely associated with obesity, type 2 diabetes and hyperlipidemia. For further understanding of NASH, development and characterization of appropriate animal models with metabolic abnormalities is important. Based on the "two hit theory", we tried to develop a new murine model of NASH with metabolic abnormalities. For the first hit to achieve metabolic abnormalities, a high-fat diet (HFD: 60 cal% fat) was fed to C57BL/6 mice for 10 weeks. For the second hit, 30mg/kg tetracycline was injected intraperitoneally once daily for 10 days. The HFD-fed mice treated with tetracycline showed robust increases in triglyceride content and expression levels of proinflammatory cytokine mRNAs in the liver. In addition, plasma ALT levels were significantly elevated by this combinational treatment. Furthermore, histological examination demonstrated that combinational treatment induced multifocal inflammatory cellular infiltration in the livers of all mice, and thus caused mild steatohepatitis. The HFD-tetracycline model could be useful for further understanding NASH.

摘要

非酒精性脂肪性肝炎(NASH)是一种与肥胖、2 型糖尿病和高脂血症密切相关的慢性肝脏疾病。为了进一步了解 NASH,开发和鉴定具有代谢异常的合适动物模型非常重要。基于“二次打击理论”,我们试图建立一种新的具有代谢异常的 NASH 小鼠模型。为了实现第一次打击以产生代谢异常,我们用高脂肪饮食(HFD:60%卡路里来自脂肪)喂养 C57BL/6 小鼠 10 周。为了进行第二次打击,我们每天用 30mg/kg 的四环素经腹腔注射 10 天。用四环素处理的 HFD 喂养的小鼠肝脏中甘油三酯含量和促炎细胞因子 mRNA 的表达水平显著增加。此外,联合治疗使血浆 ALT 水平显著升高。此外,组织学检查表明,联合治疗诱导了所有小鼠肝脏内局灶性炎症细胞浸润,从而导致轻度脂肪性肝炎。HFD-四环素模型可能有助于进一步了解 NASH。

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