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Mouse Models of Nonalcoholic Steatohepatitis: Head-to-Head Comparison of Dietary Models and Impact on Inflammation and Animal Welfare

机译:非酒精性脱脂性的小鼠模型:饮食模型的头部与炎症和对炎症和动物福利的影响

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摘要

A variety of dietary nonalcoholic steatohepatitis (NASH) mouse models are available, and choosing the appropriate mouse model is one of the most important steps in the design of NASH studies. In addition to the histopathological and metabolic findings of NASH, a sufficient mouse model should guarantee a robust clinical status and good animal welfare. Three different NASH diets, a high-fat diet (HFD60), a western diet (WD), and a cafeteria diet (CAFD), were fed for 12 or 16 weeks. Metabolic assessment was conducted at baseline and before scheduled sacrifice, and liver inflammation was analyzed via fluorescence-associated cell sorting and histopathological examination. Clinical health conditions were scored weekly to assess the impact on animal welfare. The HFD60 and WD were identified as suitable NASH mouse models without a significant strain on animal welfare. Furthermore, the progression of inflammation and liver fibrosis was associated with a decreased proportion of CD3+ NK1.1+ cells. The WD represents a model of advanced-stage NASH, and the HFD60 is a strong model of nonalcoholic fatty liver disease (NAFLD) and metabolic syndrome. However, the CAFD should not be considered a NASH model.
机译:可提供各种膳食非酒精性脂肪肝炎(NASH)小鼠模型,并选择合适的小鼠模型是纳什研究设计中最重要的步骤之一。除了NASH的组织病理学和代谢结果外,足够的小鼠模型应该保证强大的临床状态和良好的动物福利。喂养了三种不同的尿液饮食,高脂饮食(HFD60),西方饮食(WD)和自助餐厅饮食(CAFD)12或16周。在基线和预定牺牲之前进行代谢评估,通过荧光相关细胞分选和组织病理学检查分析肝脏炎症。每周评估临床健康状况,以评估对动物福利的影响。 HFD60和WD被鉴定为合适的纳什鼠标模型,没有对动物福利产生重大菌株。此外,炎症和肝纤维化的进展与CD3 + NK1.1 +细胞的比例降低有关。 WD代表了先进阶段纳什的模型,HFD60是非酒精性脂肪肝疾病(NAFLD)和代谢综合征的强大模型。但是,CAFD不应被视为纳什模型。

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