High-fat feeding rapidly induces obesity and lipid derangements in C57BL/6N mice

被引:0
|
作者
Christine Podrini
Emma L. Cambridge
Christopher J. Lelliott
Damian M. Carragher
Jeanne Estabel
Anna-Karin Gerdin
Natasha A. Karp
Cheryl L. Scudamore
Ramiro Ramirez-Solis
Jacqueline K. White
机构
[1] Wellcome Trust Sanger Institute,Epigenetics of Fatty Liver Disease Research Group
[2] Institute of Hepatology,Division of Immunoregulation
[3] Foundation for Liver Research,Department of Pathology and Infectious Diseases
[4] MRC National Institute for Medical Research (NIMR),undefined
[5] Royal Veterinary College,undefined
[6] MRC Harwell,undefined
来源
Mammalian Genome | 2013年 / 24卷
关键词
Embryonic Stem Cell; Control Diet; Nonalcoholic Fatty Liver Disease; Liver Steatosis; Fructosamine;
D O I
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中图分类号
学科分类号
摘要
C57BL/6N (B6N) is becoming the standard background for genetic manipulation of the mouse genome. The B6N, whose genome is very closely related to the reference C57BL/6J genome, is versatile in a wide range of phenotyping and experimental settings and large repositories of B6N ES cells have been developed. Here, we present a series of studies showing the baseline characteristics of B6N fed a high-fat diet (HFD) for up to 12 weeks. We show that HFD-fed B6N mice show increased weight gain, fat mass, and hypercholesterolemia compared to control diet-fed mice. In addition, HFD-fed B6N mice display a rapid onset of lipid accumulation in the liver with both macro- and microvacuolation, which became more severe with increasing duration of HFD. Our results suggest that the B6N mouse strain is a versatile background for studying diet-induced metabolic syndrome and may also represent a model for early nonalcoholic fatty liver disease.
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页码:240 / 251
页数:11
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