Literature DB >> 22105644

Gene expression in livers of BALB/C and C57BL/6J mice fed a high-fat diet.

Satomi Nishikawa1, Jiro Sugimoto, Miyoko Okada, Tetsuya Sakairi, Shiro Takagi.   

Abstract

We previously demonstrated that high-fat diet (HFD)-induced hepatic lipid accumulation is more severe in BALB/c mice than in C57BL/6J (B6) mice. To understand the changes in liver metabolism, we studied blood chemistry, gene expression, and histopathological changes of the liver in nine-week HFD-fed BALB/c and B6 mice and one- or four-week HFD-fed BALB/c mice. Serum total cholesterol and triglyceride levels were significantly increased in all HFD-fed groups, and one- and four-week HFD-fed BALB/c groups, respectively. Histopathology revealed that vacuolation of hepatocytes was severe in nine-week HFD-fed BALB/c mice, although it was less severe in the other groups. Microarray analysis of mRNA expression of nine-week HFD-fed BALB/c mice showed up-regulation of genes involved in fatty acid uptake and biosynthesis, such as Cd36, Acaca, Acly, and Fasn. Some changes were observed in the one- and four-week HFD-fed BALB/c groups and the nine-week HFD-fed B6 group, however these changes in mRNA expression were not so marked. In conclusion, the fatty accumulation observed in BALB/c mice may be caused, at least in part, by up-regulation of fatty acid uptake and biosynthesis. Cd36, Acaca, Acly and Fasn may be involved in these metabolic processes.

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Year:  2011        PMID: 22105644     DOI: 10.1177/0192623311422078

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  21 in total

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3.  Mouse strain-dependent variation in obesity and glucose homeostasis in response to high-fat feeding.

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9.  Differential Immunometabolic Phenotype in Th1 and Th2 Dominant Mouse Strains in Response to High-Fat Feeding.

Authors:  Nemanja Jovicic; Ilija Jeftic; Ivan Jovanovic; Gordana Radosavljevic; Nebojsa Arsenijevic; Miodrag L Lukic; Nada Pejnovic
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10.  Social exclusion changes histone modifications H3K4me3 and H3K27ac in liver tissue of wild house mice.

Authors:  Linda Krause; Bernhard Haubold; Angelika G Börsch-Haubold
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