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C57BL/6J and A/J Mice Fed a High‐Fat Diet Delineate Components of Metabolic Syndrome
Author(s) -
GallouKabani Catherine,
Vigé Alexandre,
Gross MarieSylvie,
Rabès JeanPierre,
Boileau Catherine,
LarueAchagiotis Christiane,
Tomé Daniel,
Jais JeanPhilippe,
Junien Claudine
Publication year - 2007
Publication title -
obesity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.438
H-Index - 199
eISSN - 1930-739X
pISSN - 1930-7381
DOI - 10.1038/oby.2007.238
Subject(s) - hyperinsulinemia , insulin resistance , metabolic syndrome , medicine , endocrinology , type 2 diabetes , impaired glucose tolerance , diabetes mellitus , obesity , biology , polyunsaturated fatty acid , fatty acid , biochemistry
Objective: The aim of this study was to assess the suitability of A/J and C57BL/6J mice of both sexes as models of some components of the human metabolic syndrome (MetS) under nutritional conditions more comparable with the actual worldwide diet responsible for the increased incidence of the MetS. Research Methods: We fed large cohorts ( n = 515) of two strains of mice, A/J and the C57BL/6J, and of both sexes a high‐fat diet (HFD; 60% fat) that, in contrast with most previous reports using saturated fats, was enriched in mono‐ and polyunsaturated fatty acids, thus more closely mimicking most Western diets, or a control diet (10% fat), for 20 weeks. Results: In sharp contrast to previous reports, weight gain and hyperleptinemia were similar in both strains and sexes. Hyperinsulinemia, glucose tolerance, insulin resistance, and hypercholesterolemia were observed, although with important differences between strains and sexes. A/J males displayed severely impaired glucose tolerance and insulin resistance. However, in contrast with C57BL6/J mice, which displayed overt type 2 diabetes, A/J mice of both sexes remained normoglycemic. Discussion: With important differences in magnitude and time course, the phenotypic and metabolic characteristics of both strains and both sexes on this HFD demonstrate that these models are very useful for identifying the mechanisms underlying progression or resistance to subsequent type 2 diabetes.

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