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C57BL/6J and A/J mice fed a high-fat diet delineate components of metabolic syndrome
Authors:Gallou-Kabani Catherine  Vigé Alexandre  Gross Marie-Sylvie  Rabès Jean-Pierre  Boileau Catherine  Larue-Achagiotis Christiane  Tomé Daniel  Jais Jean-Philippe  Junien Claudine
Institution:1. Institut National de la Santé et de la Recherche Médicale, Assistance Publique‐H?pitaux de Paris, Université Paris‐Descartes, Faculté de Médecine, H?pital Necker‐Enfants Malades, Paris, France;2. AP‐HP, Faculté de Médecine Paris Ile‐de‐France‐Ouest, Université Versailles‐Saint‐Quentin‐en‐Yvelines, Laboratoire de Biochimie, H?pital Ambroise Paré, Boulogne, France;3. Unité Mixte de Recherche, Institut National de la Recherche Agronomique 914 Physiologie de la Nutrition et du Comportement Alimentaire, Institut National Agronomique de Paris‐Grignon, Paris, France;4. Service de Biostatistique et Informatique Medicale, 75015 Paris, France;5. AP‐HP, Faculté de Médecine Paris Ile‐de‐France‐Ouest, Université Versailles‐Saint‐Quentin‐en‐Yvelines, Laboratoire de Biochimie, H?pital Ambroise Paré, Boulogne, France Institut National de la Santé et de la Recherche Médicale Unit 781, Clinique Maurice Lamy, Porte 15, H?pital Necker‐Enfants Malades, 149 rue de Sèvres, 75743 Paris, France. E‐mail:
Abstract: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.
Keywords:nutrition  type 2 diabetes  animal models
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