A novel model of type 2 diabetes mellitus based on obesity induced by high-fat diet in BDF1 mice

被引:43
作者
Karasawa, Hiroshi [1 ]
Nagata-Goto, Seiko [1 ]
Takaishi, Kiyosumi [1 ]
Kumagae, Yoshihiro [2 ]
机构
[1] Daiichi Sankyo Co Ltd, Biol Res Labs 2, Tokyo 1408710, Japan
[2] Daiichi Sankyo Co Ltd, Pharmacol Res Labs, Tokyo 1408710, Japan
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2009年 / 58卷 / 03期
关键词
INSULIN-RESISTANCE; MOUSE; PATHOGENESIS; PERSPECTIVE; PROGRESSION; EXPRESSION; MUTATIONS; C57BL/6J; FAILURE; GLUCOSE;
D O I
10.1016/j.metabol.2008.09.028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For experimental research on type 2 diabetes mellitus, a diet-induced obesity-dependent diabetes model developed using genetically normal animals is essential. However, attempts at feeding a high-fat diet (HFD) to major inbred strains of mice have not resulted in the establishment of an ideal model. Here, we show that BDF1 mice, the F, hybrids of C57BL/6 and DBA/2 normal strains, develop HFD-induced obesity-dependent, diabetes. BDF1 mice fed a HFD gained weight rapidly and developed severe diabetes characterized by hyperglycemia, glucosuria, and elevation of hemoglobin A(1C) levels in 3 to 4 months. The glucose tolerance of the diabetic mice was significantly impaired, and the elevation of plasma insulin after a glucose load was significantly reduced. Isolated pancreatic islets of HFD-fed BDF1 mice showed decreased insulin content and a reduced insulin secretory response to higher concentrations of glucose. Immunohistochemical analysis of the pancreas showed reduced staining intensity to insulin and aberrant distribution of glucagon-positive cells in diabetic BDF1 mice. These observations suggest the cause of the diabetes in HFD-fed BDF1 mice to be dysfunction of the pancreatic beta-cells, which do not produce or secrete enough insulin to compensate for insulin resistance. BDF1 mice fed a HFD showing obesity-dependent diabetes are suggested to be an appropriate animal model of type 2 diabetes mellitus. This model would be useful for exploring the mechanism of obesity-dependent type 2 diabetes mellitus and evaluating antiobesity and antidiabetic drugs. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:296 / 303
页数:8
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