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PMID: 15561913 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The high-fat diet-fed mouse: a model for studying mechanisms and treatment of impaired glucose tolerance and type 2 diabetes.

Diabetes ·Vol. 53 Suppl 3 ·2004-12-00 ·Pages S215-9

Winzell MS, Ahrén B

Abstract

This study characterizes the high-fat diet-fed mouse as a model for impaired glucose tolerance (IGT) and type 2 diabetes. Female C57BL/6J mice were fed a high-fat diet (58% energy by fat) or a normal diet (11% fat). Body weight was higher in mice fed the high-fat diet already after the first week, due to higher dietary intake in combination with lower metabolic efficiency. Circulating glucose increased after 1 week on high-fat diet and remained elevated at a level of approximately 1 mmol/l throughout the 12-month study period. In contrast, circulating insulin increased progressively by time. Intravenous glucose challenge revealed a severely compromised insulin response in association with marked glucose intolerance already after 1 week. To illustrate the usefulness of this model for the development of new treatment, mice were fed an orally active inhibitor of dipeptidyl peptidase-IV (LAF237) in the drinking water (0.3 mg/ml) for 4 weeks. This normalized glucose tolerance, as judged by an oral glucose tolerance test, in association with augmented insulin secretion. We conclude that the high-fat diet-fed C57BL/6J mouse model is a robust model for IGT and early type 2 diabetes, which may be used for studies on pathophysiology and development of new treatment.

MeSH Terms
Animals Blood Glucose/drug effects,metabolism Diabetes Mellitus, Type 2/blood,therapy Dietary Fats Dipeptidyl Peptidase 4/metabolism Disease Models, Animal Female Glucose Intolerance/blood,therapy Glucose Tolerance Test Mice Mice, Inbred C57BL Protease Inhibitors/pharmacology
Chemicals
Blood Glucose Dietary Fats Protease Inhibitors Dipeptidyl Peptidase 4
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Winzell Maria Sörhede
Dept. of Medicine, Biomedical Center (BMC), B11, S-221 84 Lund, Sweden. [email protected]
Ahrén Bo
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
2004-12-00
Pages
S215-9
Language
English
Region
United States
NLM ID
0372763
Subset
IM
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