Accelerated onset of diabetes in non‐obese diabetic mice fed a refined high‐fat diet

Author:

Batdorf Heidi M.12,Lawes Luz de Luna1,Cassagne Gabrielle A.1,Fontenot Molly S.1,Harvey Innocence C.1,Richardson Jeremy T.1,Burk David H.1,Dupuy Samuel D.3,Karlstad Michael D.3,Salbaum J. Michael1,Staszkiewicz Jaroslaw1,Beyl Robbie1,Ghosh Sujoy1,Burke Susan J.1,Collier J. Jason124ORCID

Affiliation:

1. Pennington Biomedical Research Center Baton Rouge Louisiana USA

2. Department of Biological Sciences Louisiana State University Baton Rouge Louisiana USA

3. Department of Surgery University of Tennessee Health Science Center, Graduate School of Medicine Knoxville Tennessee USA

4. Present address: Louisiana State University School of Medicine New Orleans LA USA

Abstract

AbstractAimType 1 diabetes results from autoimmune events influenced by environmental variables, including changes in diet. This study investigated how feeding refined versus unrefined (aka ‘chow’) diets affects the onset and progression of hyperglycaemia in non‐obese diabetic (NOD) mice.MethodsFemale NOD mice were fed either unrefined diets or matched refined low‐ and high‐fat diets. The onset of hyperglycaemia, glucose tolerance, food intake, energy expenditure, circulating insulin, liver gene expression and microbiome changes were measured for each dietary group.ResultsNOD mice consuming unrefined (chow) diets developed hyperglycaemia at similar frequencies. By contrast, mice consuming the defined high‐fat diet had an accelerated onset of hyperglycaemia compared to the matched low‐fat diet. There was no change in food intake, energy expenditure, or physical activity within each respective dietary group. Microbiome changes were driven by diet type, with chow diets clustering similarly, while refined low‐ and high‐fat bacterial diversity also grouped closely. In the defined dietary cohort, liver gene expression changes in high‐fat‐fed mice were consistent with a greater frequency of hyperglycaemia and impaired glucose tolerance.ConclusionGlucose intolerance is associated with an enhanced frequency of hyperglycaemia in female NOD mice fed a defined high‐fat diet. Using an appropriate matched control diet is an essential experimental variable when studying changes in microbiome composition and diet as a modifier of disease risk.

Funder

National Institute of General Medical Sciences

NIH Office of the Director

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

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