Differential levels of diabetogenic stress in two new mouse models of obesity and type 2 diabetes.
Diabetes-Mellitus-Type-II, Disease-Models-Animal, Female, Male, Mice, Mice-Inbred-Strains, Obesity, Obesity-in-Diabetes, Stress, SUPPORT-U-S-GOVT-P-H-S
Diabetes 2004 Feb; 53 (Suppl 1):S4-11.
The genetic basis for the more common forms of human obesity predisposing to insulin resistance and development of type 2 diabetes is multigenic rather than monogenic in origin. New mouse "diabesity" models have been created by combining independent diabetes risk-conferring quantitative trait loci from two unrelated parental strains: New Zealand Obese (NZO/HlLt) and Nonobese Nondiabetic (NON/Lt). F1 hybrid males, heterozygous at all polymorphic autosomal loci distinguishing the two parental strains, are driven to obesity-induced diabetes (diabesity) at high frequencies. This review focuses on two new recombinant congenic strains (RCSs) developed by introgressing multiple NZO/HlLt chromosomal segments into the nominally diabesity-resistant NON/Lt strain background. Both RCSs gain more weight than NON animals. Although exhibiting comparable weight gain and adiposity, only one of the two RCSs develops diabetes. Hence, these two RCSs will be instructive in elucidating genetic and pathophysiological differences underlying uncomplicated obesity syndromes versus diabetogenic obesity (diabesity) syndromes. Unlike mice with null mutations in a single gene producing morbid obesity, the new models develop a more moderate obesity produced by the interaction of numerous genes with relatively small effects. These RCSs are differentially sensitive to adverse side effects of thiazolidinediones and thus should be particularly useful for pharmacogenetic analyses.
Leiter, E H. and Reifsnyder, P C., " Differential levels of diabetogenic stress in two new mouse models of obesity and type 2 diabetes." (2004). Faculty Research 2000 - 2009. 728.