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Resistance to High-Fat Diet–Induced Obesity but Exacerbated Insulin Resistance in Mice Overexpressing Preadipocyte Factor-1 (Pref-1)
- Source :
- Diabetes. 57:3258-3266
- Publication Year :
- 2008
- Publisher :
- American Diabetes Association, 2008.
-
Abstract
- OBJECTIVE—White adipose tissue is a critical regulator of whole-body glucose metabolism. Preadipocyte factor-1 (Pref-1) is a secreted protein that inhibits adipocyte differentiation, both in vitro and in vivo. In this study, we have investigated the effects of Pref-1 overexpression on whole-body glucose homeostasis and its contribution to the development of insulin resistance.RESEARCH DESIGN AND METHODS—To gain insight into the role of Pref-1 on the onset of insulin resistance and type 2 diabetes, we measured body composition and whole-body insulin-stimulated glucose metabolism during a hyperinsulinemic-euglycemic clamp in Pref-1 transgenic and wild-type control mice fed a high-fat diet.RESULTS—Mice overexpressing Pref-1 were resistant to high-fat diet–induced obesity, as reflected by a marked reduction in adipose tissue mass. However, Pref-1–overexpressing mice were severely insulin resistant, mainly because of a reduction in insulin-stimulated glucose uptake in skeletal muscle and adipose tissue. The aggravated insulin resistance was associated with impaired insulin signaling and increased diacylglycerol content in skeletal muscle.CONCLUSIONS—Mice overexpressing Pref-1 are insulin resistant despite being protected from diet-induced obesity and may provide a new rodent model for the study of lipodystrophic disorders.
- Subjects :
- medicine.medical_specialty
Endocrinology, Diabetes and Metabolism
medicine.medical_treatment
Adipose tissue
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Insulin resistance
Internal medicine
Adipocyte
Internal Medicine
medicine
Glucose homeostasis
030304 developmental biology
2. Zero hunger
0303 health sciences
Glucose tolerance test
medicine.diagnostic_test
biology
Insulin
Glucose clamp technique
medicine.disease
Insulin receptor
Endocrinology
chemistry
030220 oncology & carcinogenesis
biology.protein
Subjects
Details
- ISSN :
- 1939327X and 00121797
- Volume :
- 57
- Database :
- OpenAIRE
- Journal :
- Diabetes
- Accession number :
- edsair.doi...........6795585409b700700f1545cff279ef1c