Resistance to high-fat diet-induced obesity but exacerbated insulin resistance in mice overexpressing preadipocyte factor-1 (Pref-1): a new model of partial lipodystrophy

Diabetes. 2008 Dec;57(12):3258-66. doi: 10.2337/db07-1739. Epub 2008 Oct 3.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / physiology
  • Animals
  • Blood Glucose / metabolism
  • Body Composition / physiology
  • Calcium-Binding Proteins
  • Dietary Fats / metabolism*
  • Disease Models, Animal
  • Glucose Clamp Technique
  • Glucose Tolerance Test
  • Insulin / physiology
  • Insulin Resistance / physiology*
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / physiology*
  • Leptin / physiology
  • Lipodystrophy, Familial Partial / genetics
  • Lipodystrophy, Familial Partial / physiopathology*
  • Mice
  • Mice, Transgenic
  • Obesity / etiology
  • Obesity / physiopathology*
  • Recombinant Fusion Proteins / metabolism

Substances

  • Adiponectin
  • Blood Glucose
  • Calcium-Binding Proteins
  • Dietary Fats
  • Dlk1 protein, mouse
  • Insulin
  • Intercellular Signaling Peptides and Proteins
  • Leptin
  • Recombinant Fusion Proteins