Resistance to high fat diet-induced obesity but exacerbated insulin resistance in mice overexpressing Pref-1: a new model of partial lipodystrophy
- Josep A. Villena1,
- Cheol Soo Choi2,
- Yuhui Wang1,
- Sheene Kim2,
- Yu-Jin Hwang2,
- Young-Bum Kim5,
- Gary Cline2,
- Gerald I. Shulman2,3,4 and
- Hei Sook Sul (hsul{at}nature.berkeley.edu)1
- 1Department of Nutritional Science and Toxicology, University of California, Berkeley, CA, 94720
- 2Department of Internal Medicine and
- 3Cellular & Molecular Physiology
- 4Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510
- 5Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02215
Abstract
Objective. White adipose tissue is a critical regulator of whole body glucose metabolism. 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 insights 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 due to 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.
Footnotes
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- Received December 12, 2007.
- Accepted September 17, 2008.
- Copyright © American Diabetes Association














