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

  1. Josep A. Villena1,
  2. Cheol Soo Choi2,
  3. Yuhui Wang1,
  4. Sheene Kim2,
  5. Yu-Jin Hwang2,
  6. Young-Bum Kim5,
  7. Gary Cline2,
  8. Gerald I. Shulman2,3,4 and
  9. Hei Sook Sul (hsul{at}nature.berkeley.edu)1
  1. 1Department of Nutritional Science and Toxicology, University of California, Berkeley, CA, 94720
  2. 2Department of Internal Medicine and
  3. 3Cellular & Molecular Physiology
  4. 4Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510
  5. 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

      • Received December 12, 2007.
      • Accepted September 17, 2008.