Hepatic insig-1 or -2 overexpression reduces lipogenesis in obese Zucker diabetic fatty rats and in fasted/refed normal rats

Proc Natl Acad Sci U S A. 2004 May 4;101(18):7106-11. doi: 10.1073/pnas.0401715101. Epub 2004 Apr 19.

Abstract

To determine whether the antilipogenic actions of insulin-induced gene 1 (insig-1) demonstrated in cultured preadipocytes also occur in vivo, we infected Zucker diabetic fatty (ZDF) (fa/fa) rats, with recombinant adenovirus containing insig-1 or -2 cDNA. An increase of both proteins appeared in their livers. In control ZDF (fa/fa) rats infected with adenovirus containing the beta-galactosidase (beta-gal) cDNA, triacylglycerols in the liver and plasma rose steeply whereas the insig-infected rats exhibited substantial attenuation of the increase in hepatic steatosis and hyperlipidemia. Insig overexpression was associated with a striking reduction in the elevated level of nuclear sterol regulatory element-binding protein (SREBP)-1c, the activated form of the transcription factor. The mRNA of SREBP-1c lipogenic target enzymes also fell. The mRNA of endogenous insig-1, but not -2a and -2b, was higher in the fatty livers of untreated obese ZDF (fa/fa) rats compared with controls, but the elevation was not sufficient to block the approximately 3-fold increase in SREBP-1c expression and activity. In normal animals, adenovirus-induced overexpression of the insigs reduced the increase in SREBP-1c mRNA and its target enzymes caused by refeeding. The findings demonstrated that both insigs have antilipogenic action when transgenically overexpressed in livers with increased SREBP-1c-mediated lipogenesis. However, the increase in endogenous insig-1 expression associated with augmented lipogenesis may limit it, but is insufficient to prevent it.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae
  • Animals
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / metabolism
  • Disease Models, Animal
  • Genetic Vectors
  • Humans
  • Intracellular Signaling Peptides and Proteins*
  • Lipids / biosynthesis*
  • Liver / metabolism*
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics*
  • Obesity / genetics
  • Obesity / metabolism
  • Rats
  • Rats, Zucker

Substances

  • Carrier Proteins
  • INSIG1 protein, human
  • INSIG2 protein, human
  • Insig1 protein, rat
  • Intracellular Signaling Peptides and Proteins
  • Lipids
  • Membrane Proteins