Increase in hepatic expression of SREBP-2 by gemfibrozil administration to rats

Biochem Pharmacol. 2001 Sep 15;62(6):803-9. doi: 10.1016/s0006-2952(01)00701-8.

Abstract

It is well known that gemfibrozil increases the biliary output of cholesterol and phospholipids, but we have little knowledge about the impact these changes have on liver cholesterol and phospholipid biosynthetic pathways. In the present study, no changes were detected in liver lipids and CTP:phosphocholine cytidylyltransferase after gemfibrozil administration to rats. On the contrary, 3-hydroxy-3-methylglutaryl-CoA reductase mRNA (9.9-fold) and Rd activity (16.7-fold) and phosphatidate phosphohydrolase activity (1.7-fold) increased, while plasma apo B-cholesterol (40%) and triglyceride (43%) levels decreased. As a part of a compensatory homeostatic response, we report for the first time that gemfibrozil administration to rats increased the hepatic sterol regulatory element binding protein-2 (SREBP-2) mRNA (2.9-fold) and mature protein (2.2-fold) levels. An early increase in the transcriptional activity of SREBP-2 elicited by gemfibrozil administration might be responsible for the observed changes in HMG-CoA reductase, phosphatidate phosphohydrolase, and SREBP-2 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / metabolism*
  • Gemfibrozil / pharmacology*
  • Gene Expression / drug effects*
  • Hypolipidemic Agents / pharmacology*
  • Lipid Metabolism
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Sterol Regulatory Element Binding Protein 2
  • Transcription Factors / metabolism*
  • Transcriptional Activation / drug effects

Substances

  • DNA-Binding Proteins
  • Hypolipidemic Agents
  • Sterol Regulatory Element Binding Protein 2
  • Transcription Factors
  • Gemfibrozil