The rapid induction of liver glycerophosphate acyltransferase in mice by clofibrate, a hypolipidemic agent

J Biol Chem. 1983 Mar 10;258(5):3090-3.

Abstract

Administration of clofibrate to adult mice (20-25 mg of clofibrate/day) increased liver glycerophosphate acyltransferase (EC 2.3.1.15) activity by 2.3-fold within 24 h. This increased glycerophosphate acyltransferase activity was mainly localized in the liver microsomal fraction. Three other hypolipidemic drugs, i.e. Bezafibrate (Boehringer Mannheim Co.), Gemfibrozil (Warner-Lambert Co.) and Wy-14,643 (Wyeth Laboratories), when fed to mice, also increased the liver glycerophosphate acyltransferase activity by 2-3-fold in 24 h. Simultaneous administration of inhibitors of protein biosynthesis, such as cycloheximide or actinomycin D completely abolished such stimulation of liver glycerophosphate acyltransferase by clofibrate.

Publication types

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

MeSH terms

  • Acyltransferases / genetics*
  • Animals
  • Anticholesteremic Agents / pharmacology
  • Clofibrate / pharmacology*
  • Enzyme Induction
  • Glycerol-3-Phosphate O-Acyltransferase / genetics*
  • Liver / drug effects
  • Liver / enzymology*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology

Substances

  • Anticholesteremic Agents
  • Acyltransferases
  • Glycerol-3-Phosphate O-Acyltransferase
  • Clofibrate