Fatty acid binding protein is a major determinant of hepatic pharmacokinetics of palmitate and its metabolites

Am J Physiol Gastrointest Liver Physiol. 2003 Mar;284(3):G423-33. doi: 10.1152/ajpgi.00328.2002. Epub 2002 Nov 20.

Abstract

Disposition kinetics of [(3)H]palmitate and its low-molecular-weight metabolites in perfused rat livers were studied using the multiple-indicator dilution technique, a selective assay for [(3)H]palmitate and its low-molecular-weight metabolites, and several physiologically based pharmacokinetic models. The level of liver fatty acid binding protein (L-FABP), other intrahepatic binding proteins (microsomal protein, albumin, and glutathione S-transferase) and the outflow profiles of [(3)H]palmitate and metabolites were measured in four experimental groups of rats: 1) males; 2) clofibrate-treated males; 3) females; and 4) pregnant females. A slow-diffusion/bound model was found to better describe the hepatic disposition of unchanged [(3)H]palmitate than other pharmacokinetic models. The L-FABP levels followed the order: pregnant female > clofibrate-treated male > female > male. Levels of other intrahepatic proteins did not differ significantly. The hepatic extraction ratio and mean transit time for unchanged palmitate, as well as the production of low-molecular-weight metabolites of palmitate and their retention in the liver, increased with increasing L-FABP levels. Palmitate metabolic clearance, permeability-surface area product, retention of palmitate by the liver, and cytoplasmic diffusion constant for unchanged [(3)H]palmitate also increased with increasing L-FABP levels. It is concluded that the variability in hepatic pharmacokinetics of unchanged [(3)H]palmitate and its low-molecular-weight metabolites in perfused rat livers is related to levels of L-FABP and not those of other intrahepatic proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / metabolism
  • Algorithms
  • Animals
  • Biomarkers
  • Biotransformation
  • Carrier Proteins / metabolism*
  • Clofibrate / pharmacology
  • Cytochrome P-450 Enzyme System / metabolism
  • Cytoplasm / metabolism
  • Diffusion
  • Fatty Acid-Binding Protein 7
  • Fatty Acid-Binding Proteins
  • Glutathione / metabolism
  • Hypolipidemic Agents / pharmacology
  • In Vitro Techniques
  • Liver / metabolism*
  • Male
  • Microsomes, Liver / enzymology
  • Microsomes, Liver / metabolism
  • Neoplasm Proteins*
  • Nerve Tissue Proteins*
  • Palmitates / pharmacokinetics*
  • Perfusion
  • Proteins / metabolism
  • Rats
  • Rats, Wistar
  • Tissue Distribution

Substances

  • Albumins
  • Biomarkers
  • Carrier Proteins
  • Fabp1 protein, mouse
  • Fabp1 protein, rat
  • Fabp7 protein, rat
  • Fatty Acid-Binding Protein 7
  • Fatty Acid-Binding Proteins
  • Hypolipidemic Agents
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • Palmitates
  • Proteins
  • Cytochrome P-450 Enzyme System
  • Glutathione
  • Clofibrate