Biochemical and molecular pharmacological aspects of transporters as determinants of drug disposition

Drug Metab Pharmacokinet. 2005 Apr;20(2):91-9. doi: 10.2133/dmpk.20.91.

Abstract

Membrane transporters are integral membrane proteins typically having 12 transmembrane domains. Most of the SLC family transporters consist of 300-800 amino acid residues with a molecular mass of 40-90 kDa, while the corresponding values of ABC family transporters are 1,200-1,500 residues and 140-180 kDa, respectively. Each transporter has a characteristic tissue distribution and subcellular localization. I have isolated cDNAs of various transporters, including oligopeptide transporter PEPT1, monocarboxylic acid transporter MCT1 and organic cation/carnitine transporters (OCTNs), and determined their tissue distribution and subcellular localization. I have also determined the absolute expression levels of transporters to evaluate their relative contributions to drug transport in various tissues. It is important to note that expression levels of transporters can be changed under various physiological conditions and by administration of drugs. Changes in expression level, subcellular localization and functional properties can all be involved in inter-individual differences in drug pharmacokinetics. Transporters are among the key determinants of drug disposition.

Publication types

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

MeSH terms

  • Animals
  • Biological Availability
  • Cloning, Molecular
  • DNA, Complementary / chemistry
  • Humans
  • Intestinal Mucosa / metabolism
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism*
  • Monocarboxylic Acid Transporters / genetics
  • Monocarboxylic Acid Transporters / metabolism
  • Organic Cation Transport Proteins / genetics
  • Organic Cation Transport Proteins / metabolism
  • Peptide Transporter 1
  • Pharmaceutical Preparations / administration & dosage
  • Pharmaceutical Preparations / metabolism*
  • Pharmacokinetics*
  • Pharmacology*
  • Protein Structure, Tertiary
  • Symporters / genetics
  • Symporters / metabolism
  • Tissue Distribution
  • Transduction, Genetic

Substances

  • DNA, Complementary
  • Membrane Proteins
  • Monocarboxylic Acid Transporters
  • Organic Cation Transport Proteins
  • Peptide Transporter 1
  • Pharmaceutical Preparations
  • Symporters