Nucleoside transporters in the disposition and targeting of nucleoside analogs in the kidney

Eur J Pharmacol. 2003 Oct 31;479(1-3):269-81. doi: 10.1016/j.ejphar.2003.08.076.

Abstract

Systemic disposition of nucleosides and nucleoside analogs is dependent on renal handling of these compounds. There are five known, functionally characterized nucleoside transporters with varying substrate specificities for nucleosides: concentrative nucleoside transporters (CNT1-CNT3; Solute Carrier (SLC) 28A1-28A3), which mediate the intracellular flux of nucleosides, and equilibrative nucleoside transporters (ENT1-ENT2; SLC29A1-SLC29A2), which mediate bi-directional facilitated diffusion of nucleosides. All five of these transporters are expressed in the kidney. Concentrative nucleoside transporters primarily localize to the apical membrane of renal epithelial cells while equilibrative nucleoside transporters primarily localize to the basolateral membrane. These transporters work in concert to mediate reabsorptive flux of naturally occurring nucleosides and nucleoside analogs. In addition, equilibrative transporters also participate in secretory flux of some nucleoside analogs. Nucleoside transporters also serve in the targeting of nucleoside analog therapies to renal tumors. This review examines the role that these transporters play in renal disposition of nucleosides and nucleoside analogs in both systemic and kidney-specific therapies.

Publication types

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

MeSH terms

  • Animals
  • Drug Delivery Systems / methods*
  • Humans
  • Kidney / drug effects
  • Kidney / metabolism*
  • Nucleoside Transport Proteins / chemistry
  • Nucleoside Transport Proteins / genetics
  • Nucleoside Transport Proteins / metabolism*
  • Nucleosides / administration & dosage
  • Nucleosides / chemistry
  • Nucleosides / metabolism*

Substances

  • Nucleoside Transport Proteins
  • Nucleosides