Interaction of Nucleoside Analogues with Nucleoside Transporters in Rat Brain Endothelial Cells
| Autor: | N. Joan Abbott, Mansoor Chishty, David J. Begley, Andreas Reichel |
|---|---|
| Rok vydání: | 2004 |
| Předmět: |
Adenosine
Pharmaceutical Science Nucleoside Transport Proteins Equilibrative nucleoside transporter 2 Nucleoside transporter Antiviral Agents Structure-Activity Relationship medicine Animals Structure–activity relationship Cells Cultured biology Brain Endothelial Cells Biological Transport Nucleosides Equilibrative nucleoside transporter Transporter Adenosine receptor Rats Biochemistry Blood-Brain Barrier biology.protein Nucleoside medicine.drug |
| Zdroj: | Journal of Drug Targeting. 12:265-272 |
| ISSN: | 1029-2330 1061-186X |
| DOI: | 10.1080/10611860410001731398 |
| Popis: | A number of nucleoside analogues, consisting of antiviral compounds and agents designed as adenosine A1 receptor agonists, were examined for nucleoside transporter affinity using an in vitro model of the blood-brain barrier (BBB), the rat brain endothelial cell line, RBE4. Structure-activity relationships (SAR) were also performed to identify the key structural requirements for transporter recognition and the suitability of these systems for carrier-mediated strategies to deliver therapeutics across the BBB. Adenosine receptor agonists did not show transport affinity for concentrative nucleoside carriers, but exhibited affinity for equilibrative systems (Ki=10.8-97.9 microM) within the range of Kms for natural substrates. However, none of the antiviral compounds tested in this study showed affinity for either class of nucleoside transporter. SAR studies suggest that the hydroxyl group located at the 3'-position of the ribose moiety is an essential requirement for transporter recognition. This may explain the inability of nucleoside derived anti-viral compounds to use these systems despite the significant structural homology with naturally occurring nucleosides. Sites have also been identified which accommodate structural additions with retention of carrier affinity, suggesting that compounds which fail to penetrate the BBB could be attached to these sites for carrier-mediated delivery using a prodrug strategy. |
| Databáze: | OpenAIRE |
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