INTRACELLULAR METABOLISM OF 3'-AZIDO-3'-DEOXYTHYMIDINE IN THE PRESENCE OF GANCICLOVIR OR FOSCARNET

Citation
S. Palmer et al., INTRACELLULAR METABOLISM OF 3'-AZIDO-3'-DEOXYTHYMIDINE IN THE PRESENCE OF GANCICLOVIR OR FOSCARNET, Antiviral chemistry & chemotherapy, 7(1), 1996, pp. 14-20
Citations number
49
Categorie Soggetti
Biology,"Pharmacology & Pharmacy
ISSN journal
09563202
Volume
7
Issue
1
Year of publication
1996
Pages
14 - 20
Database
ISI
SICI code
0956-3202(1996)7:1<14:IMO3IT>2.0.ZU;2-N
Abstract
Comparisons were made between the intracellular phosphorylation of 3'- azido-3'-deoxythymidine (AZT) alone and in combination with ganciclovi r (GCV) or foscarnet (PFA) in lymphocytes, uninfected fibroblasts and CMV-infected fibroblasts. The effects of AZT and the combinations of A ZT with GCV or PFA on cellular dNTP pools were also examined. The phos phorylation of AZT was not altered by the presence of GCV or PFA in ly mphocytes, and neither AZT nor the combinations of AZT with GCV or PFA changed the levels of cellular dNTP pools in these cells. AZT was pho sphorylated to a greater extent in lymphocytes when compared to fibrob lasts, but the proportion of AZT di- and triphosphates was greater in fibroblasts. The infection of fibroblasts with CMV enhanced AZT phosph orylation and increased the levels of cellular dNTP pools. GCV caused a specific reduction in AZT phosphorylation in CMV-infected fibroblast s, with a seven-fold drop in AZT triphosphate compared to AZT alone. G CV did not affect AZT phosphorylation in uninfected fibroblasts, nor d id GCV reduce the dTTP pool compared to AZT alone. The effects of GCV upon AZT phosphorylation in CMV-infected cells may shed light on the a ntagonistic effects of GCV upon the anti-HIV activity of AZT, and are of importance for the development of effective combination therapies f or the treatment of AIDS patients infected with CMV.