Toxicity of 3'-azido-3'-deoxythymidine and 9-(1,3-dihydroxy-2-propoxymethyl)guanine for normal human hematopoietic progenitor cells in vitro

Antimicrob Agents Chemother. 1987 Mar;31(3):452-4. doi: 10.1128/AAC.31.3.452.

Abstract

The effects of 3'-azido-3'-deoxythymidine (AZT) and 9-(1,3-dihydroxy-2-propoxymethyl)guanine on myeloid and erythroid colony-forming cells were studied by clonogenic assays. Both consistently inhibited granulocyte-macrophage CFU (CFU-GM) and erythroid burst-forming units in a dose-dependent fashion. Concentrations of AZT and 9-(1,3-dihydroxy-2-propoxymethyl)guanine required for 50% inhibition of CFU-GM were, respectively, 0.9 +/- 0.1 and 2.7 +/- 0.5 microM; those required for 90% inhibition were, respectively, 34.0 +/- 2.8 and 35.7 +/- 3.6 microM. Erythroid burst-forming units were less sensitive to high concentrations of AZT than were CFU-GM.

Publication types

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

MeSH terms

  • Acyclovir / analogs & derivatives*
  • Acyclovir / toxicity
  • Antiviral Agents / toxicity*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Ganciclovir
  • Hematopoietic Stem Cells / drug effects*
  • Humans
  • Thymidine / analogs & derivatives*
  • Thymidine / toxicity
  • Zidovudine

Substances

  • Antiviral Agents
  • Zidovudine
  • Ganciclovir
  • Thymidine
  • Acyclovir