Inhibition of duck hepatitis B virus replication by purine 2',3'-dideoxynucleosides

Biochem Biophys Res Commun. 1988 Nov 15;156(3):1144-51. doi: 10.1016/s0006-291x(88)80752-6.

Abstract

Primary hepatocyte cultures from duck hepatitis B virus (DHBV) infected ducklings were used to evaluate the antiviral activity of purine and pyrimidine 2',3'-dideoxynucleosides. The purine 2',3'-dideoxynucleosides were very effective inhibitors of hepadnavirus replication, whereas the pyrimidine dideoxynucleosides were not. 2',3'-Dideoxyguanosine and 2,6-diaminopurine 2',3'-dideoxyriboside (ddDAPR) were the most effective antiviral agents studied. ddDAPR given intramuscularly twice daily at 10 mg/kg rapidly cleared DHBV-DNA from the sera of persistently infected ducklings but this effect was not permanent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • DNA, Viral / analysis
  • Dideoxynucleosides / pharmacology*
  • Ducks
  • Hepatitis B virus / drug effects*
  • Liver / analysis
  • Liver / microbiology
  • Purine Nucleosides / pharmacology*
  • Purines / pharmacology
  • Pyrimidines / pharmacology
  • Virus Replication / drug effects*

Substances

  • DNA, Viral
  • Dideoxynucleosides
  • Purine Nucleosides
  • Purines
  • Pyrimidines