Fluoxetine is a potent inhibitor of coxsackievirus replication

Antimicrob Agents Chemother. 2012 Sep;56(9):4838-44. doi: 10.1128/AAC.00983-12. Epub 2012 Jul 2.

Abstract

No antiviral drugs currently exist for the treatment of enterovirus infections, which are often severe and potentially life threatening. Molecular screening of small molecule libraries identified fluoxetine, a selective serotonin reuptake inhibitor, as a potent inhibitor of coxsackievirus replication. Fluoxetine did not interfere with either viral entry or translation of the viral genome. Instead, fluoxetine and its metabolite norfluoxetine markedly reduced the synthesis of viral RNA and protein. In view of its favorable pharmacokinetics and safety profile, fluoxetine warrants additional study as a potential antiviral agent for enterovirus infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antidepressive Agents / pharmacology*
  • Antiviral Agents / pharmacology*
  • Enterovirus / drug effects*
  • Enterovirus / growth & development
  • Fluoxetine / analogs & derivatives*
  • Fluoxetine / pharmacology*
  • Genes, Reporter
  • Green Fluorescent Proteins
  • HeLa Cells
  • High-Throughput Screening Assays
  • Humans
  • Inhibitory Concentration 50
  • RNA, Viral / antagonists & inhibitors*
  • RNA, Viral / biosynthesis
  • Small Molecule Libraries / pharmacology
  • Transfection
  • Virus Replication / drug effects

Substances

  • Antidepressive Agents
  • Antiviral Agents
  • RNA, Viral
  • Small Molecule Libraries
  • Fluoxetine
  • Green Fluorescent Proteins
  • norfluoxetine