Coumarins and Hesperetin Inhibit Human Respiratory Syncytial Virus Infection

Int J Mol Sci. 2024 Dec 11;25(24):13301. doi: 10.3390/ijms252413301.

Abstract

Respiratory syncytial virus (RSV) is one of the most prevalent viruses that causes severe acute lower respiratory tract infections (ALRTIs) in the elderly and young children. There is no specific drug to treat RSV, only a broad-spectrum antiviral, ribavirin, which is only used in critical cases. Our research group is investigating antiviral agents of natural origin, such as coumarins and flavonoids, that may help reduce or prevent RSV infection. The cytotoxic concentrations of coumarins and hesperetin were tested on A549 and HEp-2 cells and used in inhibition tests in which 80% of the cells were viable. The anti-RSV action of the molecules was analyzed in A549 and HEp-2 cells and in HBE cell cultures infected with RSV-luc or rgRSV. We also encapsulated the compounds using β-cyclodextrin to improve the permeability and solubility of the molecules. Esculetin and 4-methyl inhibited rgRSV effectively on A549 and HEp-2 cells after 24 hpi, and when they were encapsulated, coumarin, esculetin, and hesperetin presented inhibition against rgRSV in HBE culture. The coumarins inhibit RSV replication in cell culture and even manage to overcome the mucus barriers of the HBE cultures, and β-cyclodextrin was essential for some of the coumarins to enter the cell and therefore to reach their targets.

Keywords: A549 cells; HBE culture; HEp-2 cells; RSV; coumarins; hesperetin.

MeSH terms

  • A549 Cells
  • Antiviral Agents* / chemistry
  • Antiviral Agents* / pharmacology
  • Cell Survival / drug effects
  • Coumarins* / chemistry
  • Coumarins* / pharmacology
  • Hesperidin* / chemistry
  • Hesperidin* / pharmacology
  • Humans
  • Respiratory Syncytial Virus Infections* / drug therapy
  • Respiratory Syncytial Virus Infections* / virology
  • Respiratory Syncytial Virus, Human* / drug effects
  • Umbelliferones / chemistry
  • Umbelliferones / pharmacology
  • Virus Replication* / drug effects
  • beta-Cyclodextrins / chemistry
  • beta-Cyclodextrins / pharmacology

Substances

  • hesperetin
  • Coumarins
  • Hesperidin
  • Antiviral Agents
  • Umbelliferones
  • beta-Cyclodextrins
  • esculetin

Grants and funding

This research received no external funding.