Inhibition of herpes simplex virus infection by tannins and related compounds

Antiviral Res. 1989 Jun-Jul;11(5-6):285-97. doi: 10.1016/0166-3542(89)90038-7.

Abstract

Several chemically defined plant extracts were investigated for their antiviral action on herpes simplex virus (HSV-1, HSV-2)-infected African green monkey kidney cells and human adenocarcinoma cells, using a plaque formation assay. Among them, the monomeric hydrolyzable tannins, oligomeric ellagitannins and condensed tannins, having galloyl groups or hexahydroxydiphenoyl groups, had the most potent anti-HSV activity. Their 50% effective doses (0.03-0.1 microgram/ml) were by two-three orders of magnitude lower than their 50% cytotoxic doses (greater than 10 micrograms/ml). On the other hand, gallic acid, neutral polysaccharides, chemically modified (N,N-dimethylaminoethyl-, carboxymethyl-, and sulfated-) glucans, sialic acid-rich glycoproteins, and uronic acid-rich pine cone polysaccharide showed little or no activity. Using radiolabeled virus particles, we demonstrated that the anti-HSV effect of the tannins is due to inhibition of virus adsorption to the cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Animals
  • Antiviral Agents*
  • Cells, Cultured
  • Chemical Phenomena
  • Chemistry
  • Dose-Response Relationship, Drug
  • Humans
  • Molecular Structure
  • Plant Extracts / pharmacology
  • Polysaccharides / pharmacology
  • Simplexvirus / drug effects*
  • Tannins / pharmacology*
  • Viral Plaque Assay

Substances

  • Antiviral Agents
  • Plant Extracts
  • Polysaccharides
  • Tannins