Antiplasmodial activity of aryltetralone lignans from Holostylis reniformis

Antimicrob Agents Chemother. 2007 Jul;51(7):2346-50. doi: 10.1128/AAC.01344-06. Epub 2007 Apr 16.

Abstract

Extracts from Holostylis reniformis were tested in vivo against Plasmodium berghei and in vitro against a chloroquine-resistant strain of Plasmodium falciparum. The hexane extract of the roots was the most active, causing 67% reduction of parasitemia in vivo. From this extract, six lignans, including a new (7'R,8S,8'S)-3',4'-methylenedioxy-4,5-dimethoxy-2,7'-cyclolignan-7-one, were isolated and tested in vitro against P. falciparum. The three most active lignans showed 50% inhibitor concentrations of < or =0.32 microM. An evaluation of minimum lethal dose (30%) values showed low toxicity for these lignans in a hepatic cell line (Hep G2A16). Therefore, these compounds are potential candidates for the development of antimalarial drugs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimalarials / isolation & purification
  • Antimalarials / pharmacology*
  • Aristolochiaceae / chemistry*
  • Cell Line, Tumor
  • Chromatography, High Pressure Liquid
  • Circular Dichroism
  • Formazans / metabolism
  • Humans
  • Inhibitory Concentration 50
  • Lignans / chemistry
  • Lignans / pharmacology*
  • Mice
  • Molecular Conformation
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Parasitemia / drug therapy
  • Plant Extracts / chemistry
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology
  • Plant Roots / chemistry
  • Plasmodium berghei / drug effects
  • Plasmodium falciparum / drug effects
  • Spectrophotometry, Ultraviolet
  • Tetralones / chemistry
  • Tetralones / pharmacology*

Substances

  • Antimalarials
  • Formazans
  • Lignans
  • Plant Extracts
  • Tetralones