Anti-inflammatory activity and sub-acute toxicity of artemetin

Planta Med. 1990 Feb;56(1):36-40. doi: 10.1055/s-2006-960879.

Abstract

The 5-hydroxy-3,6,7,3',4'-pentamethoxyflavone (artemetin) from Cordia verbenacea DC (Boraginaceae) showed marked anti-inflammatory activity using various experimental models in rats. Artemetin significantly inhibited carrageenin-induced paw edema following oral doses from 30.4 to 153.9 mg.kg-1. The doses of 102.6 and 153.9 mg.kg-1 showed an inhibitory effect similar to that of 50.0 mg.kg-1 of calcium phenylbutazone. The ED50 value of artemetin in rats was estimated to be 67.07 mg.kg-1. Repeated administration of artemetin at doses of 67.07 mg.kg-1 for a 6-day period reduced granuloma formation with a response comparable to that of 20.0 mg.kg-1 of calcium phenylbutazone. This same dose of artemetin also reduced the vascular permeability to intracutaneous histamine. Sub-acute toxicological experiments indicated a very low toxicity.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal*
  • Flavonoids / isolation & purification
  • Flavonoids / pharmacology*
  • Flavonoids / toxicity
  • Male
  • Plants, Medicinal / analysis*
  • Rats
  • Rats, Inbred Strains

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Flavonoids
  • artemetin