Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris

Planta Med. 2000 May;66(4):358-60. doi: 10.1055/s-2000-8531.

Abstract

The activity-guided fractionation of the extract of the herb of Prunella vulgaris (Labiatae) led to the isolation of four triterpenes, i.e., betulinic acid, ursolic acid, 2 alpha,3 alpha-dihydroxyurs-12-en-28-oic acid, and 2 alpha-hydroxyursolic acid. One of these compounds, 2 alpha,3 alpha-dihydroxyursolic acid, demonstrated significant inhibition on the release of beta-hexosaminidase from the cultured RBL-2H3 cells in a dose-dependent manner; the IC50 value was calculated to be 57 microM. When the isolated compounds were tested for their effects on the production of nitric oxide from cultured murine macrophages, RAW 264.7 cells, ursolic acid and 2 alpha-hydroxyursolic acid exhibited strong inhibitory activities (IC50 values, 17 and 27 microM, respectively).

Publication types

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

MeSH terms

  • Animals
  • Anti-Allergic Agents / pharmacology*
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Mast Cells / drug effects
  • Plants / chemistry*
  • Rats
  • Triterpenes / isolation & purification
  • Triterpenes / pharmacology*

Substances

  • Anti-Allergic Agents
  • Anti-Inflammatory Agents, Non-Steroidal
  • Triterpenes