Effect of ginsenoside Rb1 and compound K in chronic oxazolone-induced mouse dermatitis

Int Immunopharmacol. 2005 Jul;5(7-8):1183-91. doi: 10.1016/j.intimp.2005.02.016. Epub 2005 Mar 31.

Abstract

During the screening program to discover antipsoriatic agents from natural products, ginseng was found to show inhibitory activity in oxazolone-induced mouse ear dermatitis. Therefore, the effects of a main constituent ginsenoside Rb1 isolated from ginseng and its metabolite compound K on oxazolone-induced mouse ear dermatitis were investigated. Compound K at concentrations of 0.02% and 0.05% also potently suppressed mouse ear swelling by 54% and 76% at 16 days, respectively, although ginsenoside Rb1 did not significantly show the inhibitory activity. The compound K also significantly reduced the levels of mRNA of cyclooxygenase (COX)-2, IL-1beta, TNF-alpha, IFN-gamma and IL-4 increased in oxazolone-applied mouse ears. Based on these findings, the compound K may improve contact dermatitis or psoriasis by the regulation of COX-2 produced by macrophage cells and interferon-gamma and IL-4 induced by Th cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Chronic Disease
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Dermatitis, Contact / drug therapy*
  • Dinoprostone / biosynthesis
  • Female
  • Ginsenosides / therapeutic use*
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Membrane Proteins
  • Mice
  • Mice, Inbred ICR
  • Nitric Oxide / biosynthesis
  • Oxazolone / toxicity*
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Psoriasis / drug therapy*
  • RNA, Messenger / analysis

Substances

  • Ginsenosides
  • Membrane Proteins
  • RNA, Messenger
  • Oxazolone
  • Nitric Oxide
  • ginsenoside Rb1
  • ginsenoside M1
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Ptgs1 protein, mouse
  • Dinoprostone