COX-2 as possible target for the inhibition of PGE2 production by Rikko-san in activated macrophage

In Vivo. 2008 May-Jun;22(3):333-6.

Abstract

We have previously reported that Rikko-san (RKS) inhibited the lipopolysaccharide (LPS)-stimulated prostaglandin (PG) E2 in mouse macrophage-like RAW264.7 cells without affecting the expression of cyclooxygenase (COX)-2. Here RKS inhibition of the enzyme activity of both COX-1 and COX-2 proteins was investigated. Western blot analysis showed that RKS did not significantly change the S-nitrosylated COX-2 protein level. On the other hand, RKS inhibited the PG production catalyzed by purified COX-2, more effectively than that catalyzed by purified COX-1. These results suggest that RKS inhibits the PGE2 production by selectively inhibiting the COX-2 activity in activated macrophages.

MeSH terms

  • Animals
  • Cell Line
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase 2 Inhibitors / pharmacology*
  • Dinoprostone / biosynthesis*
  • Drugs, Chinese Herbal / pharmacology*
  • Macrophage Activation / drug effects*
  • Macrophages / drug effects*
  • Macrophages / metabolism*
  • Mice
  • Nitrogen / metabolism
  • Time Factors

Substances

  • Cyclooxygenase 2 Inhibitors
  • Drugs, Chinese Herbal
  • rikko-san
  • Cyclooxygenase 2
  • Dinoprostone
  • Nitrogen