Ginkgetin, a Biflavone from Ginko biloba leaves, inhibits cyclooxygenases-2 and 5-lipoxygenase in mouse bone marrow-derived mast cells

Biol Pharm Bull. 2005 Dec;28(12):2181-4. doi: 10.1248/bpb.28.2181.

Abstract

Ginkgetin, a biflavone from Ginkgo biloba leaves, was previously reported to be a phospholipase A(2) inhibitor and this compound showed the potent antiarthritic activity in rat adjuvant-induced arthritis as well as analgesic activity. This investigation was carried out to find effects on cyclooxygenase-2 (COX-2) in vitro effect. Ginkgetin inhibits COX-2 dependent phases of prostaglandin D(2) (PGD(2)) generation in bone marrow-derived mast cells (BMMC) in a concentration-dependent manner with IC(50) values of 0.75 microM. Western blotting probed with specific anti-COX-2 antibodies showed that the decrease in quantity of the PGD(2) product was accompanied by a decrease in the COX-2 protein level. In addition, this compound consistently inhibited the production of leukotriene C(4) (LTC(4)) in a dose dependent manner, with an IC(50) value of 0.33 microM. These results demonstrate that ginkgetin has a dual cyclooxygenase-2/5-lipoxygenase inhibitory activity. Furthermore, this compound also inhibited degranulation reaction in a dose dependent manner, with an IC(50) value of 6.52 microM. Therefore, this compound might provide a basis for novel anti-inflammatory agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonate 5-Lipoxygenase / metabolism
  • Biflavonoids / chemistry
  • Biflavonoids / isolation & purification
  • Biflavonoids / pharmacology*
  • Bone Marrow Cells / drug effects*
  • Bone Marrow Cells / metabolism
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Cyclooxygenase 2 Inhibitors / chemistry
  • Cyclooxygenase 2 Inhibitors / pharmacology*
  • Dose-Response Relationship, Drug
  • Flavonoids / chemistry
  • Flavonoids / isolation & purification
  • Flavonoids / pharmacology*
  • Ginkgo biloba*
  • Interleukin-10 / pharmacology
  • Leukotriene C4 / antagonists & inhibitors
  • Leukotriene C4 / genetics
  • Leukotriene C4 / metabolism
  • Lipopolysaccharides / pharmacology
  • Lipoxygenase Inhibitors*
  • Male
  • Mast Cells / drug effects*
  • Mast Cells / metabolism
  • Mast Cells / pathology
  • Membrane Proteins / antagonists & inhibitors
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Plant Leaves
  • Prostaglandin D2 / antagonists & inhibitors
  • Prostaglandin D2 / metabolism
  • Up-Regulation
  • beta-N-Acetylhexosaminidases / antagonists & inhibitors
  • beta-N-Acetylhexosaminidases / metabolism

Substances

  • Biflavonoids
  • Cyclooxygenase 2 Inhibitors
  • Flavonoids
  • Lipopolysaccharides
  • Lipoxygenase Inhibitors
  • Membrane Proteins
  • Interleukin-10
  • Leukotriene C4
  • ginkgetin
  • Arachidonate 5-Lipoxygenase
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • beta-N-Acetylhexosaminidases
  • Prostaglandin D2