Effects of six diterpenes on macrophage eicosanoid biosynthesis

Life Sci. 2001 Dec 7;70(3):269-78. doi: 10.1016/s0024-3205(01)01402-3.

Abstract

Six diterpenes (three clerodanes, two abietanes and one rosane) were tested for interactions with the cyclooxygenase and 5-lipoxygenase pathways of arachidonate metabolism and for effects of nitric oxide production. Two abietane diterpenes, aethiopinone and 11,12-dihydroxy-6-oxo-8,11,13-abietatriene and the rosane lagascatriol showed a remarkable effect on COX-1 pathway of PGE2 release in calcium ionophore A23187-stimulated peritoneal macrophages. Only the two latter diterpenes showed inhibition on COX-2 pathway of PGE2 release in E. coli LPS-stimulated peritoneal macrophages. In addition, all compounds assayed were inhibitors of LTC4 release with IC50 < or = 10 microM. Clerodane diterpenes were inactive in COX assay. None of the diterpenes assayed, except 11,12-dihydroxy-6-oxo-8,11,13-abietatriene, affected NO production. The results obtained suggest that the cellular mechanisms of action of some of these substances may involve inhibition of cyclooxygenase/lipoxygenase pathways and nitric oxide production.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Cyclooxygenase 2
  • Dinoprostone / biosynthesis
  • Diterpenes / pharmacology*
  • Eicosanoids / biosynthesis*
  • Isoenzymes / metabolism
  • Leukotriene C4 / biosynthesis
  • Macrophages, Peritoneal / drug effects*
  • Macrophages, Peritoneal / metabolism
  • Male
  • Mice
  • Nitric Oxide / biosynthesis
  • Nitric Oxide Synthase / metabolism
  • Prostaglandin-Endoperoxide Synthases / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Diterpenes
  • Eicosanoids
  • Isoenzymes
  • Leukotriene C4
  • Nitric Oxide
  • Nitric Oxide Synthase
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Dinoprostone