Selective inhibition of 5-lipoxygenase by natural compounds isolated from Chinese plants, Artemisia rubripes Nakai

FEBS Lett. 1983 Jul 11;158(1):41-4. doi: 10.1016/0014-5793(83)80672-3.

Abstract

Three of four natural compounds, which are caffeic acid, eupatilin and 4'-demethyleupatilin, isolated from Chinese plant, Artemisia rubripes Nakai selectively inhibited 5-lipoxygenase of cultured mastocytoma cells. Half-inhibition doses (ID50) for caffeic acid, eupatilin and 4'-demethyleupatilin were 3.7, 14 and 18 X 10(-6) M, respectively. The inhibition by caffeic acid was non-competitive types. Prostaglandin synthase activities were little inhibited by eupatilin and 4'-demethyleupatilin, but rather stimulated by caffeic acid. The formation of leukotriene C4 and D4 by mast tumor cells was almost completely suppressed by these compounds at 10(-4) M.

MeSH terms

  • Animals
  • Arachidonate Lipoxygenases
  • China
  • Clone Cells
  • Cyclooxygenase Inhibitors*
  • Lipoxygenase Inhibitors*
  • Mast-Cell Sarcoma / enzymology
  • Mice
  • Plant Extracts / pharmacology*
  • SRS-A / biosynthesis
  • Sarcoma, Experimental / enzymology

Substances

  • Cyclooxygenase Inhibitors
  • Lipoxygenase Inhibitors
  • Plant Extracts
  • SRS-A
  • Arachidonate Lipoxygenases