Inhibition of leukotriene synthesis by honokiol in rat basophilic leukemia cells

Int Arch Allergy Immunol. 1996 Jul;110(3):278-81. doi: 10.1159/000237299.

Abstract

The effects of honokiol, a diphenyl compound extracted from a Chinese herbal medicine, on leukotriene (LT) synthesis were evaluated in rat basophilic leukemia (RBL) cells. The production of LTC4 and LTB4 stimulated by the Ca2+ ionophore A23187 was measured in RBL-1 cells by high-performance liquid chromatography. Honokiol inhibited the production of LTC4 and LTB4 stimulated by A23187 in RBL-1 cells. Honokiol did not inhibit either phospholipase A2 activity, measured by the release of 3H-arachidonic acid (AA), or LTC4 synthase and LTA4 hydrolase activities, measured with LTA4-free acid as substrate. The synthesis of LTC4 and LTB4 from AA in RBL-1 cell lysates in the presence of Ca2+ was inhibited by honokiol. These results indicate that honokiol blocks LT synthesis by inhibiting 5-lipoxygenase activity. Honokiol also inhibited immunoglobulin E-mediated production of these LTs in RBL-2H3 cells, which was measured by a specific radioimmunoassay (RIA). These results suggest that honokiol may exhibit antiallergic actions by inhibiting LT synthesis in immediate-type hyperreactivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Allergic Agents / pharmacology*
  • Biphenyl Compounds / pharmacology*
  • Leukemia, Basophilic, Acute / enzymology
  • Leukemia, Basophilic, Acute / metabolism*
  • Leukotriene Antagonists*
  • Leukotrienes / biosynthesis*
  • Lignans*
  • Rats
  • Tumor Cells, Cultured

Substances

  • Anti-Allergic Agents
  • Biphenyl Compounds
  • Leukotriene Antagonists
  • Leukotrienes
  • Lignans
  • honokiol