Ketoconazole inhibits the biosynthesis of leukotrienes in vitro and in vivo

Biochem Pharmacol. 1986 Mar 15;35(6):883-91. doi: 10.1016/0006-2952(86)90072-9.

Abstract

Ketoconazole inhibits in vitro (IC50:2.6 X 10(-5) M) the formation of 5-HETE and LTB4 by isolated, carrageenin-elicited rat peritoneal PMN leukocytes, challenged with the Ca2+-ionophore A23187 in the presence of [14C]-arachidonic acid ([14C]-AA). The relative potency of various compounds tested in this respect is NDGA greater than nafazatrom greater than phenidone greater than ketoconazole greater than BW 755C. In contrast to the other compounds studies, ketoconazole in vitro, up to 1 X 10(-4) M, has no effect on the fatty acid cyclo-oxygenase or the 12-lipoxygenase-mediated metabolism of [14C]-AA by isolated human platelets; however, it stimulates the 15-lipoxygenase activity in phenylhydrazine-induced rabbit reticulocytes. After oral administration (10-40 mg/kg, -2 hr), ketoconazole inhibits in a dose-dependent way, the leukotriene-mediated anaphylactic bronchoconstriction in guinea pigs. This study demonstrates that ketoconazole is a comparatively specific and orally active inhibitor of the 5-lipoxygenase activity bearing on the production of leukotrienes derived from arachidonic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid
  • 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine
  • Animals
  • Antigens / immunology
  • Arachidonate Lipoxygenases
  • Arachidonic Acid
  • Arachidonic Acids / metabolism
  • Blood Platelets / metabolism
  • Bronchi / drug effects
  • Catechols / pharmacology
  • Cyclooxygenase Inhibitors
  • Cytochrome P-450 Enzyme Inhibitors
  • Dose-Response Relationship, Drug
  • Guinea Pigs
  • Humans
  • Hydroxyeicosatetraenoic Acids / biosynthesis
  • In Vitro Techniques
  • Ketoconazole / pharmacology*
  • Leukotriene B4 / biosynthesis*
  • Lipoxygenase Inhibitors
  • Male
  • Masoprocol
  • Neutrophils / metabolism
  • Pyrazoles / pharmacology
  • Rabbits
  • Rats
  • Rats, Inbred Strains
  • Reticulocytes / metabolism
  • SRS-A / biosynthesis*

Substances

  • Antigens
  • Arachidonic Acids
  • Catechols
  • Cyclooxygenase Inhibitors
  • Cytochrome P-450 Enzyme Inhibitors
  • Hydroxyeicosatetraenoic Acids
  • Lipoxygenase Inhibitors
  • Pyrazoles
  • SRS-A
  • Leukotriene B4
  • Arachidonic Acid
  • 5-hydroxy-6,8,11,14-eicosatetraenoic acid
  • 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid
  • 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine
  • 15-hydroxy-5,8,11,13-eicosatetraenoic acid
  • Masoprocol
  • Arachidonate Lipoxygenases
  • Ketoconazole