Hepoxilin A3 Induces Vascular Permeability in the Skin

  • Odette Laneuville
  • Cecil R. Pace-Asciak
Part of the GWUMC Department of Biochemistry Annual Spring Symposia book series (GWUN)

Abstract

Hepoxilins are 11S,12S-epoxy-8(R,S)-hydroxy metabolites of arachidonic acid formed through the 12-lipoxygenase pathway from the intermediate, 12S-HPETE (1, 2). Evidence to date shows that the hepoxilins are formed through an Fe+3 catalysed rearrangement of 12-HPETE, which although retaining both oxygen atoms of 12-HPETE through an intramolecular isomerisation, the hydroxyl group at carbon 8 is racemic (3, 4). During the past few years we have been interested in profiling the biological properties of the 8R and 8S isomers of HxA3. The present report demonstrates that the hepoxilins are active in causing vascular permeability in the rat skin, and although they are not powerful on their own, they greatly potentiate the actions of subthreshold concentrations of bradykinin.

Keywords

Arachidonic Acid Vascular Permeability Evans Blue Dorsal Skin Hydroxy Metabolite 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 1991

Authors and Affiliations

  • Odette Laneuville
    • 1
    • 2
  • Cecil R. Pace-Asciak
    • 1
    • 2
  1. 1.Research InstituteHospital for Sick ChildrenTorontoCanada
  2. 2.Department of PharmacologyUniversity of TorontoCanada

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