In vivo stimulation of 12( S)-lipoxygenase in the rat skin by bradykinin and platelet activating factor: formation of 12( S)-HETE and hepoxilins, and actions on vascular permeability

• Published in: Biochimica et biophysica acta. Molecular and cell biology of lipids 1999-01, Vol.1436 (3), p.354-362
• Main Authors: Wang, Mei Mei, Reynaud, Denis, Pace-Asciak, Cecil R.
• Format: Article
• Language: English
• Subjects: 12( S)-Hydroxy-eicosatetraenoic acid; Bradykinin; Chirality; Epidermis; Formation; Hepoxilin; Platelet activating factor; Vascular permeability
• ISSN: 1388-1981; 1879-2618
• DOI: 10.1016/S0005-2760(98)00128-3

In this study we set out to investigate whether the inflammatory agents, bradykinin (BK) and platelet activating factor (PAF), affect the lipoxygenase pathway in rat skin in vivo and whether the main products so formed may be involved in the inflammatory actions of these agents. In vitro preparations of epidermis were also investigated to determine whether lipoxygenases are stimulated by these agents. We also investigated the actions of arachidonic acid and 12( S)-HPETE as substrates for the lipoxygenases. Our results indicated that 12-lipoxygenase is actively and selectively stimulated in a dose-dependent way in both preparations by the administration of BK and PAF; the main product, 12-HETE, was shown by chiral analysis to be exclusively of the S-configuration, indicating that 12( S)-lipoxygenase was present in the rat skin and was stimulated by these inflammatory agents. Hepoxilins were also formed but to a lesser extent in both in vivo and in vitro preparations. In separate experiments, 12( S)-HETE administered intradermally on its own (40 ng/site), increased vascular permeability as also seen with bradykinin (100 ng/site) and PAF (10 ng/site). However, unlike previously observed with hepoxilin A 3 administration, 12( S)-HETE did not stimulate the action of BK on vascular permeability, suggesting that the two compounds may have different mechanisms of action to enhance inflammation. These observations suggest that the vascular permeability and plasma extravasation observed with both inflammatory agents (BK and PAF) may be mediated at least in part through the activation of 12( S)-lipoxygenase, resulting in enhanced formation of 12( S)-HETE which causes acute inflammation.