Occurrence of hepoxilins and trioxilins in psoriatic lesions

被引:27
作者
Antón, R
Puig, L
Esgleyes, T
de Moragas, JM
Vila, L
机构
[1] Inst Res, Lab Inflammat Mediators, Barcelona, Spain
[2] Santa Creu & Sant Pau Hosp, Dept Dermatol, Barcelona, Spain
关键词
arachidonic acid; eicosanoid; psoriasis; 12-lipoxygenase;
D O I
10.1046/j.1523-1747.1998.00159.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We recently found that normal human epidermis produces relatively high amounts of hepoxilins and trioxilins in vitro. Therefore, the aim of this study was to demonstrate the presence of these compounds in psoriatic lesions. Extracts front scales of patients with chronic stable plaque psoriasis were analyzed by a combination of high performance liquid chromatography and gas chromatography-mass spectrometry techniques, We found that the levels of hepoxilin B-3 were more than 16-fold higher in psoriatic scales than in normal epidermis (3.2 +/- 2.3 and < 0.2 ng per mg, respectively), whereas hepoxilin A(3) was not detected in ally sample, Trioxilins were semiquantitated and referred to 12-hydroxyeicosatetraenoic acid, ratios of trioxilins A(3) and B-3 12-hydroxyeicosatetraenoic acid in psoriatic lesions were 0.65 +/- 0.23 and 0.32 +/- 0.28, respectively, and they were not detected in normal epidermis, The presence of a great amount of trioxilin A(3) strongly suggests that hepoxilin A(3) was present in psoriatic lesions and it was totally degraded to trioxilin A(3), during the analysis procedure, Our results demonstrate that hepoxilins and trioxilins are produced by human skin in vivo and that the levels of these compounds are increased in psoriasis, The reported biologic activities of hepoxilins indicate that they could amplify and maintain the inflammatory response, Our results reinforce the idea that these compounds could play a role as mediators in the inflammatory response in skin, particularly in psoriasis.
引用
收藏
页码:303 / 310
页数:8
相关论文
共 60 条
[51]   Increased expression of inducible nitric oxide synthase in psoriatic skin and cytokine-stimulated cultured keratinocytes [J].
Sirsjo, A ;
Karlsson, M ;
Gidlof, A ;
Rollman, O ;
Torma, H .
BRITISH JOURNAL OF DERMATOLOGY, 1996, 134 (04) :643-648
[52]   EPIDERMAL CELL-POLYMORPHONUCLEAR LEUKOCYTE COOPERATION IN THE FORMATION OF LEUKOTRIENE-B4 BY TRANSCELLULAR BIOSYNTHESIS [J].
SOLA, J ;
GODESSART, N ;
VILA, L ;
PUIG, L ;
DEMORAGAS, JM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 98 (03) :333-339
[53]   LOCAL-EFFECTS OF SYNTHETIC LEUKOTRIENES (LTC4, LTD4, LTE4, AND LTB4) IN HUMAN-SKIN [J].
SOTER, NA ;
LEWIS, RA ;
COREY, EJ ;
AUSTEN, KF .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 80 (02) :115-119
[54]  
TAKAHASHI Y, 1993, J BIOL CHEM, V268, P16443
[55]   INTERLEUKIN-8 STIMULATES CALCIUM TRANSIENTS AND PROMOTES EPIDERMAL-CELL PROLIFERATION [J].
TUSCHIL, A ;
LAM, C ;
HASLBERGER, A ;
LINDLEY, I .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (03) :294-298
[56]   GENOMIC AND CDNA CLONING OF A NOVEL MOUSE LIPOXYGENASE GENE [J].
VANDIJK, KW ;
STEKETEE, K ;
HAVEKES, L ;
FRANTS, R ;
HOFKER, M .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1995, 1259 (01) :4-8
[57]   CYCLOOXYGENASE ACTIVITY IS INCREASED IN PLATELETS FROM PSORIATIC PATIENTS [J].
VILA, L ;
CULLARE, C ;
SOLA, J ;
PUIG, L ;
DECASTELLARNAU, C ;
DEMORAGAS, JM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (05) :922-926
[58]   CUTANEOUS INFLAMMATION - EFFECTS OF HYDROXY-ACIDS AND EICOSANOID PATHWAY INHIBITORS ON VASCULAR-PERMEABILITY [J].
WALDMAN, JS ;
MARCUS, AJ ;
SOTER, NA ;
LIM, HW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 92 (01) :112-116
[59]  
Wang MM, 1996, ADV EXP MED BIOL, V416, P239