Generation of eicosanoids from 15(S)-hydroxyeicosatetraenoic acid in blood monocytes from steroid-dependent asthmatic patients

被引:6
作者
Chavis, C [1 ]
Vachier, I [1 ]
Bousquet, J [1 ]
Godard, P [1 ]
Chanez, P [1 ]
机构
[1] Hop Arnaud Villeneuve, INSERM, U454, F-34295 Montpellier 5, France
关键词
monocytes; asthma; corticosteroids; leukotriene B(4); 15(S)-HETE; lipoxins;
D O I
10.1016/S0006-2952(98)00086-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to investigate eicosanoid metabolism by human peripheral blood monocytes (PBM) from steroid-dependent asthmatic patients as compared to control subjects and untreated asthmatic patients. Eicosanoid biosynthesis by PBM isolated from venous blood using Percoll gradient centrifugation was evaluated following stimulation of 5 x 10(6) cells with calcium ionophore A23187, with or without exogenous 15(S)-hydroxpeicosatetraenoic acid (15(S) HETE), and analyzed by reverse phase high performance liquid chromatography (RP-HPLC). Without 15(S)-HETE, PBM synthesized leukotriene B(4) (LTB(4)) only (40 +/- 12 ng and 59 +/- 11 ng for untreated and steroid-dependent asthmatics, respectively). In the presence of 15(S) HETE, PBM produced six-fold smaller amounts of leukotriene B(4) (P < 0.0001). They also released 5(S),15(S)-dihydroxyeicosatetraenoic acid (5(S),15(S)-diHETE) in similar amounts for all the populations, whereas low amounts of lipoxins (LXs) were produced by PBM from asthmatics only (2.7 +/- 0.7 ng and 4.6 +/- 2.8 ng for untreated and steroid dependent asthmatics, respectively). Moreover, PBM were also able to release an unknown compound containing conjugated triene chromophore. Cells from steroid dependent asthmatic patients synthesized this unknown metabolite in higher amounts than controls and untreated asthmatics (133 +/- 18 ng vs 52 +/- 19 ng and 68 +/- 15 ng, respectively, P < 0.02). This work shows for the first time that human PBM are able to metabolize 15(S)-HETE and lead to lipoxins and to an unknown metabolite, with the amounts of the latter being enhanced by long-term corticosteroid treatment, BIOCHEM PHARMACOL 56;4:535-541, 1998. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:535 / 541
页数:7
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