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用氯克罗孟(一种磷脂酶A2激活抑制剂)抑制受刺激的人多形核白细胞合成血小板活化因子。

Inhibition of PAF synthesis by stimulated human polymorphonuclear leucocytes with cloricromene, an inhibitor of phospholipase A2 activation.

作者信息

Ribaldi E, Mezzasoma A M, Francescangeli E, Prosdocimi M, Nenci G G, Goracci G, Gresele P

机构信息

Institute of Internal and Vascular Medicine, University of Perugia, Italy.

出版信息

Br J Pharmacol. 1996 Jul;118(6):1351-8. doi: 10.1111/j.1476-5381.1996.tb15544.x.

Abstract
  1. A phospholipase A2 (PLA2) represents the key enzyme in the remodelling pathway of platelet-activating factor (PAF) synthesis in human polymorphonuclear (PMN) leucocytes. 2. PLA2 activation is also the rate-limiting step for the release of the arachidonic acid utilized for the synthesis of leukotrienes in stimulated leucocytes; however, it is unknown whether the PLA2s involved in the two biosynthetic pathways are identical. 3. Cloricromene (8-monochloro-3-beta-diethylaminoethyl-4-methyl-7-ethoxy- carbonylmethoxy coumarin) is an antithrombotic coumarin derivative which inhibits platelet and leucocyte function and suppresses arachidonic acid liberation by interfering with PLA2 activation. 4. The aim of the present study was to assess whether chloricromene inhibits PAF synthesis by stimulated human polymorphonuclear leucocytes (PMNs). 5. Cloricromene (50-500 microM) inhibited in a concentration-dependent manner the release of PAF, as measured by h.p.l.c. bioassay, from A23187-stimulated PMNs. Significant inhibition (45%) of PAF-release was obtained with 50 microM cloricromene and the IC50 was 85 microM. Mepacrine (500 microM), a non-specific PLA2 inhibitor, strikingly reduced PAF release. 6. The incorporation of [3H]-acetate into [3H]-PAF induced by serum-treated zymosan in human PMNs was also inhibited concentration-dependently by cloricromene, with an IC50 of 105 microM. Mepacrine also suppressed [3H]-acetate incorporation into [3H]-PAF. 7. Cloricromene did not affect the activities of the enzymes involved in PAF-synthesis acetyltransferase or phosphocholine transferase. 8. Our data demonstrate that cloricromene, an inhibitor of PLA2-activation in human leucocytes, reduces the synthesis of PAF by stimulated PMNs. This finding has a twofold implication: the PLA2s (or the mechanisms that regulate their activation) involved in PAF synthesis and arachidonate release in human leucocytes are either identical or else indistinguishable by their sensitivity to cloricromene; the inhibition of PAF release by activated leucocytes may contribute to the antithrombotic and anti-ischaemic activities exerted by cloricromene.
摘要
  1. 磷脂酶A2(PLA2)是人类多形核(PMN)白细胞中血小板活化因子(PAF)合成重塑途径中的关键酶。2. PLA2激活也是刺激白细胞中用于白三烯合成的花生四烯酸释放的限速步骤;然而,参与这两条生物合成途径的PLA2是否相同尚不清楚。3. 氯克罗孟(8-单氯-3-β-二乙氨基乙基-4-甲基-7-乙氧基羰基甲氧基香豆素)是一种抗血栓香豆素衍生物,它通过干扰PLA2激活来抑制血小板和白细胞功能,并抑制花生四烯酸释放。4. 本研究的目的是评估氯克罗孟是否能抑制受刺激的人类多形核白细胞(PMN)合成PAF。5. 氯克罗孟(50 - 500微摩尔)以浓度依赖的方式抑制了通过高效液相色谱生物测定法测定的A23187刺激的PMN中PAF的释放。50微摩尔氯克罗孟可显著抑制(45%)PAF释放,IC50为85微摩尔。非特异性PLA2抑制剂米帕林(500微摩尔)显著降低了PAF释放。6. 氯克罗孟还以浓度依赖的方式抑制了血清处理的酵母聚糖在人类PMN中诱导的[3H] - 乙酸掺入[3H] - PAF,IC50为105微摩尔。米帕林也抑制了[3H] - 乙酸掺入[3H] - PAF。7. 氯克罗孟不影响参与PAF合成的乙酰转移酶或磷酸胆碱转移酶的活性。8. 我们的数据表明,氯克罗孟作为人类白细胞中PLA2激活的抑制剂,可减少受刺激的PMN合成PAF。这一发现有双重意义:参与人类白细胞中PAF合成和花生四烯酸释放的PLA2(或调节其激活的机制)要么相同,要么对氯克罗孟的敏感性无法区分;活化白细胞对PAF释放的抑制可能有助于氯克罗孟发挥抗血栓和抗缺血活性。

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