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血小板活化因子受体拮抗剂SM - 12502对人血小板的作用。

Effect of the PAF-receptor antagonist SM-12502 on human platelets.

作者信息

Köller M, Hilger R A, König W

机构信息

Lehrstuhl für Medizinische Mikrobiologie und Immunologie, Ruhr-Universität Bochum, Germany.

出版信息

Inflammation. 1996 Feb;20(1):71-85. doi: 10.1007/BF01487746.

Abstract

We analyzed the effect of the PAF receptor antagonist (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502) on human platelet aggregation as well as mediator release. After incubation of human platelet with different concentrations of SM-12502 the cells were subsequently stimulated with either the Ca ionophore A23187, with human thrombin, or with an activator of heterotrimeric G-proteins, sodium fluoride (NaF, in the presence of Al3+). Preincubation of platelets with the PAF receptor antagonist led to an inhibition of 12-lipoxygenase derived 12(S)-HETE and cyclooxygenase derived 12(S)-HHT. Pretreatment of platelets with the PAF receptor antagonist SM-12502 prior to activation with the Ca ionophore A23187 or PAF also inhibited platelet aggregation. Our data clearly indicate an inhibitory effect of the new PAF receptor antagonist SM-12502 on the formation of platelet derived inflammatory mediators of the lipoxygenase pathway as well as of the cyclooxygenase pathway, and furtherone, treatment with the PAF receptor antagonist diminished platelet aggregation after subsequent specific and unspecific activation.

摘要

我们分析了血小板活化因子(PAF)受体拮抗剂(+)-顺式-3,5-二甲基-2-(3-吡啶基)噻唑烷-4-酮盐酸盐(SM-12502)对人血小板聚集以及介质释放的影响。将人血小板与不同浓度的SM-12502孵育后,随后用钙离子载体A23187、人凝血酶或异源三聚体G蛋白激活剂氟化钠(NaF,在Al3+存在下)刺激细胞。血小板与PAF受体拮抗剂预孵育导致12-脂氧合酶衍生的12(S)-HETE和环氧化酶衍生的12(S)-HHT受到抑制。在用钙离子载体A23187或PAF激活之前,用PAF受体拮抗剂SM-12502预处理血小板也可抑制血小板聚集。我们的数据清楚地表明,新型PAF受体拮抗剂SM-12502对脂氧合酶途径以及环氧化酶途径的血小板衍生炎症介质的形成具有抑制作用,此外,用PAF受体拮抗剂处理可减少随后特异性和非特异性激活后的血小板聚集。

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