Hilger R A, Köller M, König W
Ruhr-Universität Bochum, Germany.
Inflammation. 1996 Feb;20(1):57-70. doi: 10.1007/BF01487745.
We analyzed the effect of the PAF receptor antagonist (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502) on the release of leukotriene B4 and IL-8 from human leukocytes. Peripheral blood from healthy donors was separated in two different fractions: polymorphonuclear leukocytes (PMN) and a lymphocyte, monocyte and basophil granulocyte cell fraction (LMB). After incubation of the cell population with different concentrations of SM-12502 the cells were subsequently stimulated with either the Ca ionophore A23187, the bacterial derived peptide fMLP, or with an activator of heterotrimetric G-proteins, the sodium fluoride (NaF, in the presence of Al3+). The PAF receptor antagonist led to a concentration and time dependent inhibition of LTB4 formation and IL-8 release from PMN and LMB. Our data clearly indicate an inhibitory effect of the PAF receptor antagonist SM-12502 on the formation of mediators of the lipoxygenase pathway and on the release of IL-8.
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)对人白细胞释放白三烯B4和白细胞介素-8的影响。将健康供体的外周血分离为两个不同部分:多形核白细胞(PMN)以及淋巴细胞、单核细胞和嗜碱性粒细胞组分(LMB)。在用不同浓度的SM-12502孵育细胞群体后,随后用钙离子载体A23187、细菌衍生肽fMLP或异三聚体G蛋白激活剂氟化钠(NaF,在Al3+存在下)刺激细胞。PAF受体拮抗剂导致PMN和LMB中白三烯B4生成和白细胞介素-8释放呈浓度和时间依赖性抑制。我们的数据清楚地表明PAF受体拮抗剂SM-12502对脂氧合酶途径介质的形成以及白细胞介素-8的释放具有抑制作用。