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The effect of inhibition of leukotriene synthesis on the activity of interleukin-8 and granulocyte-macrophage colony-stimulating factor

机译:白三烯合成抑制对白细胞介素8和粒细胞巨噬细胞集落刺激因子活性的影响

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摘要

The cytokines interleukin-8 (IL-8) and granulocyte-macrophage colony-stimulating factor (GM-CSF) enhanced the extracellular release of arachidonate metabolites from ionophore-stimulated neutrophils by 145 ± 10% (mean ± S.E.M., n = 13) and 182 ± 11% (n = 16), respectively. To determine whether enhanced leukotriene production mediates the effects of these cytokines on neutrophil activity, two different specific arachidonate 5-lipoxygenase (5-LO) inhibitors, piriprost and MK-886, were used to inhibit leukotriene synthesis. Neither inhibitor affected the upregulation of CD11b β2-integrin expression or priming of superoxide generation stimulated by IL-8 and GM-CSF. It is concluded that leukotrienes do not mediate either the direct or priming effects of these cytokines and that these classes of anti-inflammatory drugs are therefore unlikely to inhibit the effects of IL-8 and GM-CSF on neutrophil activation.
机译:细胞因子白介素8(IL-8)和粒细胞巨噬细胞集落刺激因子(GM-CSF)使离子载体刺激的中性粒细胞的花生四烯酸代谢物的细胞外释放增加145±10%(平均值±SEM,n = 13)和分别为182±11%(n = 16)。为了确定白三烯产量的增加是否能介导这些细胞因子对嗜中性粒细胞活性的影响,使用了两种不同的特异性花生四烯酸5-脂氧合酶(5-LO)抑制剂匹立前列素和MK-886来抑制白三烯的合成。两种抑制剂均未影响CD-8bβ2-整合素表达的上调或IL-8和GM-CSF刺激的超氧化物生成的启动。结论是白三烯不介导这些细胞因子的直接作用或引发作用,因此这些类型的抗炎药不太可能抑制IL-8和GM-CSF对嗜中性粒细胞活化的作用。

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