Low levels of hydrogen peroxide enhance platelet aggregation by cyclooxygenase activation.

Eicosanoids Pub Date : 1991-01-01
G Hecker, J Utz, R J Kupferschmidt, V Ullrich
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Abstract

Platelet aggregation can be triggered by addition of exogenous arachidonate owing to its conversion to endoperoxides and thromboxane A2. The dose-response curve of arachidonate-induced platelet aggregation exhibited a very steep slope. Simultaneous addition of H2O2 (1-200 microM) significantly shifted this curve to the left. H2O2 alone did not induce aggregation up to a concentration of 1 mM; however, a reversible increase of cytoplasmic Ca2+ and a small increase of the thromboxane levels could be observed. In the presence of exogenous arachidonate H2O2 led to an increased formation of arachidonate metabolites. Our data demonstrate that at threshold levels of 20:4 H2O2 is able to promote conversion of 20:4 to proaggregatory prostaglandin endoperoxides, and subsequently platelet activation is facilitated. Thus we support the evidence for a role of H2O2 in the activation of cyclooxygenase possibly by providing an adequate peroxide tone.

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低水平的过氧化氢通过环加氧酶激活增强血小板聚集。
由于外源性花生四烯酸酯转化为内过氧化物和凝血素A2,可以通过添加外源性花生四烯酸酯触发血小板聚集。花生四烯酸酯诱导血小板聚集的剂量-反应曲线呈现非常陡峭的斜率。同时加入H2O2(1-200微米)显著地使曲线向左移动。单独H2O2不能诱导聚集至1 mM;然而,可以观察到细胞质Ca2+的可逆增加和血栓素水平的小幅增加。在外源花生四烯酸存在的情况下,H2O2导致花生四烯酸代谢物的形成增加。我们的数据表明,在20:4的阈值水平下,H2O2能够促进20:4转化为促聚集性前列腺素内过氧化物,随后促进血小板活化。因此,我们支持H2O2在环加氧酶激活中的作用的证据,可能是通过提供足够的过氧化氢。
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