Lee S H, Wainscoat J S, Zeitlin H, Bolton F G, Leaver H A, Seawright A, Preece J M
Br Med J (Clin Res Ed). 1981 Nov 21;283(6303):1351-2. doi: 10.1136/bmj.283.6303.1351.
A study was conducted to find whether a deficiency in prostacyclin (prostaglandin I2; PGI2) is implicated in the pathogenesis of thrombotic thrombocytopenic purpura. Plasma samples from two patients with the disease before treatment and from 22 healthy controls were therefore assayed for concentrations of 6-oxo-PGF1 alpha and thromboxane B2, the stable metabolites of PGI2 and thromboxane A2, respectively. Neither of the patients responded to treatment, which in one case included an infusion of PGI2. Both patients had normal concentrations of 6-oxo-PGF1 alpha and thromboxane B2, thus implying that circulating amounts of PGI2 and thromboxane A2 were also normal. These findings suggest that 6-oxo-PGF1 alpha may be detectable in normal amounts in thrombotic thrombocytopenic purpura and that the condition need not be associated with a high concentration of thromboxane A2.
开展了一项研究,以确定前列环素(前列腺素I2;PGI2)缺乏是否与血栓性血小板减少性紫癜的发病机制有关。因此,对两名血栓性血小板减少性紫癜患者治疗前的血浆样本以及22名健康对照者的血浆样本进行了检测,分别测定了6-氧代-PGF1α和血栓素B2的浓度,它们分别是PGI2和血栓素A2的稳定代谢产物。两名患者均对治疗无反应,其中一名患者的治疗包括输注PGI2。两名患者的6-氧代-PGF1α和血栓素B2浓度均正常,这意味着循环中的PGI2和血栓素A2含量也正常。这些发现表明,在血栓性血小板减少性紫癜患者中,6-氧代-PGF1α的含量可能正常,且该病不一定与高浓度的血栓素A2有关。