Gerrard J M, Singhroy S, Duta E, Nosek-Cenkowska B, Israels S J, Israels E D
Department of Pediatrics, University of Manitoba, Winnipeg, Canada.
Thromb Res. 1990 Oct 1;60(1):79-85. doi: 10.1016/0049-3848(90)90342-a.
The production of thomboxane B2, the primary metabolite of thromboxane A2, and 6-keto prostaglandin F1 alpha, the primary metabolite of prostacyclin, were measured in response to a standardized vascular injury, the bleeding time, in patients with von Willebrand's disease and in patients with platelet function defects. Compared to controls, thromboxane B2 levels in bleeding time blood were significantly lower in subjects with von Willebrand's disease. In patients with platelet function defects associated with a deficient response to thromboxane A2, thromboxane B2 production in bleeding time blood was similar to controls. In subjects with other platelet function defects, thromboxane production was significantly lower than normal. 6-keto PGF1 alpha production in bleeding time blood was not significantly different in patients compared to controls. The results suggest that bleeding time thromboxane production is influenced by the extent of platelet-vessel interaction.
在血管性血友病患者和血小板功能缺陷患者中,针对标准化血管损伤(出血时间),检测了血栓素A2的主要代谢产物血栓素B2以及前列环素的主要代谢产物6-酮-前列腺素F1α的生成情况。与对照组相比,血管性血友病患者出血时间血液中的血栓素B2水平显著降低。在对血栓素A2反应不足而导致血小板功能缺陷的患者中,出血时间血液中的血栓素B2生成与对照组相似。在患有其他血小板功能缺陷的受试者中,血栓素生成显著低于正常水平。与对照组相比,患者出血时间血液中的6-酮-前列腺素F1α生成无显著差异。结果表明,出血时间时血栓素的生成受血小板与血管相互作用程度的影响。