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对血管性血友病因子、血小板糖蛋白Ib和IIb-IIIa以及储存颗粒缺乏患者出血时间血液中的血栓素B2、血小板因子4和纤维蛋白肽A的研究。

Studies of thromboxane B2, platelet factor 4, and fibrinopeptide A in bleeding-time blood of patients deficient in von Willebrand factor, platelet glycoproteins Ib and IIb-IIIa, and storage granules.

作者信息

Weiss H J, Lages B

机构信息

Department of Medicine (Division of Hematology-Oncology), St Luke's-Roosevelt Hospital Center, New York, NY 10019.

出版信息

Blood. 1993 Jul 15;82(2):481-90.

PMID:8329704
Abstract

The blood volumes and concentrations of thromboxane B2 (TxB2), platelet factor 4 (PF4), and fibrinopeptide A (FPA) were measured every 30 seconds in bleeding-time blood in normal subjects and in patients with idiopathic thrombocytopenic purpura (ITP), delta and alpha delta storage pool deficiency (SPD), Bernard-Soulier Syndrome (BSS), thrombasthenia (TSA), and von Willebrand's disease (vWD). Data were fitted to second-order (TxB2, PF4, and FPA) or third-order (volumes) polynomials. Average values for various parameters over fixed-time intervals were determined by numerical methods. The bleeding time was greater than 15 minutes in all patient groups and the initial bleeding, as reflected by the initial slope of the fitted blood volume curves, was increased in ITP, BSS, and SPD (delta-SPD in particular), but not in vWD and TSA. The increased values for both the initial slope and the volume of blood collected after 2 minutes in SPD suggest that vascular tone may be modulated, in part, by dense granule substances such as adenosine triphosphate (ATP) or serotonin. In TSA, uniquely, both platelet (TxB2 and PF4) and coagulation (FPA) values were increased in early bleeding samples (initial slope). In vitro studies of TxB2 production, together with previous flow studies of fibrin formation, also suggest enhanced activation and coagulant properties of thrombasthenic platelets. In other patients, reduced values of all substances at later times may reflect impaired platelet-fibrin plug formation in the high-shear regions at the ends of transected blood vessels. However, the initial slopes of the fitted curves for both TxB2 and PF4 were normal in vWD, suggesting that the early appearance of these substances may typically be from platelets that are adherent to collagen within the lower shear environment of the wound surface. The finding that FPA values were not decreased initially in any patient group, including ITP, but were decreased at later times (except for TSA), suggests that early fibrin formation occurs independently of platelets in the low-shear environment of the wound surface, whereas at later times fibrin is formed in a platelet-dependent manner in the high-shear regions at the ends of transected vessels.

摘要

在正常受试者以及患有特发性血小板减少性紫癜(ITP)、δ和αδ贮存池缺乏症(SPD)、伯纳德 - 索利尔综合征(BSS)、血小板无力症(TSA)和血管性血友病(vWD)的患者中,每隔30秒测量出血时间血液中的血容量以及血栓素B2(TxB2)、血小板第4因子(PF4)和纤维蛋白肽A(FPA)的浓度。数据拟合为二阶多项式(TxB2、PF4和FPA)或三阶多项式(血容量)。通过数值方法确定固定时间间隔内各种参数的平均值。所有患者组的出血时间均大于15分钟,并且如拟合血容量曲线的初始斜率所反映的,初始出血在ITP、BSS和SPD(特别是δ - SPD)中增加,但在vWD和TSA中未增加。SPD中2分钟后初始斜率和收集的血液量增加的值表明,血管张力可能部分受致密颗粒物质如三磷酸腺苷(ATP)或5 - 羟色胺调节。在TSA中,独特的是,早期出血样本(初始斜率)中血小板(TxB2和PF4)和凝血(FPA)值均增加。TxB2产生的体外研究以及先前关于纤维蛋白形成的血流研究也表明血小板无力症患者的血小板活化增强和凝血特性增强。在其他患者中,后期所有物质的值降低可能反映了在横断血管末端的高剪切区域中血小板 - 纤维蛋白凝块形成受损。然而,vWD中TxB2和PF4拟合曲线的初始斜率正常,这表明这些物质的早期出现通常可能来自在伤口表面较低剪切环境中粘附于胶原蛋白的血小板。在包括ITP在内的任何患者组中,FPA值最初均未降低,但在后期(TSA除外)降低,这一发现表明,在伤口表面的低剪切环境中,早期纤维蛋白形成独立于血小板发生,而在后期,在横断血管末端的高剪切区域中,纤维蛋白以血小板依赖的方式形成。

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