Effects of pyridoxalated polyhemoglobin and stroma-free hemoglobin on ADP-induced platelet aggregation.

F R Lalla, J Ning, T M Chang
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引用次数: 10

Abstract

Although polyhemoglobin produced from homologous sources is not immunogenic when utilized in vivo (1), effects on hemostasis and thrombosis have not been documented. In this study, we use rat platelet rich plasma (PRP) and light transmission aggregometry to measure the possible influence of stroma-free hemoglobin (SFHb) and pyridoxalated polyhemoglobin (PP-PolyHb) on platelet aggregation in response to various levels of adenosine triphosphate (ADP) activation in vitro. Our study demonstrates that PP-PolyHb and SFHb solutions, when added to PRP in volumes and concentrations likely to be administered to patients requiring perfusant therapy, do not initiate or facilitate platelet activation. Both solutions induce similar levels of aggregation (and presumably activation) inhibition, but do so only at high or maximal levels of ADP activator stimulation, late in the aggregation sequence. The apparent inability of the purified hemoglobins to stimulate platelets is a necessary characteristic if such preparations are to be used as clinical perfusants in hemorrhagic emergencies.

吡哆醛化多血红蛋白和无基质血红蛋白对adp诱导的血小板聚集的影响。
虽然同源来源产生的多血红蛋白在体内使用时不具有免疫原性(1),但对止血和血栓形成的影响尚未有文献记载。在这项研究中,我们使用大鼠富血小板血浆(PRP)和光透射聚集法来测量无基质血红蛋白(SFHb)和吡脲醛化多血红蛋白(PP-PolyHb)对血小板聚集的可能影响,以响应不同水平的三磷酸腺苷(ADP)的体外激活。我们的研究表明,当将PP-PolyHb和SFHb溶液以可能用于需要灌注治疗的患者的体积和浓度添加到PRP中时,不会启动或促进血小板激活。两种溶液都能诱导相似水平的聚集(和可能的激活)抑制,但只有在ADP激活剂刺激的高或最大水平时,在聚集序列的后期才会产生这种抑制。纯化的血红蛋白明显不能刺激血小板,如果这种制剂在出血紧急情况下用作临床灌注剂,这是一个必要的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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