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Effects of surface-bound and intravenously administered heparin on cell-surface interactions: Inflammation and coagulation

机译:表面结合和静脉内给予肝素对细胞-表面相互作用的影响:炎症和凝血

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Intravenous administration of heparin and heparin-bonded extracorporeal circuits are frequently used to mitigate the deleterious effects of blood contact with synthetic materials. The work described here utilized human blood in a micro-perfusion circuit to experimentally examine the effects of intravenous and surface-bound heparin on cellular activation. Activation markers of coagulation and of the inflammatory response were examined using flow cytometry; specifically, markers of platelet, monocyte, polymorphonuclear leukocyte (PMN), and lymphocyte activation were quantified. The results indicate that surface-bound heparin reduces the inflammatory response whereas systemically administered heparin does not. This finding has important implications for blood-contacting devices, particularly within the context of recently elucidated connections between inflammation pathways and coagulation disorders. Data presented indicate that surface-bound heparin and intravenously administered heparin play distinct, but vital roles in rendering biomaterial surfaces compatible with blood.
机译:静脉内给予肝素和与肝素结合的体外回路通常用于减轻血液与合成材料的接触所产生的有害影响。此处描述的工作是在微灌注回路中利用人体血液来实验性地检查静脉内和表面结合的肝素对细胞活化的影响。使用流式细胞仪检测凝血和炎症反应的激活标志物。具体来说,对血小板,单核细胞,多形核白细胞(PMN)和淋巴细胞活化的标记物进行了定量。结果表明,表面结合的肝素可降低炎症反应,而全身给药的肝素则不能。这一发现对血液接触设备具有重要意义,特别是在最近阐明的炎症途径与凝血功能障碍之间的联系的背景下。所提供的数据表明,表面结合的肝素和静脉内给予的肝素在使生物材料表面与血液相容方面起着独特但至关重要的作用。

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