首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Hyperacute renal allograft rejection in the primate. Therapeutic limitations of antiplatelet agents alone and combined with heparin.
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Hyperacute renal allograft rejection in the primate. Therapeutic limitations of antiplatelet agents alone and combined with heparin.

机译:灵长类动物的超急性肾移植排斥反应。单独和与肝素联合使用抗血小板药的治疗局限性。

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摘要

Two antiplatelet drugs, pyridinolcarbamate and Sudoxicam, were tested separately and in combination with heparin for their ability to modify experimental hyperacute renal allograft rejection in primates. Pyridinolcarbamate delayed and amerliorated tissue injury and obstructive thrombosis but only minimally prolonged renal blood flow over that seen in untreated allografts, suggesting that graft failure was primarily due to vasoconstriction. Sudoxicam, an antiinflammatory agent, resulted in higher initial blood flow, but the duration of flow and graft survival were again only minimally prolonged. However, functional changes including C3, Factor II and X consumption were prevented, a net increase in Factor VIII activity was minimized, and fibrinolysis was inhibited. The combined effects of pyridinolcarbamate and heparin resembled those of heparin alone. Combination of Sudoxicam with heparin was more effective than heparin along in preventing intrarenal complement consumption, sequestration of formed elements, activation of coagulation, and inhibition of fibrinolysis. However, the latter combination also failed to prolong venous flow and graft survival over that seen with heparin alone.
机译:分别测试了两种抗血小板药物吡啶醇氨基甲酸酯和Sudoxicam,并与肝素联合测试了它们修饰灵长类动物实验性超急性肾移植排斥反应的能力。吡啶甲酸氨基甲酸酯可延迟和减轻组织损伤和阻塞性血栓形成,但与未治疗的同种异体移植相比,肾血流的延长时间极短,这表明移植失败主要归因于血管收缩。抗炎药Sudoxicam导致较高的初始血流量,但血流持续时间和移植物存活时间再次仅有极短的延长。但是,可以防止功能变化(包括C3,因子II和X消耗),使因子VIII活性的净增加减至最小,并抑制纤维蛋白溶解。吡啶醇氨基甲酸酯和肝素的联合作用类似于单独的肝素。 Sudoxicam与肝素的结合在预防肾内补体消耗,隔离形成的元素,激活凝血和抑制纤维蛋白溶解方面比肝素更有效。然而,与单独使用肝素相比,后一种组合也未能延长静脉血流和移植物存活。

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