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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Chrono-lume and magnesium potentiate aggregation of canine but not human platelets in citrated platelet-rich plasma.
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Chrono-lume and magnesium potentiate aggregation of canine but not human platelets in citrated platelet-rich plasma.

机译:在富含柠檬酸盐的血浆中,慢性烟气和镁会增强犬的聚集,但不会增强人的血小板。

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摘要

The effects of Chrono-lume (CL) and magnesium sulfate (Mg2+), a component of this luciferin-luciferase reagent, on platelet aggregation were studied in platelet-rich plasma (PRP) obtained from blood anticoagulated with sodium citrate from humans, dogs, cats, horses, and cows. The final added Mg2+ concentration of both solutions ranged from 0.75-3.7 mM. CL and Mg2+ had no effect on maximum aggregation of platelets from humans induced by sub-threshold concentrations of collagen and ADP. In contrast, addition of CL or Mg2+ to canine PRP resulted in a dose-dependent and equal potentiation of platelet aggregation in response to sub-threshold concentrations of collagen, ADP, and thrombin in normal and thrombopathic dogs. The effect of CL on platelet aggregation induced by sub-threshold concentrations of agonists was less pronounced and varied in other species according to the agonist. The reason for the marked difference in sensitivity of human and canine platelets to CL or Mg2+ is not clear, although a difference in releasable cation pools of the platelets from these two species has been recognized. Platelet aggregation studies of animals with suspected thrombopathias should be performed without CL to prevent masking of a platelet function defect.
机译:在富含血小板的血浆(PRP)中研究了慢性荧光素(CL)和硫酸镁(Mg2 +)(这种荧光素-荧光素酶试剂的成分)对血小板聚集的影响,血浆富含PRP的血液是用人,狗,猫,老鼠,猫,马和牛。两种溶液最终添加的Mg2 +浓度范围为0.75-3.7 mM。 CL和Mg2 +对低于阈值浓度的胶原蛋白和ADP诱导的人血小板最大聚集没有影响。相比之下,在正常和血栓形成性犬中,对胶原蛋白,ADP和凝血酶的亚阈值浓度以下的反应,在犬PRP中添加CL或Mg2 +会导致剂量依赖性的血小板聚集增强作用,并具有相同的增强作用。 CL对由亚阈值浓度的激动剂诱导的血小板聚集的影响不太明显,并且根据激动剂在其他物种中也有所不同。尽管人们已经认识到人和犬血小板对CL或Mg2 +的敏感性显着不同的原因,但已认识到这两种物种的血小板可释放阳离子池的差异。应该对没有血栓形成的可疑血栓形成动物进行血小板聚集研究,以防止掩盖血小板功能缺陷。

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