首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Postprandial changes in the phospholipid composition of circulating microparticles are not associated with coagulation activation
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Postprandial changes in the phospholipid composition of circulating microparticles are not associated with coagulation activation

机译:餐后循环中微粒的磷脂成分变化与凝血活化无关

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Introduction: Evidence is present that the phospholipid composition of circulating cell-derived microparticles (MP) affects coagulation in vivo, and that postprandial metabolic alterations may be associated with hypercoagulable state. Our objective was to investigate whether postprandial metabolic responses affect the phospholipid composition of MP, and whether such changes are associated with coagulation activation. Materials and Methods: Twelve healthy males were studied twice and randomly received two consecutive meals or remained fasted. Blood was collected before and at 2, 4, 6 and 8 h following breakfast. Plasma concentrations of prothrombin-F 1 + 2 and thrombin- antithrombin-complexes were measured. Numbers and cellular origin of MP were determined by flowcytometry. The phospholipid composition of MP was determined by hpTLC. In vitro procoagulant activity of MP was studied by fibrin generation. Results: During the meal visit, plasma glucose, triglyceride and insulin levels increased, compared to baseline and the fasting visit (all P 0.05). Postprandially, the total numbers of MP increased in time compared to the fasting visit (P 0.05). Erythrocyte-derived MP increased (6-fold) during the meal visit, but remained constant on the fasting day (P 0.001). On the meal versus fasting day circulating MP contained increased phosphatidylcholine (P 0.05) and decreased sphingomyelin (P 0.05) amounts. The amount of phosphatidylserine did not change. Concentrations of plasma F 1 + 2 and thrombin-antithrombin were similar on both days, as was the ability of MP to generate fibrin in vitro. Conclusion: Although numbers, cellular origin and phospholipid composition of MP alter during exposure to two consecutive meals in healthy subjects, this does not lead to changes in the coagulation activation in vivo.
机译:简介:目前有证据表明循环细胞来源的微粒(MP)的磷脂成分会影响体内凝血,并且餐后代谢改变可能与高凝状态有关。我们的目的是研究餐后代谢反应是否影响MP的磷脂组成,以及这种变化是否与凝血激活有关。材料和方法:对十二名健康男性进行了两次研究,随机接受连续两餐或禁食。在早餐前,早餐后2、4、6和8小时收集血液。测量了凝血酶原-F 1 + 2和凝血酶-抗凝血酶复合物的血浆浓度。 MP的数目和细胞起源通过流式细胞术确定。通过hpTLC确定MP的磷脂组成。通过纤维蛋白生成研究了MP的体外促凝活性。结果:在就餐期间,与基线和空腹就诊相比,血浆葡萄糖,甘油三酯和胰岛素水平升高(所有P <0.05)。餐后,与空腹访视相比,MP的总数随时间增加(P <0.05)。进餐期间,源自红细胞的MP增加(6倍),但在禁食日保持不变(P <0.001)。进餐与空腹相比,循环中的MP含有增加的磷脂酰胆碱(P <0.05)和减少的鞘磷脂(P <0.05)。磷脂酰丝氨酸的量没有改变。这两天血浆F 1 + 2和凝血酶-抗凝血酶的浓度相似,MP在体外产生纤维蛋白的能力也相似。结论:尽管健康受试者连续两次进餐期间MP的数量,细胞来源和磷脂成分发生变化,但这并不会导致体内凝血激活的改变。

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