TY - JOUR
T1 - Postprandial changes in the phospholipid composition of circulating microparticles are not associated with coagulation activation
AU - Tushuizen, Maarten E.
AU - Diamant, Michaela
AU - Peypers, Erik G.
AU - Hoek, Frans J.
AU - Heine, Robert J.
AU - Sturk, Augueste
AU - Nieuwland, Rienk
PY - 2012
Y1 - 2012
N2 - 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-F1+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 F1+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. (C) 2011 Elsevier Ltd. All rights reserved
AB - 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-F1+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 F1+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. (C) 2011 Elsevier Ltd. All rights reserved
U2 - https://doi.org/10.1016/j.thromres.2011.09.003
DO - https://doi.org/10.1016/j.thromres.2011.09.003
M3 - Article
C2 - 21962986
SN - 0049-3848
VL - 130
SP - 115
EP - 121
JO - Thrombosis research
JF - Thrombosis research
IS - 1
ER -