Loss of Endothelial Glycocalyx During Acute Hyperglycemia Coincides With Endothelial Dysfunction and Coagulation Activation In Vivo

Max Nieuwdorp(Amsterdam UMC Location University of Amsterdam), Timon W. van Haeften(University Medical Center Utrecht), Mirella Gouverneur(Amsterdam UMC Location University of Amsterdam), Hans L. Mooij(Amsterdam UMC Location University of Amsterdam), Miriam H. P. van Lieshout(Amsterdam UMC Location University of Amsterdam), Marcel Levi(Amsterdam UMC Location University of Amsterdam), Joost C.M. Meijers(Amsterdam UMC Location University of Amsterdam), F. Holleman(Amsterdam UMC Location University of Amsterdam), J. B. L. Hoekstra(Amsterdam UMC Location University of Amsterdam), Hans Vink(Amsterdam UMC Location University of Amsterdam), John J.P. Kastelein(Amsterdam UMC Location University of Amsterdam), Erik S.G. Stroes(Amsterdam UMC Location University of Amsterdam)
Diabetes
February 1, 2006
Cited by 626Open Access
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Abstract

Hyperglycemia is associated with increased susceptibility to atherothrombotic stimuli. The glycocalyx, a layer of proteoglycans covering the endothelium, is involved in the protective capacity of the vessel wall. We therefore evaluated whether hyperglycemia affects the glycocalyx, thereby increasing vascular vulnerability. The systemic glycocalyx volume was estimated by comparing the distribution volume of a glycocalyx permeable tracer (dextran 40) with that of a glycocalyx impermeable tracer (labeled erythrocytes) in 10 healthy male subjects. Measurements were performed in random order on five occasions: two control measurements, two measurements during normoinsulinemic hyperglycemia with or without N-acetylcysteine (NAC) infusion, and one during mannitol infusion. Glycocalyx measurements were reproducible (1.7 +/- 0.2 vs. 1.7 +/- 0.3 l). Hyperglycemia reduced glycocalyx volume (to 0.8 +/- 0.2 l; P < 0.05), and NAC was able to prevent the reduction (1.4 +/- 0.2 l). Mannitol infusion had no effect on glycocalyx volume (1.6 +/- 0.1 l). Hyperglycemia resulted in endothelial dysfunction, increased plasma hyaluronan levels (from 70 +/- 6 to 112 +/- 16 ng/ml; P < 0.05) and coagulation activation (prothrombin activation fragment 1 + 2: from 0.4 +/- 0.1 to 1.1 +/- 0.2 nmol/l; d-dimer: from 0.27 +/- 0.1 to 0.55 +/- 0.2 g/l; P < 0.05). Taken together, these data indicate a potential role for glycocalyx perturbation in mediating vascular dysfunction during hyperglycemia.


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