Ascorbate reverses high glucose- and RAGE-induced leak of the endothelial permeability barrier |
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Authors: | M. Elizabeth Meredith Zhi-Chao Qu James M. May |
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Affiliation: | 1. Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232-0475, United States;2. Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232-0475, United States |
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Abstract: | High glucose concentrations due to diabetes increase leakage of plasma constituents across the endothelial permeability barrier. We sought to determine whether vitamin C, or ascorbic acid (ascorbate), could reverse such high glucose-induced increases in endothelial barrier permeability. Human umbilical vein endothelial cells and two brain endothelial cell lines cultured at 25 mM glucose showed increases in endothelial barrier permeability to radiolabeled inulin compared to cells cultured at 5 mM glucose. Acute loading of the cells for 30–60 min with ascorbate before the permeability assay prevented the high glucose-induced increase in permeability and decreased basal permeability at 5 mM glucose. High glucose-induced barrier leakage was mediated largely by activation of the receptor for advanced glycation end products (RAGE), since it was prevented by RAGE blockade and mimicked by RAGE ligands. Intracellular ascorbate completely prevented RAGE ligand-induced increases in barrier permeability. The high glucose-induced increase in endothelial barrier permeability was also acutely decreased by several cell-penetrant antioxidants, suggesting that at least part of the ascorbate effect could be due to its ability to act as an antioxidant. |
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Keywords: | AGE, advanced glycation end-products FPS-ZM1, N-benzyl-4-chloro-N-cyclohexylbenzamide Hepes, N-2-hydroxyethylpiperazine-N&prime -2-ethanesulfonic acid HMGB1, high mobility group box 1 KRH, Krebs-Ringer Hepes NAC, N-acetylcysteine RAGE, receptor for advanced glycation end-products SVCT2, sodium-dependent vitamin C transporter-2 |
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