Sevelamer reduces endothelial inflammatory response to advanced glycation end products.

Background: Advanced glycation end products (AGEs) have been related to the pathogenesis of cardiovascular diseases (CVD), chronic kidney disease (CKD) and diabetes mellitus. We sought to investigate the binding capacity of sevelamer to both AGEs and uremic serum in vitro and then test this pharmaceutical effect as a potential vascular anti-inflammatory strategy.

Methods: AGEs were prepared by albumin glycation and characterized by absorbance and electrophoresis. Human endothelial cells were incubated in culture media containing AGEs and uremic serum with or without sevelamer. Receptor for advanced glycation end product (RAGE) expression was evaluated through immunocytochemistry and western blot to explore the interactions between AGEs and the endothelium. Inflammatory and endothelial dysfunction biomarkers, such as interleukin 6 (IL-6) and IL-8, monocyte chemoattractant protein-1 (MCP-1), plasminogen activator inhibitor-1 (PAI-1) and serum amyloid A (SAA) were also measured in cell supernatant. The chemotactic property of the supernatant was evaluated.

Results: AGEs significantly induced the expression of RAGE, inflammatory and endothelial activation biomarkers [IL-6, (P   <   0.005); IL-8, MCP-1, PAI-1 and SAA (P   <   0.001)] and monocyte chemotaxis as compared with controls. In addition, AGEs increased the levels of inflammatory biomarkers, which were observed after 6 h of endothelial cell incubation with uremic serum [IL-6 (P  <  0.001) IL-8, MCP-1 and PAI-1 (P  <  0.05)]. On the other hand, after 6 h of endothelial cell treatment with sevelamer, RAGE expression (P  <  0.05) and levels of inflammatory biomarkers [IL-6 and IL-8 (P   <   0.001), MCP-1 (P   <   0.01), PAI-1 and SAA (P   <   0.005)] significantly decreased compared with the AGEs/uremic serum treatment alone.

Conclusions: Sevelamer decreased both endothelial expression of RAGE and endothelial dysfunction biomarkers, induced by AGEs, and uremic serum. Further studies are necessary for a better understanding of the potential protective role of sevelamer on uremic serum and AGEs-mediated endothelial dysfunction.