Advanced glycation end products in diabetic patients with optimized glycaemic control and their effects on endothelial reactivity: Possible implications in venous graft failure

Massimo Chello, Cristiano Spadaccio, Mario Lusini, Elvio Covino, Carla Blarzino, Federico De Marco, Fabio Di Domenico, Raffaella Coccia

Research output: Contribution to journalArticle

Abstract

Background: Diabetic patients exhibit an increased risk of saphenous graft occlusion after coronary bypass. Advanced glycation end products (AGEs) are ubiquitous signalling proteins that are associated with vascular and neurological complication of diabetes. The aim of this study is to verify whether AGE levels may promote endothelial cell alterations responsible for vein graft failure. Methods: Segments of saphenous vein were obtained from both normal people and diabetic patients (HbA1c <6.0%) at the time of coronary surgery. Cultured endothelial cells were incubated in the absence/presence of AGEs (2 and 20 μM), and mRNA and protein for both receptor of AGEs (RAGE) and peroxisome proliferator-activated receptors-γ (PPAR-γ) were analysed by real-time polymerised chain reaction (PCR) and Western blot analysis. In the same fashion, the cell release of reactive oxygen species (ROS) was estimated in the absence/presence of AGEs by spectrofluorimetric analysis. Finally, neutrophil-endothelial adhesion was evaluated in saphenous vein segments with and without the addition of AGEs. Results AGEs activated in a dose-dependent manner the expression of RAGE and inhibited PPAR-γ expression in endothelial cells as testified by both reverse transcription-PCR (RT-PCR) and Western blot analysis. Stimulation of cultured endothelial cells with AGEs significantly enhanced intracellular ROS formation in a dose-dependent manner. Finally, neutrophil-endothelial adhesion was significantly increased after incubation of control veins with AGEs. Conclusions: These findings indicate that even in diabetic patients with HbA1c <6.0%, elevated serum levels of AGE determine a sort of a prothrombotic state, providing a common mechanism that could explain the increased rate of vein graft occlusion in this population.

Original languageEnglish
Pages (from-to)420-426
Number of pages7
JournalDiabetes/Metabolism Research and Reviews
Volume25
Issue number5
DOIs
Publication statusPublished - Jul 2009

Keywords

  • Coronary bypass
  • Diabetes
  • Leukocytes
  • Thrombosis
  • Venous grafts

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism
  • Internal Medicine

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