High Glucose Induces Oxidative Stress That Alters Glycocalyx Proteoglycan Levels in Primary Rat Retinal Microvascular Endothelial Cells and in Isolated Ophthalmic Arteries.
Ivan A AlvarezMinsup LeeRanda S EshaqWendy LeskovaNorman R HarrisPublished in: Pathophysiology : the official journal of the International Society for Pathophysiology (2024)
Our purpose in this study was to identify the role played by oxidative stress in the changes to proteoglycans that occur under hyperglycemic conditions, using primary rat retinal microvascular endothelial cells (RRMEC) and cultured ophthalmic arteries. The cells and blood vessels obtained from rats were cultured in normal glucose (5.6 mM) and high glucose (25 mM) with or without N-acetylcysteine (NAC), an antioxidant. Intracellular oxidative stress was determined by measuring dihydroethidium (DHE) fluorescence and malondialdehyde (MDA)-modified protein levels. mRNA and protein levels were evaluated using quantitative real-time polymerase chain reaction and immunoblot, respectively. High glucose increased levels of glypican-1 mRNA and protein. The level of syndecan-1 mRNA also was increased, but its protein level was decreased, by high glucose. Evaluation of DHE and MDA showed that high glucose increased oxidative stress. These changes caused by high glucose were significantly reversed by NAC treatment. Matrix metalloproteinase-9 (MMP-9) levels, which increased under high glucose conditions, were suppressed by NAC treatment. Oxidative stress caused by hyperglycemia may be responsible for significant changes to the ocular endothelial glycocalyx.
Keyphrases
- high glucose
- endothelial cells
- oxidative stress
- induced apoptosis
- diabetic rats
- dna damage
- binding protein
- transcription factor
- vascular endothelial growth factor
- protein protein
- optical coherence tomography
- cell cycle arrest
- amino acid
- signaling pathway
- heat shock
- skeletal muscle
- blood pressure
- diabetic retinopathy
- type diabetes
- mass spectrometry
- optic nerve
- blood glucose
- insulin resistance
- cell death
- heat shock protein