Determination of Advanced Glycation End Products in Serum by Fluorescence Spectroscopy and Competitive ELISA
- 1 January 1997
- journal article
- research article
- Published by Walter de Gruyter GmbH in cclm
- Vol. 35 (9), 669-678
- https://doi.org/10.1515/cclm.1997.35.9.669
Abstract
Recent studies suggest that advanced glycation endproducts play an important role in cardiovascular complications of ageing, diabetes and end-stage renal failure. Since highly elevated levels of advanced glycation endproducts are present in serum of patients on maintenance haemodialysis, an accurate and rapid assay for their determination would be useful. This would be particularly valuable for monitoring the removal of advanced glycation endproducts by novel dialysis membranes, as well as the effect of new drugs for the inhibition of their formation. Measurement of advanced glycation endproducts in serum was performed by two competitive ELISAs, using a monoclonal antibody directed against imidazolone, an advanced glycation endproduct formed by the reaction of arginine with 3-deoxyglucosone, and a polyclonal antibody directed against keyhole limpet haemocyanin-advanced glycation endproduct, as well as by quantitative fluorescence spectroscopy. Each of the assays showed significant differences between the controls and the maintenance haemodialysis patients. Advanced glycation endproduct levels determined by each of the ELISAs correlated with total and protein-bound fluorescence, but not with each other, suggesting a variable distribution of advanced glycation endproducts on serum proteins among the maintenance haemodialysis patients.Keywords
This publication has 24 references indexed in Scilit:
- Amyloid β2-microglobulin is modified with imidazolone, a novel advanced glycation end product, in dialysis-related amyloidosisKidney International, 1997
- Advanced glycation endproducts interacting with their endothelial receptor induce expression of vascular cell adhesion molecule-1 (VCAM-1) in cultured human endothelial cells and in mice. A potential mechanism for the accelerated vasculopathy of diabetes.Journal of Clinical Investigation, 1995
- N.epsilon.-(Carboxymethyl)lysine Is a Dominant Advanced Glycation End Product (AGE) Antigen in Tissue ProteinsBiochemistry, 1995
- Radical AGEing in Alzheimer's diseaseTrends in Neurosciences, 1995
- Influence of dialysis modality on plasma and tissue concentrations of pentosidine in patients with end-stage renal diseaseAmerican Journal of Kidney Diseases, 1995
- ADVANCED PROTEIN GLYCOSYLATION IN DIABETES AND AGINGAnnual Review of Medicine, 1995
- Advanced glycation end products induce glomerular sclerosis and albuminuria in normal rats.Proceedings of the National Academy of Sciences, 1994
- Immunological quantification of advanced glycosylation end-products in the serum of patients on hemodialysis or CAPDKidney International, 1994
- Advanced Glycosylation: Chemistry, Biology, and Implications for Diabetes and AgingPublished by Elsevier ,1992
- Nonenzymatic Browning in Vivo: Possible Process for Aging of Long-Lived ProteinsScience, 1981