Arteriosclerosis Thrombosis and Vascular Biology · 1998 · 54 citations · 42 references
Life SciencesBiochemistryCardiologyAgingGlycobiologyHistopathologyCardiovascular AgingCardiovascular PathologyExtracellular Matrix GlycansGlycan AnalysisGlycan StructureVascular PathologyAge-related Cardiovascular ChangesAge-related Vascular ChangesArterial Wall ThickeningDermatan SulfateGlycosaminoglycan AccumulationGlycosaminoglycan ContentGlycosaminoglycansHeparan Sulfate Proteoglycans
Glycosaminoglycans were extracted from the intima and media layers of normal human thoracic aortas from donors of different ages. The arterial segments were devoid of macroscopically visible lesions obtained from patients who had no clinically evident cardiovascular disease. Total glycosaminoglycan content increases during the first 40 years of life. Changes in the content of hyaluronic acid and heparan sulfate are less noticeable. The content of chondroitin sulfate (mainly the 6-isomer) increases, whereas dermatan sulfate remains constant. Plasma LDL-affinity chromatography of dermatan sulfate+chondroitin 4/6-sulfate fractions allowed the separation of LDL high- and low-affinity glycosaminoglycan species. Remarkably, only glycosaminoglycan species with low affinity for plasma LDL increase with age in the disease-free areas of human thoracic aortas studied. These results suggest that age-related changes in glycosaminoglycan composition of the arterial wall do not contribute to increased deposition of plasma LDL. However, the alternative explanation that individuals with arterial glycosaminoglycans that avidly bind LDL would develop early and severe cardiovascular disease and would thus be excluded from our analysis cannot be ruled out.
42
A modified uronic acid carbazole reaction
Thomas Bitter, H. M. Muir · Analytical Biochemistry · 1962 · 6.3K citations
Hyperlipidemia and Atherosclerosis
Russell Ross, Laurence A. Harker · Science · 1976 · 763 citations