SIMPLE METHODS OF QUANTIFYING OXIDATION-PRODUCTS AND ANTIOXIDANT POTENTIAL OF LOW-DENSITY LIPOPROTEINS

Citation
M. Ahotupa et al., SIMPLE METHODS OF QUANTIFYING OXIDATION-PRODUCTS AND ANTIOXIDANT POTENTIAL OF LOW-DENSITY LIPOPROTEINS, Clinical biochemistry, 29(2), 1996, pp. 139-144
Citations number
23
Categorie Soggetti
Biology,"Chemistry Medicinal
Journal title
ISSN journal
00099120
Volume
29
Issue
2
Year of publication
1996
Pages
139 - 144
Database
ISI
SICI code
0009-9120(1996)29:2<139:SMOQOA>2.0.ZU;2-X
Abstract
Objectives: The present study describes new methods for the measuremen t of oxidation products and antioxidant potential of low density lipop roteins (LDL). Design and methods: LDL is isolated by precipitation wi th buffered heparin. The assay for LDL oxidation products (LDL-BDC) is based on determination of baseline levels of conjugated dienes (BDC) in lipids extracted from LDL. The assay for antioxidant potential of L DL (LDL-TRAP) is based on the ability of LDL to trap peroxyl radicals. Results: LDL-BDC was found to increase linearly over a range from 100 to 1750 mu L, LDL-TRAP from 250 to 1750 mu L of serum taken for preci pitation. For LDL-BDC, the CV was 4.4% and 4.5% for within- and betwee n-assay precision, respectively. For the LDL-TRAP, the CV was 8.1% and 8.7% for within- and between-assay precisions, respectively. Freezing of the serum (2 weeks at -70 degrees C) did not affect LDL-BDC or LDL -TRAP levels. A negative correlation was found to exist between the LD L-BDC and LDL-TRAP values. LDL-BDC and LDL-TRAP values were at the sam e level in both sexes. The LDL-BDC was found to increase with age. Sho rt-term intervention with antioxidants increased LDL-TRAP substantiall y, but did not affect the LDL-BDC level. Conclusions: These methods ar e fast and simple to perform, and can, therefore, be applied to clinic al purposes.