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Selected Publication:

Esterbauer, H; Striegl, G; Puhl, H; Rotheneder, M.
Continuous monitoring of in vitro oxidation of human low density lipoprotein.
Free Radic Res Commun. 1989; 6(1): 67-75. Doi: 10.3109/10715768909073429
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Co-authors Med Uni Graz
Dieber-Rotheneder Martina
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Abstract:
The kinetics of the oxidation of human low density lipoprotein (LDL) can be measured continuously by monitoring the change of the 234 nm diene absorption. The time-course shows three consecutive phases, a lag-phase during which the diene absorption increases only weakly, a propagation phase with a rapid increase of the diene absorption and finally a decomposition phase. The increase of the dienes is highly correlated with the increase of MDA or lipid hydroperoxides. The duration of the lag-phase is determined by the endogenous antioxidants contained in LDL (vitamin E, carotenoids, retinylstearate). Water-soluble antioxidants (ascorbic acid, urate) added in micromolar concentrations prolong the lag-phase in a concentration-dependent manner. The determination of the lag-phase is a convenient and objective procedure for determining the susceptibility of LDL from different donors towards oxidation as well as effects of pro- and antioxidants.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Antioxidants - pharmacology
Carotenoids - blood
Chromatography, High Pressure Liquid - blood
Humans - blood
Kinetics - blood
Lipoproteins, LDL - blood
Monitoring, Physiologic - blood
Oxidation-Reduction - blood
Spectrophotometry, Ultraviolet - methods
Vitamin E - blood

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