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Journal of Lipid Research, Vol 28, 495-509, Copyright © 1987 by Lipid Research, Inc.
H Esterbauer, G Jurgens, O Quehenberger and E Koller
The alteration of structural and biological properties of human plasma low
density lipoprotein (LDL) exposed to oxidative conditions is in part
ascribed to lipid peroxidation. The objective of this investigation was to
measure quantitatively several parameters in oxidizing LDL indicative for
lipid peroxidation. Exposure of freshly prepared EDTA-free LDL to an
oxygen-saturated buffer led to a complete depletion of alpha- and
gamma-tocopherol within 6 hr, thereafter lipid peroxidation commenced as
indicated by the kinetics of the loss of linoleic (18:2) and arachidonic
(20:4) acids, the formation of aldehydic lipid peroxidation products and
fluorescent apoB. Within 24 hr of oxidation, on average 79 nmol of 18:2
(initial 345) and 12.8 nmol of 20.4 (initial 25.6) were oxidized per mg of
LDL and the sample contained in total 7.1 nmol of aldehydes with the
following molar distribution: 36.6% malonaldehyde, 25% hexanal, 8.9%
propanal, 8.2% 4- hydroxynonenal, 7.6% butanal, 4.1% 2.4-heptadienal, 3.4%
pentanal, 3.4% 4-hydroxyhexenal, and 2.5% 4-hydroxyoctenal. Malonaldehyde
was predominantly (93%) in the aqueous phase, whereas the other aldehydes
remained mostly (34-98%) within the LDL particle, where the total aldehyde
concentration was in the range of 12 mM. Oxidized LDL exhibited a 1.6-fold
enhanced electrophoretic mobility. Similarily, native LDL incubated for 5
hr with aldehydes showed increased electrophoretic mobility. At equal
concentrations (5 mM) 4- hydroxynonenal was most effective, followed by
2,4-heptadienal, hexanal, and malonaldehyde. This study reports for the
first time the rate and extent of the change of LDL constituents occurring
during lipid peroxidation.
ARTICLES
Autoxidation of human low density lipoprotein: loss of polyunsaturated fatty acids and vitamin E and generation of aldehydes
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