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Journal of Lipid Research, Vol 37, 2650-2661, Copyright © 1996 by Lipid Research, Inc.
JM Upston, J Neuzil and R Stocker
Various lipoxygenases (LO) oxidize low density lipoprotein (LDL) in vitro
and 15-LO has been implicated in the development of atherosclerosis in
vivo. Direct oxidation of phospholipids (PL) and cholesteryl esters (CE) by
LO has been proposed as a mechanism whereby these enzymes cause or
contribute to LDL lipid peroxidation. Herein we show that the extent to
which recombinant human 15-LO (rhLO) caused peroxidation of LDL's
esterified core and surface lipids depended on, and directly related to,
the alpha-tocopherol (alpha-TOH) content of the lipoprotein. Thus, CE and
PL of in vivo alpha-TOH-depleted LDL, isolated from a patient with familial
isolated vitamin E deficiency, were resistant to oxidation by rhLO, whereas
those in alpha-TOH- containing LDL from the same patient receiving vitamin
E supplements readily oxidized. The extent to which rhLO caused oxidation
of CE and PL directly and linearly correlated with LDL's content of vitamin
E, as demonstrated by studies with in vitro alpha-TOH-depleted
lipoproteins. The geometric isomers of oxidized cholesteryl linoleate
formed in LDL during oxidation initiated by rhLO, matched those obtained
during non- enzymic, peroxyl radical-initiated oxidation of LDL whilst
alpha-TOH was present. Ascorbate, an efficient co-antioxidant for
alpha-TOH, completely prevented rhLO-initiated oxidation of LDL's CE, but
did not inhibit rhLO-mediated oxidation of unesterified linoleate. These
results are inconsistent with direct oxidation of LDL esterified lipids by
rhLO. Isolated LDL contained free fatty acids (FFA), and its exposure to
rhLO caused a rapid formation of linoleate hydroperoxide. To reconcile
these data, we propose that during rhLO-initiated oxidation of LDL, enzymic
oxidation of FFA preceeds the oxidation of CE and PL, which occurs largely
via a tocopherol-dependent process.
ARTICLES
Oxidation of LDL by recombinant human 15-lipoxygenase: evidence for alpha-tocopherol-dependent oxidation of esterified core and surface lipids
Biochemistry Unit, Heart Research Institute, Camperdown, NSW, Australia.
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