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Journal of Lipid Research, Vol 37, 1978-1986, Copyright © 1996 by Lipid Research, Inc.
D Li, S Devaraj, C Fuller, R Bucala and I Jialal
Much data support a role for both low density lipoprotein (LDL) oxidation
and glycation in atherogenesis. While alpha-tocopherol decreases the
oxidative susceptibility of LDL, its role in decreasing LDL glycation is
unclear. Hence we tested the effect of alpha- tocopherol both in vitro and
in vivo on LDL oxidation and glycation. LDL was isolated after enrichment
of plasma with alpha-tocopherol. This resulted in a 2-fold increase in
alpha-tocopherol in LDL (AT-LDL). During a 6-day incubation of control LDL
(C-LDL) and AT-LDL with 25 mM glucose, there were no significant
differences in the degree of glycation on days 1, 3, and 6. Also, apoB
advanced glycosylation end product levels were not significantly different
between C-LDL and AT- LDL. There was a progressive increase in the
susceptibility of LDL to oxidation with increasing LDL glycation as
evidenced by reduced lag time of copper-catalyzed LDL oxidation. However,
AT-LDL was more resistant to copper-catalyzed oxidation. Similar findings
were observed when the LDLs were incubated with endothelial cells. The data
from the alpha-tocopherol supplementation study confirmed our in vitro
findings that alpha-tocopherol significantly decreases oxidative
susceptibility of LDL, but does not affect its glycation. Therefore, while
glycation increases LDL oxidative susceptibility, alpha-tocopherol
decreases the oxidation of glycated LDL but not LDL glycation.
ARTICLES
Effect of alpha-tocopherol on LDL oxidation and glycation: in vitro and in vivo studies
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235, USA.
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