© 2003 by European Society of Cardiology
Copyright © 2003, European Society of Cardiology
Vitamin E inhibits lipid peroxidation-induced adhesion molecule expression in endothelial cells and decreases soluble cell adhesion molecules in healthy subjects
aDepartment of Internal Medicine, Vrije Universiteit Medical Centre, Amsterdam, The Netherlands
bDepartment of Clinical Chemistry, Institute for Cardiovascular Research, Vrije Universiteit Medical Centre, De Boelelaan 1117, 1007 MB Amsterdam, The Netherlands
cDepartment of Oncology, Vrije Universiteit Medical Centre, Amsterdam, The Netherlands
dInstitute for Cardiovascular Research, Vrije Universiteit Medical Centre, Amsterdam, The Netherlands
eGaubius Laboratory TNO-PG, Leiden, The Netherlands
c.schalkwijk{at}vumc.nl
* Corresponding author. Tel.: +31-20-444-3680; fax: +31-20-444-3895.
Objective: In a combination of in vivo and in vitro studies, we investigated mechanisms via which
-tocopherol, a lipid soluble form of vitamin E, can directly affect endothelial activation as induced by H2O2 and TNF
. Methods: We measured effects of
-tocopherol on H2O2-induced lipid peroxidation as determined with a fluorescent C-11 BODIPY581/591 probe and on adhesion molecule expression in cultured endothelial cells. In 20 healthy volunteers treated with increasing doses of
-tocopherol up to 800 IU/ml for 12 weeks, plasma levels of soluble cell adhesion molecules (sCAMs) and C-reactive protein were measured. Results: We showed that
-tocopherol protects cultured endothelial cells against H2O2-induced lipid peroxidation, while TNF
did not induce lipid peroxidation. Moreover,
-tocopherol attenuated H2O2-, but not TNF
-induced increases in adhesion molecule expression. In healthy persons,
-tocopherol decreased plasma levels of sE-selectin from 65±6 to 60±6 ng/ml (P=0.002), sVCAM from 893±31 to 853±23 ng/ml (P=0.022), and sICAM from 483±21 to 463±16 ng/ml (P=0.048). C-Reactive protein, as a sensitive marker of low grade inflammation, was not significantly affected. Conclusion:
-Tocopherol specifically inhibits lipid peroxidation-induced endothelial activation in vitro. The observed vitamin E-induced decrease in sCAMs in control subjects suggests that lipid peroxidation can take place in healthy individuals. Although vitamin E supplementation may be especially effective in specific groups of patients exposed to increased oxidative stress, our study suggests that vitamin E supplementation can be of benefit in healthy individuals as well.
KEYWORDS Endothelial function; Free radicals; Lipid metabolism
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