17beta-estradiol affects in vivo the low density lipoprotein composition, particle size, and oxidizability

The aim of this study was to explore the possible modifications induced by 17beta-estradiol (E(2)) in vivo on low-density lipoprotein (LDL) lipid composition, particle size, and oxidizability. For this purpose, women were recruited from an in vitro fertilization program, ranging their plasma E(2) le...

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Veröffentlicht in:Free radical biology & medicine 2001-08, Vol.31 (3), p.391-397
Hauptverfasser: Ruiz-Sanz, J I, Navarro, R, Martínez, R, Martín, C, Lacort, M, Matorras, R, Ruiz-Larrea, M B
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container_end_page 397
container_issue 3
container_start_page 391
container_title Free radical biology & medicine
container_volume 31
creator Ruiz-Sanz, J I
Navarro, R
Martínez, R
Martín, C
Lacort, M
Matorras, R
Ruiz-Larrea, M B
description The aim of this study was to explore the possible modifications induced by 17beta-estradiol (E(2)) in vivo on low-density lipoprotein (LDL) lipid composition, particle size, and oxidizability. For this purpose, women were recruited from an in vitro fertilization program, ranging their plasma E(2) levels from less than 12 pg/ml to more than 2000 pg/ml at the end of the treatment. The LDL lipid constituents were analyzed by thin layer chromatography and image analysis, and the LDL diameter was calculated from the lipid data. The results showed that high plasma E(2) levels were associated with smaller LDL particles, with lower amounts of free and esterified cholesterol and an increased relative content of alpha-tocopherol. The hormonal treatment produced a remodelation of the LDL acyl composition, rendering a lipoprotein enriched in saturated fatty acids, with a poorer polyunsaturated fatty acid content. These alterations in the physicochemical properties of LDL paralleled changes in the susceptibility of LDL to in vitro oxidation induced by both Cu(2+) and the peroxyl radical generator, 2,2'-azobis (2-amidinopropane), these changes being mainly reflected in a reduced maximum oxidation rate. The in vivo changes in the physicochemical properties of LDL induced by E(2) could explain some of the antiatherogenic actions of estrogens.
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These alterations in the physicochemical properties of LDL paralleled changes in the susceptibility of LDL to in vitro oxidation induced by both Cu(2+) and the peroxyl radical generator, 2,2'-azobis (2-amidinopropane), these changes being mainly reflected in a reduced maximum oxidation rate. 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These alterations in the physicochemical properties of LDL paralleled changes in the susceptibility of LDL to in vitro oxidation induced by both Cu(2+) and the peroxyl radical generator, 2,2'-azobis (2-amidinopropane), these changes being mainly reflected in a reduced maximum oxidation rate. 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These alterations in the physicochemical properties of LDL paralleled changes in the susceptibility of LDL to in vitro oxidation induced by both Cu(2+) and the peroxyl radical generator, 2,2'-azobis (2-amidinopropane), these changes being mainly reflected in a reduced maximum oxidation rate. The in vivo changes in the physicochemical properties of LDL induced by E(2) could explain some of the antiatherogenic actions of estrogens.</abstract><cop>United States</cop><pmid>11461777</pmid><tpages>7</tpages></addata></record>
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subjects Adult
Estradiol - pharmacology
Fatty Acids, Nonesterified - blood
Fatty Acids, Unsaturated - blood
Female
Fertilization in Vitro
Humans
Lipoproteins, LDL - blood
Lipoproteins, LDL - chemistry
Lipoproteins, LDL - drug effects
Oxidation-Reduction
Premenopause
Triglycerides - blood
Triglycerides - chemistry
Vitamin A - blood
title 17beta-estradiol affects in vivo the low density lipoprotein composition, particle size, and oxidizability
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