Estradiol as an antioxidant: incompatible with its physiological concentrations and function

Estradiol has been documented to inhibit the oxidation of low density lipoprotein (LDL). We show that physiological concentrations of estradiol do not inhibit the oxidation of LDL by copper. LDL samples isolated from a) premenopausal and postmenopausal women and from b) women at different time perio...

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Main Authors: Nalini Santanam, Robin Shern-Brewer, Ruth McClatchey, Penny Z. Castellano, Ana A. Murphy, Steve Voelkel, Sampath Parthasarathy
Format: Article
Language:English
Published: Elsevier 1998-11-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520324652
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author Nalini Santanam
Robin Shern-Brewer
Ruth McClatchey
Penny Z. Castellano
Ana A. Murphy
Steve Voelkel
Sampath Parthasarathy
author_facet Nalini Santanam
Robin Shern-Brewer
Ruth McClatchey
Penny Z. Castellano
Ana A. Murphy
Steve Voelkel
Sampath Parthasarathy
author_sort Nalini Santanam
collection DOAJ
description Estradiol has been documented to inhibit the oxidation of low density lipoprotein (LDL). We show that physiological concentrations of estradiol do not inhibit the oxidation of LDL by copper. LDL samples isolated from a) premenopausal and postmenopausal women and from b) women at different time periods during their menstrual cycle, who differ vastly in plasma estradiol levels, were also oxidized at the same rates by copper. In contrast, LDL samples isolated from c) women who were hyperstimulated during in vitro fertilization (IVF), with estradiol concentrations above 2000 pg/ml, were resistant to oxidation by copper. However, these LDL samples were also oxidized at a higher rate by peroxidases. More importantly, subjects with high estradiol levels also showed an increase in myeloperoxidase (MPO) protein in the plasma. Based on these results, we conclude that at physiologic concentrations, it is unlikely that estradiol could act as an antioxidant. In fact, the ability of estradiol to induce MPO and become a prooxidant might instead suggest that MPO-mediated oxidative clearance of LDL from plasma by liver might favorably influence the outcome of atherosclerosis. —Santanam, N., R. Shern-Brewer, R. McClatchey, P. Z. Castellano, A. A. Murphy, S. Voelkel, and S. Parthasarathy. Estradiol as an antioxidant: incompatible with its physiological concentrations and function. J. Lipid Res. 1998. 39: 2111–2118.
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spelling doaj.art-03fef592f42943bd9b5d341b5d986f492022-12-21T19:41:13ZengElsevierJournal of Lipid Research0022-22751998-11-01391121112118Estradiol as an antioxidant: incompatible with its physiological concentrations and functionNalini Santanam0Robin Shern-Brewer1Ruth McClatchey2Penny Z. Castellano3Ana A. Murphy4Steve Voelkel5Sampath Parthasarathy6Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322To whom correspondence should be addressed.; Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA 30322Estradiol has been documented to inhibit the oxidation of low density lipoprotein (LDL). We show that physiological concentrations of estradiol do not inhibit the oxidation of LDL by copper. LDL samples isolated from a) premenopausal and postmenopausal women and from b) women at different time periods during their menstrual cycle, who differ vastly in plasma estradiol levels, were also oxidized at the same rates by copper. In contrast, LDL samples isolated from c) women who were hyperstimulated during in vitro fertilization (IVF), with estradiol concentrations above 2000 pg/ml, were resistant to oxidation by copper. However, these LDL samples were also oxidized at a higher rate by peroxidases. More importantly, subjects with high estradiol levels also showed an increase in myeloperoxidase (MPO) protein in the plasma. Based on these results, we conclude that at physiologic concentrations, it is unlikely that estradiol could act as an antioxidant. In fact, the ability of estradiol to induce MPO and become a prooxidant might instead suggest that MPO-mediated oxidative clearance of LDL from plasma by liver might favorably influence the outcome of atherosclerosis. —Santanam, N., R. Shern-Brewer, R. McClatchey, P. Z. Castellano, A. A. Murphy, S. Voelkel, and S. Parthasarathy. Estradiol as an antioxidant: incompatible with its physiological concentrations and function. J. Lipid Res. 1998. 39: 2111–2118.http://www.sciencedirect.com/science/article/pii/S0022227520324652atherosclerosismenopausecoronary artery diseaselipid peroxidationmyeloperoxidaseoxidized low-density lipoprotein
spellingShingle Nalini Santanam
Robin Shern-Brewer
Ruth McClatchey
Penny Z. Castellano
Ana A. Murphy
Steve Voelkel
Sampath Parthasarathy
Estradiol as an antioxidant: incompatible with its physiological concentrations and function
Journal of Lipid Research
atherosclerosis
menopause
coronary artery disease
lipid peroxidation
myeloperoxidase
oxidized low-density lipoprotein
title Estradiol as an antioxidant: incompatible with its physiological concentrations and function
title_full Estradiol as an antioxidant: incompatible with its physiological concentrations and function
title_fullStr Estradiol as an antioxidant: incompatible with its physiological concentrations and function
title_full_unstemmed Estradiol as an antioxidant: incompatible with its physiological concentrations and function
title_short Estradiol as an antioxidant: incompatible with its physiological concentrations and function
title_sort estradiol as an antioxidant incompatible with its physiological concentrations and function
topic atherosclerosis
menopause
coronary artery disease
lipid peroxidation
myeloperoxidase
oxidized low-density lipoprotein
url http://www.sciencedirect.com/science/article/pii/S0022227520324652
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