Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content

Apolipoproteins E and C-III are modulators of lipoprotein metabolism that could affect development of atherosclerosis. The prevalence in plasma of apoB-containing particles (LpB) that contain either apoE or apoC-III, both or neither, and the effect of estrogen on these lipoproteins are unknown. The...

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Main Authors: Christina Khoo, Hannia Campos, Helena Judge, Frank M. Sacks
Format: Article
Language:English
Published: Elsevier 1999-02-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520333587
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spelling doaj-29db745bc1844744b53c4e5e52cafe832021-04-26T05:46:40ZengElsevierJournal of Lipid Research0022-22751999-02-01402202212Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III contentChristina Khoo0Hannia Campos1Helena Judge2Frank M. Sacks3Department of Nutrition, Harvard School of Public Health, Boston, MA 02115Department of Nutrition, Harvard School of Public Health, Boston, MA 02115Department of Nutrition, Harvard School of Public Health, Boston, MA 02115To whom correspondence should be addressed.; Department of Nutrition, Harvard School of Public Health, Boston, MA 02115; Departments of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115Apolipoproteins E and C-III are modulators of lipoprotein metabolism that could affect development of atherosclerosis. The prevalence in plasma of apoB-containing particles (LpB) that contain either apoE or apoC-III, both or neither, and the effect of estrogen on these lipoproteins are unknown. The LpB particle system, defined by the presence or absence of apoE or C-III, was studied in 13 normolipidemic women, 7 nonusers and 6 users of oral contraceptives. Fasting plasma was separated by anti-apoE and C-III affinity chromatography and ultracentrifugation into four types of VLDL, IDL, and LDL particles: with apoE but not apoC-III (E+C−), apoC-III but not apoE (E−C+), both (E+C+) or neither (E−C−). The predominant VLDL particles were E−C− (42% in nonusers, 56% in users) and E+C+ (39% in nonusers, 24% in users), suggesting that apoE and apoC-III mainly exist together in VLDL. In IDL, E−C− was the major fraction (74% nonusers, 81% users), and in LDL, it was 99% in both groups. The triglycerides in VLDL and IDL were mainly contained in C+ particles (79% and 66% of the total VLDL and IDL triglycerides, respectively). Within VLDL, IDL, and LDL, E−C− particles had the smallest size and E+C+ or E−C+ the largest. Users had higher concentrations of VLDL E−C− (280%) and IDL E−C− (90%) particles than nonusers. They also had higher free cholesterol and cholesteryl ester concentrations associated with these fractions and with VLDL E−C+. The triglyceride contents of VLDL E−C− particles were lower in users of oral contraceptives than in nonusers. This study demonstrates that the elevated VLDL TG concentrations in users of estrogen-dominant oral contraceptives is mainly caused by an increased concentration of small VLDL particles that have reduced TG content, and that do not have apoE and C-III. These particles may have lower atherogenicity than particles enriched with apoE and C-III.—Khoo, C., H. Campos, H. Judge, and F. M. Sacks. Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content. J. Lipid Res. 1999. 40: 202–212.http://www.sciencedirect.com/science/article/pii/S0022227520333587apoBapoEapoC-IIIestrogenoral contraceptivesatherosclerosis
collection DOAJ
language English
format Article
sources DOAJ
author Christina Khoo
Hannia Campos
Helena Judge
Frank M. Sacks
spellingShingle Christina Khoo
Hannia Campos
Helena Judge
Frank M. Sacks
Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content
Journal of Lipid Research
apoB
apoE
apoC-III
estrogen
oral contraceptives
atherosclerosis
author_facet Christina Khoo
Hannia Campos
Helena Judge
Frank M. Sacks
author_sort Christina Khoo
title Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content
title_short Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content
title_full Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content
title_fullStr Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content
title_full_unstemmed Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content
title_sort effects of estrogenic oral contraceptives on the lipoprotein b particle system defined by apolipoproteins e and c-iii content
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1999-02-01
description Apolipoproteins E and C-III are modulators of lipoprotein metabolism that could affect development of atherosclerosis. The prevalence in plasma of apoB-containing particles (LpB) that contain either apoE or apoC-III, both or neither, and the effect of estrogen on these lipoproteins are unknown. The LpB particle system, defined by the presence or absence of apoE or C-III, was studied in 13 normolipidemic women, 7 nonusers and 6 users of oral contraceptives. Fasting plasma was separated by anti-apoE and C-III affinity chromatography and ultracentrifugation into four types of VLDL, IDL, and LDL particles: with apoE but not apoC-III (E+C−), apoC-III but not apoE (E−C+), both (E+C+) or neither (E−C−). The predominant VLDL particles were E−C− (42% in nonusers, 56% in users) and E+C+ (39% in nonusers, 24% in users), suggesting that apoE and apoC-III mainly exist together in VLDL. In IDL, E−C− was the major fraction (74% nonusers, 81% users), and in LDL, it was 99% in both groups. The triglycerides in VLDL and IDL were mainly contained in C+ particles (79% and 66% of the total VLDL and IDL triglycerides, respectively). Within VLDL, IDL, and LDL, E−C− particles had the smallest size and E+C+ or E−C+ the largest. Users had higher concentrations of VLDL E−C− (280%) and IDL E−C− (90%) particles than nonusers. They also had higher free cholesterol and cholesteryl ester concentrations associated with these fractions and with VLDL E−C+. The triglyceride contents of VLDL E−C− particles were lower in users of oral contraceptives than in nonusers. This study demonstrates that the elevated VLDL TG concentrations in users of estrogen-dominant oral contraceptives is mainly caused by an increased concentration of small VLDL particles that have reduced TG content, and that do not have apoE and C-III. These particles may have lower atherogenicity than particles enriched with apoE and C-III.—Khoo, C., H. Campos, H. Judge, and F. M. Sacks. Effects of estrogenic oral contraceptives on the lipoprotein B particle system defined by apolipoproteins E and C-III content. J. Lipid Res. 1999. 40: 202–212.
topic apoB
apoE
apoC-III
estrogen
oral contraceptives
atherosclerosis
url http://www.sciencedirect.com/science/article/pii/S0022227520333587
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