Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1

Moderate alcohol consumption increases HDL cholesterol, which is involved in reverse cholesterol transport (RCT). The aim of this study was to investigate the effect of moderate alcohol consumption on cholesterol efflux, using J774 mouse macrophages and Fu5AH cells, and on other parameters in the RC...

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Main Authors: J.W.J. Beulens, A. Sierksma, A. van Tol, N. Fournier, T. van Gent, J-L. Paul, H.F.J. Hendriks
Format: Article
Language:English
Published: Elsevier 2004-09-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520312888
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language English
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author J.W.J. Beulens
A. Sierksma
A. van Tol
N. Fournier
T. van Gent
J-L. Paul
H.F.J. Hendriks
spellingShingle J.W.J. Beulens
A. Sierksma
A. van Tol
N. Fournier
T. van Gent
J-L. Paul
H.F.J. Hendriks
Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1
Journal of Lipid Research
ATP binding cassette transporter 1
reverse cholesterol transport
J774 macrophages
Fu5AH cells
preβ-high density lipoprotein
body mass index
author_facet J.W.J. Beulens
A. Sierksma
A. van Tol
N. Fournier
T. van Gent
J-L. Paul
H.F.J. Hendriks
author_sort J.W.J. Beulens
title Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1
title_short Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1
title_full Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1
title_fullStr Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1
title_full_unstemmed Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1
title_sort moderate alcohol consumption increases cholesterol efflux mediated by abca1
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 2004-09-01
description Moderate alcohol consumption increases HDL cholesterol, which is involved in reverse cholesterol transport (RCT). The aim of this study was to investigate the effect of moderate alcohol consumption on cholesterol efflux, using J774 mouse macrophages and Fu5AH cells, and on other parameters in the RCT pathway. Twenty-three healthy men (45–65 years) participated in a randomized, partially diet-controlled, crossover trial. They consumed four glasses of whisky (40 g of alcohol) or water daily for 17 days. After 17 days of whisky consumption, serum capacity to induce ABCA1-dependent cholesterol efflux from J774 mouse macrophages was increased by 17.5% (P = 0.027) compared with water consumption. Plasma capacity to induce cholesterol efflux from Fu5AH cells increased by 4.6% (P = 0.002). Preβ-HDL, apolipoprotein A-I (apoA-I), and lipoprotein A-I:A-II also increased by 31.6, 6.2, and 5.7% (P < 0.05), respectively, after whisky consumption compared with water consumption. Changes of cAMP-stimulated cholesterol efflux correlated (r = 0.65, P < 0.05) with changes of apoA-I but not with changes of preβ-HDL (r = 0.30, P = 0.18). Cholesterol efflux capacities from serum of lean men were higher than those from overweight men.In conclusion, this study shows that moderate alcohol consumption increases the capacity of serum to induce cholesterol efflux from J774 mouse macrophages, which may be mediated by ABCA1.
topic ATP binding cassette transporter 1
reverse cholesterol transport
J774 macrophages
Fu5AH cells
preβ-high density lipoprotein
body mass index
url http://www.sciencedirect.com/science/article/pii/S0022227520312888
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spelling doaj-c1957cfd5b274580a000c96992e11bf82021-04-27T04:39:35ZengElsevierJournal of Lipid Research0022-22752004-09-0145917161723Moderate alcohol consumption increases cholesterol efflux mediated by ABCA1J.W.J. Beulens0A. Sierksma1A. van Tol2N. Fournier3T. van Gent4J-L. Paul5H.F.J. Hendriks6Netherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceNetherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceNetherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceNetherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceNetherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceNetherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceNetherlands Organization for Applied Scientific Research (TNO), Nutrition and Food Research, Zeist, The Netherlands; Wageningen University, Wageningen, The Netherlands; Departments of Biochemistry and Cell Biology &amp; Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands; Laboratoire de Biochimie, Faculté des Sciences Pharmaceutiques, Châtenay-Malabry, FranceModerate alcohol consumption increases HDL cholesterol, which is involved in reverse cholesterol transport (RCT). The aim of this study was to investigate the effect of moderate alcohol consumption on cholesterol efflux, using J774 mouse macrophages and Fu5AH cells, and on other parameters in the RCT pathway. Twenty-three healthy men (45–65 years) participated in a randomized, partially diet-controlled, crossover trial. They consumed four glasses of whisky (40 g of alcohol) or water daily for 17 days. After 17 days of whisky consumption, serum capacity to induce ABCA1-dependent cholesterol efflux from J774 mouse macrophages was increased by 17.5% (P = 0.027) compared with water consumption. Plasma capacity to induce cholesterol efflux from Fu5AH cells increased by 4.6% (P = 0.002). Preβ-HDL, apolipoprotein A-I (apoA-I), and lipoprotein A-I:A-II also increased by 31.6, 6.2, and 5.7% (P < 0.05), respectively, after whisky consumption compared with water consumption. Changes of cAMP-stimulated cholesterol efflux correlated (r = 0.65, P < 0.05) with changes of apoA-I but not with changes of preβ-HDL (r = 0.30, P = 0.18). Cholesterol efflux capacities from serum of lean men were higher than those from overweight men.In conclusion, this study shows that moderate alcohol consumption increases the capacity of serum to induce cholesterol efflux from J774 mouse macrophages, which may be mediated by ABCA1.http://www.sciencedirect.com/science/article/pii/S0022227520312888ATP binding cassette transporter 1reverse cholesterol transportJ774 macrophagesFu5AH cellspreβ-high density lipoproteinbody mass index