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Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid

BACKGROUND: Sphingolipids (SL), in particular sphingomyelin (SM) are important components of milk fat polar lipids. Dietary SM inhibits cholesterol absorption in rats (Nyberg et al. J Nutr Biochem. 2000) and SLs decrease both cholesterol and TG concentrations in lipid- and cholesterol fed APOE*3Leid...

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Autores principales: Ohlsson, Lena, Burling, Hans, Nilsson, Åke
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768711/
https://www.ncbi.nlm.nih.gov/pubmed/19835602
http://dx.doi.org/10.1186/1476-511X-8-44
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author Ohlsson, Lena
Burling, Hans
Nilsson, Åke
author_facet Ohlsson, Lena
Burling, Hans
Nilsson, Åke
author_sort Ohlsson, Lena
collection PubMed
description BACKGROUND: Sphingolipids (SL), in particular sphingomyelin (SM) are important components of milk fat polar lipids. Dietary SM inhibits cholesterol absorption in rats (Nyberg et al. J Nutr Biochem. 2000) and SLs decrease both cholesterol and TG concentrations in lipid- and cholesterol fed APOE*3Leiden mice (Duivenvoorden et al. Am J Clin Nutr. 2006). This human study examines effects of a butter milk formulation enriched in milk fat globule membrane material, and thereby in SLs, on blood lipids in healthy volunteers. In a four week parallel group study with 33 men and 15 women we examined the effects of an SL-enriched butter milk formulation (A) and an equivalent control formulation (B) on plasma lipid levels. Plasma concentrations of HDL and LDL cholesterol, triacylglycerols (TG), apolipoproteins AI and B, and lipoprotein (a) were measured. The daily dose of SL in A was 975 mg of which 700 mg was SM. The participants registered food and drink intake four days before introducing the test formula and the last four days of the test period. RESULTS: A daily increase of SL intake did not significantly influence fasting plasma lipids or lipoproteins. In group B TG, cholesterol, LDL, HDL and apolipoprotein B concentrations increased, however, but not in group A after four weeks. The difference in LDL cholesterol was seen primarily in women and difference in TG primarily in men. No significant side effects were observed. CONCLUSION: The study did not show any significant decrease on plasma lipids or lipoprotein levels of an SL-enriched formulation containing 2-3 times more SL than the normal dietary intake on cholesterol, other plasma lipids or on energy intake. The formulation A may, however, have counteracted the trend towards increased blood lipid concentrations caused by increased energy intake that was seen with the B formulation.
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spelling pubmed-27687112009-10-28 Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid Ohlsson, Lena Burling, Hans Nilsson, Åke Lipids Health Dis Research BACKGROUND: Sphingolipids (SL), in particular sphingomyelin (SM) are important components of milk fat polar lipids. Dietary SM inhibits cholesterol absorption in rats (Nyberg et al. J Nutr Biochem. 2000) and SLs decrease both cholesterol and TG concentrations in lipid- and cholesterol fed APOE*3Leiden mice (Duivenvoorden et al. Am J Clin Nutr. 2006). This human study examines effects of a butter milk formulation enriched in milk fat globule membrane material, and thereby in SLs, on blood lipids in healthy volunteers. In a four week parallel group study with 33 men and 15 women we examined the effects of an SL-enriched butter milk formulation (A) and an equivalent control formulation (B) on plasma lipid levels. Plasma concentrations of HDL and LDL cholesterol, triacylglycerols (TG), apolipoproteins AI and B, and lipoprotein (a) were measured. The daily dose of SL in A was 975 mg of which 700 mg was SM. The participants registered food and drink intake four days before introducing the test formula and the last four days of the test period. RESULTS: A daily increase of SL intake did not significantly influence fasting plasma lipids or lipoproteins. In group B TG, cholesterol, LDL, HDL and apolipoprotein B concentrations increased, however, but not in group A after four weeks. The difference in LDL cholesterol was seen primarily in women and difference in TG primarily in men. No significant side effects were observed. CONCLUSION: The study did not show any significant decrease on plasma lipids or lipoprotein levels of an SL-enriched formulation containing 2-3 times more SL than the normal dietary intake on cholesterol, other plasma lipids or on energy intake. The formulation A may, however, have counteracted the trend towards increased blood lipid concentrations caused by increased energy intake that was seen with the B formulation. BioMed Central 2009-10-16 /pmc/articles/PMC2768711/ /pubmed/19835602 http://dx.doi.org/10.1186/1476-511X-8-44 Text en Copyright © 2009 Ohlsson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ohlsson, Lena
Burling, Hans
Nilsson, Åke
Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
title Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
title_full Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
title_fullStr Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
title_full_unstemmed Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
title_short Long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
title_sort long term effects on human plasma lipoproteins of a formulation enriched in butter milk polar lipid
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768711/
https://www.ncbi.nlm.nih.gov/pubmed/19835602
http://dx.doi.org/10.1186/1476-511X-8-44
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