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Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation

Dietary fatty acid (FA) composition in early postnatal life can modulate growth and development and later metabolic health. Investigating programming effects of early dietary FA manipulations in rodents may be stressful and complicated due to the need of artificial feeding techniques. It is largely...

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Autores principales: Oosting, Annemarie, Verkade, Henkjan J., Kegler, Diane, van de Heijning, Bert J. M., van der Beek, Eline M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462764/
https://www.ncbi.nlm.nih.gov/pubmed/26097702
http://dx.doi.org/10.1017/jns.2015.13
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author Oosting, Annemarie
Verkade, Henkjan J.
Kegler, Diane
van de Heijning, Bert J. M.
van der Beek, Eline M.
author_facet Oosting, Annemarie
Verkade, Henkjan J.
Kegler, Diane
van de Heijning, Bert J. M.
van der Beek, Eline M.
author_sort Oosting, Annemarie
collection PubMed
description Dietary fatty acid (FA) composition in early postnatal life can modulate growth and development and later metabolic health. Investigating programming effects of early dietary FA manipulations in rodents may be stressful and complicated due to the need of artificial feeding techniques. It is largely unknown to what extent breast milk (BM) FA composition can be directly manipulated by the diet. We exposed dams to different dietary FA compositions from postnatal day (PN) 2 until PN28. Dams with litters were randomly assigned to control (CTRL), high-medium-chain FA (MCFA), low-linoleic acid (LowLA), high-n-3 long-chain PUFA (n-3LCP) or high-n-3LCP and MCFA (n-3LCP/MCFA) diets, and diets were continued after weaning until PN28. FA compositions were determined in feeds, milk and in erythrocytes. BM MCFA content was independent from dietary MCFA intake. In contrast, the LowLA diet reduced BM LA content by about 50 % compared with the CTRL diet at PN7. BM of dams fed the n-3LCP or n-3LCP/MCFA diet contained about 6-fold more n-3 LCP than BM of the dams fed the CTRL diet at PN7. These changes in milk FA composition established after 5 d of dietary exposure did not further change over the lactation period. At PN28, the erythrocyte FA composition of the male pups correlated with analysed milk FA profiles. In conclusion, manipulation of the diet of lactating mice can strongly and rapidly affect BM FA composition, in particular of n-6 LA and n-3 LCP. Our present findings will facilitate mechanistic studies on the programming of adult metabolic health by dietary FA in the early postnatal period via direct and selective manipulation of the maternal diet.
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spelling pubmed-44627642015-06-19 Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation Oosting, Annemarie Verkade, Henkjan J. Kegler, Diane van de Heijning, Bert J. M. van der Beek, Eline M. J Nutr Sci Research Article Dietary fatty acid (FA) composition in early postnatal life can modulate growth and development and later metabolic health. Investigating programming effects of early dietary FA manipulations in rodents may be stressful and complicated due to the need of artificial feeding techniques. It is largely unknown to what extent breast milk (BM) FA composition can be directly manipulated by the diet. We exposed dams to different dietary FA compositions from postnatal day (PN) 2 until PN28. Dams with litters were randomly assigned to control (CTRL), high-medium-chain FA (MCFA), low-linoleic acid (LowLA), high-n-3 long-chain PUFA (n-3LCP) or high-n-3LCP and MCFA (n-3LCP/MCFA) diets, and diets were continued after weaning until PN28. FA compositions were determined in feeds, milk and in erythrocytes. BM MCFA content was independent from dietary MCFA intake. In contrast, the LowLA diet reduced BM LA content by about 50 % compared with the CTRL diet at PN7. BM of dams fed the n-3LCP or n-3LCP/MCFA diet contained about 6-fold more n-3 LCP than BM of the dams fed the CTRL diet at PN7. These changes in milk FA composition established after 5 d of dietary exposure did not further change over the lactation period. At PN28, the erythrocyte FA composition of the male pups correlated with analysed milk FA profiles. In conclusion, manipulation of the diet of lactating mice can strongly and rapidly affect BM FA composition, in particular of n-6 LA and n-3 LCP. Our present findings will facilitate mechanistic studies on the programming of adult metabolic health by dietary FA in the early postnatal period via direct and selective manipulation of the maternal diet. Cambridge University Press 2015-05-06 /pmc/articles/PMC4462764/ /pubmed/26097702 http://dx.doi.org/10.1017/jns.2015.13 Text en © The Author(s) 2015 This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Oosting, Annemarie
Verkade, Henkjan J.
Kegler, Diane
van de Heijning, Bert J. M.
van der Beek, Eline M.
Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
title Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
title_full Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
title_fullStr Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
title_full_unstemmed Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
title_short Rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
title_sort rapid and selective manipulation of milk fatty acid composition in mice through the maternal diet during lactation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462764/
https://www.ncbi.nlm.nih.gov/pubmed/26097702
http://dx.doi.org/10.1017/jns.2015.13
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