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Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet

BACKGROUND: In the past several years, the use of resistant starch (RS) as prebiotic has extensively been studied in pigs, and this mostly in the critical period around weaning. RS is believed to exert beneficial effects on the gastrointestinal tract mainly due to higher levels of short chain fatty...

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Autores principales: Schroyen, Martine, Leblois, Julie, Uerlings, Julie, Li, Bing, Sureda, Ester Arévalo, Massart, Sébastien, Wavreille, José, Bindelle, Jérôme, Everaert, Nadia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318506/
https://www.ncbi.nlm.nih.gov/pubmed/32590936
http://dx.doi.org/10.1186/s12864-020-06854-x
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author Schroyen, Martine
Leblois, Julie
Uerlings, Julie
Li, Bing
Sureda, Ester Arévalo
Massart, Sébastien
Wavreille, José
Bindelle, Jérôme
Everaert, Nadia
author_facet Schroyen, Martine
Leblois, Julie
Uerlings, Julie
Li, Bing
Sureda, Ester Arévalo
Massart, Sébastien
Wavreille, José
Bindelle, Jérôme
Everaert, Nadia
author_sort Schroyen, Martine
collection PubMed
description BACKGROUND: In the past several years, the use of resistant starch (RS) as prebiotic has extensively been studied in pigs, and this mostly in the critical period around weaning. RS is believed to exert beneficial effects on the gastrointestinal tract mainly due to higher levels of short chain fatty acids (SCFAs) and an improved microbiota profile. In this study, sows were fed digestible starch (DS) or RS during late gestation and lactation and the possible maternal effect of RS on the overall health of the progeny was assessed. Since RS is also described to have a positive effect on metabolism, and to investigate a metabolic programming of the progeny, half of the piglets per maternal diet were assigned to a high fat diet from weaning on to 10 weeks after. RESULTS: No bodyweight differences were found between the four experimental piglet groups. The high fat diet did however impact back fat thickness and meat percentage whereas maternal diet did not influence these parameters. The impact of the high fat diet was also reflected in higher levels of serum cholesterol. No major differences in microbiota could be distinguished, although higher levels of SCFA were seen in the colon of piglets born from RS fed sows, and some differences in SCFA production were observed in the caecum, mainly due to piglet diet. RNA-sequencing on liver and colon scrapings revealed minor differences between the maternal diet groups. Merely a handful of genes was differentially expressed between piglets from DS and RS sows, and network analysis showed only one significant cluster of genes in the liver due to the maternal diet that did not point to meaningful biological pathways. However, the high fat diet resulted in liver gene clusters that were significantly correlated with piglet diet, of which one is annotated for lipid metabolic processes. These clusters were not correlated with maternal diet. CONCLUSIONS: There is only a minor impact of maternal dietary RS on the progeny, reflected in SCFA changes. A high fat diet given to the progeny directly evokes metabolic changes in the liver, without any maternal programming by a RS diet.
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spelling pubmed-73185062020-06-29 Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet Schroyen, Martine Leblois, Julie Uerlings, Julie Li, Bing Sureda, Ester Arévalo Massart, Sébastien Wavreille, José Bindelle, Jérôme Everaert, Nadia BMC Genomics Research Article BACKGROUND: In the past several years, the use of resistant starch (RS) as prebiotic has extensively been studied in pigs, and this mostly in the critical period around weaning. RS is believed to exert beneficial effects on the gastrointestinal tract mainly due to higher levels of short chain fatty acids (SCFAs) and an improved microbiota profile. In this study, sows were fed digestible starch (DS) or RS during late gestation and lactation and the possible maternal effect of RS on the overall health of the progeny was assessed. Since RS is also described to have a positive effect on metabolism, and to investigate a metabolic programming of the progeny, half of the piglets per maternal diet were assigned to a high fat diet from weaning on to 10 weeks after. RESULTS: No bodyweight differences were found between the four experimental piglet groups. The high fat diet did however impact back fat thickness and meat percentage whereas maternal diet did not influence these parameters. The impact of the high fat diet was also reflected in higher levels of serum cholesterol. No major differences in microbiota could be distinguished, although higher levels of SCFA were seen in the colon of piglets born from RS fed sows, and some differences in SCFA production were observed in the caecum, mainly due to piglet diet. RNA-sequencing on liver and colon scrapings revealed minor differences between the maternal diet groups. Merely a handful of genes was differentially expressed between piglets from DS and RS sows, and network analysis showed only one significant cluster of genes in the liver due to the maternal diet that did not point to meaningful biological pathways. However, the high fat diet resulted in liver gene clusters that were significantly correlated with piglet diet, of which one is annotated for lipid metabolic processes. These clusters were not correlated with maternal diet. CONCLUSIONS: There is only a minor impact of maternal dietary RS on the progeny, reflected in SCFA changes. A high fat diet given to the progeny directly evokes metabolic changes in the liver, without any maternal programming by a RS diet. BioMed Central 2020-06-26 /pmc/articles/PMC7318506/ /pubmed/32590936 http://dx.doi.org/10.1186/s12864-020-06854-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Schroyen, Martine
Leblois, Julie
Uerlings, Julie
Li, Bing
Sureda, Ester Arévalo
Massart, Sébastien
Wavreille, José
Bindelle, Jérôme
Everaert, Nadia
Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
title Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
title_full Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
title_fullStr Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
title_full_unstemmed Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
title_short Maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
title_sort maternal dietary resistant starch does not improve piglet’s gut and liver metabolism when challenged with a high fat diet
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318506/
https://www.ncbi.nlm.nih.gov/pubmed/32590936
http://dx.doi.org/10.1186/s12864-020-06854-x
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