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Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch

The metabolome and gut microbiota were investigated in a juvenile Göttingen minipig model. This study aimed to explore the metabolic effects of two carbohydrate sources with different degrees of risk in obesity development when associated with a high fat intake. A high-risk (HR) high-fat diet contai...

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Autores principales: Curtasu, Mihai V., Tafintseva, Valeria, Bendiks, Zachary A., Marco, Maria L., Kohler, Achim, Xu, Yetong, Nørskov, Natalja P., Nygaard Lærke, Helle, Bach Knudsen, Knud Erik, Hedemann, Mette Skou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697781/
https://www.ncbi.nlm.nih.gov/pubmed/33198236
http://dx.doi.org/10.3390/metabo10110456
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author Curtasu, Mihai V.
Tafintseva, Valeria
Bendiks, Zachary A.
Marco, Maria L.
Kohler, Achim
Xu, Yetong
Nørskov, Natalja P.
Nygaard Lærke, Helle
Bach Knudsen, Knud Erik
Hedemann, Mette Skou
author_facet Curtasu, Mihai V.
Tafintseva, Valeria
Bendiks, Zachary A.
Marco, Maria L.
Kohler, Achim
Xu, Yetong
Nørskov, Natalja P.
Nygaard Lærke, Helle
Bach Knudsen, Knud Erik
Hedemann, Mette Skou
author_sort Curtasu, Mihai V.
collection PubMed
description The metabolome and gut microbiota were investigated in a juvenile Göttingen minipig model. This study aimed to explore the metabolic effects of two carbohydrate sources with different degrees of risk in obesity development when associated with a high fat intake. A high-risk (HR) high-fat diet containing 20% fructose was compared to a control lower-risk (LR) high-fat diet where a similar amount of carbohydrate was provided as a mix of digestible and resistant starch from high amylose maize. Both diets were fed ad libitum. Non-targeted metabolomics was used to explore plasma, urine, and feces samples over five months. Plasma and fecal short-chain fatty acids were targeted and quantified. Fecal microbiota was analyzed using genomic sequencing. Data analysis was performed using sparse multi-block partial least squares regression. The LR diet increased concentrations of fecal and plasma total short-chain fatty acids, primarily acetate, and there was a higher relative abundance of microbiota associated with acetate production such as Bacteroidetes and Ruminococcus. A higher proportion of Firmicutes was measured with the HR diet, together with a lower alpha diversity compared to the LR diet. Irrespective of diet, the ad libitum exposure to the high-energy diets was accompanied by well-known biomarkers associated with obesity and diabetes, particularly branched-chain amino acids, keto acids, and other catabolism metabolites.
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spelling pubmed-76977812020-11-29 Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch Curtasu, Mihai V. Tafintseva, Valeria Bendiks, Zachary A. Marco, Maria L. Kohler, Achim Xu, Yetong Nørskov, Natalja P. Nygaard Lærke, Helle Bach Knudsen, Knud Erik Hedemann, Mette Skou Metabolites Article The metabolome and gut microbiota were investigated in a juvenile Göttingen minipig model. This study aimed to explore the metabolic effects of two carbohydrate sources with different degrees of risk in obesity development when associated with a high fat intake. A high-risk (HR) high-fat diet containing 20% fructose was compared to a control lower-risk (LR) high-fat diet where a similar amount of carbohydrate was provided as a mix of digestible and resistant starch from high amylose maize. Both diets were fed ad libitum. Non-targeted metabolomics was used to explore plasma, urine, and feces samples over five months. Plasma and fecal short-chain fatty acids were targeted and quantified. Fecal microbiota was analyzed using genomic sequencing. Data analysis was performed using sparse multi-block partial least squares regression. The LR diet increased concentrations of fecal and plasma total short-chain fatty acids, primarily acetate, and there was a higher relative abundance of microbiota associated with acetate production such as Bacteroidetes and Ruminococcus. A higher proportion of Firmicutes was measured with the HR diet, together with a lower alpha diversity compared to the LR diet. Irrespective of diet, the ad libitum exposure to the high-energy diets was accompanied by well-known biomarkers associated with obesity and diabetes, particularly branched-chain amino acids, keto acids, and other catabolism metabolites. MDPI 2020-11-12 /pmc/articles/PMC7697781/ /pubmed/33198236 http://dx.doi.org/10.3390/metabo10110456 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Curtasu, Mihai V.
Tafintseva, Valeria
Bendiks, Zachary A.
Marco, Maria L.
Kohler, Achim
Xu, Yetong
Nørskov, Natalja P.
Nygaard Lærke, Helle
Bach Knudsen, Knud Erik
Hedemann, Mette Skou
Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch
title Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch
title_full Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch
title_fullStr Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch
title_full_unstemmed Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch
title_short Obesity-Related Metabolome and Gut Microbiota Profiles of Juvenile Göttingen Minipigs—Long-Term Intake of Fructose and Resistant Starch
title_sort obesity-related metabolome and gut microbiota profiles of juvenile göttingen minipigs—long-term intake of fructose and resistant starch
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697781/
https://www.ncbi.nlm.nih.gov/pubmed/33198236
http://dx.doi.org/10.3390/metabo10110456
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