Lipo‐Protein Emulsion Structure in the Diet Affects Protein Digestion Kinetics, Intestinal Mucosa Parameters and Microbiota Composition
Scope Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes. Methods & Results Rats (n = 40) are fed for 3 weeks with two diets chemically identical but based...
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Published in | Molecular nutrition & food research Vol. 62; no. 2 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.01.2018
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Abstract | Scope
Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes.
Methods & Results
Rats (n = 40) are fed for 3 weeks with two diets chemically identical but based on lipid–protein liquid‐fine (LFE) or gelled‐coarse (GCE) emulsions that differ at the macro‐ and microstructure levels. After an overnight fasting, they ingest a 15N‐labeled LFE or GCE test meal and are euthanized 0, 15 min, 1 h, and 5 h later. 15N enrichment in intestinal contents and blood are measured. Gastric emptying, protein digestion kinetics, 15N absorption, and incorporation in blood protein and urea are faster with LFE than GCE. At 15 min time point, LFE group shows higher increase in GIP portal levels than GCE. Three weeks of dietary adaptation leads to higher expression of cationic amino acid transporters in ileum of LFE compared to GCE. LFE diet raises cecal butyrate and isovalerate proportion relative to GCE, suggesting increased protein fermentation. LFE diet increases fecal Parabacteroides relative abundance but decreases Bifidobacterium, Sutterella, Parasutterella genera, and Clostridium cluster XIV abundance.
Conclusion
Protein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value.
Food processing alters food structure, raising the question how that affects its digestion. To investigate this, we created two chemically identical diets which differed in macro‐ and microstructure of protein–lipid emulsion. It was found that these structural differences in lipoprotein matrix incorporated in the diet had major effects on dietary protein digestion kinetics, nitrogenous compound absorption, and incorporation in blood proteins. This was associated with changes in endocrine response of the proximal intestine and modification and activity of the gut microbiota. |
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AbstractList | ScopeFood structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes.Methods & ResultsRats (n = 40) are fed for 3 weeks with two diets chemically identical but based on lipid–protein liquid‐fine (LFE) or gelled‐coarse (GCE) emulsions that differ at the macro‐ and microstructure levels. After an overnight fasting, they ingest a 15N‐labeled LFE or GCE test meal and are euthanized 0, 15 min, 1 h, and 5 h later. 15N enrichment in intestinal contents and blood are measured. Gastric emptying, protein digestion kinetics, 15N absorption, and incorporation in blood protein and urea are faster with LFE than GCE. At 15 min time point, LFE group shows higher increase in GIP portal levels than GCE. Three weeks of dietary adaptation leads to higher expression of cationic amino acid transporters in ileum of LFE compared to GCE. LFE diet raises cecal butyrate and isovalerate proportion relative to GCE, suggesting increased protein fermentation. LFE diet increases fecal Parabacteroides relative abundance but decreases Bifidobacterium, Sutterella, Parasutterella genera, and Clostridium cluster XIV abundance.ConclusionProtein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value. Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes. Rats (n = 40) are fed for 3 weeks with two diets chemically identical but based on lipid-protein liquid-fine (LFE) or gelled-coarse (GCE) emulsions that differ at the macro- and microstructure levels. After an overnight fasting, they ingest a N-labeled LFE or GCE test meal and are euthanized 0, 15 min, 1 h, and 5 h later. N enrichment in intestinal contents and blood are measured. Gastric emptying, protein digestion kinetics, N absorption, and incorporation in blood protein and urea are faster with LFE than GCE. At 15 min time point, LFE group shows higher increase in GIP portal levels than GCE. Three weeks of dietary adaptation leads to higher expression of cationic amino acid transporters in ileum of LFE compared to GCE. LFE diet raises cecal butyrate and isovalerate proportion relative to GCE, suggesting increased protein fermentation. LFE diet increases fecal Parabacteroides relative abundance but decreases Bifidobacterium, Sutterella, Parasutterella genera, and Clostridium cluster XIV abundance. Protein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value. Scope Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes. Methods & Results Rats (n = 40) are fed for 3 weeks with two diets chemically identical but based on lipid–protein liquid‐fine (LFE) or gelled‐coarse (GCE) emulsions that differ at the macro‐ and microstructure levels. After an overnight fasting, they ingest a 15N‐labeled LFE or GCE test meal and are euthanized 0, 15 min, 1 h, and 5 h later. 15N enrichment in intestinal contents and blood are measured. Gastric emptying, protein digestion kinetics, 15N absorption, and incorporation in blood protein and urea are faster with LFE than GCE. At 15 min time point, LFE group shows higher increase in GIP portal levels than GCE. Three weeks of dietary adaptation leads to higher expression of cationic amino acid transporters in ileum of LFE compared to GCE. LFE diet raises cecal butyrate and isovalerate proportion relative to GCE, suggesting increased protein fermentation. LFE diet increases fecal Parabacteroides relative abundance but decreases Bifidobacterium, Sutterella, Parasutterella genera, and Clostridium cluster XIV abundance. Conclusion Protein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value. Food processing alters food structure, raising the question how that affects its digestion. To investigate this, we created two chemically identical diets which differed in macro‐ and microstructure of protein–lipid emulsion. It was found that these structural differences in lipoprotein matrix incorporated in the diet had major effects on dietary protein digestion kinetics, nitrogenous compound absorption, and incorporation in blood proteins. This was associated with changes in endocrine response of the proximal intestine and modification and activity of the gut microbiota. Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes.SCOPEFood structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect digestive and absorptive processes.Rats (n = 40) are fed for 3 weeks with two diets chemically identical but based on lipid-protein liquid-fine (LFE) or gelled-coarse (GCE) emulsions that differ at the macro- and microstructure levels. After an overnight fasting, they ingest a 15 N-labeled LFE or GCE test meal and are euthanized 0, 15 min, 1 h, and 5 h later. 15 N enrichment in intestinal contents and blood are measured. Gastric emptying, protein digestion kinetics, 15 N absorption, and incorporation in blood protein and urea are faster with LFE than GCE. At 15 min time point, LFE group shows higher increase in GIP portal levels than GCE. Three weeks of dietary adaptation leads to higher expression of cationic amino acid transporters in ileum of LFE compared to GCE. LFE diet raises cecal butyrate and isovalerate proportion relative to GCE, suggesting increased protein fermentation. LFE diet increases fecal Parabacteroides relative abundance but decreases Bifidobacterium, Sutterella, Parasutterella genera, and Clostridium cluster XIV abundance.METHODS & RESULTSRats (n = 40) are fed for 3 weeks with two diets chemically identical but based on lipid-protein liquid-fine (LFE) or gelled-coarse (GCE) emulsions that differ at the macro- and microstructure levels. After an overnight fasting, they ingest a 15 N-labeled LFE or GCE test meal and are euthanized 0, 15 min, 1 h, and 5 h later. 15 N enrichment in intestinal contents and blood are measured. Gastric emptying, protein digestion kinetics, 15 N absorption, and incorporation in blood protein and urea are faster with LFE than GCE. At 15 min time point, LFE group shows higher increase in GIP portal levels than GCE. Three weeks of dietary adaptation leads to higher expression of cationic amino acid transporters in ileum of LFE compared to GCE. LFE diet raises cecal butyrate and isovalerate proportion relative to GCE, suggesting increased protein fermentation. LFE diet increases fecal Parabacteroides relative abundance but decreases Bifidobacterium, Sutterella, Parasutterella genera, and Clostridium cluster XIV abundance.Protein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value.CONCLUSIONProtein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value. |
Author | Leclerc, Marion Gaudichon, Claire Chaumontet, Catherine Beaumont, Martin Feunteun, Steven Fromentin, Gilles Michon, Camille Douard, Véronique Laurent, Sandy Souchon, Isabelle Devime, Fabienne Blachier, François Mat, Damien Oberli, Marion Davila, Anne‐Marie Jaoui, Daphné Tomé, Daniel |
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Keywords | dietary protein gut peptides stomach emptying gut microbiota food structure digestion |
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Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may... Food structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may affect... ScopeFood structure is a key factor controlling digestion and nutrient absorption. We test the hypothesis that protein emulsion structure in the diet may... |
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SubjectTerms | Absorption Absorptivity Abundance Amino Acid Transport Systems, Neutral - genetics Amino Acid Transport Systems, Neutral - metabolism Amino acids Amino Acids - pharmacokinetics Animals Blood Body Weight - drug effects Cecum Clostridium Diet dietary protein Dietary Proteins - pharmacokinetics Digestion Digestive system Emulsions Emulsions - chemistry Emulsions - pharmacology Fermentation Food and Nutrition Food composition food structure Gastric emptying Gastrointestinal Microbiome - drug effects Gastrointestinal tract gut microbiota gut peptides Ileum Intestinal Mucosa - drug effects Intestinal Mucosa - physiology Intestine Intestine, Small - drug effects Intestine, Small - metabolism Kinetics Life Sciences Lipoproteins - chemistry Lipoproteins - pharmacology Male Microbiota Mucosa Nitrogen Isotopes - analysis Nitrogen Isotopes - pharmacokinetics Protein structure Proteins Rats Rats, Wistar Relative abundance Rodents stomach emptying Urea |
Title | Lipo‐Protein Emulsion Structure in the Diet Affects Protein Digestion Kinetics, Intestinal Mucosa Parameters and Microbiota Composition |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmnfr.201700570 https://www.ncbi.nlm.nih.gov/pubmed/28994235 https://www.proquest.com/docview/1989598804 https://www.proquest.com/docview/1949695543 https://agroparistech.hal.science/hal-01619023 |
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