Camille Michon
Université Paris-Saclay
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Featured researches published by Camille Michon.
Food Chemistry | 2018
Damien Mat; Thomas Cattenoz; Isabelle Souchon; Camille Michon; Steven Le Feunteun
This study intends to demonstrate that acid titration at low pH is very well adapted to the monitoring of pepsin activity. After a description of the underlying principles, this approach was used during in vitro gastric digestions of a model of complex food containing 15wt% of whey proteins, according to both static (2h at pHxa0=xa03, Infogest protocol) and dynamic pH conditions (from pH 6.3 down to 2 in 1h). Pepsin activity was quantitatively assessed in all experiments through the calculation of degrees of hydrolysis (DH). Final values of 3.7 and 3.0% were obtained in static and dynamic pH conditions, respectively, and validated using an independent method. Results also show that about 92% of the peptides were detected at pHxa0=xa03, and 100% for pH≤2.5. Overall, the proposed approach proved to be very worthy to study protein hydrolysis during in vitro gastric digestions.
Molecular Nutrition & Food Research | 2018
Marion Oberli; Véronique Douard; Martin Beaumont; Daphné Jaoui; Fabienne Devime; Sandy Laurent; Catherine Chaumontet; Damien Mat; Steven Le Feunteun; Camille Michon; Anne-Marie Davila; G. Fromentin; Daniel Tomé; Isabelle Souchon; Marion Leclerc; Claire Gaudichon; François Blachier
SCOPEnFood 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.nnnMETHODS & RESULTSnRats (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, 15xa0min, 1xa0h, and 5xa0h 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 15xa0min 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.nnnCONCLUSIONnProtein emulsion structure regulates digestion kinetics and gastrointestinal physiology, and could be targeted to improve food health value.
Molecular Nutrition & Food Research | 2017
Martin Beaumont; Daphné Jaoui; Véronique Douard; Damien Mat; Fanny Koeth; Bénédicte Goustard; Camille Mayeur; Stanislas Mondot; Anais Hovaghimian; Steven Le Feunteun; Catherine Chaumontet; Anne-Marie Davila; Daniel Tomé; Isabelle Souchon; Camille Michon; G. Fromentin; François Blachier; Marion Leclerc
SCOPEnFew studies have evaluated in vivo the impact of food structure on digestion, absorption of nutrients and on microbiota composition and metabolism. In this study we evaluated in rat the impact of two structures of protein emulsion in food on gut microbiota, luminal content composition, and intestinal characteristics.nnnMETHODS AND RESULTSnRats received for 3 weeks two diets of identical composition but based on lipid-protein matrices of liquid fine (LFE) or gelled coarse (GCE) emulsion. LFE diet led to higher abundance, when compared to the GCE, of Lactobacillaceae (Lactobacillus reuteri) in the ileum, higher β-diversity of the caecum mucus-associated bacteria. In contrast, the LFE diet led to a decrease in Akkermansia municiphila in the caecum. This coincided with heavier caecum content and higher amount of isovalerate in the LFE group. LFE diet induced an increased expression of (i) amino acid transporters in the ileum (ii) glucagon in the caecum, together with an elevated level of GLP-1 in portal plasma. However, these intestinal effects were not associated with modification of food intake or body weight gain.nnnCONCLUSIONnOverall, the structure of protein emulsion in food affects the expression of amino acid transporters and gut peptides concomitantly with modification of the gut microbiota composition and activity. Our data suggest that these effects of the emulsion structure are the result of a modification of protein digestion properties.
Journal of Texture Studies | 2018
Marine Dewaest; Cindy Villemejane; Sophie Berland; Stéphane Néron; Jérôme Clement; Aliette Verel; Camille Michon
Sponge cake is a cereal product characterized by an aerated crumb and appreciated for its softness. When formulating such product, it is interesting to be able to characterize the crumb structure using image analysis and to bring knowledge about the effects of the crumb cellular structure on its mechanical properties which contribute to softness. An image analysis method based on mathematical morphology was adapted from the one developed for bread crumb. In order to evaluate its ability to discriminate cellular structures, series of cakes were prepared using two rather similar emulsifiers but also using flours with different aging times before use. The mechanical properties of the crumbs of these different cakes were also characterized. It allowed a cell structure classification taking into account cell size and homogeneity, but also cell wall thickness and the number of holes in the walls. Interestingly, the cellular structure differences had a larger impact on the aerated crumb Young modulus than the wall firmness. Increasing the aging time of flour before use leads to the production of firmer crumbs due to coarser and inhomogeneous cellular structures. Changing the composition of the emulsifier may change the cellular structure and, depending on the type of the structural changes, have an impact on the firmness of the crumb.nnnPRACTICAL APPLICATIONSnCellular structure rather than cell wall firmness was found to impact cake crumb firmness. The new fast and automated tool for cake crumb structure analysis allows detecting quickly any change in cell size or homogeneity but also cell wall thickness and number of holes in the walls (openness degree). To obtain a softer crumb, it seems that options are to decrease the cell size and the cell wall thickness and/or to increase the openness degree. It is then possible to easily evaluate the effects of ingredients (flour composition, emulsifier …) or change in the process on the crumb structure and thus its softness. Moreover, this image analysis is a very efficient tool for quality control.
Agricultural Systems | 2017
Jean Marc Meynard; Marie-Hélène Jeuffroy; Marianne Le Bail; Amélie Lefevre; Marie-Benoît Magrini; Camille Michon
Food Research International | 2016
Damien Mat; Steven Le Feunteun; Camille Michon; Isabelle Souchon
Food Hydrocolloids | 2017
J. Bousquières; C. Bonazzi; Camille Michon
Food Hydrocolloids | 2017
J. Bousquières; Camille Michon; C. Bonazzi
Food Hydrocolloids | 2017
S. Ben-Harb; Maud Panouillé; Delphine Huc-Mathis; G. Moulin; A. Saint-Eve; F. Irlinger; P. Bonnarme; Camille Michon; Isabelle Souchon
Lwt - Food Science and Technology | 2017
Marine Dewaest; Cindy Villemejane; Sophie Berland; Camille Michon; Aliette Verel; Marie Helene Morel