Casein structure differently impacts satiety by modulating plasma aminoacid kinetic
2024
Guerin, Sylvie | Le Normand, Laurence | Cahu, Armelle | Boulier, Audrey | Hiolle, Manon | Baniel, Alain | Dupont, Didier | Boudry, Gaëlle | Henry, Gwenaëlle | Nutrition, Métabolismes et Cancer (NuMeCan) ; Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE) | INGREDIA SA, F-62000 Arras, France ; Partenaires INRAE | Science et Technologie du Lait et de l'Oeuf (STLO) ; Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut Agro Rennes Angers ; Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro) | https://www.icfd2024.com/
International audience
Afficher plus [+] Moins [-]anglais. Dietary protein is strong appetite inhibitor as it reduces food intake in following meals by signalingdirectly or indirectly to the brain, modulating eating behavior. However, the type of protein in snacksor pre-loads differently influences food intake, likely due to differences in dietary protein hydrolysisand amino acid bioavailability. We recently observed striking differences in plasma amino acidkinetics as well as intra-gastric behavior between micellar casein (MC) and sodium caseinate (SC).Gastric distension and plasma amino acid levels, in particular that of leucine, both impact foodintake. The objective of the present study was therefore to clarify whether the structure of caseinimpacts its preload effect on subsequent food intake in the pig model.Overnight fasted pigs (21.5 ± 1.5 kg) equipped with jugular catheters were allowed to consumewithin 5 min casein drinks differing in casein structure (SC vs. MC, 350 kcal, 10% casein, 1.2% glucosein water) in a cross-over study. Ad libitum intake of their regular feed was assessed during 1hr, either1 or 4hr after casein drink ingestion. Gastric emptying of the casein drinks radiolabeled with 99Tc-colloïd was followed during 2hr using gamma-scintigraphy. Plasma kinetics of hormones related toeating behavior (ghrelin, GLP-1, insulin) and of free amino acids were evaluated for 2hr followingcasein drink ingestion.The amount of feed consumed 1hr, but not 4hr, after SC ingestion was lower than the amount offeed consumed after MC ingestion (feed consumed at 1h: SC 1306 ± 138 vs. MC 1513 ± 79 g, P=0.03).Gastric emptying parameters after both types of casein ingestion were not significantly different(t1/2: SC 103 ± 12 vs. MC 116 ± 18 min, β: SC 0.67 ± 0.14 vs. MC 0.52 ± 0.04, P>0.05). Plasma ghrelin,GLP-1 and insulin kinetics were similar after casein drink ingestion (SC vs. MC, P>0.05 for allhormones). Free plasma amino acid concentrations, in particular that of leucine, increased after bothSC and MC ingestion but was greater after SC than MC ingestion from 60 to 120 min (plasma leucineat 60 min: SC 87.8 ± 4.8 vs. MC 66.0 ± 3.5 mg/L, P=0.009).In conclusion, ingestion of casein differing in their structure impacts subsequent food intake likelydue to difference in amino acid bioavailability. Casein exhibits less anorectic effect when consumedas micellar casein than as sodium caseinate. Such differences might be of importance when designingfood dedicated to people with low appetite.
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