Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/73612
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorHutchison, A.-
dc.contributor.authorFeinle-Bisset, C.-
dc.contributor.authorKallas, A.-
dc.contributor.authorWishart, J.-
dc.contributor.authorClifton, P.-
dc.contributor.authorHorowitz, M.-
dc.contributor.authorLuscombe-Marsh, N.-
dc.date.issued2012-
dc.identifier.citationAmerican Journal of Clinical Nutrition, 2012; 96(3):474-482-
dc.identifier.issn0002-9165-
dc.identifier.issn1938-3207-
dc.identifier.urihttp://hdl.handle.net/2440/73612-
dc.description.abstractBACKGROUND: Intraduodenal fat and carbohydrate modulate antropyloroduodenal motility and hormone release and suppress appetite and energy intake in a load-dependent manner. Protein also suppresses energy intake, but its effects on these gastrointestinal factors and their role in the appetite-suppressive effects of protein remain unclear. OBJECTIVE: We aimed to characterize the effects of different intraduodenal protein loads on antropyloroduodenal pressures, gastrointestinal hormone release, glucose and insulin concentrations, appetite perceptions, and energy intake. DESIGN: Sixteen lean, healthy men were studied on 4 occasions in a randomized, double-blind fashion. Antropyloroduodenal pressures, plasma glucagon-like peptide 1 (GLP-1), cholecystokinin, peptide YY, ghrelin, blood glucose, serum insulin, and appetite were measured during 60-min, 4-mL/min intraduodenal infusions of protein at 0.5, 1.5, or 3 kcal/min or saline (control). Energy intakes at a buffet lunch consumed immediately after the infusion were quantified. RESULTS: Increases in the load of protein resulted in greater suppression of antral motility, greater stimulation of basal and isolated pyloric pressures and plasma cholecystokinin and GLP-1 concentrations, and greater suppression of energy intake. However, energy intake was reduced only after a protein load of 3 kcal/min compared with after all other treatments (P< 0.05). The suppression of energy intake after adjustment for cholecystokinin, GLP-1, and insulin was related inversely with basal pyloric pressure (r = 20.51, P < 0.001). CONCLUSION: The acute effects of intraduodenal protein on antropyloroduodenal motility, gastrointestinal hormone release, glucose, and insulin are load dependent and contribute to the suppression of energy intake.-
dc.description.statementofresponsibilityAmy T. Ryan, Christine Feinle-Bisset, Asimina Kallas, Judith M. Wishart, Peter M. Clifton, Michael Horowitz and Natalie D. Luscombe-Marsh-
dc.language.isoen-
dc.publisherAmer Soc Clinical Nutrition-
dc.rights© 2012 American Society for Nutrition-
dc.source.urihttp://dx.doi.org/10.3945/ajcn.112.038133-
dc.subjectDuodenum-
dc.subjectPyloric Antrum-
dc.subjectHumans-
dc.subjectGastrointestinal Hormones-
dc.subjectInsulin-
dc.subjectBlood Glucose-
dc.subjectDietary Proteins-
dc.subjectMilk Proteins-
dc.subjectProtein Hydrolysates-
dc.subjectCross-Over Studies-
dc.subjectDouble-Blind Method-
dc.subjectEnergy Intake-
dc.subjectAppetite Regulation-
dc.subjectGastrointestinal Motility-
dc.subjectPostprandial Period-
dc.subjectAdult-
dc.subjectMiddle Aged-
dc.subjectNew Zealand-
dc.subjectMale-
dc.subjectYoung Adult-
dc.subjectWhey Proteins-
dc.titleIntraduodenal protein modulates antropyloroduodenal motility, hormone release, glycemia, appetite, and energy intake in lean men-
dc.typeJournal article-
dc.identifier.doi10.3945/ajcn.112.038133-
pubs.publication-statusPublished-
dc.identifier.orcidHutchison, A. [0000-0002-6393-3671]-
dc.identifier.orcidFeinle-Bisset, C. [0000-0001-6848-0125]-
dc.identifier.orcidClifton, P. [0000-0002-6411-626X]-
dc.identifier.orcidHorowitz, M. [0000-0002-0942-0306]-
dc.identifier.orcidLuscombe-Marsh, N. [0000-0001-9690-4722]-
Appears in Collections:Aurora harvest 5
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.