Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17455
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dc.contributor.authorBrennan, I.-
dc.contributor.authorFeltrin, K.-
dc.contributor.authorHorowitz, M.-
dc.contributor.authorSmout, A.-
dc.contributor.authorMeyer, J.-
dc.contributor.authorWishart, J.-
dc.contributor.authorFeinle-Bisset, C.-
dc.date.issued2005-
dc.identifier.citationAmerican Journal of Physiology: Regulatory, Integrative and Comparative Physiology, 2005; 288(6):R1477-R1485-
dc.identifier.issn0363-6119-
dc.identifier.issn1522-1490-
dc.identifier.urihttp://hdl.handle.net/2440/17455-
dc.descriptionPublished abstract used with permission of the copyright owner.-
dc.description.abstractThere is evidence that CCK and glucagon-like peptide-1 (GLP-1) mediate the effects of nutrients on appetite and gastrointestinal function and that their interaction may be synergistic. We hypothesized that intravenous CCK-8 and GLP-1 would have synergistic effects on appetite, energy intake, and antropyloroduodenal (APD) motility. Nine healthy males (age 22 ± 1 yr) were studied on four separate days in a double-blind, randomized fashion. Appetite and APD pressures were measured during 150-min intravenous infusions of 1) isotonic saline (control), 2) CCK-8 (1.8 pmol·kg–1·min–1), 3) GLP-1 (0.9 pmol·kg–1·min–1), or 4) both CCK-8 (1.8 pmol·kg–1·min–1) and GLP-1 (0.9 pmol·kg–1·min–1). At 120 min, energy intake at a buffet meal was quantified. CCK-8, but not GLP-1, increased fullness, decreased desire to eat and subsequent energy intake, and increased the number and amplitude of isolated pyloric pressure waves and basal pyloric pressure (P < 0.05). Both CCK-8 and GLP-1 decreased the number of antral and duodenal pressure waves (PWs) (P < 0.05), and CCK-8+GLP-1 decreased the number of duodenal PWs more than either CCK-8 or GLP-1 alone (P < 0.02). This was not the case for appetite or isolated pyloric PWs. In conclusion, at the doses evaluated, exogenously administered CCK-8 and GLP-1 had discrepant effects on appetite, energy intake, and APD pressures, and the effects of CCK-8+GLP-1, in combination, did not exceed the sum of the effects of CCK-8 and GLP-1, providing no evidence of synergism.-
dc.description.statementofresponsibilityIxchel M. Brennan, Kate L. Feltrin, Michael Horowitz, Andre J. P. M. Smout, James H. Meyer, Judith Wishart, and Christine Feinle-Bisset-
dc.language.isoen-
dc.publisherAmer Physiological Soc-
dc.rightsCopyright © 2005 American Physiological Society-
dc.source.urihttp://dx.doi.org/10.1152/ajpregu.00732.2004-
dc.subjectDuodenum-
dc.subjectPyloric Antrum-
dc.subjectHumans-
dc.subjectNausea-
dc.subjectCholecystokinin-
dc.subjectGlucagon-
dc.subjectPeptide Fragments-
dc.subjectProtein Precursors-
dc.subjectInfusions, Intravenous-
dc.subjectDouble-Blind Method-
dc.subjectAppetite-
dc.subjectSatiety Response-
dc.subjectEnergy Intake-
dc.subjectGastrointestinal Motility-
dc.subjectDrug Synergism-
dc.subjectPressure-
dc.subjectReference Values-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectMale-
dc.subjectGlucagon-Like Peptide 1-
dc.titleEvaluation of interactions between CCK and GLP-1 in their effects on appetite, energy intake, and antropyloroduodenal motility in healthy men-
dc.typeJournal article-
dc.identifier.doi10.1152/ajpregu.00732.2004-
pubs.publication-statusPublished-
dc.identifier.orcidHorowitz, M. [0000-0002-0942-0306]-
dc.identifier.orcidFeinle-Bisset, C. [0000-0001-6848-0125]-
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