2012
DOI: 10.1016/j.neuropharm.2011.10.008
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The role of the gut/brain axis in modulating food intake

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Cited by 134 publications
(105 citation statements)
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References 172 publications
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“…Clarification of the interactions between these drivers is just beginning to emerge. From 2000 to the present, much has been learned about the peripheral hormonal signals and central targets that influence energy intake (20)(21)(22). Dietary protein is an effective stimulus for the release or inhibition of many of these peptides (23)(24)(25).…”
Section: Nonspecific Appetitementioning
confidence: 99%
“…Clarification of the interactions between these drivers is just beginning to emerge. From 2000 to the present, much has been learned about the peripheral hormonal signals and central targets that influence energy intake (20)(21)(22). Dietary protein is an effective stimulus for the release or inhibition of many of these peptides (23)(24)(25).…”
Section: Nonspecific Appetitementioning
confidence: 99%
“…These anorexic hormones include cholecystokinin (CCK), glucogon-like peptide 1 (GLP1), vasoactive intestinal polypeptide (VIP), peptide YY (PYY), neurotensin (NT), oxyntomodulin (OXM), enterostatin, apolipoprotein A-IV (APO), gastrin-releasing peptide (GRP), and neuromedin B (NMB) (reviewed in Refs. 3, 13,16,31,48,53,59). L-cells in the alimentary tract that secrete some of these hormones have been shown to have taste receptors and short-chain fatty acid receptors on their luminal surfaces, which detect digested nutrients and mediate the release of the hormones (32).…”
Section: Short-term Regulation Of Food Intake and Energy Balancementioning
confidence: 99%
“…While these results suggest that OEA inhibits food intake by recruiting vagal sensory afferents (27), a recent report showing that subdiaphrag- An integrated view Gut peptide hormones are differentially distributed along the longitudinal axis of the alimentary canal and serve complementary functions in the control of feeding behavior. For example, ghrelin released from specialized cells in the stomach stimulates food intake during fasting, whereas cholecystokinin and GLP1 secreted from enteroendocrine cells in the small intestine inhibit intake after feeding (126,127). The evidence summarized in this article suggests that two chemically distinct classes of lipid-derived mediatorsglycerol esters and ethanolamides of LCFUs -may act in parallel and presumably in concert with peptide hormones to regulate the ingestion of fat-containing foods ( Figure 2).…”
Section: Lipid-derived Signals Of Satietymentioning
confidence: 95%