Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/115583
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Type: Journal article
Title: Role of intestinal bitter sensing in enteroendocrine hormone secretion and metabolic control
Author: Xie, C.
Wang, X.
Young, R.L.
Horowitz, M.
Rayner, C.K.
Wu, T.
Citation: Frontiers in Endocrinology, 2018; 9:576-1-576-10
Publisher: Frontiers Media
Issue Date: 2018
ISSN: 1664-2392
1664-2392
Statement of
Responsibility: 
Cong Xie, Xuyi Wang, Richard L. Young, Michael Horowitz, Christopher K. Rayner and Tongzhi Wu
Abstract: The gastrointestinal tract stores ingested nutrients in the stomach which are then delivered to the small intestine at a controlled rate to optimize their digestion and absorption. The interaction of nutrients with the small and large intestine generates feedback that slows gastric emptying, induces satiation, and reduces postprandial glycemic excursions. The mechanisms underlying these nutrient-gut interactions are complex; it has only recently been appreciated that the gut has the capacity to detect intraluminal contents in much the same way as the tongue, via activation of specific G-protein-coupled receptors, and that ensuing signaling mechanisms modulate the release of an array of gut hormones that influence gastrointestinal motility, appetite and glycemia. Interestingly, evidence from preclinical models supports a functional link between intestinal bitter taste receptor (BTRs) and gastrointestinal hormone secretion, and the outcomes of recent studies indicate that stimulation of intestinal BTRs may be used to modulate gastrointestinal function, to diminish energy intake and limit postprandial blood glucose excursions in humans. This review summarizes current evidence about the expression and function of intestinal BTRs in relation to enteroendocrine hormone release and discusses the clinical implications of this pathway for the management of obesity and type 2 diabetes.
Keywords: bitter taste receptors; gut hormones; enteroendocrine cells; energy intake; blood glucose; obesity; type 2 diabetes
Description: Published: 27 September 2018
Rights: Copyright © 2018 Xie, Wang, Young, Horowitz, Rayner and Wu. This is an openaccess article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
RMID: 0030099337
DOI: 10.3389/fendo.2018.00576
Grant ID: http://purl.org/au-research/grants/nhmrc/1147333
Appears in Collections:Medicine publications

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