Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/106997
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Type: Journal article
Title: Mapping glucose-mediated gut-to-brain signalling pathways in humans
Author: Little, T.
McKie, S.
Jones, R.
D'Amato, M.
Smith, C.
Kiss, O.
Thompson, D.
McLaughlin, J.
Citation: NeuroImage, 2014; 96:1-11
Publisher: Elsevier
Issue Date: 2014
ISSN: 1053-8119
1095-9572
Statement of
Responsibility: 
Tanya J. Little, Shane McKie, Richard B. Jones, Massimo D'Amato, Craig Smith, Orsolya Kiss, David G. Thompson, John T. McLaughlin
Abstract: Objectives: Previous fMRI studies have demonstrated that glucose decreases the hypothalamic BOLD response in humans. However, the mechanisms underlying the CNS response to glucose have not been defined. We recently demonstrated that the slowing of gastric emptying by glucose is dependent on activation of the gut peptide cholecystokinin (CCK1) receptor. Using physiological functional magnetic resonance imaging this study aimed to determine the whole brain response to glucose, and whether CCK plays a central role. Experimental design: Changes in blood oxygenation level-dependent (BOLD) signalwere monitored using fMRI in 12 healthy subjects following intragastric infusion (250 ml) of: 1 M glucose + predosing with dexloxiglumide (CCK1 receptor antagonist), 1 M glucose + placebo, or 0.9% saline (control) + placebo, in a single-blind, randomised fashion. Gallbladder volume, blood glucose, insulin, and GLP-1 and CCK concentrations were determined. Hunger, fullness and nausea scores were also recorded. Principal observations: Intragastric glucose elevated plasma glucose, insulin, and GLP-1, and reduced gall bladder volume (an in vivo assay for CCK secretion). Glucose decreased BOLD signal, relative to saline, in the brainstemand hypothalamus as well as the cerebellum, right occipital cortex, putamen and thalamus. The timing of the BOLD signal decreasewas negatively correlatedwith the rise in blood glucose and insulin levels. The glucose+dex armhighlighted a CCK1-receptor dependent increase in BOLD signal only in the motor cortex. Conclusions: Glucose induces site-specific differences in BOLD response in the human brain; the brainstem and hypothalamus show a CCK1 receptor-independent reductionwhich is likely to be mediated by a circulatory effect of glucose and insulin, whereas the motor cortex shows an early dexloxiglumide-reversible increase in signal, suggesting a CCK1 receptor-dependent neural pathway.
Keywords: Glucose; cholecystokinin (CCK); dexloxiglumide; physMRI; nutrient
Description: Available online 28 March 2014
Rights: © 2014 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
RMID: 0030074019
DOI: 10.1016/j.neuroimage.2014.03.059
Grant ID: http://purl.org/au-research/grants/nhmrc/1022706
Appears in Collections:Medicine publications

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