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Functional interaction between Ghrelin and GLP-1 regulates feeding through the vagal afferent system
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Functional interaction between Ghrelin and GLP-1 regulates feeding through the vagal afferent system
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Journal Article
Functional interaction between Ghrelin and GLP-1 regulates feeding through the vagal afferent system
2020
Overview
The gastrointestinal tract transmits feeding-regulatory signals to the brain via neuronal and hormonal pathways. Here we studied the interaction between the orexigenic gastric peptide, ghrelin, and the anorectic intestinal peptide, glucagon-like peptide 1 (GLP-1), in terms of feeding regulation via the vagal afferents. GLP-1 preadministration 30 min before ghrelin administration to rats and mice abolished ghrelin-induced food intake, while ghrelin preadministration abolished the anorectic effect of GLP-1. Ghrelin preadministration suppressed GLP-1-induced Fos expression in the nodose ganglia (NG). Electrophysiological assessment confirmed that the initially administered peptide abolished the vagal afferent electrical alteration induced by the subsequently administered peptide. Both the growth hormone secretagogue receptor (GHSR) and the GLP-1 receptor (GLP-1R) are co-localised in a major proportion of NG neurons that innervate the stomach. In these
Ghsr
+
Glp1r
+
neurons, ghrelin preadministration abolished the GLP-1-induced calcium response. Ghrelin generated a hyperpolarising current and GLP-1 generated a depolarising current in isolated NG neurons in a patch-clamp experiment. Ghrelin and GLP-1 potently influenced each other in terms of vagally mediated feeding regulation. This peptidergic interaction allows for fine control of the electrophysiological properties of NG neurons.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 631/443
/ 692/163
/ 692/4020
/ 692/617
/ Afferent Pathways - physiology
/ Animals
/ Calcium
/ Feeding
/ Ghrelin
/ Glucagon
/ Glucagon-Like Peptide 1 - physiology
/ Glucagon-Like Peptide-1 Receptor - physiology
/ Humanities and Social Sciences
/ Male
/ Neurons
/ Nodose Ganglion - physiology
/ Peptides
/ Receptors, Ghrelin - metabolism
/ Science
