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©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 28, 2017; 23(40): 7211-7220
Published online Oct 28, 2017. doi: 10.3748/wjg.v23.i40.7211
Published online Oct 28, 2017. doi: 10.3748/wjg.v23.i40.7211
Glucagon-like peptide-2 modulates the nitrergic neurotransmission in strips from the mouse gastric fundus
Rachele Garella, Eglantina Idrizaj, Roberta Squecco, Maria Caterina Baccari, Department of Experimental and Clinical Medicine, Section of Physiology, University of Florence, 50134 Florence, Italy
Chiara Traini, Maria Giuliana Vannucchi, Department of Experimental and Clinical Medicine, Histology and Embryology Research Unit, University of Florence, 50134 Florence, Italy
Author contributions: Garella R and Idrizaj E contributed equally to this work; Garella R, Idrizaj E and Squecco R performed the functional experiments; Traini C performed the immunohistochemical experiments and the image analysis; Baccari MC, Garella R and Idrizaj E designed the research study and analyzed the data; Vannucchi MG contributed to design the research study and analyzed the data; Baccari MC wrote the paper; Garella R, Idrizaj E, Traini C, Vannucchi MG and Baccari MC critically revised the manuscript.
Supported by University of Florence (ex 60%) RICATEN14-16 to Baccari MC.
Institutional animal care and use committee statement: The experimental protocol was designed in compliance with the guidelines of the European Communities Council Directive 2010/63/UE and the recommendations for the care and use of laboratory animals approved by the Animal Care Committee of the University of Florence, Italy, with authorization from the Italian Ministry of Health No. 787/2016-PR.
Conflict-of-interest statement: No conflicts of interest, financial or otherwise, are declared by the authors.
Data sharing statement: No additional data are available.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Maria Caterina Baccari, PhD, Associate Professor, Department of Experimental and Clinical Medicine, Section of Physiology, University of Florence, Viale G.B. Morgagni 63, 50134 Florence, Italy. mcaterina.baccari@unifi.it
Telephone: +39-55-2751600 Fax: +39-55-4379506
Received: June 8, 2017
Peer-review started: June 8, 2017
First decision: August 10, 2017
Revised: August 4, 2017
Accepted: September 26, 2017
Article in press: September 26, 2017
Published online: October 28, 2017
Processing time: 143 Days and 16.5 Hours
Peer-review started: June 8, 2017
First decision: August 10, 2017
Revised: August 4, 2017
Accepted: September 26, 2017
Article in press: September 26, 2017
Published online: October 28, 2017
Processing time: 143 Days and 16.5 Hours
Core Tip
Core tip:The results of the present study demonstrate for the first time that, in strips from the mouse gastric fundus, glucagon-like peptide-2 (GLP-2) depresses the amplitude of the neurally-induced contractile responses and enhances the amplitude of the relaxant ones through the modulation of the nitrergic neurotransmission. GLP-2 also increases neuronal nitric oxide synthase immunoreactivity in the nerve structures. All these inhibitory effects might contribute to gastric relaxation, thus increasing the organ capacity. Since gastric distension represents a peripheral satiety signal from a physiological point of view, it could be speculated that the relaxant effects of GLP-2 might concur to suppress feeding behavior in rodents.