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Effects of prucalopride on esophageal secondary peristalsis in humans

OBJECTIVES: Prucalopride, a high-affinity 5-hydroxytrypatamine 4 (5-HT(4)) receptors agonist, has been shown to improve colon motility in adults. Secondary peristalsis helps the clearance of retained food bolus and refluxate from the esophagus, but the effects of prucalopride on esophageal secondary...

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Autores principales: Yi, Chih-Hsun, Lei, Wei-Yi, Hung, Jui-Sheng, Liu, Tso-Tsai, Chen, Chien-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288569/
https://www.ncbi.nlm.nih.gov/pubmed/27831544
http://dx.doi.org/10.1038/ctg.2016.58
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author Yi, Chih-Hsun
Lei, Wei-Yi
Hung, Jui-Sheng
Liu, Tso-Tsai
Chen, Chien-Lin
author_facet Yi, Chih-Hsun
Lei, Wei-Yi
Hung, Jui-Sheng
Liu, Tso-Tsai
Chen, Chien-Lin
author_sort Yi, Chih-Hsun
collection PubMed
description OBJECTIVES: Prucalopride, a high-affinity 5-hydroxytrypatamine 4 (5-HT(4)) receptors agonist, has been shown to improve colon motility in adults. Secondary peristalsis helps the clearance of retained food bolus and refluxate from the esophagus, but the effects of prucalopride on esophageal secondary peristalsis are unknown. We aimed to assess the effects of prucalopride on distension-induced secondary peristalsis in healthy adults. METHODS: Two separate sessions with prucalopride and placebo were performed in 11 healthy adults to test the effects on secondary peristalsis. Secondary peristalsis was performed with slow and rapid mid-esophageal injections of air after a baseline recording of esophageal motility. RESULTS: Prucalopride significantly decreased the threshold volume to generate secondary peristalsis during slow air injection (9.8±1.4 vs. 14.4±0.9 ml, P=0.005) and rapid air injection (3.9±0.3 vs. 5.2±0.4 ml, P=0.008). Secondary peristalsis was generated more frequently after application of prucalopride (80% (70–100%) vs. 70% (60–73%), P=0.01). Prucalopride increased the wave amplitude of distal esophagus during slow air injection (147.9±28.5 vs. 104.2±16.8 mm Hg, P=0.048) and rapid air injection (128.0±13.3 vs. 105.7±12.3 mm Hg, P=0.016). Primary peristaltic amplitudes were also significantly increased by the application of prucalopride. CONCLUSIONS: Acute administration of prucalopride enhances mechanosensitivity of distension-induced secondary peristalsis and promotes esophageal contractility in healthy adults. Whether prucalopride could be a therapeutic option for the treatment of subjects with esophageal hypomotility needs further study.
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spelling pubmed-52885692017-02-07 Effects of prucalopride on esophageal secondary peristalsis in humans Yi, Chih-Hsun Lei, Wei-Yi Hung, Jui-Sheng Liu, Tso-Tsai Chen, Chien-Lin Clin Transl Gastroenterol Original Contributions OBJECTIVES: Prucalopride, a high-affinity 5-hydroxytrypatamine 4 (5-HT(4)) receptors agonist, has been shown to improve colon motility in adults. Secondary peristalsis helps the clearance of retained food bolus and refluxate from the esophagus, but the effects of prucalopride on esophageal secondary peristalsis are unknown. We aimed to assess the effects of prucalopride on distension-induced secondary peristalsis in healthy adults. METHODS: Two separate sessions with prucalopride and placebo were performed in 11 healthy adults to test the effects on secondary peristalsis. Secondary peristalsis was performed with slow and rapid mid-esophageal injections of air after a baseline recording of esophageal motility. RESULTS: Prucalopride significantly decreased the threshold volume to generate secondary peristalsis during slow air injection (9.8±1.4 vs. 14.4±0.9 ml, P=0.005) and rapid air injection (3.9±0.3 vs. 5.2±0.4 ml, P=0.008). Secondary peristalsis was generated more frequently after application of prucalopride (80% (70–100%) vs. 70% (60–73%), P=0.01). Prucalopride increased the wave amplitude of distal esophagus during slow air injection (147.9±28.5 vs. 104.2±16.8 mm Hg, P=0.048) and rapid air injection (128.0±13.3 vs. 105.7±12.3 mm Hg, P=0.016). Primary peristaltic amplitudes were also significantly increased by the application of prucalopride. CONCLUSIONS: Acute administration of prucalopride enhances mechanosensitivity of distension-induced secondary peristalsis and promotes esophageal contractility in healthy adults. Whether prucalopride could be a therapeutic option for the treatment of subjects with esophageal hypomotility needs further study. Nature Publishing Group 2016-11 2016-11-10 /pmc/articles/PMC5288569/ /pubmed/27831544 http://dx.doi.org/10.1038/ctg.2016.58 Text en Copyright © 2016 The Author(s) the American College of Gastroenterology http://creativecommons.org/licenses/by-nc-nd/4.0/ Clinical and Translational Gastroenterology is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Contributions
Yi, Chih-Hsun
Lei, Wei-Yi
Hung, Jui-Sheng
Liu, Tso-Tsai
Chen, Chien-Lin
Effects of prucalopride on esophageal secondary peristalsis in humans
title Effects of prucalopride on esophageal secondary peristalsis in humans
title_full Effects of prucalopride on esophageal secondary peristalsis in humans
title_fullStr Effects of prucalopride on esophageal secondary peristalsis in humans
title_full_unstemmed Effects of prucalopride on esophageal secondary peristalsis in humans
title_short Effects of prucalopride on esophageal secondary peristalsis in humans
title_sort effects of prucalopride on esophageal secondary peristalsis in humans
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288569/
https://www.ncbi.nlm.nih.gov/pubmed/27831544
http://dx.doi.org/10.1038/ctg.2016.58
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