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Characterization of Esophageal Physiology Using Mechanical State Analysis

The esophagus functions to transport swallowed fluids and food from the pharynx to the stomach. The esophageal muscles governing bolus transport comprise circular striated muscle of the proximal esophagus and circular smooth muscle of the distal esophagus. Longitudinal smooth muscle contraction prov...

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Autores principales: Leibbrandt, Richard E., Dinning, Phil G., Costa, Marcello, Cock, Charles, Wiklendt, Lukasz, Wang, Guangsong, Tack, Jan, van Beckevoort, Dirk, Rommel, Nathalie, Omari, Taher I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756108/
https://www.ncbi.nlm.nih.gov/pubmed/26924967
http://dx.doi.org/10.3389/fnsys.2016.00010
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author Leibbrandt, Richard E.
Dinning, Phil G.
Costa, Marcello
Cock, Charles
Wiklendt, Lukasz
Wang, Guangsong
Tack, Jan
van Beckevoort, Dirk
Rommel, Nathalie
Omari, Taher I.
author_facet Leibbrandt, Richard E.
Dinning, Phil G.
Costa, Marcello
Cock, Charles
Wiklendt, Lukasz
Wang, Guangsong
Tack, Jan
van Beckevoort, Dirk
Rommel, Nathalie
Omari, Taher I.
author_sort Leibbrandt, Richard E.
collection PubMed
description The esophagus functions to transport swallowed fluids and food from the pharynx to the stomach. The esophageal muscles governing bolus transport comprise circular striated muscle of the proximal esophagus and circular smooth muscle of the distal esophagus. Longitudinal smooth muscle contraction provides a mechanical advantage to bolus transit during circular smooth muscle contraction. Esophageal striated muscle is directly controlled by neural circuits originating in the central nervous system, resulting in coordinated contractions. In contrast, the esophageal smooth muscle is controlled by enteric circuits modulated by extrinsic central neural connections resulting in neural relaxation and contraction. The esophageal muscles are modulated by sensory information arising from within the lumen. Contraction or relaxation, which changes the diameter of the lumen, alters the intraluminal pressure and ultimately inhibits or promotes flow of content. This relationship that exists between the changes in diameter and concurrent changes in intraluminal pressure has been used previously to identify the “mechanical states” of the circular muscle; that is when the muscles are passively or actively, relaxing or contracting. Detecting these changes in the mechanical state of the muscle has been difficult and as the current interpretation of esophageal motility is based largely upon pressure measurement (manometry), subtle changes in the muscle function during peristalsis can be missed. We hypothesized that quantification of mechanical states of the esophageal circular muscles and the pressure-diameter properties that define them, would allow objective characterization of the mechanisms that govern esophageal peristalsis. To achieve this we analyzed barium swallows captured by simultaneous videofluoroscopy and pressure with impedance recording. From these data we demonstrated that intraluminal impedance measurements could be used to determine changes in the internal diameter of the lumen comparable with measurements from videofluoroscopy. Our data indicated that identification of mechanical state of esophageal muscle was simple to apply and revealed patterns consistent with the known neural inputs activating the different muscles during swallowing.
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spelling pubmed-47561082016-02-26 Characterization of Esophageal Physiology Using Mechanical State Analysis Leibbrandt, Richard E. Dinning, Phil G. Costa, Marcello Cock, Charles Wiklendt, Lukasz Wang, Guangsong Tack, Jan van Beckevoort, Dirk Rommel, Nathalie Omari, Taher I. Front Syst Neurosci Neuroscience The esophagus functions to transport swallowed fluids and food from the pharynx to the stomach. The esophageal muscles governing bolus transport comprise circular striated muscle of the proximal esophagus and circular smooth muscle of the distal esophagus. Longitudinal smooth muscle contraction provides a mechanical advantage to bolus transit during circular smooth muscle contraction. Esophageal striated muscle is directly controlled by neural circuits originating in the central nervous system, resulting in coordinated contractions. In contrast, the esophageal smooth muscle is controlled by enteric circuits modulated by extrinsic central neural connections resulting in neural relaxation and contraction. The esophageal muscles are modulated by sensory information arising from within the lumen. Contraction or relaxation, which changes the diameter of the lumen, alters the intraluminal pressure and ultimately inhibits or promotes flow of content. This relationship that exists between the changes in diameter and concurrent changes in intraluminal pressure has been used previously to identify the “mechanical states” of the circular muscle; that is when the muscles are passively or actively, relaxing or contracting. Detecting these changes in the mechanical state of the muscle has been difficult and as the current interpretation of esophageal motility is based largely upon pressure measurement (manometry), subtle changes in the muscle function during peristalsis can be missed. We hypothesized that quantification of mechanical states of the esophageal circular muscles and the pressure-diameter properties that define them, would allow objective characterization of the mechanisms that govern esophageal peristalsis. To achieve this we analyzed barium swallows captured by simultaneous videofluoroscopy and pressure with impedance recording. From these data we demonstrated that intraluminal impedance measurements could be used to determine changes in the internal diameter of the lumen comparable with measurements from videofluoroscopy. Our data indicated that identification of mechanical state of esophageal muscle was simple to apply and revealed patterns consistent with the known neural inputs activating the different muscles during swallowing. Frontiers Media S.A. 2016-02-17 /pmc/articles/PMC4756108/ /pubmed/26924967 http://dx.doi.org/10.3389/fnsys.2016.00010 Text en Copyright © 2016 Leibbrandt, Dinning, Costa, Cock, Wiklendt, Wang, Tack, van Beckevoort, Rommel and Omari. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor 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.
spellingShingle Neuroscience
Leibbrandt, Richard E.
Dinning, Phil G.
Costa, Marcello
Cock, Charles
Wiklendt, Lukasz
Wang, Guangsong
Tack, Jan
van Beckevoort, Dirk
Rommel, Nathalie
Omari, Taher I.
Characterization of Esophageal Physiology Using Mechanical State Analysis
title Characterization of Esophageal Physiology Using Mechanical State Analysis
title_full Characterization of Esophageal Physiology Using Mechanical State Analysis
title_fullStr Characterization of Esophageal Physiology Using Mechanical State Analysis
title_full_unstemmed Characterization of Esophageal Physiology Using Mechanical State Analysis
title_short Characterization of Esophageal Physiology Using Mechanical State Analysis
title_sort characterization of esophageal physiology using mechanical state analysis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756108/
https://www.ncbi.nlm.nih.gov/pubmed/26924967
http://dx.doi.org/10.3389/fnsys.2016.00010
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