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Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening

The swallowing muscles that influence upper esophageal sphincter (UES) opening are centrally controlled and modulated by sensory information. Activation of neural inputs to these muscles, the intrinsic cricopharyngeus muscle and extrinsic suprahyoid muscles, results in their contraction or relaxatio...

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Autores principales: Omari, Taher I., Wiklendt, Lukasz, Dinning, Philip, Costa, Marcello, Rommel, Nathalie, Cock, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285690/
https://www.ncbi.nlm.nih.gov/pubmed/25610376
http://dx.doi.org/10.3389/fnsys.2014.00241
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author Omari, Taher I.
Wiklendt, Lukasz
Dinning, Philip
Costa, Marcello
Rommel, Nathalie
Cock, Charles
author_facet Omari, Taher I.
Wiklendt, Lukasz
Dinning, Philip
Costa, Marcello
Rommel, Nathalie
Cock, Charles
author_sort Omari, Taher I.
collection PubMed
description The swallowing muscles that influence upper esophageal sphincter (UES) opening are centrally controlled and modulated by sensory information. Activation of neural inputs to these muscles, the intrinsic cricopharyngeus muscle and extrinsic suprahyoid muscles, results in their 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 calculate the “mechanical states” of the muscle; that is when the muscles are passively or actively, relaxing or contracting. Diseases that alter the neural pathways to these muscles can result in weakening the muscle contractility and/or decreasing the muscle compliance, all of which can cause dysphagia. Detecting these changes in the mechanical state of the muscle is difficult and as the current interpretation of UES motility is based largely upon pressure measurement (manometry), subtle changes in the muscle function during swallow can be missed. We hypothesized that quantification of mechanical states of the UES and the pressure-diameter properties that define them, would allow objective characterization of the mechanisms that govern the timing and extent of UES opening during swallowing. To achieve this we initially analyzed swallows captured by simultaneous videofluoroscopy and UES 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 when compared to videofluoroscopy. Then using a database of pressure-impedance studies, recorded from young and aged healthy controls and patients with motor neuron disease, we calculated the UES mechanical states in relation to a standardized swallowed bolus volume, normal aging and dysphagia pathology. Our results indicated that eight different mechanical states were almost always seen during healthy swallowing and some of these calculated changes in muscle function were consistent with the known neurally dependent phasic discharge patterns of cricopharyngeus muscle activity during swallowing. Clearly defined changes in the mechanical states were observed in motor neuron disease when compared to age matched healthy controls. Our data indicate that mechanical state predictions were simple to apply and revealed patterns consistent with the known neural inputs activating the different muscles during swallowing.
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spelling pubmed-42856902015-01-21 Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening Omari, Taher I. Wiklendt, Lukasz Dinning, Philip Costa, Marcello Rommel, Nathalie Cock, Charles Front Syst Neurosci Neuroscience The swallowing muscles that influence upper esophageal sphincter (UES) opening are centrally controlled and modulated by sensory information. Activation of neural inputs to these muscles, the intrinsic cricopharyngeus muscle and extrinsic suprahyoid muscles, results in their 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 calculate the “mechanical states” of the muscle; that is when the muscles are passively or actively, relaxing or contracting. Diseases that alter the neural pathways to these muscles can result in weakening the muscle contractility and/or decreasing the muscle compliance, all of which can cause dysphagia. Detecting these changes in the mechanical state of the muscle is difficult and as the current interpretation of UES motility is based largely upon pressure measurement (manometry), subtle changes in the muscle function during swallow can be missed. We hypothesized that quantification of mechanical states of the UES and the pressure-diameter properties that define them, would allow objective characterization of the mechanisms that govern the timing and extent of UES opening during swallowing. To achieve this we initially analyzed swallows captured by simultaneous videofluoroscopy and UES 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 when compared to videofluoroscopy. Then using a database of pressure-impedance studies, recorded from young and aged healthy controls and patients with motor neuron disease, we calculated the UES mechanical states in relation to a standardized swallowed bolus volume, normal aging and dysphagia pathology. Our results indicated that eight different mechanical states were almost always seen during healthy swallowing and some of these calculated changes in muscle function were consistent with the known neurally dependent phasic discharge patterns of cricopharyngeus muscle activity during swallowing. Clearly defined changes in the mechanical states were observed in motor neuron disease when compared to age matched healthy controls. Our data indicate that mechanical state predictions were simple to apply and revealed patterns consistent with the known neural inputs activating the different muscles during swallowing. Frontiers Media S.A. 2015-01-07 /pmc/articles/PMC4285690/ /pubmed/25610376 http://dx.doi.org/10.3389/fnsys.2014.00241 Text en Copyright © 2015 Omari, Wiklendt, Dinning, Costa, Rommel and Cock. 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 or 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
Omari, Taher I.
Wiklendt, Lukasz
Dinning, Philip
Costa, Marcello
Rommel, Nathalie
Cock, Charles
Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening
title Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening
title_full Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening
title_fullStr Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening
title_full_unstemmed Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening
title_short Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening
title_sort upper esophageal sphincter mechanical states analysis: a novel methodology to describe ues relaxation and opening
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285690/
https://www.ncbi.nlm.nih.gov/pubmed/25610376
http://dx.doi.org/10.3389/fnsys.2014.00241
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