Cargando…

Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies

Pharyngolaryngeal hypesthesia is a major reason for dysphagia in various neurological diseases. Emerging neuromodulation devices have shown potential to foster dysphagia rehabilitation, but the optimal treatment strategy is unknown. Because functional imaging studies are difficult to conduct in seve...

Descripción completa

Detalles Bibliográficos
Autores principales: Muhle, Paul, Labeit, Bendix, Wollbrink, Andreas, Claus, Inga, Warnecke, Tobias, Wolters, Carsten H., Gross, Joachim, Dziewas, Rainer, Suntrup‐Krueger, Sonja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776007/
https://www.ncbi.nlm.nih.gov/pubmed/33068056
http://dx.doi.org/10.1002/hbm.25233
_version_ 1783630580144930816
author Muhle, Paul
Labeit, Bendix
Wollbrink, Andreas
Claus, Inga
Warnecke, Tobias
Wolters, Carsten H.
Gross, Joachim
Dziewas, Rainer
Suntrup‐Krueger, Sonja
author_facet Muhle, Paul
Labeit, Bendix
Wollbrink, Andreas
Claus, Inga
Warnecke, Tobias
Wolters, Carsten H.
Gross, Joachim
Dziewas, Rainer
Suntrup‐Krueger, Sonja
author_sort Muhle, Paul
collection PubMed
description Pharyngolaryngeal hypesthesia is a major reason for dysphagia in various neurological diseases. Emerging neuromodulation devices have shown potential to foster dysphagia rehabilitation, but the optimal treatment strategy is unknown. Because functional imaging studies are difficult to conduct in severely ill patients, we induced a virtual sensory lesion in healthy volunteers and evaluated the effects of central and peripheral neurostimulation techniques. In a sham‐controlled intervention study with crossover design on 10 participants, we tested the potential of (peripheral) pharyngeal electrical stimulation (PES) and (central) transcranial direct current stimulation (tDCS) to revert the effects of lidocaine‐induced pharyngolaryngeal hypesthesia on central sensorimotor processing. Changes were observed during pharyngeal air‐pulse stimulation and voluntary swallowing applying magnetoencephalography before and after the interventions. PES induced a significant (p < .05) increase of activation during swallowing in the bihemispheric sensorimotor network in alpha and low gamma frequency ranges, peaking in the right premotor and left primary sensory area, respectively. With pneumatic stimulation, significant activation increase was found after PES in high gamma peaking in the left premotor area. Significant changes of brain activation after tDCS could neither be detected for pneumatic stimulation nor for swallowing. Due to the peripheral cause of dysphagia in this model, PES was able to revert the detrimental effects of reduced sensory input on central processing, whereas tDCS was not. Results may have implications for therapeutic decisions in the clinical context.
format Online
Article
Text
id pubmed-7776007
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-77760072021-01-07 Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies Muhle, Paul Labeit, Bendix Wollbrink, Andreas Claus, Inga Warnecke, Tobias Wolters, Carsten H. Gross, Joachim Dziewas, Rainer Suntrup‐Krueger, Sonja Hum Brain Mapp Research Articles Pharyngolaryngeal hypesthesia is a major reason for dysphagia in various neurological diseases. Emerging neuromodulation devices have shown potential to foster dysphagia rehabilitation, but the optimal treatment strategy is unknown. Because functional imaging studies are difficult to conduct in severely ill patients, we induced a virtual sensory lesion in healthy volunteers and evaluated the effects of central and peripheral neurostimulation techniques. In a sham‐controlled intervention study with crossover design on 10 participants, we tested the potential of (peripheral) pharyngeal electrical stimulation (PES) and (central) transcranial direct current stimulation (tDCS) to revert the effects of lidocaine‐induced pharyngolaryngeal hypesthesia on central sensorimotor processing. Changes were observed during pharyngeal air‐pulse stimulation and voluntary swallowing applying magnetoencephalography before and after the interventions. PES induced a significant (p < .05) increase of activation during swallowing in the bihemispheric sensorimotor network in alpha and low gamma frequency ranges, peaking in the right premotor and left primary sensory area, respectively. With pneumatic stimulation, significant activation increase was found after PES in high gamma peaking in the left premotor area. Significant changes of brain activation after tDCS could neither be detected for pneumatic stimulation nor for swallowing. Due to the peripheral cause of dysphagia in this model, PES was able to revert the detrimental effects of reduced sensory input on central processing, whereas tDCS was not. Results may have implications for therapeutic decisions in the clinical context. John Wiley & Sons, Inc. 2020-10-17 /pmc/articles/PMC7776007/ /pubmed/33068056 http://dx.doi.org/10.1002/hbm.25233 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Muhle, Paul
Labeit, Bendix
Wollbrink, Andreas
Claus, Inga
Warnecke, Tobias
Wolters, Carsten H.
Gross, Joachim
Dziewas, Rainer
Suntrup‐Krueger, Sonja
Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
title Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
title_full Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
title_fullStr Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
title_full_unstemmed Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
title_short Targeting the sensory feedback within the swallowing network—Reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
title_sort targeting the sensory feedback within the swallowing network—reversing artificially induced pharyngolaryngeal hypesthesia by central and peripheral stimulation strategies
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776007/
https://www.ncbi.nlm.nih.gov/pubmed/33068056
http://dx.doi.org/10.1002/hbm.25233
work_keys_str_mv AT muhlepaul targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT labeitbendix targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT wollbrinkandreas targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT clausinga targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT warnecketobias targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT wolterscarstenh targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT grossjoachim targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT dziewasrainer targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies
AT suntrupkruegersonja targetingthesensoryfeedbackwithintheswallowingnetworkreversingartificiallyinducedpharyngolaryngealhypesthesiabycentralandperipheralstimulationstrategies