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...
Autores principales: | , , , , , , , , |
---|---|
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 |