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Compensatory recombination phenomena of neurological functions in central dysphagia patients

We speculate that cortical reactions evoked by swallowing activity may be abnormal in patients with central infarction with dysphagia. The present study aimed to detect functional imaging features of cerebral cortex in central dysphagia patients by using blood oxygen level-dependent functional magne...

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Autores principales: Yuan, Xiao-dong, Zhou, Li-fu, Wang, Shu-juan, Zhao, Yan-sheng, Wang, Xiao-jie, Zhang, Li-li, Wang, Shou-hong, Zhang, Ya-jie, Chen, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396115/
https://www.ncbi.nlm.nih.gov/pubmed/25878601
http://dx.doi.org/10.4103/1673-5374.153701
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author Yuan, Xiao-dong
Zhou, Li-fu
Wang, Shu-juan
Zhao, Yan-sheng
Wang, Xiao-jie
Zhang, Li-li
Wang, Shou-hong
Zhang, Ya-jie
Chen, Li
author_facet Yuan, Xiao-dong
Zhou, Li-fu
Wang, Shu-juan
Zhao, Yan-sheng
Wang, Xiao-jie
Zhang, Li-li
Wang, Shou-hong
Zhang, Ya-jie
Chen, Li
author_sort Yuan, Xiao-dong
collection PubMed
description We speculate that cortical reactions evoked by swallowing activity may be abnormal in patients with central infarction with dysphagia. The present study aimed to detect functional imaging features of cerebral cortex in central dysphagia patients by using blood oxygen level-dependent functional magnetic resonance imaging techniques. The results showed that when normal controls swallowed, primary motor cortex (BA4), insula (BA13), premotor cortex (BA6/8), supramarginal gyrus (BA40), and anterior cingulate cortex (BA24/32) were activated, and that the size of the activated areas were larger in the left hemisphere compared with the right. In recurrent cerebral infarction patients with central dysphagia, BA4, BA13, BA40 and BA6/8 areas were activated, while the degree of activation in BA24/32 was decreased. Additionally, more areas were activated, including posterior cingulate cortex (BA23/31), visual association cortex (BA18/19), primary auditory cortex (BA41) and parahippocampal cortex (BA36). Somatosensory association cortex (BA7) and left cerebellum in patients with recurrent cerebral infarction with central dysphagia were also activated. Experimental findings suggest that the cerebral cortex has obvious hemisphere lateralization in response to swallowing, and patients with recurrent cerebral infarction with central dysphagia show compensatory recombination phenomena of neurological functions. In rehabilitative treatment, using the favorite food of patients can stimulate swallowing through visual, auditory, and other nerve conduction pathways, thus promoting compensatory recombination of the central cortex functions.
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spelling pubmed-43961152015-04-15 Compensatory recombination phenomena of neurological functions in central dysphagia patients Yuan, Xiao-dong Zhou, Li-fu Wang, Shu-juan Zhao, Yan-sheng Wang, Xiao-jie Zhang, Li-li Wang, Shou-hong Zhang, Ya-jie Chen, Li Neural Regen Res Research Article We speculate that cortical reactions evoked by swallowing activity may be abnormal in patients with central infarction with dysphagia. The present study aimed to detect functional imaging features of cerebral cortex in central dysphagia patients by using blood oxygen level-dependent functional magnetic resonance imaging techniques. The results showed that when normal controls swallowed, primary motor cortex (BA4), insula (BA13), premotor cortex (BA6/8), supramarginal gyrus (BA40), and anterior cingulate cortex (BA24/32) were activated, and that the size of the activated areas were larger in the left hemisphere compared with the right. In recurrent cerebral infarction patients with central dysphagia, BA4, BA13, BA40 and BA6/8 areas were activated, while the degree of activation in BA24/32 was decreased. Additionally, more areas were activated, including posterior cingulate cortex (BA23/31), visual association cortex (BA18/19), primary auditory cortex (BA41) and parahippocampal cortex (BA36). Somatosensory association cortex (BA7) and left cerebellum in patients with recurrent cerebral infarction with central dysphagia were also activated. Experimental findings suggest that the cerebral cortex has obvious hemisphere lateralization in response to swallowing, and patients with recurrent cerebral infarction with central dysphagia show compensatory recombination phenomena of neurological functions. In rehabilitative treatment, using the favorite food of patients can stimulate swallowing through visual, auditory, and other nerve conduction pathways, thus promoting compensatory recombination of the central cortex functions. Medknow Publications & Media Pvt Ltd 2015-03 /pmc/articles/PMC4396115/ /pubmed/25878601 http://dx.doi.org/10.4103/1673-5374.153701 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yuan, Xiao-dong
Zhou, Li-fu
Wang, Shu-juan
Zhao, Yan-sheng
Wang, Xiao-jie
Zhang, Li-li
Wang, Shou-hong
Zhang, Ya-jie
Chen, Li
Compensatory recombination phenomena of neurological functions in central dysphagia patients
title Compensatory recombination phenomena of neurological functions in central dysphagia patients
title_full Compensatory recombination phenomena of neurological functions in central dysphagia patients
title_fullStr Compensatory recombination phenomena of neurological functions in central dysphagia patients
title_full_unstemmed Compensatory recombination phenomena of neurological functions in central dysphagia patients
title_short Compensatory recombination phenomena of neurological functions in central dysphagia patients
title_sort compensatory recombination phenomena of neurological functions in central dysphagia patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396115/
https://www.ncbi.nlm.nih.gov/pubmed/25878601
http://dx.doi.org/10.4103/1673-5374.153701
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