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Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting
While the pathogenesis of cervical dystonia remains unknown, recent animal and clinical experimental studies have indicated its probable mechanisms. Abnormal temporal discrimination is a mediational endophenotype of cervical dystonia and informs new concepts of disease pathogenesis. Our hypothesis i...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009446/ https://www.ncbi.nlm.nih.gov/pubmed/24803911 http://dx.doi.org/10.3389/fneur.2014.00054 |
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author | Hutchinson, Michael Isa, Tadashi Molloy, Anna Kimmich, Okka Williams, Laura Molloy, Fiona Moore, Helena Healy, Daniel G. Lynch, Tim Walsh, Cathal Butler, John Reilly, Richard B. Walsh, Richard O’Riordan, Sean |
author_facet | Hutchinson, Michael Isa, Tadashi Molloy, Anna Kimmich, Okka Williams, Laura Molloy, Fiona Moore, Helena Healy, Daniel G. Lynch, Tim Walsh, Cathal Butler, John Reilly, Richard B. Walsh, Richard O’Riordan, Sean |
author_sort | Hutchinson, Michael |
collection | PubMed |
description | While the pathogenesis of cervical dystonia remains unknown, recent animal and clinical experimental studies have indicated its probable mechanisms. Abnormal temporal discrimination is a mediational endophenotype of cervical dystonia and informs new concepts of disease pathogenesis. Our hypothesis is that both abnormal temporal discrimination and cervical dystonia are due to a disorder of the midbrain network for covert attentional orienting caused by reduced gamma-aminobutyric acid (GABA) inhibition, resulting, in turn, from as yet undetermined, genetic mutations. Such disinhibition is (a) subclinically manifested by abnormal temporal discrimination due to prolonged duration firing of the visual sensory neurons in the superficial laminae of the superior colliculus and (b) clinically manifested by cervical dystonia due to disinhibited burst activity of the cephalomotor neurons of the intermediate and deep laminae of the superior colliculus. Abnormal temporal discrimination in unaffected first-degree relatives of patients with cervical dystonia represents a subclinical manifestation of defective GABA activity both within the superior colliculus and from the substantia nigra pars reticulata. A number of experiments are required to prove or disprove this hypothesis. |
format | Online Article Text |
id | pubmed-4009446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40094462014-05-06 Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting Hutchinson, Michael Isa, Tadashi Molloy, Anna Kimmich, Okka Williams, Laura Molloy, Fiona Moore, Helena Healy, Daniel G. Lynch, Tim Walsh, Cathal Butler, John Reilly, Richard B. Walsh, Richard O’Riordan, Sean Front Neurol Neuroscience While the pathogenesis of cervical dystonia remains unknown, recent animal and clinical experimental studies have indicated its probable mechanisms. Abnormal temporal discrimination is a mediational endophenotype of cervical dystonia and informs new concepts of disease pathogenesis. Our hypothesis is that both abnormal temporal discrimination and cervical dystonia are due to a disorder of the midbrain network for covert attentional orienting caused by reduced gamma-aminobutyric acid (GABA) inhibition, resulting, in turn, from as yet undetermined, genetic mutations. Such disinhibition is (a) subclinically manifested by abnormal temporal discrimination due to prolonged duration firing of the visual sensory neurons in the superficial laminae of the superior colliculus and (b) clinically manifested by cervical dystonia due to disinhibited burst activity of the cephalomotor neurons of the intermediate and deep laminae of the superior colliculus. Abnormal temporal discrimination in unaffected first-degree relatives of patients with cervical dystonia represents a subclinical manifestation of defective GABA activity both within the superior colliculus and from the substantia nigra pars reticulata. A number of experiments are required to prove or disprove this hypothesis. Frontiers Media S.A. 2014-04-28 /pmc/articles/PMC4009446/ /pubmed/24803911 http://dx.doi.org/10.3389/fneur.2014.00054 Text en Copyright © 2014 Hutchinson, Isa, Molloy, Kimmich, Williams, Molloy, Moore, Healy, Lynch, Walsh, Butler, Reilly, Walsh and O’Riordan. http://creativecommons.org/licenses/by/3.0/ 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 Hutchinson, Michael Isa, Tadashi Molloy, Anna Kimmich, Okka Williams, Laura Molloy, Fiona Moore, Helena Healy, Daniel G. Lynch, Tim Walsh, Cathal Butler, John Reilly, Richard B. Walsh, Richard O’Riordan, Sean Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting |
title | Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting |
title_full | Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting |
title_fullStr | Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting |
title_full_unstemmed | Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting |
title_short | Cervical Dystonia: A Disorder of the Midbrain Network for Covert Attentional Orienting |
title_sort | cervical dystonia: a disorder of the midbrain network for covert attentional orienting |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009446/ https://www.ncbi.nlm.nih.gov/pubmed/24803911 http://dx.doi.org/10.3389/fneur.2014.00054 |
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