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DYT1 dystonia increases risk taking in humans
It has been difficult to link synaptic modification to overt behavioral changes. Rodent models of DYT1 dystonia, a motor disorder caused by a single gene mutation, demonstrate increased long-term potentiation and decreased long-term depression in corticostriatal synapses. Computationally, such asymm...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951192/ https://www.ncbi.nlm.nih.gov/pubmed/27249418 http://dx.doi.org/10.7554/eLife.14155 |
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author | Arkadir, David Radulescu, Angela Raymond, Deborah Lubarr, Naomi Bressman, Susan B Mazzoni, Pietro Niv, Yael |
author_facet | Arkadir, David Radulescu, Angela Raymond, Deborah Lubarr, Naomi Bressman, Susan B Mazzoni, Pietro Niv, Yael |
author_sort | Arkadir, David |
collection | PubMed |
description | It has been difficult to link synaptic modification to overt behavioral changes. Rodent models of DYT1 dystonia, a motor disorder caused by a single gene mutation, demonstrate increased long-term potentiation and decreased long-term depression in corticostriatal synapses. Computationally, such asymmetric learning predicts risk taking in probabilistic tasks. Here we demonstrate abnormal risk taking in DYT1 dystonia patients, which is correlated with disease severity, thereby supporting striatal plasticity in shaping choice behavior in humans. DOI: http://dx.doi.org/10.7554/eLife.14155.001 |
format | Online Article Text |
id | pubmed-4951192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49511922016-07-21 DYT1 dystonia increases risk taking in humans Arkadir, David Radulescu, Angela Raymond, Deborah Lubarr, Naomi Bressman, Susan B Mazzoni, Pietro Niv, Yael eLife Neuroscience It has been difficult to link synaptic modification to overt behavioral changes. Rodent models of DYT1 dystonia, a motor disorder caused by a single gene mutation, demonstrate increased long-term potentiation and decreased long-term depression in corticostriatal synapses. Computationally, such asymmetric learning predicts risk taking in probabilistic tasks. Here we demonstrate abnormal risk taking in DYT1 dystonia patients, which is correlated with disease severity, thereby supporting striatal plasticity in shaping choice behavior in humans. DOI: http://dx.doi.org/10.7554/eLife.14155.001 eLife Sciences Publications, Ltd 2016-06-01 /pmc/articles/PMC4951192/ /pubmed/27249418 http://dx.doi.org/10.7554/eLife.14155 Text en © 2016, Arkadir et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Arkadir, David Radulescu, Angela Raymond, Deborah Lubarr, Naomi Bressman, Susan B Mazzoni, Pietro Niv, Yael DYT1 dystonia increases risk taking in humans |
title | DYT1 dystonia increases risk taking in humans |
title_full | DYT1 dystonia increases risk taking in humans |
title_fullStr | DYT1 dystonia increases risk taking in humans |
title_full_unstemmed | DYT1 dystonia increases risk taking in humans |
title_short | DYT1 dystonia increases risk taking in humans |
title_sort | dyt1 dystonia increases risk taking in humans |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951192/ https://www.ncbi.nlm.nih.gov/pubmed/27249418 http://dx.doi.org/10.7554/eLife.14155 |
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