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GABA concentrations in the anterior temporal lobe predict human semantic processing
There is now considerable convergent evidence from multiple methodologies and clinical studies that the human anterior temporal lobe (ATL) is a semantic representational hub. However, the neurochemical nature of the ATL in the semantic processing remains unclear. The current study investigated the n...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691052/ https://www.ncbi.nlm.nih.gov/pubmed/29146995 http://dx.doi.org/10.1038/s41598-017-15981-7 |
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author | Jung, JeYoung Williams, Stephen R. Sanaei Nezhad, Faezeh Lambon Ralph, Matthew A. |
author_facet | Jung, JeYoung Williams, Stephen R. Sanaei Nezhad, Faezeh Lambon Ralph, Matthew A. |
author_sort | Jung, JeYoung |
collection | PubMed |
description | There is now considerable convergent evidence from multiple methodologies and clinical studies that the human anterior temporal lobe (ATL) is a semantic representational hub. However, the neurochemical nature of the ATL in the semantic processing remains unclear. The current study investigated the neurochemical mechanism underlying semantic processing in the ATL. We combined functional magnetic resonance imaging (fMRI) with resting-state magnetic resonance spectroscopy (MRS) to measure task-related blood-oxygen level-dependent (BOLD) signal changes during sematic processing and resting-state GABA concentrations in the ATL. Our combined fMRI and MRS investigation showed that the stronger ATL BOLD response induced by the semantic task, the lower GABA concentration in the same region. Moreover, individuals with higher GABA concentration in the ATL showed better semantic performance and stronger BOLD-related fluctuations in the semantic network. Our data demonstrated that the resting-state GABA concentration predicts neural changes in the human ATL and task performance during semantic processing. Our findings indicate that individuals with higher GABA may have a more efficient semantic processing leading to better task performance and imply that GABAergic neurochemical processes are potentially crucial to the neurobiological contribution of the ATL to semantic cognition. |
format | Online Article Text |
id | pubmed-5691052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56910522017-11-24 GABA concentrations in the anterior temporal lobe predict human semantic processing Jung, JeYoung Williams, Stephen R. Sanaei Nezhad, Faezeh Lambon Ralph, Matthew A. Sci Rep Article There is now considerable convergent evidence from multiple methodologies and clinical studies that the human anterior temporal lobe (ATL) is a semantic representational hub. However, the neurochemical nature of the ATL in the semantic processing remains unclear. The current study investigated the neurochemical mechanism underlying semantic processing in the ATL. We combined functional magnetic resonance imaging (fMRI) with resting-state magnetic resonance spectroscopy (MRS) to measure task-related blood-oxygen level-dependent (BOLD) signal changes during sematic processing and resting-state GABA concentrations in the ATL. Our combined fMRI and MRS investigation showed that the stronger ATL BOLD response induced by the semantic task, the lower GABA concentration in the same region. Moreover, individuals with higher GABA concentration in the ATL showed better semantic performance and stronger BOLD-related fluctuations in the semantic network. Our data demonstrated that the resting-state GABA concentration predicts neural changes in the human ATL and task performance during semantic processing. Our findings indicate that individuals with higher GABA may have a more efficient semantic processing leading to better task performance and imply that GABAergic neurochemical processes are potentially crucial to the neurobiological contribution of the ATL to semantic cognition. Nature Publishing Group UK 2017-11-16 /pmc/articles/PMC5691052/ /pubmed/29146995 http://dx.doi.org/10.1038/s41598-017-15981-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jung, JeYoung Williams, Stephen R. Sanaei Nezhad, Faezeh Lambon Ralph, Matthew A. GABA concentrations in the anterior temporal lobe predict human semantic processing |
title | GABA concentrations in the anterior temporal lobe predict human semantic processing |
title_full | GABA concentrations in the anterior temporal lobe predict human semantic processing |
title_fullStr | GABA concentrations in the anterior temporal lobe predict human semantic processing |
title_full_unstemmed | GABA concentrations in the anterior temporal lobe predict human semantic processing |
title_short | GABA concentrations in the anterior temporal lobe predict human semantic processing |
title_sort | gaba concentrations in the anterior temporal lobe predict human semantic processing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691052/ https://www.ncbi.nlm.nih.gov/pubmed/29146995 http://dx.doi.org/10.1038/s41598-017-15981-7 |
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