Cargando…
Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability
Perceptual organisation must select one interpretation from several alternatives to guide behaviour. Computational models suggest that this could be achieved through an interplay between inhibition and excitation across competing types of neural population coding for each interpretation. Here, to te...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162284/ https://www.ncbi.nlm.nih.gov/pubmed/30267021 http://dx.doi.org/10.1038/s41598-018-32892-3 |
_version_ | 1783359110442385408 |
---|---|
author | Kondo, Hirohito M. Pressnitzer, Daniel Shimada, Yasuhiro Kochiyama, Takanori Kashino, Makio |
author_facet | Kondo, Hirohito M. Pressnitzer, Daniel Shimada, Yasuhiro Kochiyama, Takanori Kashino, Makio |
author_sort | Kondo, Hirohito M. |
collection | PubMed |
description | Perceptual organisation must select one interpretation from several alternatives to guide behaviour. Computational models suggest that this could be achieved through an interplay between inhibition and excitation across competing types of neural population coding for each interpretation. Here, to test for such models, we used magnetic resonance spectroscopy to measure non-invasively the concentrations of inhibitory γ-aminobutyric acid (GABA) and excitatory glutamate-glutamine (Glx) in several brain regions. Human participants first performed auditory and visual multistability tasks that produced spontaneous switching between percepts. Then, we observed that longer percept durations during behaviour were associated with higher GABA/Glx ratios in the sensory area coding for each modality. When participants were asked to voluntarily modulate their perception, a common factor across modalities emerged: the GABA/Glx ratio in the posterior parietal cortex tended to be positively correlated with the amount of effective volitional control. Our results provide direct evidence implicating that the balance between neural inhibition and excitation within sensory regions resolves perceptual competition. This powerful computational principle appears to be leveraged by both audition and vision, implemented independently across modalities, but modulated by an integrated control process. |
format | Online Article Text |
id | pubmed-6162284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61622842018-10-02 Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability Kondo, Hirohito M. Pressnitzer, Daniel Shimada, Yasuhiro Kochiyama, Takanori Kashino, Makio Sci Rep Article Perceptual organisation must select one interpretation from several alternatives to guide behaviour. Computational models suggest that this could be achieved through an interplay between inhibition and excitation across competing types of neural population coding for each interpretation. Here, to test for such models, we used magnetic resonance spectroscopy to measure non-invasively the concentrations of inhibitory γ-aminobutyric acid (GABA) and excitatory glutamate-glutamine (Glx) in several brain regions. Human participants first performed auditory and visual multistability tasks that produced spontaneous switching between percepts. Then, we observed that longer percept durations during behaviour were associated with higher GABA/Glx ratios in the sensory area coding for each modality. When participants were asked to voluntarily modulate their perception, a common factor across modalities emerged: the GABA/Glx ratio in the posterior parietal cortex tended to be positively correlated with the amount of effective volitional control. Our results provide direct evidence implicating that the balance between neural inhibition and excitation within sensory regions resolves perceptual competition. This powerful computational principle appears to be leveraged by both audition and vision, implemented independently across modalities, but modulated by an integrated control process. Nature Publishing Group UK 2018-09-28 /pmc/articles/PMC6162284/ /pubmed/30267021 http://dx.doi.org/10.1038/s41598-018-32892-3 Text en © The Author(s) 2018 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 Kondo, Hirohito M. Pressnitzer, Daniel Shimada, Yasuhiro Kochiyama, Takanori Kashino, Makio Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
title | Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
title_full | Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
title_fullStr | Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
title_full_unstemmed | Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
title_short | Inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
title_sort | inhibition-excitation balance in the parietal cortex modulates volitional control for auditory and visual multistability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162284/ https://www.ncbi.nlm.nih.gov/pubmed/30267021 http://dx.doi.org/10.1038/s41598-018-32892-3 |
work_keys_str_mv | AT kondohirohitom inhibitionexcitationbalanceintheparietalcortexmodulatesvolitionalcontrolforauditoryandvisualmultistability AT pressnitzerdaniel inhibitionexcitationbalanceintheparietalcortexmodulatesvolitionalcontrolforauditoryandvisualmultistability AT shimadayasuhiro inhibitionexcitationbalanceintheparietalcortexmodulatesvolitionalcontrolforauditoryandvisualmultistability AT kochiyamatakanori inhibitionexcitationbalanceintheparietalcortexmodulatesvolitionalcontrolforauditoryandvisualmultistability AT kashinomakio inhibitionexcitationbalanceintheparietalcortexmodulatesvolitionalcontrolforauditoryandvisualmultistability |