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A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences
Inhibitory control is an important component of executive function that allows organisms to abort emerging behavioral plans or ongoing actions on the fly as new sensory information becomes available. Current models treat inhibitory control as a race between a Go- and a Stop process that may be media...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500928/ https://www.ncbi.nlm.nih.gov/pubmed/26236226 http://dx.doi.org/10.3389/fncom.2015.00087 |
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author | Teichert, Tobias Ferrera, Vincent P. |
author_facet | Teichert, Tobias Ferrera, Vincent P. |
author_sort | Teichert, Tobias |
collection | PubMed |
description | Inhibitory control is an important component of executive function that allows organisms to abort emerging behavioral plans or ongoing actions on the fly as new sensory information becomes available. Current models treat inhibitory control as a race between a Go- and a Stop process that may be mediated by partially distinct neural substrates, i.e., the direct and the hyper-direct pathway of the basal ganglia. The fact that finishing times of the Stop process (Stop-Signal Reaction Time, SSRT) cannot be observed directly has precluded a precise comparison of the functional properties that govern the initiation (GoRT) and inhibition (SSRT) of a motor response. To solve this problem, we modified an existing inhibitory paradigm and developed a non-parametric framework to measure the trial-by-trial variability of SSRT. A series of simulations verified that the non-parametric approach is on par with a parametric approach and yields accurate estimates of the entire SSRT distribution from as few as ~750 trials. Our results show that in identical settings, the distribution of SSRT is very similar to the distribution of GoRT albeit somewhat shorter, wider and significantly less right-skewed. The ability to measure the precise shapes of SSRT distributions opens new avenues for research into the functional properties of the hyper-direct pathway that is believed to mediate inhibitory control. |
format | Online Article Text |
id | pubmed-4500928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45009282015-07-31 A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences Teichert, Tobias Ferrera, Vincent P. Front Comput Neurosci Neuroscience Inhibitory control is an important component of executive function that allows organisms to abort emerging behavioral plans or ongoing actions on the fly as new sensory information becomes available. Current models treat inhibitory control as a race between a Go- and a Stop process that may be mediated by partially distinct neural substrates, i.e., the direct and the hyper-direct pathway of the basal ganglia. The fact that finishing times of the Stop process (Stop-Signal Reaction Time, SSRT) cannot be observed directly has precluded a precise comparison of the functional properties that govern the initiation (GoRT) and inhibition (SSRT) of a motor response. To solve this problem, we modified an existing inhibitory paradigm and developed a non-parametric framework to measure the trial-by-trial variability of SSRT. A series of simulations verified that the non-parametric approach is on par with a parametric approach and yields accurate estimates of the entire SSRT distribution from as few as ~750 trials. Our results show that in identical settings, the distribution of SSRT is very similar to the distribution of GoRT albeit somewhat shorter, wider and significantly less right-skewed. The ability to measure the precise shapes of SSRT distributions opens new avenues for research into the functional properties of the hyper-direct pathway that is believed to mediate inhibitory control. Frontiers Media S.A. 2015-07-14 /pmc/articles/PMC4500928/ /pubmed/26236226 http://dx.doi.org/10.3389/fncom.2015.00087 Text en Copyright © 2015 Teichert and Ferrera. http://creativecommons.org/licenses/by/4.0/ 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 Teichert, Tobias Ferrera, Vincent P. A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
title | A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
title_full | A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
title_fullStr | A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
title_full_unstemmed | A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
title_short | A new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
title_sort | new paradigm and computational framework to estimate stop-signal reaction time distributions from the inhibition of complex motor sequences |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500928/ https://www.ncbi.nlm.nih.gov/pubmed/26236226 http://dx.doi.org/10.3389/fncom.2015.00087 |
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