Cargando…
Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation
Primate studies show slow ramping activity in posterior parietal cortex (PPC) neurons during perceptual decision-making. These findings have inspired a rich theoretical literature to account for this activity. These accounts are largely unrelated to Bayesian theories of perception and predictive cod...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306525/ https://www.ncbi.nlm.nih.gov/pubmed/25512038 http://dx.doi.org/10.1016/j.neuroimage.2014.12.015 |
_version_ | 1782354339090661376 |
---|---|
author | FitzGerald, Thomas H.B. Moran, Rosalyn J. Friston, Karl J. Dolan, Raymond J. |
author_facet | FitzGerald, Thomas H.B. Moran, Rosalyn J. Friston, Karl J. Dolan, Raymond J. |
author_sort | FitzGerald, Thomas H.B. |
collection | PubMed |
description | Primate studies show slow ramping activity in posterior parietal cortex (PPC) neurons during perceptual decision-making. These findings have inspired a rich theoretical literature to account for this activity. These accounts are largely unrelated to Bayesian theories of perception and predictive coding, a related formulation of perceptual inference in the cortical hierarchy. Here, we tested a key prediction of such hierarchical inference, namely that the estimated precision (reliability) of information ascending the cortical hierarchy plays a key role in determining both the speed of decision-making and the rate of increase of PPC activity. Using dynamic causal modelling of magnetoencephalographic (MEG) evoked responses, recorded during a simple perceptual decision-making task, we recover ramping-activity from an anatomically and functionally plausible network of regions, including early visual cortex, the middle temporal area (MT) and PPC. Precision, as reflected by the gain on pyramidal cell activity, was strongly correlated with both the speed of decision making and the slope of PPC ramping activity. Our findings indicate that the dynamics of neuronal activity in the human PPC during perceptual decision-making recapitulate those observed in the macaque, and in so doing we link observations from primate electrophysiology and human choice behaviour. Moreover, the synaptic gain control modulating these dynamics is consistent with predictive coding formulations of evidence accumulation. |
format | Online Article Text |
id | pubmed-4306525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43065252015-02-15 Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation FitzGerald, Thomas H.B. Moran, Rosalyn J. Friston, Karl J. Dolan, Raymond J. Neuroimage Article Primate studies show slow ramping activity in posterior parietal cortex (PPC) neurons during perceptual decision-making. These findings have inspired a rich theoretical literature to account for this activity. These accounts are largely unrelated to Bayesian theories of perception and predictive coding, a related formulation of perceptual inference in the cortical hierarchy. Here, we tested a key prediction of such hierarchical inference, namely that the estimated precision (reliability) of information ascending the cortical hierarchy plays a key role in determining both the speed of decision-making and the rate of increase of PPC activity. Using dynamic causal modelling of magnetoencephalographic (MEG) evoked responses, recorded during a simple perceptual decision-making task, we recover ramping-activity from an anatomically and functionally plausible network of regions, including early visual cortex, the middle temporal area (MT) and PPC. Precision, as reflected by the gain on pyramidal cell activity, was strongly correlated with both the speed of decision making and the slope of PPC ramping activity. Our findings indicate that the dynamics of neuronal activity in the human PPC during perceptual decision-making recapitulate those observed in the macaque, and in so doing we link observations from primate electrophysiology and human choice behaviour. Moreover, the synaptic gain control modulating these dynamics is consistent with predictive coding formulations of evidence accumulation. Academic Press 2015-02-15 /pmc/articles/PMC4306525/ /pubmed/25512038 http://dx.doi.org/10.1016/j.neuroimage.2014.12.015 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article FitzGerald, Thomas H.B. Moran, Rosalyn J. Friston, Karl J. Dolan, Raymond J. Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
title | Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
title_full | Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
title_fullStr | Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
title_full_unstemmed | Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
title_short | Precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
title_sort | precision and neuronal dynamics in the human posterior parietal cortex during evidence accumulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306525/ https://www.ncbi.nlm.nih.gov/pubmed/25512038 http://dx.doi.org/10.1016/j.neuroimage.2014.12.015 |
work_keys_str_mv | AT fitzgeraldthomashb precisionandneuronaldynamicsinthehumanposteriorparietalcortexduringevidenceaccumulation AT moranrosalynj precisionandneuronaldynamicsinthehumanposteriorparietalcortexduringevidenceaccumulation AT fristonkarlj precisionandneuronaldynamicsinthehumanposteriorparietalcortexduringevidenceaccumulation AT dolanraymondj precisionandneuronaldynamicsinthehumanposteriorparietalcortexduringevidenceaccumulation |