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Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity

In many brain areas, sensory responses are heavily modulated by factors including attentional state, context, reward history, motor preparation, learned associations, and other cognitive variables. Modelling the effect of these modulatory factors on sensory responses has proven challenging, mostly d...

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Autores principales: Niknam, Kaiser, Akbarian, Amir, Clark, Kelsey, Zamani, Yasin, Noudoost, Behrad, Nategh, Neda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759185/
https://www.ncbi.nlm.nih.gov/pubmed/31513570
http://dx.doi.org/10.1371/journal.pcbi.1007275
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author Niknam, Kaiser
Akbarian, Amir
Clark, Kelsey
Zamani, Yasin
Noudoost, Behrad
Nategh, Neda
author_facet Niknam, Kaiser
Akbarian, Amir
Clark, Kelsey
Zamani, Yasin
Noudoost, Behrad
Nategh, Neda
author_sort Niknam, Kaiser
collection PubMed
description In many brain areas, sensory responses are heavily modulated by factors including attentional state, context, reward history, motor preparation, learned associations, and other cognitive variables. Modelling the effect of these modulatory factors on sensory responses has proven challenging, mostly due to the time-varying and nonlinear nature of the underlying computations. Here we present a computational model capable of capturing and dissociating multiple time-varying modulatory effects on neuronal responses on the order of milliseconds. The model’s performance is tested on extrastriate perisaccadic visual responses in nonhuman primates. Visual neurons respond to stimuli presented around the time of saccades differently than during fixation. These perisaccadic changes include sensitivity to the stimuli presented at locations outside the neuron’s receptive field, which suggests a contribution of multiple sources to perisaccadic response generation. Current computational approaches cannot quantitatively characterize the contribution of each modulatory source in response generation, mainly due to the very short timescale on which the saccade takes place. In this study, we use a high spatiotemporal resolution experimental paradigm along with a novel extension of the generalized linear model framework (GLM), termed the sparse-variable GLM, to allow for time-varying model parameters representing the temporal evolution of the system with a resolution on the order of milliseconds. We used this model framework to precisely map the temporal evolution of the spatiotemporal receptive field of visual neurons in the middle temporal area during the execution of a saccade. Moreover, an extended model based on a factorization of the sparse-variable GLM allowed us to disassociate and quantify the contribution of individual sources to the perisaccadic response. Our results show that our novel framework can precisely capture the changes in sensitivity of neurons around the time of saccades, and provide a general framework to quantitatively track the role of multiple modulatory sources over time.
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spelling pubmed-67591852019-10-04 Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity Niknam, Kaiser Akbarian, Amir Clark, Kelsey Zamani, Yasin Noudoost, Behrad Nategh, Neda PLoS Comput Biol Research Article In many brain areas, sensory responses are heavily modulated by factors including attentional state, context, reward history, motor preparation, learned associations, and other cognitive variables. Modelling the effect of these modulatory factors on sensory responses has proven challenging, mostly due to the time-varying and nonlinear nature of the underlying computations. Here we present a computational model capable of capturing and dissociating multiple time-varying modulatory effects on neuronal responses on the order of milliseconds. The model’s performance is tested on extrastriate perisaccadic visual responses in nonhuman primates. Visual neurons respond to stimuli presented around the time of saccades differently than during fixation. These perisaccadic changes include sensitivity to the stimuli presented at locations outside the neuron’s receptive field, which suggests a contribution of multiple sources to perisaccadic response generation. Current computational approaches cannot quantitatively characterize the contribution of each modulatory source in response generation, mainly due to the very short timescale on which the saccade takes place. In this study, we use a high spatiotemporal resolution experimental paradigm along with a novel extension of the generalized linear model framework (GLM), termed the sparse-variable GLM, to allow for time-varying model parameters representing the temporal evolution of the system with a resolution on the order of milliseconds. We used this model framework to precisely map the temporal evolution of the spatiotemporal receptive field of visual neurons in the middle temporal area during the execution of a saccade. Moreover, an extended model based on a factorization of the sparse-variable GLM allowed us to disassociate and quantify the contribution of individual sources to the perisaccadic response. Our results show that our novel framework can precisely capture the changes in sensitivity of neurons around the time of saccades, and provide a general framework to quantitatively track the role of multiple modulatory sources over time. Public Library of Science 2019-09-12 /pmc/articles/PMC6759185/ /pubmed/31513570 http://dx.doi.org/10.1371/journal.pcbi.1007275 Text en © 2019 Niknam et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Niknam, Kaiser
Akbarian, Amir
Clark, Kelsey
Zamani, Yasin
Noudoost, Behrad
Nategh, Neda
Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
title Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
title_full Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
title_fullStr Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
title_full_unstemmed Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
title_short Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
title_sort characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759185/
https://www.ncbi.nlm.nih.gov/pubmed/31513570
http://dx.doi.org/10.1371/journal.pcbi.1007275
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