Cargando…

Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making

How do neurons in a decision circuit integrate time-varying signals, in favor of or against alternative choice options? To address this question, we used a recurrent neural circuit model to simulate an experiment in which monkeys performed a direction-discrimination task on a visual motion stimulus....

Descripción completa

Detalles Bibliográficos
Autores principales: Wong, Kong-Fatt, Huk, Alexander C., Shadlen, Michael N., Wang, Xiao-Jing
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525934/
https://www.ncbi.nlm.nih.gov/pubmed/18946528
http://dx.doi.org/10.3389/neuro.10.006.2007
_version_ 1782158700718325760
author Wong, Kong-Fatt
Huk, Alexander C.
Shadlen, Michael N.
Wang, Xiao-Jing
author_facet Wong, Kong-Fatt
Huk, Alexander C.
Shadlen, Michael N.
Wang, Xiao-Jing
author_sort Wong, Kong-Fatt
collection PubMed
description How do neurons in a decision circuit integrate time-varying signals, in favor of or against alternative choice options? To address this question, we used a recurrent neural circuit model to simulate an experiment in which monkeys performed a direction-discrimination task on a visual motion stimulus. In a recent study, it was found that brief pulses of motion perturbed neural activity in the lateral intraparietal area (LIP), and exerted corresponding effects on the monkey's choices and response times. Our model reproduces the behavioral observations and replicates LIP activity which, depending on whether the direction of the pulse is the same or opposite to that of a preferred motion stimulus, increases or decreases persistently over a few hundred milliseconds. Furthermore, our model accounts for the observation that the pulse exerts a weaker influence on LIP neuronal responses when the pulse is late relative to motion stimulus onset. We show that this violation of time-shift invariance (TSI) is consistent with a recurrent circuit mechanism of time integration. We further examine time integration using two consecutive pulses of the same or opposite motion directions. The induced changes in the performance are not additive, and the second of the paired pulses is less effective than its standalone impact, a prediction that is experimentally testable. Taken together, these findings lend further support for an attractor network model of time integration in perceptual decision making.
format Text
id pubmed-2525934
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Frontiers Research Foundation
record_format MEDLINE/PubMed
spelling pubmed-25259342008-10-22 Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making Wong, Kong-Fatt Huk, Alexander C. Shadlen, Michael N. Wang, Xiao-Jing Front Comput Neurosci Neuroscience How do neurons in a decision circuit integrate time-varying signals, in favor of or against alternative choice options? To address this question, we used a recurrent neural circuit model to simulate an experiment in which monkeys performed a direction-discrimination task on a visual motion stimulus. In a recent study, it was found that brief pulses of motion perturbed neural activity in the lateral intraparietal area (LIP), and exerted corresponding effects on the monkey's choices and response times. Our model reproduces the behavioral observations and replicates LIP activity which, depending on whether the direction of the pulse is the same or opposite to that of a preferred motion stimulus, increases or decreases persistently over a few hundred milliseconds. Furthermore, our model accounts for the observation that the pulse exerts a weaker influence on LIP neuronal responses when the pulse is late relative to motion stimulus onset. We show that this violation of time-shift invariance (TSI) is consistent with a recurrent circuit mechanism of time integration. We further examine time integration using two consecutive pulses of the same or opposite motion directions. The induced changes in the performance are not additive, and the second of the paired pulses is less effective than its standalone impact, a prediction that is experimentally testable. Taken together, these findings lend further support for an attractor network model of time integration in perceptual decision making. Frontiers Research Foundation 2007-11-02 /pmc/articles/PMC2525934/ /pubmed/18946528 http://dx.doi.org/10.3389/neuro.10.006.2007 Text en Copyright: © 2007 Wong, Huk, Shadlen, Wang. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Wong, Kong-Fatt
Huk, Alexander C.
Shadlen, Michael N.
Wang, Xiao-Jing
Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making
title Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making
title_full Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making
title_fullStr Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making
title_full_unstemmed Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making
title_short Neural Circuit Dynamics Underlying Accumulation of Time-Varying Evidence During Perceptual Decision Making
title_sort neural circuit dynamics underlying accumulation of time-varying evidence during perceptual decision making
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525934/
https://www.ncbi.nlm.nih.gov/pubmed/18946528
http://dx.doi.org/10.3389/neuro.10.006.2007
work_keys_str_mv AT wongkongfatt neuralcircuitdynamicsunderlyingaccumulationoftimevaryingevidenceduringperceptualdecisionmaking
AT hukalexanderc neuralcircuitdynamicsunderlyingaccumulationoftimevaryingevidenceduringperceptualdecisionmaking
AT shadlenmichaeln neuralcircuitdynamicsunderlyingaccumulationoftimevaryingevidenceduringperceptualdecisionmaking
AT wangxiaojing neuralcircuitdynamicsunderlyingaccumulationoftimevaryingevidenceduringperceptualdecisionmaking