Stochastic Dynamics Underlying Cognitive Stability and Flexibility
Cognitive stability and flexibility are core functions in the successful pursuit of behavioral goals. While there is evidence for a common frontoparietal network underlying both functions and for a key role of dopamine in the modulation of flexible versus stable behavior, the exact neurocomputationa...
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description | Cognitive stability and flexibility are core functions in the successful pursuit of behavioral goals. While there is evidence for a common frontoparietal network underlying both functions and for a key role of dopamine in the modulation of flexible versus stable behavior, the exact neurocomputational mechanisms underlying those executive functions and their adaptation to environmental demands are still unclear. In this work we study the neurocomputational mechanisms underlying cue based task switching (flexibility) and distractor inhibition (stability) in a paradigm specifically designed to probe both functions. We develop a physiologically plausible, explicit model of neural networks that maintain the currently active task rule in working memory and implement the decision process. We simplify the four-choice decision network to a nonlinear drift-diffusion process that we canonically derive from a generic winner-take-all network model. By fitting our model to the behavioral data of individual subjects, we can reproduce their full behavior in terms of decisions and reaction time distributions in baseline as well as distractor inhibition and switch conditions. Furthermore, we predict the individual hemodynamic response timecourse of the rule-representing network and localize it to a frontoparietal network including the inferior frontal junction area and the intraparietal sulcus, using functional magnetic resonance imaging. This refines the understanding of task-switch-related frontoparietal brain activity as reflecting attractor-like working memory representations of task rules. Finally, we estimate the subject-specific stability of the rule-representing attractor states in terms of the minimal action associated with a transition between different rule states in the phase-space of the fitted models. This stability measure correlates with switching-specific thalamocorticostriatal activation, i.e., with a system associated with flexible working memory updating and dopaminergic modulation of cognitive flexibility. These results show that stochastic dynamical systems can implement the basic computations underlying cognitive stability and flexibility and explain neurobiological bases of individual differences. |
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By fitting our model to the behavioral data of individual subjects, we can reproduce their full behavior in terms of decisions and reaction time distributions in baseline as well as distractor inhibition and switch conditions. Furthermore, we predict the individual hemodynamic response timecourse of the rule-representing network and localize it to a frontoparietal network including the inferior frontal junction area and the intraparietal sulcus, using functional magnetic resonance imaging. This refines the understanding of task-switch-related frontoparietal brain activity as reflecting attractor-like working memory representations of task rules. Finally, we estimate the subject-specific stability of the rule-representing attractor states in terms of the minimal action associated with a transition between different rule states in the phase-space of the fitted models. This stability measure correlates with switching-specific thalamocorticostriatal activation, i.e., with a system associated with flexible working memory updating and dopaminergic modulation of cognitive flexibility. 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While there is evidence for a common frontoparietal network underlying both functions and for a key role of dopamine in the modulation of flexible versus stable behavior, the exact neurocomputational mechanisms underlying those executive functions and their adaptation to environmental demands are still unclear. In this work we study the neurocomputational mechanisms underlying cue based task switching (flexibility) and distractor inhibition (stability) in a paradigm specifically designed to probe both functions. We develop a physiologically plausible, explicit model of neural networks that maintain the currently active task rule in working memory and implement the decision process. We simplify the four-choice decision network to a nonlinear drift-diffusion process that we canonically derive from a generic winner-take-all network model. By fitting our model to the behavioral data of individual subjects, we can reproduce their full behavior in terms of decisions and reaction time distributions in baseline as well as distractor inhibition and switch conditions. Furthermore, we predict the individual hemodynamic response timecourse of the rule-representing network and localize it to a frontoparietal network including the inferior frontal junction area and the intraparietal sulcus, using functional magnetic resonance imaging. This refines the understanding of task-switch-related frontoparietal brain activity as reflecting attractor-like working memory representations of task rules. Finally, we estimate the subject-specific stability of the rule-representing attractor states in terms of the minimal action associated with a transition between different rule states in the phase-space of the fitted models. This stability measure correlates with switching-specific thalamocorticostriatal activation, i.e., with a system associated with flexible working memory updating and dopaminergic modulation of cognitive flexibility. These results show that stochastic dynamical systems can implement the basic computations underlying cognitive stability and flexibility and explain neurobiological bases of individual differences.</description><subject>Adult</subject><subject>Behavior</subject><subject>Brain - physiology</subject><subject>Brain Mapping</subject><subject>Cognition - physiology</subject><subject>Computational Biology</subject><subject>Energy consumption</subject><subject>Female</subject><subject>Flexibility</subject><subject>Funding</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Memory</subject><subject>Memory, Short-Term - physiology</subject><subject>Models, Neurological</subject><subject>Neural networks</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Reaction Time - physiology</subject><subject>Task Performance and Analysis</subject><subject>Young Adult</subject><issn>1553-7358</issn><issn>1553-734X</issn><issn>1553-7358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNpVUctu2zAQJIoWzat_ULQ65mKXNB8iLwUaN2kDBOghyZlYUSuHBi26pBzEf1-qVoLkxOVydmaWQ8hnRueM1-zbOu5SD2G-dY2fM0oF5-wdOWZS8lnNpX7_qj4iJzmvKS2lUR_J0UJRpRkzx-TidojuAfLgXfVz38PGu1zd9y2msPf9qlrGVe8H_4jV7QCND37YV9C31VXAJ3-4n5EPHYSMn6bzlNxfXd4tf89u_vy6Xv64mTlh9DADBk0LBjrgnaOMY4cCZcc7phSYVqPkXCxQM9rK1iG6WjpnOFWsgQUXkp-SrwfebYjZTutny5RRWirJR8T1AdFGWNtt8htIexvB2_-NmFYWUtk0oC2_1cnipG10I8BprZxYUM4o1KpmOHJ9n9R2zQaLoX5IEN6Qvn3p_YNdxUcrhFLSqEJwPhGk-HeHebAbnx2GAD3G3ehbm6KnWV2g4gB1KeacsHuRYdSOYT9va8ew7RR2Gfvy2uLL0HO6_B8-BKm-</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Ueltzhöffer, Kai</creator><creator>Armbruster-Genç, Diana J N</creator><creator>Fiebach, Christian J</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150601</creationdate><title>Stochastic Dynamics Underlying Cognitive Stability and Flexibility</title><author>Ueltzhöffer, Kai ; Armbruster-Genç, Diana J N ; Fiebach, Christian J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-a1abda9afa3fc013efe4e5f3f166a9d8e53342e810d5dceec75cc93061ba23453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Behavior</topic><topic>Brain - physiology</topic><topic>Brain Mapping</topic><topic>Cognition - physiology</topic><topic>Computational Biology</topic><topic>Energy consumption</topic><topic>Female</topic><topic>Flexibility</topic><topic>Funding</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Memory</topic><topic>Memory, Short-Term - physiology</topic><topic>Models, Neurological</topic><topic>Neural networks</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Reaction Time - physiology</topic><topic>Task Performance and Analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ueltzhöffer, Kai</creatorcontrib><creatorcontrib>Armbruster-Genç, Diana J N</creatorcontrib><creatorcontrib>Fiebach, Christian J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS computational biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ueltzhöffer, Kai</au><au>Armbruster-Genç, Diana J N</au><au>Fiebach, Christian J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stochastic Dynamics Underlying Cognitive Stability and Flexibility</atitle><jtitle>PLoS computational biology</jtitle><addtitle>PLoS Comput Biol</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>11</volume><issue>6</issue><spage>e1004331</spage><epage>e1004331</epage><pages>e1004331-e1004331</pages><issn>1553-7358</issn><issn>1553-734X</issn><eissn>1553-7358</eissn><abstract>Cognitive stability and flexibility are core functions in the successful pursuit of behavioral goals. While there is evidence for a common frontoparietal network underlying both functions and for a key role of dopamine in the modulation of flexible versus stable behavior, the exact neurocomputational mechanisms underlying those executive functions and their adaptation to environmental demands are still unclear. In this work we study the neurocomputational mechanisms underlying cue based task switching (flexibility) and distractor inhibition (stability) in a paradigm specifically designed to probe both functions. We develop a physiologically plausible, explicit model of neural networks that maintain the currently active task rule in working memory and implement the decision process. We simplify the four-choice decision network to a nonlinear drift-diffusion process that we canonically derive from a generic winner-take-all network model. By fitting our model to the behavioral data of individual subjects, we can reproduce their full behavior in terms of decisions and reaction time distributions in baseline as well as distractor inhibition and switch conditions. Furthermore, we predict the individual hemodynamic response timecourse of the rule-representing network and localize it to a frontoparietal network including the inferior frontal junction area and the intraparietal sulcus, using functional magnetic resonance imaging. This refines the understanding of task-switch-related frontoparietal brain activity as reflecting attractor-like working memory representations of task rules. Finally, we estimate the subject-specific stability of the rule-representing attractor states in terms of the minimal action associated with a transition between different rule states in the phase-space of the fitted models. This stability measure correlates with switching-specific thalamocorticostriatal activation, i.e., with a system associated with flexible working memory updating and dopaminergic modulation of cognitive flexibility. These results show that stochastic dynamical systems can implement the basic computations underlying cognitive stability and flexibility and explain neurobiological bases of individual differences.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26068119</pmid><doi>10.1371/journal.pcbi.1004331</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Behavior Brain - physiology Brain Mapping Cognition - physiology Computational Biology Energy consumption Female Flexibility Funding Humans Magnetic Resonance Imaging Male Memory Memory, Short-Term - physiology Models, Neurological Neural networks NMR Nuclear magnetic resonance Reaction Time - physiology Task Performance and Analysis Young Adult |
title | Stochastic Dynamics Underlying Cognitive Stability and Flexibility |
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