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Beyond the evoked/intrinsic neural process dichotomy

Contemporary functional neuroimaging research has increasingly focused on characterization of intrinsic or “spontaneous” brain activity. Analysis of intrinsic activity is often contrasted with analysis of task-evoked activity that has traditionally been the focus of cognitive neuroscience. But does...

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Detalles Bibliográficos
Autores principales: Bolt, Taylor, Anderson, Michael L., Uddin, Lucina Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MIT Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989985/
https://www.ncbi.nlm.nih.gov/pubmed/29911670
http://dx.doi.org/10.1162/NETN_a_00028
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author Bolt, Taylor
Anderson, Michael L.
Uddin, Lucina Q.
author_facet Bolt, Taylor
Anderson, Michael L.
Uddin, Lucina Q.
author_sort Bolt, Taylor
collection PubMed
description Contemporary functional neuroimaging research has increasingly focused on characterization of intrinsic or “spontaneous” brain activity. Analysis of intrinsic activity is often contrasted with analysis of task-evoked activity that has traditionally been the focus of cognitive neuroscience. But does this evoked/intrinsic dichotomy adequately characterize human brain function? Based on empirical data demonstrating a close functional interdependence between intrinsic and task-evoked activity, we argue that the dichotomy between intrinsic and task-evoked activity as unobserved contributions to brain activity is artificial. We present an alternative picture of brain function in which the brain’s spatiotemporal dynamics do not consist of separable intrinsic and task-evoked components, but reflect the enaction of a system of mutual constraints to move the brain into and out of task-appropriate functional configurations. According to this alternative picture, cognitive neuroscientists are tasked with describing both the temporal trajectory of brain activity patterns across time, and the modulation of this trajectory by task states, without separating this process into intrinsic and task-evoked components. We argue that this alternative picture of brain function is best captured in a novel explanatory framework called enabling constraint. Overall, these insights call for a reconceptualization of functional brain activity, and should drive future methodological and empirical efforts.
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spelling pubmed-59899852018-06-15 Beyond the evoked/intrinsic neural process dichotomy Bolt, Taylor Anderson, Michael L. Uddin, Lucina Q. Netw Neurosci Perspective Contemporary functional neuroimaging research has increasingly focused on characterization of intrinsic or “spontaneous” brain activity. Analysis of intrinsic activity is often contrasted with analysis of task-evoked activity that has traditionally been the focus of cognitive neuroscience. But does this evoked/intrinsic dichotomy adequately characterize human brain function? Based on empirical data demonstrating a close functional interdependence between intrinsic and task-evoked activity, we argue that the dichotomy between intrinsic and task-evoked activity as unobserved contributions to brain activity is artificial. We present an alternative picture of brain function in which the brain’s spatiotemporal dynamics do not consist of separable intrinsic and task-evoked components, but reflect the enaction of a system of mutual constraints to move the brain into and out of task-appropriate functional configurations. According to this alternative picture, cognitive neuroscientists are tasked with describing both the temporal trajectory of brain activity patterns across time, and the modulation of this trajectory by task states, without separating this process into intrinsic and task-evoked components. We argue that this alternative picture of brain function is best captured in a novel explanatory framework called enabling constraint. Overall, these insights call for a reconceptualization of functional brain activity, and should drive future methodological and empirical efforts. MIT Press 2018-03-01 /pmc/articles/PMC5989985/ /pubmed/29911670 http://dx.doi.org/10.1162/NETN_a_00028 Text en © 2017 Massachusetts Institute of Technology http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Perspective
Bolt, Taylor
Anderson, Michael L.
Uddin, Lucina Q.
Beyond the evoked/intrinsic neural process dichotomy
title Beyond the evoked/intrinsic neural process dichotomy
title_full Beyond the evoked/intrinsic neural process dichotomy
title_fullStr Beyond the evoked/intrinsic neural process dichotomy
title_full_unstemmed Beyond the evoked/intrinsic neural process dichotomy
title_short Beyond the evoked/intrinsic neural process dichotomy
title_sort beyond the evoked/intrinsic neural process dichotomy
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989985/
https://www.ncbi.nlm.nih.gov/pubmed/29911670
http://dx.doi.org/10.1162/NETN_a_00028
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