Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain

Although optimizing decisions between drives to avoid pain and to obtain reward are critical for survival, understanding the neuronal circuit activity that regulates choice during approach-avoidance conflicts is limited. Here, we recorded neuronal activity in the infralimbic (IL) cortex and nucleus...

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Main Authors: Neil Schwartz, Catriona Miller, Howard L. Fields
Format: Article
Language:English
Published: Elsevier 2017-05-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124717306022
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spelling doaj-f017138f9c734b76b460956de88078fc2020-11-25T01:09:08ZengElsevierCell Reports2211-12472017-05-011981522153110.1016/j.celrep.2017.04.073Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic PainNeil Schwartz0Catriona Miller1Howard L. Fields2Department of Neurology, the Weill Institute for Neuroscience, University of California, San Francisco, San Francisco, CA 94143, USADepartment of Neurology, the Weill Institute for Neuroscience, University of California, San Francisco, San Francisco, CA 94143, USADepartment of Neurology, the Weill Institute for Neuroscience, University of California, San Francisco, San Francisco, CA 94143, USAAlthough optimizing decisions between drives to avoid pain and to obtain reward are critical for survival, understanding the neuronal circuit activity that regulates choice during approach-avoidance conflicts is limited. Here, we recorded neuronal activity in the infralimbic (IL) cortex and nucleus accumbens (NAc) during an approach-avoidance task. In this task, disruption of approach by a pain-predictive cue (PPC-avoidance) is extinguished by experience and reinstated in a model of chronic pain. In the IL-NAc circuit, the activity of distinct subpopulations of neurons predicts the extent of PPC-avoidance observed. Furthermore, chemogenetic and optogenetic manipulations establish that IL-NAc circuitry regulates PPC-avoidance behavior. Our results indicate that IL-NAc circuitry is engaged during approach-avoidance conflicts, and modifications of this circuit by experience and chronic pain determine whether approach or avoidance occurs.http://www.sciencedirect.com/science/article/pii/S2211124717306022approach-avoidancepainchronic paininfralimbicaccumbensventral striatummotivationchoicevmPFC
collection DOAJ
language English
format Article
sources DOAJ
author Neil Schwartz
Catriona Miller
Howard L. Fields
spellingShingle Neil Schwartz
Catriona Miller
Howard L. Fields
Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain
Cell Reports
approach-avoidance
pain
chronic pain
infralimbic
accumbens
ventral striatum
motivation
choice
vmPFC
author_facet Neil Schwartz
Catriona Miller
Howard L. Fields
author_sort Neil Schwartz
title Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain
title_short Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain
title_full Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain
title_fullStr Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain
title_full_unstemmed Cortico-Accumbens Regulation of Approach-Avoidance Behavior Is Modified by Experience and Chronic Pain
title_sort cortico-accumbens regulation of approach-avoidance behavior is modified by experience and chronic pain
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2017-05-01
description Although optimizing decisions between drives to avoid pain and to obtain reward are critical for survival, understanding the neuronal circuit activity that regulates choice during approach-avoidance conflicts is limited. Here, we recorded neuronal activity in the infralimbic (IL) cortex and nucleus accumbens (NAc) during an approach-avoidance task. In this task, disruption of approach by a pain-predictive cue (PPC-avoidance) is extinguished by experience and reinstated in a model of chronic pain. In the IL-NAc circuit, the activity of distinct subpopulations of neurons predicts the extent of PPC-avoidance observed. Furthermore, chemogenetic and optogenetic manipulations establish that IL-NAc circuitry regulates PPC-avoidance behavior. Our results indicate that IL-NAc circuitry is engaged during approach-avoidance conflicts, and modifications of this circuit by experience and chronic pain determine whether approach or avoidance occurs.
topic approach-avoidance
pain
chronic pain
infralimbic
accumbens
ventral striatum
motivation
choice
vmPFC
url http://www.sciencedirect.com/science/article/pii/S2211124717306022
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AT catrionamiller corticoaccumbensregulationofapproachavoidancebehaviorismodifiedbyexperienceandchronicpain
AT howardlfields corticoaccumbensregulationofapproachavoidancebehaviorismodifiedbyexperienceandchronicpain
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