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Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking

Fear can potently inhibit ongoing behavior, including reward-seeking, yet the neural circuits that underlie such suppression remain to be clarified. Prior studies have demonstrated that distinct subregions of the rodent medial prefrontal cortex (mPFC) differentially affect fear behavior, whereby fea...

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Detalles Bibliográficos
Autores principales: Piantadosi, Patrick T., Yeates, Dylan C.M., Floresco, Stan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497111/
https://www.ncbi.nlm.nih.gov/pubmed/32934096
http://dx.doi.org/10.1101/lm.051912.120
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author Piantadosi, Patrick T.
Yeates, Dylan C.M.
Floresco, Stan B.
author_facet Piantadosi, Patrick T.
Yeates, Dylan C.M.
Floresco, Stan B.
author_sort Piantadosi, Patrick T.
collection PubMed
description Fear can potently inhibit ongoing behavior, including reward-seeking, yet the neural circuits that underlie such suppression remain to be clarified. Prior studies have demonstrated that distinct subregions of the rodent medial prefrontal cortex (mPFC) differentially affect fear behavior, whereby fear expression is promoted by the more dorsal prelimbic cortex (PL) and inhibited by the more ventral infralimbic cortex (IL). These mPFC regions project to subregions of the nucleus accumbens, the core (NAcC) and shell (NAcS), that differentially contribute to reward-seeking as well as affective processes that may be relevant to fear expression. Here, we investigated how these mPFC and NAc subregions contribute to discriminative fear conditioning, assessed by conditioned suppression of reward-seeking. Bilateral inactivation of the NAcS or PL reduced the expression of conditioned suppression to a shock-associated CS+, whereas NAcC inactivation reduced reward-seeking without affecting suppression. IL inactivation caused a general reduction in conditioned suppression following discriminative conditioning, but not when using a single-stimulus design. Pharmacological disconnection of the PL → NAcS pathway revealed that this projection mediates conditioned suppression. These data add to a growing literature implicating discrete cortico-striatal pathways in the suppression of reward-seeking in response to aversive stimuli. Dysfunction within related structures may contribute to aberrant patterns of behavior in psychiatric illnesses including substance use disorders.
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spelling pubmed-74971112021-10-01 Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking Piantadosi, Patrick T. Yeates, Dylan C.M. Floresco, Stan B. Learn Mem Research Fear can potently inhibit ongoing behavior, including reward-seeking, yet the neural circuits that underlie such suppression remain to be clarified. Prior studies have demonstrated that distinct subregions of the rodent medial prefrontal cortex (mPFC) differentially affect fear behavior, whereby fear expression is promoted by the more dorsal prelimbic cortex (PL) and inhibited by the more ventral infralimbic cortex (IL). These mPFC regions project to subregions of the nucleus accumbens, the core (NAcC) and shell (NAcS), that differentially contribute to reward-seeking as well as affective processes that may be relevant to fear expression. Here, we investigated how these mPFC and NAc subregions contribute to discriminative fear conditioning, assessed by conditioned suppression of reward-seeking. Bilateral inactivation of the NAcS or PL reduced the expression of conditioned suppression to a shock-associated CS+, whereas NAcC inactivation reduced reward-seeking without affecting suppression. IL inactivation caused a general reduction in conditioned suppression following discriminative conditioning, but not when using a single-stimulus design. Pharmacological disconnection of the PL → NAcS pathway revealed that this projection mediates conditioned suppression. These data add to a growing literature implicating discrete cortico-striatal pathways in the suppression of reward-seeking in response to aversive stimuli. Dysfunction within related structures may contribute to aberrant patterns of behavior in psychiatric illnesses including substance use disorders. Cold Spring Harbor Laboratory Press 2020-10 /pmc/articles/PMC7497111/ /pubmed/32934096 http://dx.doi.org/10.1101/lm.051912.120 Text en © 2020 Piantadosi et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Piantadosi, Patrick T.
Yeates, Dylan C.M.
Floresco, Stan B.
Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
title Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
title_full Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
title_fullStr Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
title_full_unstemmed Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
title_short Prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
title_sort prefrontal cortical and nucleus accumbens contributions to discriminative conditioned suppression of reward-seeking
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497111/
https://www.ncbi.nlm.nih.gov/pubmed/32934096
http://dx.doi.org/10.1101/lm.051912.120
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