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Interplay of prefrontal cortex and amygdala during extinction of drug seeking
Extinction of Pavlovian conditioning is a complex process that involves brain regions such as the medial prefrontal cortex (mPFC), the amygdala and the locus coeruleus. In particular, noradrenaline (NA) coming from the locus coeruleus has been recently shown to play a different role in two subregion...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869906/ https://www.ncbi.nlm.nih.gov/pubmed/29081007 http://dx.doi.org/10.1007/s00429-017-1533-9 |
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author | Oliva, Valeria Cartoni, Emilio Latagliata, Emanuele Claudio Puglisi-Allegra, Stefano Baldassarre, Gianluca |
author_facet | Oliva, Valeria Cartoni, Emilio Latagliata, Emanuele Claudio Puglisi-Allegra, Stefano Baldassarre, Gianluca |
author_sort | Oliva, Valeria |
collection | PubMed |
description | Extinction of Pavlovian conditioning is a complex process that involves brain regions such as the medial prefrontal cortex (mPFC), the amygdala and the locus coeruleus. In particular, noradrenaline (NA) coming from the locus coeruleus has been recently shown to play a different role in two subregions of the mPFC, the prelimbic (PL) and the infralimbic (IL) regions. How these regions interact in conditioning and subsequent extinction is an open issue. We studied these processes using two approaches: computational modelling and NA manipulation in a conditioned place preference paradigm (CPP) in mice. In the computational model, NA in PL and IL causes inputs arriving to these regions to be amplified, thus allowing them to modulate learning processes in amygdala. The model reproduces results from studies involving depletion of NA from PL, IL, or both in CPP. In addition, we simulated new experiments of NA manipulations in mPFC, making predictions on the possible results. We searched the parameters of the model and tested the robustness of the predictions by performing a sensitivity analysis. We also present an empirical experiment where, in accord with the model, a double depletion of NA from both PL and IL in CPP with amphetamine impairs extinction. Overall the proposed model, supported by anatomical, physiological, and behavioural data, explains the differential role of NA in PL and IL and opens up the possibility to understand extinction mechanisms more in depth and hence to aid the development of treatments for disorders such as addiction. |
format | Online Article Text |
id | pubmed-5869906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-58699062018-03-28 Interplay of prefrontal cortex and amygdala during extinction of drug seeking Oliva, Valeria Cartoni, Emilio Latagliata, Emanuele Claudio Puglisi-Allegra, Stefano Baldassarre, Gianluca Brain Struct Funct Original Article Extinction of Pavlovian conditioning is a complex process that involves brain regions such as the medial prefrontal cortex (mPFC), the amygdala and the locus coeruleus. In particular, noradrenaline (NA) coming from the locus coeruleus has been recently shown to play a different role in two subregions of the mPFC, the prelimbic (PL) and the infralimbic (IL) regions. How these regions interact in conditioning and subsequent extinction is an open issue. We studied these processes using two approaches: computational modelling and NA manipulation in a conditioned place preference paradigm (CPP) in mice. In the computational model, NA in PL and IL causes inputs arriving to these regions to be amplified, thus allowing them to modulate learning processes in amygdala. The model reproduces results from studies involving depletion of NA from PL, IL, or both in CPP. In addition, we simulated new experiments of NA manipulations in mPFC, making predictions on the possible results. We searched the parameters of the model and tested the robustness of the predictions by performing a sensitivity analysis. We also present an empirical experiment where, in accord with the model, a double depletion of NA from both PL and IL in CPP with amphetamine impairs extinction. Overall the proposed model, supported by anatomical, physiological, and behavioural data, explains the differential role of NA in PL and IL and opens up the possibility to understand extinction mechanisms more in depth and hence to aid the development of treatments for disorders such as addiction. Springer Berlin Heidelberg 2017-10-28 2018 /pmc/articles/PMC5869906/ /pubmed/29081007 http://dx.doi.org/10.1007/s00429-017-1533-9 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Oliva, Valeria Cartoni, Emilio Latagliata, Emanuele Claudio Puglisi-Allegra, Stefano Baldassarre, Gianluca Interplay of prefrontal cortex and amygdala during extinction of drug seeking |
title | Interplay of prefrontal cortex and amygdala during extinction of drug seeking |
title_full | Interplay of prefrontal cortex and amygdala during extinction of drug seeking |
title_fullStr | Interplay of prefrontal cortex and amygdala during extinction of drug seeking |
title_full_unstemmed | Interplay of prefrontal cortex and amygdala during extinction of drug seeking |
title_short | Interplay of prefrontal cortex and amygdala during extinction of drug seeking |
title_sort | interplay of prefrontal cortex and amygdala during extinction of drug seeking |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869906/ https://www.ncbi.nlm.nih.gov/pubmed/29081007 http://dx.doi.org/10.1007/s00429-017-1533-9 |
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