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Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience

Intense motivational salience attribution is considered to have a major role in the development of different psychopathologies. Numerous brain areas are involved in “normal” motivational salience attribution processes; however, it is not clear whether common or different neural mechanisms also under...

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Autores principales: Ventura, Rossella, Latagliata, Emanuele Claudio, Morrone, Cristina, La Mela, Immacolata, Puglisi-Allegra, Stefano
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2516177/
https://www.ncbi.nlm.nih.gov/pubmed/18725944
http://dx.doi.org/10.1371/journal.pone.0003044
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author Ventura, Rossella
Latagliata, Emanuele Claudio
Morrone, Cristina
La Mela, Immacolata
Puglisi-Allegra, Stefano
author_facet Ventura, Rossella
Latagliata, Emanuele Claudio
Morrone, Cristina
La Mela, Immacolata
Puglisi-Allegra, Stefano
author_sort Ventura, Rossella
collection PubMed
description Intense motivational salience attribution is considered to have a major role in the development of different psychopathologies. Numerous brain areas are involved in “normal” motivational salience attribution processes; however, it is not clear whether common or different neural mechanisms also underlie intense motivational salience attribution. To elucidate this a brain area and a neural system had to be envisaged that were involved only in motivational salience attribution to highly salient stimuli. Using intracerebral microdialysis, we found that natural stimuli induced an increase in norepinephrine release in the medial prefrontal cortex of mice proportional to their salience, and that selective prefrontal norepinephrine depletion abolished the increase of norepinephrine release in the medial prefrontal cortex induced by exposure to appetitive (palatable food) or aversive (light) stimuli independently of salience. However, selective norepinephrine depletion in the medial prefrontal cortex impaired the place conditioning induced exclusively by highly salient stimuli, thus indicating that prefrontal noradrenergic transmission determines approach or avoidance responses to both reward- and aversion-related natural stimuli only when the salience of the unconditioned natural stimulus is high enough to induce sustained norepinephrine outflow. This affirms that prefrontal noradrenergic transmission determines motivational salience attribution selectively when intense motivational salience is processed, as in conditions that characterize psychopathological outcomes.
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spelling pubmed-25161772008-08-22 Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience Ventura, Rossella Latagliata, Emanuele Claudio Morrone, Cristina La Mela, Immacolata Puglisi-Allegra, Stefano PLoS One Research Article Intense motivational salience attribution is considered to have a major role in the development of different psychopathologies. Numerous brain areas are involved in “normal” motivational salience attribution processes; however, it is not clear whether common or different neural mechanisms also underlie intense motivational salience attribution. To elucidate this a brain area and a neural system had to be envisaged that were involved only in motivational salience attribution to highly salient stimuli. Using intracerebral microdialysis, we found that natural stimuli induced an increase in norepinephrine release in the medial prefrontal cortex of mice proportional to their salience, and that selective prefrontal norepinephrine depletion abolished the increase of norepinephrine release in the medial prefrontal cortex induced by exposure to appetitive (palatable food) or aversive (light) stimuli independently of salience. However, selective norepinephrine depletion in the medial prefrontal cortex impaired the place conditioning induced exclusively by highly salient stimuli, thus indicating that prefrontal noradrenergic transmission determines approach or avoidance responses to both reward- and aversion-related natural stimuli only when the salience of the unconditioned natural stimulus is high enough to induce sustained norepinephrine outflow. This affirms that prefrontal noradrenergic transmission determines motivational salience attribution selectively when intense motivational salience is processed, as in conditions that characterize psychopathological outcomes. Public Library of Science 2008-08-22 /pmc/articles/PMC2516177/ /pubmed/18725944 http://dx.doi.org/10.1371/journal.pone.0003044 Text en Ventura et al. http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Ventura, Rossella
Latagliata, Emanuele Claudio
Morrone, Cristina
La Mela, Immacolata
Puglisi-Allegra, Stefano
Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience
title Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience
title_full Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience
title_fullStr Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience
title_full_unstemmed Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience
title_short Prefrontal Norepinephrine Determines Attribution of “High” Motivational Salience
title_sort prefrontal norepinephrine determines attribution of “high” motivational salience
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2516177/
https://www.ncbi.nlm.nih.gov/pubmed/18725944
http://dx.doi.org/10.1371/journal.pone.0003044
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