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Temporal Rewiring of Striatal Circuits Initiated by Nicotine

Drug addiction has been conceptualized as maladaptive recruitment of integrative circuits coursing through the striatum, facilitating drug-seeking and drug-taking behavior. The aim of this study was to define temporal neuroadaptations in striatal subregions initiated by 3 weeks of intermittent nicot...

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Autores principales: Adermark, Louise, Morud, Julia, Lotfi, Amir, Danielsson, Klara, Ulenius, Lisa, Söderpalm, Bo, Ericson, Mia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101553/
https://www.ncbi.nlm.nih.gov/pubmed/27388328
http://dx.doi.org/10.1038/npp.2016.118
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author Adermark, Louise
Morud, Julia
Lotfi, Amir
Danielsson, Klara
Ulenius, Lisa
Söderpalm, Bo
Ericson, Mia
author_facet Adermark, Louise
Morud, Julia
Lotfi, Amir
Danielsson, Klara
Ulenius, Lisa
Söderpalm, Bo
Ericson, Mia
author_sort Adermark, Louise
collection PubMed
description Drug addiction has been conceptualized as maladaptive recruitment of integrative circuits coursing through the striatum, facilitating drug-seeking and drug-taking behavior. The aim of this study was to define temporal neuroadaptations in striatal subregions initiated by 3 weeks of intermittent nicotine exposure followed by protracted abstinence. Enhanced rearing activity was assessed in motor activity boxes as a measurement of behavioral change induced by nicotine (0.36 mg/kg), whereas electrophysiological field potential recordings were performed to evaluate treatment effects on neuronal activity. Dopamine receptor mRNA expression was quantified by qPCR, and nicotine-induced dopamine release was measured in striatal subregions using in vivo microdialysis. Golgi staining was performed to assess nicotine-induced changes in spine density of medium spiny neurons. The data presented here show that a brief period of nicotine exposure followed by abstinence leads to temporal changes in synaptic efficacy, dopamine receptor expression, and spine density in a subregion-specific manner. Nicotine may thus initiate a reorganization of striatal circuits that continues to develop despite protracted abstinence. We also show that the response to nicotine is modulated in previously exposed rats even after 6 months of abstinence. The data presented here suggests that, even though not self-administered, nicotine may produce progressive neuronal alterations in brain regions associated with goal-directed and habitual performance, which might contribute to the development of compulsive drug seeking and the increased vulnerability to relapse, which are hallmarks of drug addiction.
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spelling pubmed-51015532016-12-01 Temporal Rewiring of Striatal Circuits Initiated by Nicotine Adermark, Louise Morud, Julia Lotfi, Amir Danielsson, Klara Ulenius, Lisa Söderpalm, Bo Ericson, Mia Neuropsychopharmacology Original Article Drug addiction has been conceptualized as maladaptive recruitment of integrative circuits coursing through the striatum, facilitating drug-seeking and drug-taking behavior. The aim of this study was to define temporal neuroadaptations in striatal subregions initiated by 3 weeks of intermittent nicotine exposure followed by protracted abstinence. Enhanced rearing activity was assessed in motor activity boxes as a measurement of behavioral change induced by nicotine (0.36 mg/kg), whereas electrophysiological field potential recordings were performed to evaluate treatment effects on neuronal activity. Dopamine receptor mRNA expression was quantified by qPCR, and nicotine-induced dopamine release was measured in striatal subregions using in vivo microdialysis. Golgi staining was performed to assess nicotine-induced changes in spine density of medium spiny neurons. The data presented here show that a brief period of nicotine exposure followed by abstinence leads to temporal changes in synaptic efficacy, dopamine receptor expression, and spine density in a subregion-specific manner. Nicotine may thus initiate a reorganization of striatal circuits that continues to develop despite protracted abstinence. We also show that the response to nicotine is modulated in previously exposed rats even after 6 months of abstinence. The data presented here suggests that, even though not self-administered, nicotine may produce progressive neuronal alterations in brain regions associated with goal-directed and habitual performance, which might contribute to the development of compulsive drug seeking and the increased vulnerability to relapse, which are hallmarks of drug addiction. Nature Publishing Group 2016-12 2016-08-10 /pmc/articles/PMC5101553/ /pubmed/27388328 http://dx.doi.org/10.1038/npp.2016.118 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Adermark, Louise
Morud, Julia
Lotfi, Amir
Danielsson, Klara
Ulenius, Lisa
Söderpalm, Bo
Ericson, Mia
Temporal Rewiring of Striatal Circuits Initiated by Nicotine
title Temporal Rewiring of Striatal Circuits Initiated by Nicotine
title_full Temporal Rewiring of Striatal Circuits Initiated by Nicotine
title_fullStr Temporal Rewiring of Striatal Circuits Initiated by Nicotine
title_full_unstemmed Temporal Rewiring of Striatal Circuits Initiated by Nicotine
title_short Temporal Rewiring of Striatal Circuits Initiated by Nicotine
title_sort temporal rewiring of striatal circuits initiated by nicotine
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101553/
https://www.ncbi.nlm.nih.gov/pubmed/27388328
http://dx.doi.org/10.1038/npp.2016.118
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