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Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell

INTRODUCTION: Using yoked animals as the control when monitoring operant drug-self-administration is considered the golden standard. However, instrumental learning per se recruits several neurocircuits that may produce distinct or overlapping neuroadaptations with drugs of abuse. The aim of this pro...

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Autores principales: Domi, Ana, Lucente, Erika, Cadeddu, Davide, Adermark, Louise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907443/
https://www.ncbi.nlm.nih.gov/pubmed/36760603
http://dx.doi.org/10.3389/fnmol.2023.1105388
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author Domi, Ana
Lucente, Erika
Cadeddu, Davide
Adermark, Louise
author_facet Domi, Ana
Lucente, Erika
Cadeddu, Davide
Adermark, Louise
author_sort Domi, Ana
collection PubMed
description INTRODUCTION: Using yoked animals as the control when monitoring operant drug-self-administration is considered the golden standard. However, instrumental learning per se recruits several neurocircuits that may produce distinct or overlapping neuroadaptations with drugs of abuse. The aim of this project was to assess if contingent responding for nicotine or saline in the presence of a light stimulus as a conditioned reinforcer is associated with sustained neurophysiological adaptations in the nucleus accumbens shell (nAcS), a brain region repeatedly associated with reward related behaviors. METHODS: To this end, nicotine-or saline-administrating rats and yoked-saline stimulus-unpaired training conditions were assessed in operant boxes over four consecutive weeks. After four additional weeks of home cage forced abstinence and subsequent cue reinforced responding under extinction conditions, ex vivo electrophysiology was performed in the nAcS medium spiny neurons (MSNs). RESULTS: Whole cell recordings conducted in voltage and current-clamp mode showed that excitatory synapses in the nAcS were altered after prolonged forced abstinence from nicotine self-administration. We observed an increase in sEPSC amplitude in animals with a history of contingent nicotine SA potentially indicating higher excitability of accumbal MSNs, which was further supported by current clamp recordings. Interestingly no sustained neuroadaptations were elicited in saline exposed rats from nicotine associated visual cues compared to the yoked controls. CONCLUSION: The data presented here indicate that nicotine self-administration produces sustained neuroadaptations in the nAcS while operant responding driven by nicotine visual stimuli has no long-term effects on MSNs in nAcS.
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spelling pubmed-99074432023-02-08 Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell Domi, Ana Lucente, Erika Cadeddu, Davide Adermark, Louise Front Mol Neurosci Molecular Neuroscience INTRODUCTION: Using yoked animals as the control when monitoring operant drug-self-administration is considered the golden standard. However, instrumental learning per se recruits several neurocircuits that may produce distinct or overlapping neuroadaptations with drugs of abuse. The aim of this project was to assess if contingent responding for nicotine or saline in the presence of a light stimulus as a conditioned reinforcer is associated with sustained neurophysiological adaptations in the nucleus accumbens shell (nAcS), a brain region repeatedly associated with reward related behaviors. METHODS: To this end, nicotine-or saline-administrating rats and yoked-saline stimulus-unpaired training conditions were assessed in operant boxes over four consecutive weeks. After four additional weeks of home cage forced abstinence and subsequent cue reinforced responding under extinction conditions, ex vivo electrophysiology was performed in the nAcS medium spiny neurons (MSNs). RESULTS: Whole cell recordings conducted in voltage and current-clamp mode showed that excitatory synapses in the nAcS were altered after prolonged forced abstinence from nicotine self-administration. We observed an increase in sEPSC amplitude in animals with a history of contingent nicotine SA potentially indicating higher excitability of accumbal MSNs, which was further supported by current clamp recordings. Interestingly no sustained neuroadaptations were elicited in saline exposed rats from nicotine associated visual cues compared to the yoked controls. CONCLUSION: The data presented here indicate that nicotine self-administration produces sustained neuroadaptations in the nAcS while operant responding driven by nicotine visual stimuli has no long-term effects on MSNs in nAcS. Frontiers Media S.A. 2023-01-25 /pmc/articles/PMC9907443/ /pubmed/36760603 http://dx.doi.org/10.3389/fnmol.2023.1105388 Text en Copyright © 2023 Domi, Lucente, Cadeddu and Adermark. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Neuroscience
Domi, Ana
Lucente, Erika
Cadeddu, Davide
Adermark, Louise
Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
title Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
title_full Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
title_fullStr Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
title_full_unstemmed Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
title_short Nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
title_sort nicotine but not saline self-administering or yoked control conditions produces sustained neuroadaptations in the accumbens shell
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907443/
https://www.ncbi.nlm.nih.gov/pubmed/36760603
http://dx.doi.org/10.3389/fnmol.2023.1105388
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