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Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences

Adolescent cocaine use increases the likelihood of drug abuse and addiction in adulthood, and etiological factors may include a cocaine-induced bias towards so-called ‘reward-seeking' habits. To determine whether adolescent cocaine exposure indeed impacts decision-making strategies in adulthood...

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Autores principales: DePoy, L M, Allen, A G, Gourley, S L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022090/
https://www.ncbi.nlm.nih.gov/pubmed/27576164
http://dx.doi.org/10.1038/tp.2016.150
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author DePoy, L M
Allen, A G
Gourley, S L
author_facet DePoy, L M
Allen, A G
Gourley, S L
author_sort DePoy, L M
collection PubMed
description Adolescent cocaine use increases the likelihood of drug abuse and addiction in adulthood, and etiological factors may include a cocaine-induced bias towards so-called ‘reward-seeking' habits. To determine whether adolescent cocaine exposure indeed impacts decision-making strategies in adulthood, we trained adolescent mice to orally self-administer cocaine. In adulthood, males with a history of escalating self-administration developed a bias towards habit-based behaviors. In contrast, escalating females did not develop habit biases; rather, low response rates were associated with later behavioral inflexibility, independent of cocaine dose. We focused the rest of our report on understanding how individual differences in young-adolescent females predicted long-term behavioral outcomes. Low, ‘stable' cocaine-reinforced response rates during adolescence were associated with cocaine-conditioned object preference and enlarged dendritic spine head size in the medial (prelimbic) prefrontal cortex in adulthood. Meanwhile, cocaine resilience was associated with enlarged spine heads in deep-layer orbitofrontal cortex. Re-exposure to the cocaine-associated context in adulthood energized responding in ‘stable responders', which could then be reduced by the GABA(B) agonist baclofen and the putative tyrosine receptor kinase B (trkB) agonist, 7,8-dihydroxyflavone. Together, our findings highlight resilience to cocaine-induced habits in females relative to males when intake escalates. However, failures in instrumental conditioning in adolescent females may precipitate reward-seeking behaviors in adulthood, particularly in the context of cocaine exposure.
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spelling pubmed-50220902016-09-19 Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences DePoy, L M Allen, A G Gourley, S L Transl Psychiatry Original Article Adolescent cocaine use increases the likelihood of drug abuse and addiction in adulthood, and etiological factors may include a cocaine-induced bias towards so-called ‘reward-seeking' habits. To determine whether adolescent cocaine exposure indeed impacts decision-making strategies in adulthood, we trained adolescent mice to orally self-administer cocaine. In adulthood, males with a history of escalating self-administration developed a bias towards habit-based behaviors. In contrast, escalating females did not develop habit biases; rather, low response rates were associated with later behavioral inflexibility, independent of cocaine dose. We focused the rest of our report on understanding how individual differences in young-adolescent females predicted long-term behavioral outcomes. Low, ‘stable' cocaine-reinforced response rates during adolescence were associated with cocaine-conditioned object preference and enlarged dendritic spine head size in the medial (prelimbic) prefrontal cortex in adulthood. Meanwhile, cocaine resilience was associated with enlarged spine heads in deep-layer orbitofrontal cortex. Re-exposure to the cocaine-associated context in adulthood energized responding in ‘stable responders', which could then be reduced by the GABA(B) agonist baclofen and the putative tyrosine receptor kinase B (trkB) agonist, 7,8-dihydroxyflavone. Together, our findings highlight resilience to cocaine-induced habits in females relative to males when intake escalates. However, failures in instrumental conditioning in adolescent females may precipitate reward-seeking behaviors in adulthood, particularly in the context of cocaine exposure. Nature Publishing Group 2016-08 2016-08-30 /pmc/articles/PMC5022090/ /pubmed/27576164 http://dx.doi.org/10.1038/tp.2016.150 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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/4.0/
spellingShingle Original Article
DePoy, L M
Allen, A G
Gourley, S L
Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
title Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
title_full Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
title_fullStr Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
title_full_unstemmed Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
title_short Adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
title_sort adolescent cocaine self-administration induces habit behavior in adulthood: sex differences and structural consequences
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022090/
https://www.ncbi.nlm.nih.gov/pubmed/27576164
http://dx.doi.org/10.1038/tp.2016.150
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