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Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats

RATIONALE: The endocannabinoid system makes critical contributions to reward processing, motivation, and behavioral control. Repeated exposure to THC or other cannabinoid drugs can cause persistent adaptions in the endocannabinoid system and associated neural circuitry. It remains unclear how such t...

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Autores principales: Halbout, Briac, Hutson, Collin, Hua, Leann, Inshishian, Victoria, Mahler, Stephen V., Ostlund, Sean B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10102061/
https://www.ncbi.nlm.nih.gov/pubmed/36933028
http://dx.doi.org/10.1007/s00213-023-06352-4
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author Halbout, Briac
Hutson, Collin
Hua, Leann
Inshishian, Victoria
Mahler, Stephen V.
Ostlund, Sean B.
author_facet Halbout, Briac
Hutson, Collin
Hua, Leann
Inshishian, Victoria
Mahler, Stephen V.
Ostlund, Sean B.
author_sort Halbout, Briac
collection PubMed
description RATIONALE: The endocannabinoid system makes critical contributions to reward processing, motivation, and behavioral control. Repeated exposure to THC or other cannabinoid drugs can cause persistent adaptions in the endocannabinoid system and associated neural circuitry. It remains unclear how such treatments affect the way rewards are processed and pursued. OBJECTIVE AND METHODS: We examined if repeated THC exposure (5 mg/kg/day for 14 days) during adolescence or adulthood led to long-term changes in rats’ capacity to flexibly encode and use action-outcome associations for goal-directed decision making. Effects on hedonic feeding and progressive ratio responding were also assessed. RESULTS: THC exposure had no effect on rats’ ability to flexibly select actions following reward devaluation. However, instrumental contingency degradation learning, which involves avoiding an action that is unnecessary for reward delivery, was augmented in rats with a history of adult but not adolescent THC exposure. THC-exposed rats also displayed more vigorous instrumental behavior in this study, suggesting a motivational enhancement. A separate experiment found that while THC exposure had no effect on hedonic feeding behavior, it increased rats’ willingness to work for food on a progressive ratio schedule, an effect that was more pronounced when THC was administered to adults. Adolescent and adult THC exposure had opposing effects on the CB1 receptor dependence of progressive ratio performance, decreasing and increasing sensitivity to rimonabant-induced behavioral suppression, respectively. CONCLUSIONS: Our findings reveal that exposure to a translationally relevant THC exposure regimen induces long-lasting, age-dependent alterations in cognitive and motivational processes that regulate the pursuit of rewards. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00213-023-06352-4.
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spelling pubmed-101020612023-04-15 Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats Halbout, Briac Hutson, Collin Hua, Leann Inshishian, Victoria Mahler, Stephen V. Ostlund, Sean B. Psychopharmacology (Berl) Original Investigation RATIONALE: The endocannabinoid system makes critical contributions to reward processing, motivation, and behavioral control. Repeated exposure to THC or other cannabinoid drugs can cause persistent adaptions in the endocannabinoid system and associated neural circuitry. It remains unclear how such treatments affect the way rewards are processed and pursued. OBJECTIVE AND METHODS: We examined if repeated THC exposure (5 mg/kg/day for 14 days) during adolescence or adulthood led to long-term changes in rats’ capacity to flexibly encode and use action-outcome associations for goal-directed decision making. Effects on hedonic feeding and progressive ratio responding were also assessed. RESULTS: THC exposure had no effect on rats’ ability to flexibly select actions following reward devaluation. However, instrumental contingency degradation learning, which involves avoiding an action that is unnecessary for reward delivery, was augmented in rats with a history of adult but not adolescent THC exposure. THC-exposed rats also displayed more vigorous instrumental behavior in this study, suggesting a motivational enhancement. A separate experiment found that while THC exposure had no effect on hedonic feeding behavior, it increased rats’ willingness to work for food on a progressive ratio schedule, an effect that was more pronounced when THC was administered to adults. Adolescent and adult THC exposure had opposing effects on the CB1 receptor dependence of progressive ratio performance, decreasing and increasing sensitivity to rimonabant-induced behavioral suppression, respectively. CONCLUSIONS: Our findings reveal that exposure to a translationally relevant THC exposure regimen induces long-lasting, age-dependent alterations in cognitive and motivational processes that regulate the pursuit of rewards. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00213-023-06352-4. Springer Berlin Heidelberg 2023-03-18 2023 /pmc/articles/PMC10102061/ /pubmed/36933028 http://dx.doi.org/10.1007/s00213-023-06352-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Investigation
Halbout, Briac
Hutson, Collin
Hua, Leann
Inshishian, Victoria
Mahler, Stephen V.
Ostlund, Sean B.
Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats
title Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats
title_full Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats
title_fullStr Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats
title_full_unstemmed Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats
title_short Long-term effects of THC exposure on reward learning and motivated behavior in adolescent and adult male rats
title_sort long-term effects of thc exposure on reward learning and motivated behavior in adolescent and adult male rats
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10102061/
https://www.ncbi.nlm.nih.gov/pubmed/36933028
http://dx.doi.org/10.1007/s00213-023-06352-4
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