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Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice
Regular use of marijuana during adolescence enhances the risk of long‐lasting neurobiological changes in adulthood. The present study was aimed at assessing the effect of long‐term administration of the synthetic cannabinoid WIN55212.2 during adolescence in young adult mice. Adolescent mice aged 5 w...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697667/ https://www.ncbi.nlm.nih.gov/pubmed/27578457 http://dx.doi.org/10.1111/adb.12446 |
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author | Tomas‐Roig, J Benito, E Agis‐Balboa, RC Piscitelli, F Hoyer‐Fender, S Di Marzo, V Havemann‐Reinecke, U |
author_facet | Tomas‐Roig, J Benito, E Agis‐Balboa, RC Piscitelli, F Hoyer‐Fender, S Di Marzo, V Havemann‐Reinecke, U |
author_sort | Tomas‐Roig, J |
collection | PubMed |
description | Regular use of marijuana during adolescence enhances the risk of long‐lasting neurobiological changes in adulthood. The present study was aimed at assessing the effect of long‐term administration of the synthetic cannabinoid WIN55212.2 during adolescence in young adult mice. Adolescent mice aged 5 weeks were subjected daily to the pharmacological action of WIN55212.2 for 3 weeks and were then left undisturbed in their home cage for a 5‐week period and finally evaluated by behavioral testing. Mice that received the drug during adolescence showed memory impairment in the Morris water maze, as well as a dose‐dependent memory impairment in fear conditioning. In addition, the administration of 3 mg/kg WIN55212.2 in adolescence increased adult hippocampal AEA levels and promoted DNA hypermethylation at the intragenic region of the intracellular signaling modulator Rgs7, which was accompanied by a lower rate of mRNA transcription of this gene, suggesting a potential causal relation. Although the concrete mechanisms underlying the behavioral observations remain to be elucidated, we demonstrate that long‐term administration of 3 mg/kg of WIN during adolescence leads to increased endocannabinoid levels and altered Rgs7 expression in adulthood and establish a potential link to epigenetic changes. |
format | Online Article Text |
id | pubmed-5697667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56976672017-11-28 Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice Tomas‐Roig, J Benito, E Agis‐Balboa, RC Piscitelli, F Hoyer‐Fender, S Di Marzo, V Havemann‐Reinecke, U Addict Biol Preclinical Studies Regular use of marijuana during adolescence enhances the risk of long‐lasting neurobiological changes in adulthood. The present study was aimed at assessing the effect of long‐term administration of the synthetic cannabinoid WIN55212.2 during adolescence in young adult mice. Adolescent mice aged 5 weeks were subjected daily to the pharmacological action of WIN55212.2 for 3 weeks and were then left undisturbed in their home cage for a 5‐week period and finally evaluated by behavioral testing. Mice that received the drug during adolescence showed memory impairment in the Morris water maze, as well as a dose‐dependent memory impairment in fear conditioning. In addition, the administration of 3 mg/kg WIN55212.2 in adolescence increased adult hippocampal AEA levels and promoted DNA hypermethylation at the intragenic region of the intracellular signaling modulator Rgs7, which was accompanied by a lower rate of mRNA transcription of this gene, suggesting a potential causal relation. Although the concrete mechanisms underlying the behavioral observations remain to be elucidated, we demonstrate that long‐term administration of 3 mg/kg of WIN during adolescence leads to increased endocannabinoid levels and altered Rgs7 expression in adulthood and establish a potential link to epigenetic changes. John Wiley and Sons Inc. 2016-08-31 2017-11 /pmc/articles/PMC5697667/ /pubmed/27578457 http://dx.doi.org/10.1111/adb.12446 Text en © 2016 The Authors.Addiction Biology published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Preclinical Studies Tomas‐Roig, J Benito, E Agis‐Balboa, RC Piscitelli, F Hoyer‐Fender, S Di Marzo, V Havemann‐Reinecke, U Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
title | Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
title_full | Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
title_fullStr | Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
title_full_unstemmed | Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
title_short | Chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
title_sort | chronic exposure to cannabinoids during adolescence causes long‐lasting behavioral deficits in adult mice |
topic | Preclinical Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697667/ https://www.ncbi.nlm.nih.gov/pubmed/27578457 http://dx.doi.org/10.1111/adb.12446 |
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