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Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice
Adolescence represents a developmental period with the highest risk for initiating cannabis use. Little is known about whether genetic variation in the endocannabinoid system alters mesolimbic reward circuitry to produce vulnerability to the rewarding properties of the exogenous cannabinoid Δ(9)-tet...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015690/ https://www.ncbi.nlm.nih.gov/pubmed/32095523 http://dx.doi.org/10.1126/sciadv.aay1502 |
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author | Burgdorf, Caitlin E. Jing, Deqiang Yang, Ruirong Huang, Chienchun Hill, Matthew N. Mackie, Ken Milner, Teresa A. Pickel, Virginia M. Lee, Francis S. Rajadhyaksha, Anjali M. |
author_facet | Burgdorf, Caitlin E. Jing, Deqiang Yang, Ruirong Huang, Chienchun Hill, Matthew N. Mackie, Ken Milner, Teresa A. Pickel, Virginia M. Lee, Francis S. Rajadhyaksha, Anjali M. |
author_sort | Burgdorf, Caitlin E. |
collection | PubMed |
description | Adolescence represents a developmental period with the highest risk for initiating cannabis use. Little is known about whether genetic variation in the endocannabinoid system alters mesolimbic reward circuitry to produce vulnerability to the rewarding properties of the exogenous cannabinoid Δ(9)-tetrahydrocannabinol (THC). Using a genetic knock-in mouse model (FAAH(C/A)) that biologically recapitulates the human polymorphism associated with problematic drug use, we find that in adolescent female mice, but not male mice, this FAAH polymorphism enhances the mesolimbic dopamine circuitry projecting from the ventral tegmental area (VTA) to the nucleus accumbens (NAc) and alters cannabinoid receptor 1 (CB(1)R) levels at inhibitory and excitatory terminals in the VTA. These developmental changes collectively increase vulnerability of adolescent female FAAH(C/A) mice to THC preference that persists into adulthood. Together, these findings suggest that this endocannabinoid genetic variant is a contributing factor for increased susceptibility to cannabis dependence in adolescent females. |
format | Online Article Text |
id | pubmed-7015690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70156902020-02-24 Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice Burgdorf, Caitlin E. Jing, Deqiang Yang, Ruirong Huang, Chienchun Hill, Matthew N. Mackie, Ken Milner, Teresa A. Pickel, Virginia M. Lee, Francis S. Rajadhyaksha, Anjali M. Sci Adv Research Articles Adolescence represents a developmental period with the highest risk for initiating cannabis use. Little is known about whether genetic variation in the endocannabinoid system alters mesolimbic reward circuitry to produce vulnerability to the rewarding properties of the exogenous cannabinoid Δ(9)-tetrahydrocannabinol (THC). Using a genetic knock-in mouse model (FAAH(C/A)) that biologically recapitulates the human polymorphism associated with problematic drug use, we find that in adolescent female mice, but not male mice, this FAAH polymorphism enhances the mesolimbic dopamine circuitry projecting from the ventral tegmental area (VTA) to the nucleus accumbens (NAc) and alters cannabinoid receptor 1 (CB(1)R) levels at inhibitory and excitatory terminals in the VTA. These developmental changes collectively increase vulnerability of adolescent female FAAH(C/A) mice to THC preference that persists into adulthood. Together, these findings suggest that this endocannabinoid genetic variant is a contributing factor for increased susceptibility to cannabis dependence in adolescent females. American Association for the Advancement of Science 2020-02-12 /pmc/articles/PMC7015690/ /pubmed/32095523 http://dx.doi.org/10.1126/sciadv.aay1502 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Burgdorf, Caitlin E. Jing, Deqiang Yang, Ruirong Huang, Chienchun Hill, Matthew N. Mackie, Ken Milner, Teresa A. Pickel, Virginia M. Lee, Francis S. Rajadhyaksha, Anjali M. Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice |
title | Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice |
title_full | Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice |
title_fullStr | Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice |
title_full_unstemmed | Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice |
title_short | Endocannabinoid genetic variation enhances vulnerability to THC reward in adolescent female mice |
title_sort | endocannabinoid genetic variation enhances vulnerability to thc reward in adolescent female mice |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015690/ https://www.ncbi.nlm.nih.gov/pubmed/32095523 http://dx.doi.org/10.1126/sciadv.aay1502 |
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