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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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.
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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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