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A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction
The striatum plays a critical role in regulating addiction-related behaviors. The conventional dichotomy model suggests that striatal D1/D2 medium spiny neurons (MSNs) positively/negatively regulate addiction-related behaviors. However, this model does not account for the neuronal heterogeneity and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374336/ https://www.ncbi.nlm.nih.gov/pubmed/35960793 http://dx.doi.org/10.1126/sciadv.abn3552 |
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author | Zhao, Zheng-dong Han, Xiao Chen, Renchao Liu, Yiqiong Bhattacherjee, Aritra Chen, Wenqiang Zhang, Yi |
author_facet | Zhao, Zheng-dong Han, Xiao Chen, Renchao Liu, Yiqiong Bhattacherjee, Aritra Chen, Wenqiang Zhang, Yi |
author_sort | Zhao, Zheng-dong |
collection | PubMed |
description | The striatum plays a critical role in regulating addiction-related behaviors. The conventional dichotomy model suggests that striatal D1/D2 medium spiny neurons (MSNs) positively/negatively regulate addiction-related behaviors. However, this model does not account for the neuronal heterogeneity and functional diversity of the striatum, and whether MSN subtypes beyond the pan-D1/D2 populations play distinct roles in drug addiction remains unknown. We characterized the role of a tachykinin 2–expressing D1 MSN subtype (Tac2(+)), present in both rodent and primate striatum, using cocaine addiction mouse models. We found that acute cocaine administration reduces Tac2 neuronal activity, and cocaine conditioning alters neuronal response related to cocaine reward contextual associations. In addition, activation/inhibition of Tac2(+) neurons attenuates/promotes cocaine-induced conditioned place preference and cocaine intravenous self-administration. Furthermore, stimulation of the NAc-to-lateral hypothalamic projection of Tac2(+) neurons suppresses cocaine reward behavior. Our study reveals an unconventional negative regulatory function of D1 MSNs in drug addiction that operates in a subtype- and projection-specific manner. |
format | Online Article Text |
id | pubmed-9374336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-93743362022-08-18 A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction Zhao, Zheng-dong Han, Xiao Chen, Renchao Liu, Yiqiong Bhattacherjee, Aritra Chen, Wenqiang Zhang, Yi Sci Adv Neuroscience The striatum plays a critical role in regulating addiction-related behaviors. The conventional dichotomy model suggests that striatal D1/D2 medium spiny neurons (MSNs) positively/negatively regulate addiction-related behaviors. However, this model does not account for the neuronal heterogeneity and functional diversity of the striatum, and whether MSN subtypes beyond the pan-D1/D2 populations play distinct roles in drug addiction remains unknown. We characterized the role of a tachykinin 2–expressing D1 MSN subtype (Tac2(+)), present in both rodent and primate striatum, using cocaine addiction mouse models. We found that acute cocaine administration reduces Tac2 neuronal activity, and cocaine conditioning alters neuronal response related to cocaine reward contextual associations. In addition, activation/inhibition of Tac2(+) neurons attenuates/promotes cocaine-induced conditioned place preference and cocaine intravenous self-administration. Furthermore, stimulation of the NAc-to-lateral hypothalamic projection of Tac2(+) neurons suppresses cocaine reward behavior. Our study reveals an unconventional negative regulatory function of D1 MSNs in drug addiction that operates in a subtype- and projection-specific manner. American Association for the Advancement of Science 2022-08-12 /pmc/articles/PMC9374336/ /pubmed/35960793 http://dx.doi.org/10.1126/sciadv.abn3552 Text en Copyright © 2022 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 License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience Zhao, Zheng-dong Han, Xiao Chen, Renchao Liu, Yiqiong Bhattacherjee, Aritra Chen, Wenqiang Zhang, Yi A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction |
title | A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction |
title_full | A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction |
title_fullStr | A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction |
title_full_unstemmed | A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction |
title_short | A molecularly defined D1 medium spiny neuron subtype negatively regulates cocaine addiction |
title_sort | molecularly defined d1 medium spiny neuron subtype negatively regulates cocaine addiction |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374336/ https://www.ncbi.nlm.nih.gov/pubmed/35960793 http://dx.doi.org/10.1126/sciadv.abn3552 |
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