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Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area

The initiation of psychostimulant sensitization depends on the mesocorticolimbic dopamine (DA) system. Although many cellular adaptations has been reported to be associated with this addictive behavior, the overall influence of these adaptations on the network regulation of DA neurons has not been e...

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Autores principales: Liu, Chang-Liang, Wang, Ya-Kun, Jin, Guo-Zhang, Shi, Wei-Xing, Gao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818474/
https://www.ncbi.nlm.nih.gov/pubmed/29459754
http://dx.doi.org/10.1038/s41598-018-21592-7
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author Liu, Chang-Liang
Wang, Ya-Kun
Jin, Guo-Zhang
Shi, Wei-Xing
Gao, Ming
author_facet Liu, Chang-Liang
Wang, Ya-Kun
Jin, Guo-Zhang
Shi, Wei-Xing
Gao, Ming
author_sort Liu, Chang-Liang
collection PubMed
description The initiation of psychostimulant sensitization depends on the mesocorticolimbic dopamine (DA) system. Although many cellular adaptations has been reported to be associated with this addictive behavior, the overall influence of these adaptations on the network regulation of DA neurons has not been established. Here, we profile a network-driven slow oscillation (SO) in the firing activity of ventral tegmental area (VTA) putative DA and non-DA neurons and their correlation with locomotor sensitization induced by repeated administration of cocaine. One day after the last cocaine injection, the power of SO (Pso) significantly increased both in DA and non-DA neurons. Interestingly, the Pso in DA neurons was positively correlated, while Pso in non-DA neurons was negatively correlated with the level of locomotor sensitization. On the other hand, the firing rates of DA and non-DA neurons were both elevated, but none exhibited any correlation with the level of sensitization. Fourteen days after the last injection, the Pso of DA neurons dissipated but still positively correlated with the level of sensitization. In contrast, the Pso in non-DA neurons lost correlation with locomotor sensitization. These results suggest that cocaine-induced locomotor sensitization is associated with long-term network adaptation in DA system and that DA and non-DA neurons may corporately facilitate/hamper the initiation of locomotor sensitization.
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spelling pubmed-58184742018-02-26 Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area Liu, Chang-Liang Wang, Ya-Kun Jin, Guo-Zhang Shi, Wei-Xing Gao, Ming Sci Rep Article The initiation of psychostimulant sensitization depends on the mesocorticolimbic dopamine (DA) system. Although many cellular adaptations has been reported to be associated with this addictive behavior, the overall influence of these adaptations on the network regulation of DA neurons has not been established. Here, we profile a network-driven slow oscillation (SO) in the firing activity of ventral tegmental area (VTA) putative DA and non-DA neurons and their correlation with locomotor sensitization induced by repeated administration of cocaine. One day after the last cocaine injection, the power of SO (Pso) significantly increased both in DA and non-DA neurons. Interestingly, the Pso in DA neurons was positively correlated, while Pso in non-DA neurons was negatively correlated with the level of locomotor sensitization. On the other hand, the firing rates of DA and non-DA neurons were both elevated, but none exhibited any correlation with the level of sensitization. Fourteen days after the last injection, the Pso of DA neurons dissipated but still positively correlated with the level of sensitization. In contrast, the Pso in non-DA neurons lost correlation with locomotor sensitization. These results suggest that cocaine-induced locomotor sensitization is associated with long-term network adaptation in DA system and that DA and non-DA neurons may corporately facilitate/hamper the initiation of locomotor sensitization. Nature Publishing Group UK 2018-02-19 /pmc/articles/PMC5818474/ /pubmed/29459754 http://dx.doi.org/10.1038/s41598-018-21592-7 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Chang-Liang
Wang, Ya-Kun
Jin, Guo-Zhang
Shi, Wei-Xing
Gao, Ming
Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
title Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
title_full Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
title_fullStr Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
title_full_unstemmed Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
title_short Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
title_sort cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818474/
https://www.ncbi.nlm.nih.gov/pubmed/29459754
http://dx.doi.org/10.1038/s41598-018-21592-7
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