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Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra
We examined the contribution of the nigrostriatal DA system to instrumental learning and behavior using optogenetics in awake, behaving mice. Using Cre-inducible channelrhodopsin-2 (ChR2) in mice expressing Cre recombinase driven by the tyrosine hydroxylase promoter (Th-Cre), we tested whether selec...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673941/ https://www.ncbi.nlm.nih.gov/pubmed/23755282 http://dx.doi.org/10.1371/journal.pone.0065799 |
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author | Rossi, Mark A. Sukharnikova, Tatyana Hayrapetyan, Volodya Y. Yang, Lucie Yin, Henry H. |
author_facet | Rossi, Mark A. Sukharnikova, Tatyana Hayrapetyan, Volodya Y. Yang, Lucie Yin, Henry H. |
author_sort | Rossi, Mark A. |
collection | PubMed |
description | We examined the contribution of the nigrostriatal DA system to instrumental learning and behavior using optogenetics in awake, behaving mice. Using Cre-inducible channelrhodopsin-2 (ChR2) in mice expressing Cre recombinase driven by the tyrosine hydroxylase promoter (Th-Cre), we tested whether selective stimulation of DA neurons in the substantia nigra pars compacta (SNC), in the absence of any natural rewards, was sufficient to promote instrumental learning in naive mice. Mice expressing ChR2 in SNC DA neurons readily learned to press a lever to receive laser stimulation, but unlike natural food rewards the lever pressing did not decline with satiation. When the number of presses required to receive a stimulation was altered, mice adjusted their rate of pressing accordingly, suggesting that the rate of stimulation was a controlled variable. Moreover, extinction, i.e. the cessation of action-contingent stimulation, and the complete reversal of the relationship between action and outcome by the imposition of an omission contingency, rapidly abolished lever pressing. Together these results suggest that selective activation of SNC DA neurons can be sufficient for acquisition and maintenance of a new instrumental action. |
format | Online Article Text |
id | pubmed-3673941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36739412013-06-10 Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra Rossi, Mark A. Sukharnikova, Tatyana Hayrapetyan, Volodya Y. Yang, Lucie Yin, Henry H. PLoS One Research Article We examined the contribution of the nigrostriatal DA system to instrumental learning and behavior using optogenetics in awake, behaving mice. Using Cre-inducible channelrhodopsin-2 (ChR2) in mice expressing Cre recombinase driven by the tyrosine hydroxylase promoter (Th-Cre), we tested whether selective stimulation of DA neurons in the substantia nigra pars compacta (SNC), in the absence of any natural rewards, was sufficient to promote instrumental learning in naive mice. Mice expressing ChR2 in SNC DA neurons readily learned to press a lever to receive laser stimulation, but unlike natural food rewards the lever pressing did not decline with satiation. When the number of presses required to receive a stimulation was altered, mice adjusted their rate of pressing accordingly, suggesting that the rate of stimulation was a controlled variable. Moreover, extinction, i.e. the cessation of action-contingent stimulation, and the complete reversal of the relationship between action and outcome by the imposition of an omission contingency, rapidly abolished lever pressing. Together these results suggest that selective activation of SNC DA neurons can be sufficient for acquisition and maintenance of a new instrumental action. Public Library of Science 2013-06-05 /pmc/articles/PMC3673941/ /pubmed/23755282 http://dx.doi.org/10.1371/journal.pone.0065799 Text en © 2013 Rossi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rossi, Mark A. Sukharnikova, Tatyana Hayrapetyan, Volodya Y. Yang, Lucie Yin, Henry H. Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra |
title | Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra |
title_full | Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra |
title_fullStr | Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra |
title_full_unstemmed | Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra |
title_short | Operant Self-Stimulation of Dopamine Neurons in the Substantia Nigra |
title_sort | operant self-stimulation of dopamine neurons in the substantia nigra |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3673941/ https://www.ncbi.nlm.nih.gov/pubmed/23755282 http://dx.doi.org/10.1371/journal.pone.0065799 |
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