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...

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Main Authors: Mark A Rossi, Tatyana Sukharnikova, Volodya Y Hayrapetyan, Lucie Yang, Henry H Yin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3673941?pdf=render
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spelling doaj-2525577b09734a399ce383a436f5db4b2020-11-25T01:55:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6579910.1371/journal.pone.0065799Operant self-stimulation of dopamine neurons in the substantia nigra.Mark A RossiTatyana SukharnikovaVolodya Y HayrapetyanLucie YangHenry H YinWe 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.http://europepmc.org/articles/PMC3673941?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mark A Rossi
Tatyana Sukharnikova
Volodya Y Hayrapetyan
Lucie Yang
Henry H Yin
spellingShingle Mark A Rossi
Tatyana Sukharnikova
Volodya Y Hayrapetyan
Lucie Yang
Henry H Yin
Operant self-stimulation of dopamine neurons in the substantia nigra.
PLoS ONE
author_facet Mark A Rossi
Tatyana Sukharnikova
Volodya Y Hayrapetyan
Lucie Yang
Henry H Yin
author_sort Mark A Rossi
title Operant self-stimulation of dopamine neurons in the substantia nigra.
title_short 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_sort operant self-stimulation of dopamine neurons in the substantia nigra.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
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.
url http://europepmc.org/articles/PMC3673941?pdf=render
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