Optogenetic interrogation of dopaminergic modulation of the multiple phases of reward-seeking behavior
Phasic activation of dopaminergic neurons is associated with reward-predicting cues and supports learning during behavioral adaptation. While noncontingent activation of dopaminergic neurons in the ventral tegmental are (VTA) is sufficient for passive behavioral conditioning, it remains unknown whet...
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Published in | The Journal of neuroscience Vol. 31; no. 30; pp. 10829 - 10835 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society for Neuroscience
27.07.2011
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Subjects | |
Online Access | Get full text |
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Summary: | Phasic activation of dopaminergic neurons is associated with reward-predicting cues and supports learning during behavioral adaptation. While noncontingent activation of dopaminergic neurons in the ventral tegmental are (VTA) is sufficient for passive behavioral conditioning, it remains unknown whether the phasic dopaminergic signal is truly reinforcing. In this study, we first targeted the expression of channelrhodopsin-2 to dopaminergic neurons of the VTA and optimized optogenetically evoked dopamine transients. Second, we showed that phasic activation of dopaminergic neurons in freely moving mice causally enhances positive reinforcing actions in a food-seeking operant task. Interestingly, such effect was not found in the absence of food reward. We further found that phasic activation of dopaminergic neurons is sufficient to reactivate previously extinguished food-seeking behavior in the absence of external cues. This was also confirmed using a single-session reversal paradigm. Collectively, these data suggest that activation of dopaminergic neurons facilitates the development of positive reinforcement during reward-seeking and behavioral flexibility. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 A.R.A. and H.-C.T. contributed equally to this work. A. Bonci's present address: NIDA Intramural Research Program, Johns Hopkins Bayview Campus, 251 Bayview Boulevard, Baltimore, MD 21224. Author contributions: A.R.A., H.-C.T., B.B., F.Z., G.D.S., A.B., K.D., and L.d.L. designed research; A.R.A., H.-C.T., F.Z., G.D.S., E.A.B., and C.T. performed research; A.R.A., H.-C.T., F.Z., G.D.S., E.A.B., A.B., K.D., and L.d.L. contributed unpublished reagents/analytic tools; A.R.A., H.-C.T., F.Z., G.D.S., and E.A.B. analyzed data; A.R.A., H.-C.T., B.B., G.D.S., K.D., and L.d.L. wrote the paper. A. R. Adamantidis's present address: McGill University, Department of Psychiatry, Douglas Mental Health University Institute, Montreal, QC H4H 1R3, Canada. |
ISSN: | 0270-6474 1529-2401 |
DOI: | 10.1523/jneurosci.2246-11.2011 |